16-4462447-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4462447
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4462447
    reference: chr 16
allele count: 16
allele frequency: 1.325688529479999e-4
allele num: 120692
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458459
  ensembl transcript: ENST00000571227
  gene symbol: CORO7
  hgvsc: ENST00000571227.1:c.*155-16C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458411
  ensembl transcript: ENST00000572044
  gene symbol: CORO7
  hgvsc: ENST00000572044.1:c.60+4013C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461051
  ensembl transcript: ENST00000572153
  gene symbol: CORO7
  hgvsc: ENST00000572153.1:c.61-16C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000251166
  ensembl transcript: ENST00000251166
  gene symbol: CORO7
  hgvsc: ENST00000251166.4:c.158-16C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458828
  ensembl transcript: ENST00000571756
  gene symbol: CORO7
  hgvsc: ENST00000571756.1:c.158-16C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000460885
  ensembl transcript: ENST00000572467
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000572467.1:c.158-16C>T
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000576457
  gene symbol: CORO7
  hgvsc: ENST00000576457.1:n.218-16C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460901
  ensembl transcript: ENST00000570645
  gene symbol: CORO7
  hgvsc: ENST00000570645.1:c.-214+4034C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000572518
  gene symbol: CORO7
  hgvsc: ENST00000572518.1:n.406-16C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460199
  ensembl transcript: ENST00000570928
  gene symbol: CORO7
  hgvsc: ENST00000570928.1:c.158-16C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000391530
  ensembl transcript: ENST00000423908
  gene symbol: CORO7
  hgvsc: ENST00000423908.2:c.60+4013C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459286
  ensembl transcript: ENST00000572549
  gene symbol: CORO7
  hgvsc: ENST00000572549.1:c.99+4339C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000446221
  ensembl transcript: ENST00000539968
  gene symbol: CORO7
  hgvsc: ENST00000539968.1:c.-442-16C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000577144
  gene symbol: CORO7
  hgvsc: ENST00000577144.1:n.266-16C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461797
  ensembl transcript: ENST00000575038
  gene symbol: CORO7
  hgvsc: ENST00000575038.1:c.158-16C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460910
  ensembl transcript: ENST00000575850
  gene symbol: CORO7
  hgvsc: ENST00000575850.1:c.197-16C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460036
  ensembl transcript: ENST00000571059
  gene symbol: CORO7
  hgvsc: ENST00000571059.1:c.158-16C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000458607
  ensembl transcript: ENST00000575334
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000575334.1:c.158-16C>T
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461187
  ensembl transcript: ENST00000574311
  gene symbol: CORO7
  hgvsc: ENST00000574311.1:c.60+4013C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000440460
  ensembl transcript: ENST00000537233
  gene symbol: CORO7
  hgvsc: ENST00000537233.2:c.158-16C>T
  variant of: http://identifiers.org/hgnc/26161
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: South Asian
population: Other
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQ

16-4462448-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4462448
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4462448
    reference: chr 16
allele count: 1
allele frequency: 8.285965232089886e-6
allele num: 120686
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458411
  ensembl transcript: ENST00000572044
  gene symbol: CORO7
  hgvsc: ENST00000572044.1:c.60+4012C>G
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000440460
  ensembl transcript: ENST00000537233
  gene symbol: CORO7
  hgvsc: ENST00000537233.2:c.158-17C>G
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000446221
  ensembl transcript: ENST00000539968
  gene symbol: CORO7
  hgvsc: ENST00000539968.1:c.-442-17C>G
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000577144
  gene symbol: CORO7
  hgvsc: ENST00000577144.1:n.266-17C>G
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461702
  ensembl transcript: ENST00000574025
  gene symbol: CORO7
  hgvsc: ENST00000574025.1:c.158-17C>G
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461187
  ensembl transcript: ENST00000574311
  gene symbol: CORO7
  hgvsc: ENST00000574311.1:c.60+4012C>G
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458935
  ensembl transcript: ENST00000572898
  gene symbol: CORO7
  hgvsc: ENST00000572898.1:c.158-17C>G
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461051
  ensembl transcript: ENST00000572153
  gene symbol: CORO7
  hgvsc: ENST00000572153.1:c.61-17C>G
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460199
  ensembl transcript: ENST00000570928
  gene symbol: CORO7
  hgvsc: ENST00000570928.1:c.158-17C>G
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000458607
  ensembl transcript: ENST00000575334
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000575334.1:c.158-17C>G
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459888
  ensembl transcript: ENST00000576051
  gene symbol: CORO7
  hgvsc: ENST00000576051.1:c.-342-17C>G
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460901
  ensembl transcript: ENST00000570645
  gene symbol: CORO7
  hgvsc: ENST00000570645.1:c.-214+4033C>G
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460910
  ensembl transcript: ENST00000575850
  gene symbol: CORO7
  hgvsc: ENST00000575850.1:c.197-17C>G
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460036
  ensembl transcript: ENST00000571059
  gene symbol: CORO7
  hgvsc: ENST00000571059.1:c.158-17C>G
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459286
  ensembl transcript: ENST00000572549
  gene symbol: CORO7
  hgvsc: ENST00000572549.1:c.99+4338C>G
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000460885
  ensembl transcript: ENST00000572467
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000572467.1:c.158-17C>G
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461797
  ensembl transcript: ENST00000575038
  gene symbol: CORO7
  hgvsc: ENST00000575038.1:c.158-17C>G
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458459
  ensembl transcript: ENST00000571227
  gene symbol: CORO7
  hgvsc: ENST00000571227.1:c.*155-17C>G
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000576457
  gene symbol: CORO7
  hgvsc: ENST00000576457.1:n.218-17C>G
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459228
  ensembl transcript: ENST00000576437
  gene symbol: CORO7
  hgvsc: ENST00000576437.1:c.-214+4033C>G
  variant of: http://identifiers.org/hgnc/26161
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
population: African
population: East Asian
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: DP

16-4462450-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4462450
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4462450
    reference: chr 16
allele count: 5
allele frequency: 4.145043357153516e-5
allele num: 120626
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459228
  ensembl transcript: ENST00000576437
  gene symbol: CORO7
  hgvsc: ENST00000576437.1:c.-214+4031C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000460885
  ensembl transcript: ENST00000572467
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000572467.1:c.158-19C>T
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461702
  ensembl transcript: ENST00000574025
  gene symbol: CORO7
  hgvsc: ENST00000574025.1:c.158-19C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460901
  ensembl transcript: ENST00000570645
  gene symbol: CORO7
  hgvsc: ENST00000570645.1:c.-214+4031C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460036
  ensembl transcript: ENST00000571059
  gene symbol: CORO7
  hgvsc: ENST00000571059.1:c.158-19C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000577144
  gene symbol: CORO7
  hgvsc: ENST00000577144.1:n.266-19C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000251166
  ensembl transcript: ENST00000251166
  gene symbol: CORO7
  hgvsc: ENST00000251166.4:c.158-19C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458459
  ensembl transcript: ENST00000571227
  gene symbol: CORO7
  hgvsc: ENST00000571227.1:c.*155-19C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000391530
  ensembl transcript: ENST00000423908
  gene symbol: CORO7
  hgvsc: ENST00000423908.2:c.60+4010C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458828
  ensembl transcript: ENST00000571756
  gene symbol: CORO7
  hgvsc: ENST00000571756.1:c.158-19C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000446221
  ensembl transcript: ENST00000539968
  gene symbol: CORO7
  hgvsc: ENST00000539968.1:c.-442-19C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459286
  ensembl transcript: ENST00000572549
  gene symbol: CORO7
  hgvsc: ENST00000572549.1:c.99+4336C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458411
  ensembl transcript: ENST00000572044
  gene symbol: CORO7
  hgvsc: ENST00000572044.1:c.60+4010C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460910
  ensembl transcript: ENST00000575850
  gene symbol: CORO7
  hgvsc: ENST00000575850.1:c.197-19C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000458607
  ensembl transcript: ENST00000575334
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000575334.1:c.158-19C>T
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461051
  ensembl transcript: ENST00000572153
  gene symbol: CORO7
  hgvsc: ENST00000572153.1:c.61-19C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459085
  ensembl transcript: ENST00000571052
  gene symbol: CORO7
  hgvsc: ENST00000571052.1:c.-268+4010C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460199
  ensembl transcript: ENST00000570928
  gene symbol: CORO7
  hgvsc: ENST00000570928.1:c.158-19C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000576457
  gene symbol: CORO7
  hgvsc: ENST00000576457.1:n.218-19C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458935
  ensembl transcript: ENST00000572898
  gene symbol: CORO7
  hgvsc: ENST00000572898.1:c.158-19C>T
  variant of: http://identifiers.org/hgnc/26161
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
population: Latino
population: African
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD

16-4462457-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4462457
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4462457
    reference: chr 16
allele count: 1
allele frequency: 8.302062232258493e-6
allele num: 120452
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459228
  ensembl transcript: ENST00000576437
  gene symbol: CORO7
  hgvsc: ENST00000576437.1:c.-214+4024T>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458411
  ensembl transcript: ENST00000572044
  gene symbol: CORO7
  hgvsc: ENST00000572044.1:c.60+4003T>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000446221
  ensembl transcript: ENST00000539968
  gene symbol: CORO7
  hgvsc: ENST00000539968.1:c.-442-26T>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000576457
  gene symbol: CORO7
  hgvsc: ENST00000576457.1:n.218-26T>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461187
  ensembl transcript: ENST00000574311
  gene symbol: CORO7
  hgvsc: ENST00000574311.1:c.60+4003T>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461702
  ensembl transcript: ENST00000574025
  gene symbol: CORO7
  hgvsc: ENST00000574025.1:c.158-26T>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459085
  ensembl transcript: ENST00000571052
  gene symbol: CORO7
  hgvsc: ENST00000571052.1:c.-268+4003T>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000577144
  gene symbol: CORO7
  hgvsc: ENST00000577144.1:n.266-26T>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460910
  ensembl transcript: ENST00000575850
  gene symbol: CORO7
  hgvsc: ENST00000575850.1:c.197-26T>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461051
  ensembl transcript: ENST00000572153
  gene symbol: CORO7
  hgvsc: ENST00000572153.1:c.61-26T>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000458607
  ensembl transcript: ENST00000575334
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000575334.1:c.158-26T>C
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460036
  ensembl transcript: ENST00000571059
  gene symbol: CORO7
  hgvsc: ENST00000571059.1:c.158-26T>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000391530
  ensembl transcript: ENST00000423908
  gene symbol: CORO7
  hgvsc: ENST00000423908.2:c.60+4003T>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459286
  ensembl transcript: ENST00000572549
  gene symbol: CORO7
  hgvsc: ENST00000572549.1:c.99+4329T>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000572518
  gene symbol: CORO7
  hgvsc: ENST00000572518.1:n.406-26T>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458828
  ensembl transcript: ENST00000571756
  gene symbol: CORO7
  hgvsc: ENST00000571756.1:c.158-26T>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460901
  ensembl transcript: ENST00000570645
  gene symbol: CORO7
  hgvsc: ENST00000570645.1:c.-214+4024T>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000460885
  ensembl transcript: ENST00000572467
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000572467.1:c.158-26T>C
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461797
  ensembl transcript: ENST00000575038
  gene symbol: CORO7
  hgvsc: ENST00000575038.1:c.158-26T>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458459
  ensembl transcript: ENST00000571227
  gene symbol: CORO7
  hgvsc: ENST00000571227.1:c.*155-26T>C
  variant of: http://identifiers.org/hgnc/26161
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Other
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: DP

16-4462458-CT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4462458
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4462457
    reference: chr 16
allele count: 5
allele frequency: 4.153168867846167e-5
allele num: 120390
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000251166
  ensembl transcript: ENST00000251166
  gene symbol: CORO7
  hgvsc: ENST00000251166.4:c.158-28delA
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460910
  ensembl transcript: ENST00000575850
  gene symbol: CORO7
  hgvsc: ENST00000575850.1:c.197-28delA
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000440460
  ensembl transcript: ENST00000537233
  gene symbol: CORO7
  hgvsc: ENST00000537233.2:c.158-28delA
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000460885
  ensembl transcript: ENST00000572467
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000572467.1:c.158-28delA
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461797
  ensembl transcript: ENST00000575038
  gene symbol: CORO7
  hgvsc: ENST00000575038.1:c.158-28delA
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460199
  ensembl transcript: ENST00000570928
  gene symbol: CORO7
  hgvsc: ENST00000570928.1:c.158-28delA
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458411
  ensembl transcript: ENST00000572044
  gene symbol: CORO7
  hgvsc: ENST00000572044.1:c.60+4001delA
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000458607
  ensembl transcript: ENST00000575334
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000575334.1:c.158-28delA
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000446221
  ensembl transcript: ENST00000539968
  gene symbol: CORO7
  hgvsc: ENST00000539968.1:c.-442-28delA
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000391530
  ensembl transcript: ENST00000423908
  gene symbol: CORO7
  hgvsc: ENST00000423908.2:c.60+4001delA
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458935
  ensembl transcript: ENST00000572898
  gene symbol: CORO7
  hgvsc: ENST00000572898.1:c.158-28delA
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461187
  ensembl transcript: ENST00000574311
  gene symbol: CORO7
  hgvsc: ENST00000574311.1:c.60+4001delA
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458828
  ensembl transcript: ENST00000571756
  gene symbol: CORO7
  hgvsc: ENST00000571756.1:c.158-28delA
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459286
  ensembl transcript: ENST00000572549
  gene symbol: CORO7
  hgvsc: ENST00000572549.1:c.99+4327delA
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459888
  ensembl transcript: ENST00000576051
  gene symbol: CORO7
  hgvsc: ENST00000576051.1:c.-342-28delA
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460036
  ensembl transcript: ENST00000571059
  gene symbol: CORO7
  hgvsc: ENST00000571059.1:c.158-28delA
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000572518
  gene symbol: CORO7
  hgvsc: ENST00000572518.1:n.406-28delA
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458459
  ensembl transcript: ENST00000571227
  gene symbol: CORO7
  hgvsc: ENST00000571227.1:c.*155-28delA
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461051
  ensembl transcript: ENST00000572153
  gene symbol: CORO7
  hgvsc: ENST00000572153.1:c.61-28delA
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000577144
  gene symbol: CORO7
  hgvsc: ENST00000577144.1:n.266-28delA
  variant of: http://identifiers.org/hgnc/26161
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
population: African
population: Other
population: European (Non-Finnish)
reference allele: CT
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: QD

16-4462462-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4462462
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4462462
    reference: chr 16
allele count: 5
allele frequency: 4.157727552428944e-5
allele num: 120258
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000572518
  gene symbol: CORO7
  hgvsc: ENST00000572518.1:n.406-31T>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461797
  ensembl transcript: ENST00000575038
  gene symbol: CORO7
  hgvsc: ENST00000575038.1:c.158-31T>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460901
  ensembl transcript: ENST00000570645
  gene symbol: CORO7
  hgvsc: ENST00000570645.1:c.-214+4019T>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459085
  ensembl transcript: ENST00000571052
  gene symbol: CORO7
  hgvsc: ENST00000571052.1:c.-268+3998T>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000460885
  ensembl transcript: ENST00000572467
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000572467.1:c.158-31T>A
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460036
  ensembl transcript: ENST00000571059
  gene symbol: CORO7
  hgvsc: ENST00000571059.1:c.158-31T>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000251166
  ensembl transcript: ENST00000251166
  gene symbol: CORO7
  hgvsc: ENST00000251166.4:c.158-31T>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000440460
  ensembl transcript: ENST00000537233
  gene symbol: CORO7
  hgvsc: ENST00000537233.2:c.158-31T>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000446221
  ensembl transcript: ENST00000539968
  gene symbol: CORO7
  hgvsc: ENST00000539968.1:c.-442-31T>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460910
  ensembl transcript: ENST00000575850
  gene symbol: CORO7
  hgvsc: ENST00000575850.1:c.197-31T>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000577144
  gene symbol: CORO7
  hgvsc: ENST00000577144.1:n.266-31T>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461702
  ensembl transcript: ENST00000574025
  gene symbol: CORO7
  hgvsc: ENST00000574025.1:c.158-31T>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000458607
  ensembl transcript: ENST00000575334
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000575334.1:c.158-31T>A
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000576457
  gene symbol: CORO7
  hgvsc: ENST00000576457.1:n.218-31T>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458828
  ensembl transcript: ENST00000571756
  gene symbol: CORO7
  hgvsc: ENST00000571756.1:c.158-31T>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458935
  ensembl transcript: ENST00000572898
  gene symbol: CORO7
  hgvsc: ENST00000572898.1:c.158-31T>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459888
  ensembl transcript: ENST00000576051
  gene symbol: CORO7
  hgvsc: ENST00000576051.1:c.-342-31T>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460199
  ensembl transcript: ENST00000570928
  gene symbol: CORO7
  hgvsc: ENST00000570928.1:c.158-31T>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458411
  ensembl transcript: ENST00000572044
  gene symbol: CORO7
  hgvsc: ENST00000572044.1:c.60+3998T>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461187
  ensembl transcript: ENST00000574311
  gene symbol: CORO7
  hgvsc: ENST00000574311.1:c.60+3998T>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000572026
  gene symbol: CORO7
  hgvsc: ENST00000572026.1:n.281-31T>A
  variant of: http://identifiers.org/hgnc/26161
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: A
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum

16-4462464-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4462464
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4462464
    reference: chr 16
allele count: 5
allele frequency: 4.160841488582651e-5
allele num: 120168
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000391530
  ensembl transcript: ENST00000423908
  gene symbol: CORO7
  hgvsc: ENST00000423908.2:c.60+3996C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000458607
  ensembl transcript: ENST00000575334
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000575334.1:c.158-33C>T
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458411
  ensembl transcript: ENST00000572044
  gene symbol: CORO7
  hgvsc: ENST00000572044.1:c.60+3996C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459228
  ensembl transcript: ENST00000576437
  gene symbol: CORO7
  hgvsc: ENST00000576437.1:c.-214+4017C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461187
  ensembl transcript: ENST00000574311
  gene symbol: CORO7
  hgvsc: ENST00000574311.1:c.60+3996C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461051
  ensembl transcript: ENST00000572153
  gene symbol: CORO7
  hgvsc: ENST00000572153.1:c.61-33C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000251166
  ensembl transcript: ENST00000251166
  gene symbol: CORO7
  hgvsc: ENST00000251166.4:c.158-33C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000576457
  gene symbol: CORO7
  hgvsc: ENST00000576457.1:n.218-33C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000572518
  gene symbol: CORO7
  hgvsc: ENST00000572518.1:n.406-33C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000460885
  ensembl transcript: ENST00000572467
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000572467.1:c.158-33C>T
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460910
  ensembl transcript: ENST00000575850
  gene symbol: CORO7
  hgvsc: ENST00000575850.1:c.197-33C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000446221
  ensembl transcript: ENST00000539968
  gene symbol: CORO7
  hgvsc: ENST00000539968.1:c.-442-33C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459286
  ensembl transcript: ENST00000572549
  gene symbol: CORO7
  hgvsc: ENST00000572549.1:c.99+4322C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458828
  ensembl transcript: ENST00000571756
  gene symbol: CORO7
  hgvsc: ENST00000571756.1:c.158-33C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461797
  ensembl transcript: ENST00000575038
  gene symbol: CORO7
  hgvsc: ENST00000575038.1:c.158-33C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460036
  ensembl transcript: ENST00000571059
  gene symbol: CORO7
  hgvsc: ENST00000571059.1:c.158-33C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461702
  ensembl transcript: ENST00000574025
  gene symbol: CORO7
  hgvsc: ENST00000574025.1:c.158-33C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000440460
  ensembl transcript: ENST00000537233
  gene symbol: CORO7
  hgvsc: ENST00000537233.2:c.158-33C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460199
  ensembl transcript: ENST00000570928
  gene symbol: CORO7
  hgvsc: ENST00000570928.1:c.158-33C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459888
  ensembl transcript: ENST00000576051
  gene symbol: CORO7
  hgvsc: ENST00000576051.1:c.-342-33C>T
  variant of: http://identifiers.org/hgnc/26161
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: African
reference allele: G
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ

16-4462470-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4462470
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4462470
    reference: chr 16
allele count: 10
allele frequency: 8.337363058811759e-5
allele num: 119942
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000391530
  ensembl transcript: ENST00000423908
  gene symbol: CORO7
  hgvsc: ENST00000423908.2:c.60+3990G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460036
  ensembl transcript: ENST00000571059
  gene symbol: CORO7
  hgvsc: ENST00000571059.1:c.158-39G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000460885
  ensembl transcript: ENST00000572467
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000572467.1:c.158-39G>A
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000572518
  gene symbol: CORO7
  hgvsc: ENST00000572518.1:n.406-39G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459888
  ensembl transcript: ENST00000576051
  gene symbol: CORO7
  hgvsc: ENST00000576051.1:c.-342-39G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461797
  ensembl transcript: ENST00000575038
  gene symbol: CORO7
  hgvsc: ENST00000575038.1:c.158-39G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460910
  ensembl transcript: ENST00000575850
  gene symbol: CORO7
  hgvsc: ENST00000575850.1:c.197-39G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459286
  ensembl transcript: ENST00000572549
  gene symbol: CORO7
  hgvsc: ENST00000572549.1:c.99+4316G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000577144
  gene symbol: CORO7
  hgvsc: ENST00000577144.1:n.266-39G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458935
  ensembl transcript: ENST00000572898
  gene symbol: CORO7
  hgvsc: ENST00000572898.1:c.158-39G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000458607
  ensembl transcript: ENST00000575334
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000575334.1:c.158-39G>A
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460901
  ensembl transcript: ENST00000570645
  gene symbol: CORO7
  hgvsc: ENST00000570645.1:c.-214+4011G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458459
  ensembl transcript: ENST00000571227
  gene symbol: CORO7
  hgvsc: ENST00000571227.1:c.*155-39G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458411
  ensembl transcript: ENST00000572044
  gene symbol: CORO7
  hgvsc: ENST00000572044.1:c.60+3990G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460199
  ensembl transcript: ENST00000570928
  gene symbol: CORO7
  hgvsc: ENST00000570928.1:c.158-39G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458828
  ensembl transcript: ENST00000571756
  gene symbol: CORO7
  hgvsc: ENST00000571756.1:c.158-39G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000572026
  gene symbol: CORO7
  hgvsc: ENST00000572026.1:n.281-39G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461187
  ensembl transcript: ENST00000574311
  gene symbol: CORO7
  hgvsc: ENST00000574311.1:c.60+3990G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461702
  ensembl transcript: ENST00000574025
  gene symbol: CORO7
  hgvsc: ENST00000574025.1:c.158-39G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459085
  ensembl transcript: ENST00000571052
  gene symbol: CORO7
  hgvsc: ENST00000571052.1:c.-268+3990G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000446221
  ensembl transcript: ENST00000539968
  gene symbol: CORO7
  hgvsc: ENST00000539968.1:c.-442-39G>A
  variant of: http://identifiers.org/hgnc/26161
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: African
population: Latino
population: Other
reference allele: C
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum

16-4462478-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4462478
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4462478
    reference: chr 16
allele count: 5
allele frequency: 4.177458434288579e-5
allele num: 119690
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000446221
  ensembl transcript: ENST00000539968
  gene symbol: CORO7
  hgvsc: ENST00000539968.1:c.-442-47G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458411
  ensembl transcript: ENST00000572044
  gene symbol: CORO7
  hgvsc: ENST00000572044.1:c.60+3982G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000576457
  gene symbol: CORO7
  hgvsc: ENST00000576457.1:n.218-47G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460036
  ensembl transcript: ENST00000571059
  gene symbol: CORO7
  hgvsc: ENST00000571059.1:c.158-47G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460910
  ensembl transcript: ENST00000575850
  gene symbol: CORO7
  hgvsc: ENST00000575850.1:c.197-47G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461187
  ensembl transcript: ENST00000574311
  gene symbol: CORO7
  hgvsc: ENST00000574311.1:c.60+3982G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000460885
  ensembl transcript: ENST00000572467
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000572467.1:c.158-47G>A
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000440460
  ensembl transcript: ENST00000537233
  gene symbol: CORO7
  hgvsc: ENST00000537233.2:c.158-47G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459888
  ensembl transcript: ENST00000576051
  gene symbol: CORO7
  hgvsc: ENST00000576051.1:c.-342-47G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460901
  ensembl transcript: ENST00000570645
  gene symbol: CORO7
  hgvsc: ENST00000570645.1:c.-214+4003G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000577144
  gene symbol: CORO7
  hgvsc: ENST00000577144.1:n.266-47G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461702
  ensembl transcript: ENST00000574025
  gene symbol: CORO7
  hgvsc: ENST00000574025.1:c.158-47G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458459
  ensembl transcript: ENST00000571227
  gene symbol: CORO7
  hgvsc: ENST00000571227.1:c.*155-47G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459228
  ensembl transcript: ENST00000576437
  gene symbol: CORO7
  hgvsc: ENST00000576437.1:c.-214+4003G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459286
  ensembl transcript: ENST00000572549
  gene symbol: CORO7
  hgvsc: ENST00000572549.1:c.99+4308G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458935
  ensembl transcript: ENST00000572898
  gene symbol: CORO7
  hgvsc: ENST00000572898.1:c.158-47G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461051
  ensembl transcript: ENST00000572153
  gene symbol: CORO7
  hgvsc: ENST00000572153.1:c.61-47G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000251166
  ensembl transcript: ENST00000251166
  gene symbol: CORO7
  hgvsc: ENST00000251166.4:c.158-47G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000458607
  ensembl transcript: ENST00000575334
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000575334.1:c.158-47G>A
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000391530
  ensembl transcript: ENST00000423908
  gene symbol: CORO7
  hgvsc: ENST00000423908.2:c.60+3982G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458828
  ensembl transcript: ENST00000571756
  gene symbol: CORO7
  hgvsc: ENST00000571756.1:c.158-47G>A
  variant of: http://identifiers.org/hgnc/26161
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: African
reference allele: C
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum

16-4462480-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4462480
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4462480
    reference: chr 16
allele count: 1
allele frequency: 8.375630266177531e-6
allele num: 119394
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459286
  ensembl transcript: ENST00000572549
  gene symbol: CORO7
  hgvsc: ENST00000572549.1:c.99+4306G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461051
  ensembl transcript: ENST00000572153
  gene symbol: CORO7
  hgvsc: ENST00000572153.1:c.61-49G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459085
  ensembl transcript: ENST00000571052
  gene symbol: CORO7
  hgvsc: ENST00000571052.1:c.-268+3980G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000391530
  ensembl transcript: ENST00000423908
  gene symbol: CORO7
  hgvsc: ENST00000423908.2:c.60+3980G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460910
  ensembl transcript: ENST00000575850
  gene symbol: CORO7
  hgvsc: ENST00000575850.1:c.197-49G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458411
  ensembl transcript: ENST00000572044
  gene symbol: CORO7
  hgvsc: ENST00000572044.1:c.60+3980G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461702
  ensembl transcript: ENST00000574025
  gene symbol: CORO7
  hgvsc: ENST00000574025.1:c.158-49G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460036
  ensembl transcript: ENST00000571059
  gene symbol: CORO7
  hgvsc: ENST00000571059.1:c.158-49G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000572518
  gene symbol: CORO7
  hgvsc: ENST00000572518.1:n.406-49G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461797
  ensembl transcript: ENST00000575038
  gene symbol: CORO7
  hgvsc: ENST00000575038.1:c.158-49G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000576457
  gene symbol: CORO7
  hgvsc: ENST00000576457.1:n.218-49G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460901
  ensembl transcript: ENST00000570645
  gene symbol: CORO7
  hgvsc: ENST00000570645.1:c.-214+4001G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000446221
  ensembl transcript: ENST00000539968
  gene symbol: CORO7
  hgvsc: ENST00000539968.1:c.-442-49G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460199
  ensembl transcript: ENST00000570928
  gene symbol: CORO7
  hgvsc: ENST00000570928.1:c.158-49G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000458607
  ensembl transcript: ENST00000575334
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000575334.1:c.158-49G>A
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000460885
  ensembl transcript: ENST00000572467
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000572467.1:c.158-49G>A
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458935
  ensembl transcript: ENST00000572898
  gene symbol: CORO7
  hgvsc: ENST00000572898.1:c.158-49G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000440460
  ensembl transcript: ENST00000537233
  gene symbol: CORO7
  hgvsc: ENST00000537233.2:c.158-49G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000577144
  gene symbol: CORO7
  hgvsc: ENST00000577144.1:n.266-49G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458459
  ensembl transcript: ENST00000571227
  gene symbol: CORO7
  hgvsc: ENST00000571227.1:c.*155-49G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000572026
  gene symbol: CORO7
  hgvsc: ENST00000572026.1:n.281-49G>A
  variant of: http://identifiers.org/hgnc/26161
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: African
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
reference allele: C
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum

16-4463261-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4463261
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4463261
    reference: chr 16
allele count: 0
allele frequency: 0.0e0
allele num: 21924
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000460885
  ensembl transcript: ENST00000572467
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000572467.1:c.157+48C>T
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000458607
  ensembl transcript: ENST00000575334
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000575334.1:c.157+48C>T
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000576457
  gene symbol: CORO7
  hgvsc: ENST00000576457.1:n.217+48C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460901
  ensembl transcript: ENST00000570645
  gene symbol: CORO7
  hgvsc: ENST00000570645.1:c.-214+3220C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459888
  ensembl transcript: ENST00000576051
  gene symbol: CORO7
  hgvsc: ENST00000576051.1:c.-343+48C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459085
  ensembl transcript: ENST00000571052
  gene symbol: CORO7
  hgvsc: ENST00000571052.1:c.-268+3199C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459286
  ensembl transcript: ENST00000572549
  gene symbol: CORO7
  hgvsc: ENST00000572549.1:c.99+3525C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461702
  ensembl transcript: ENST00000574025
  gene symbol: CORO7
  hgvsc: ENST00000574025.1:c.157+48C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000251166
  ensembl transcript: ENST00000251166
  gene symbol: CORO7
  hgvsc: ENST00000251166.4:c.157+48C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458411
  ensembl transcript: ENST00000572044
  gene symbol: CORO7
  hgvsc: ENST00000572044.1:c.60+3199C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000446221
  ensembl transcript: ENST00000539968
  gene symbol: CORO7
  hgvsc: ENST00000539968.1:c.-443+48C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460910
  ensembl transcript: ENST00000575850
  gene symbol: CORO7
  hgvsc: ENST00000575850.1:c.196+48C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000572026
  gene symbol: CORO7
  hgvsc: ENST00000572026.1:n.280+48C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460036
  ensembl transcript: ENST00000571059
  gene symbol: CORO7
  hgvsc: ENST00000571059.1:c.157+48C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461187
  ensembl transcript: ENST00000574311
  gene symbol: CORO7
  hgvsc: ENST00000574311.1:c.60+3199C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460199
  ensembl transcript: ENST00000570928
  gene symbol: CORO7
  hgvsc: ENST00000570928.1:c.157+48C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461797
  ensembl transcript: ENST00000575038
  gene symbol: CORO7
  hgvsc: ENST00000575038.1:c.157+48C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458828
  ensembl transcript: ENST00000571756
  gene symbol: CORO7
  hgvsc: ENST00000571756.1:c.157+48C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000440460
  ensembl transcript: ENST00000537233
  gene symbol: CORO7
  hgvsc: ENST00000537233.2:c.157+48C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000577144
  gene symbol: CORO7
  hgvsc: ENST00000577144.1:n.265+48C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000391530
  ensembl transcript: ENST00000423908
  gene symbol: CORO7
  hgvsc: ENST00000423908.2:c.60+3199C>T
  variant of: http://identifiers.org/hgnc/26161
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
population: Latino
reference allele: G
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD

16-4463267-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4463267
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4463267
    reference: chr 16
allele count: 6
allele frequency: 2.729505959421344e-4
allele num: 21982
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458935
  ensembl transcript: ENST00000572898
  gene symbol: CORO7
  hgvsc: ENST00000572898.1:c.157+42G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000458607
  ensembl transcript: ENST00000575334
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000575334.1:c.157+42G>A
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000446221
  ensembl transcript: ENST00000539968
  gene symbol: CORO7
  hgvsc: ENST00000539968.1:c.-443+42G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000577144
  gene symbol: CORO7
  hgvsc: ENST00000577144.1:n.265+42G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461051
  ensembl transcript: ENST00000572153
  gene symbol: CORO7
  hgvsc: ENST00000572153.1:c.61-836G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000572026
  gene symbol: CORO7
  hgvsc: ENST00000572026.1:n.280+42G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000460885
  ensembl transcript: ENST00000572467
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000572467.1:c.157+42G>A
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460901
  ensembl transcript: ENST00000570645
  gene symbol: CORO7
  hgvsc: ENST00000570645.1:c.-214+3214G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459228
  ensembl transcript: ENST00000576437
  gene symbol: CORO7
  hgvsc: ENST00000576437.1:c.-214+3214G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459888
  ensembl transcript: ENST00000576051
  gene symbol: CORO7
  hgvsc: ENST00000576051.1:c.-343+42G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458828
  ensembl transcript: ENST00000571756
  gene symbol: CORO7
  hgvsc: ENST00000571756.1:c.157+42G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000440460
  ensembl transcript: ENST00000537233
  gene symbol: CORO7
  hgvsc: ENST00000537233.2:c.157+42G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458411
  ensembl transcript: ENST00000572044
  gene symbol: CORO7
  hgvsc: ENST00000572044.1:c.60+3193G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460036
  ensembl transcript: ENST00000571059
  gene symbol: CORO7
  hgvsc: ENST00000571059.1:c.157+42G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460910
  ensembl transcript: ENST00000575850
  gene symbol: CORO7
  hgvsc: ENST00000575850.1:c.196+42G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461797
  ensembl transcript: ENST00000575038
  gene symbol: CORO7
  hgvsc: ENST00000575038.1:c.157+42G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461187
  ensembl transcript: ENST00000574311
  gene symbol: CORO7
  hgvsc: ENST00000574311.1:c.60+3193G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458459
  ensembl transcript: ENST00000571227
  gene symbol: CORO7
  hgvsc: ENST00000571227.1:c.*154+42G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461702
  ensembl transcript: ENST00000574025
  gene symbol: CORO7
  hgvsc: ENST00000574025.1:c.157+42G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000576457
  gene symbol: CORO7
  hgvsc: ENST00000576457.1:n.217+42G>A
  variant of: http://identifiers.org/hgnc/26161
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: East Asian
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum

16-4463268-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4463268
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4463268
    reference: chr 16
allele count: 1
allele frequency: 4.512635379061372e-5
allele num: 22160
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458411
  ensembl transcript: ENST00000572044
  gene symbol: CORO7
  hgvsc: ENST00000572044.1:c.60+3192C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459085
  ensembl transcript: ENST00000571052
  gene symbol: CORO7
  hgvsc: ENST00000571052.1:c.-268+3192C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460901
  ensembl transcript: ENST00000570645
  gene symbol: CORO7
  hgvsc: ENST00000570645.1:c.-214+3213C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458935
  ensembl transcript: ENST00000572898
  gene symbol: CORO7
  hgvsc: ENST00000572898.1:c.157+41C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458828
  ensembl transcript: ENST00000571756
  gene symbol: CORO7
  hgvsc: ENST00000571756.1:c.157+41C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461797
  ensembl transcript: ENST00000575038
  gene symbol: CORO7
  hgvsc: ENST00000575038.1:c.157+41C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458459
  ensembl transcript: ENST00000571227
  gene symbol: CORO7
  hgvsc: ENST00000571227.1:c.*154+41C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000251166
  ensembl transcript: ENST00000251166
  gene symbol: CORO7
  hgvsc: ENST00000251166.4:c.157+41C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000458607
  ensembl transcript: ENST00000575334
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000575334.1:c.157+41C>T
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461187
  ensembl transcript: ENST00000574311
  gene symbol: CORO7
  hgvsc: ENST00000574311.1:c.60+3192C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459228
  ensembl transcript: ENST00000576437
  gene symbol: CORO7
  hgvsc: ENST00000576437.1:c.-214+3213C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460036
  ensembl transcript: ENST00000571059
  gene symbol: CORO7
  hgvsc: ENST00000571059.1:c.157+41C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000576457
  gene symbol: CORO7
  hgvsc: ENST00000576457.1:n.217+41C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000460885
  ensembl transcript: ENST00000572467
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000572467.1:c.157+41C>T
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459286
  ensembl transcript: ENST00000572549
  gene symbol: CORO7
  hgvsc: ENST00000572549.1:c.99+3518C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000446221
  ensembl transcript: ENST00000539968
  gene symbol: CORO7
  hgvsc: ENST00000539968.1:c.-443+41C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460910
  ensembl transcript: ENST00000575850
  gene symbol: CORO7
  hgvsc: ENST00000575850.1:c.196+41C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461702
  ensembl transcript: ENST00000574025
  gene symbol: CORO7
  hgvsc: ENST00000574025.1:c.157+41C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459888
  ensembl transcript: ENST00000576051
  gene symbol: CORO7
  hgvsc: ENST00000576051.1:c.-343+41C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000391530
  ensembl transcript: ENST00000423908
  gene symbol: CORO7
  hgvsc: ENST00000423908.2:c.60+3192C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000440460
  ensembl transcript: ENST00000537233
  gene symbol: CORO7
  hgvsc: ENST00000537233.2:c.157+41C>T
  variant of: http://identifiers.org/hgnc/26161
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff

16-4463278-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4463278
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4463278
    reference: chr 16
allele count: 0
allele frequency: 0.0e0
allele num: 22840
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000460885
  ensembl transcript: ENST00000572467
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000572467.1:c.157+31C>T
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459085
  ensembl transcript: ENST00000571052
  gene symbol: CORO7
  hgvsc: ENST00000571052.1:c.-268+3182C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458935
  ensembl transcript: ENST00000572898
  gene symbol: CORO7
  hgvsc: ENST00000572898.1:c.157+31C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458411
  ensembl transcript: ENST00000572044
  gene symbol: CORO7
  hgvsc: ENST00000572044.1:c.60+3182C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000391530
  ensembl transcript: ENST00000423908
  gene symbol: CORO7
  hgvsc: ENST00000423908.2:c.60+3182C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458828
  ensembl transcript: ENST00000571756
  gene symbol: CORO7
  hgvsc: ENST00000571756.1:c.157+31C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460910
  ensembl transcript: ENST00000575850
  gene symbol: CORO7
  hgvsc: ENST00000575850.1:c.196+31C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459228
  ensembl transcript: ENST00000576437
  gene symbol: CORO7
  hgvsc: ENST00000576437.1:c.-214+3203C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000446221
  ensembl transcript: ENST00000539968
  gene symbol: CORO7
  hgvsc: ENST00000539968.1:c.-443+31C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460901
  ensembl transcript: ENST00000570645
  gene symbol: CORO7
  hgvsc: ENST00000570645.1:c.-214+3203C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461187
  ensembl transcript: ENST00000574311
  gene symbol: CORO7
  hgvsc: ENST00000574311.1:c.60+3182C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000440460
  ensembl transcript: ENST00000537233
  gene symbol: CORO7
  hgvsc: ENST00000537233.2:c.157+31C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461702
  ensembl transcript: ENST00000574025
  gene symbol: CORO7
  hgvsc: ENST00000574025.1:c.157+31C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000576457
  gene symbol: CORO7
  hgvsc: ENST00000576457.1:n.217+31C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000577144
  gene symbol: CORO7
  hgvsc: ENST00000577144.1:n.265+31C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460036
  ensembl transcript: ENST00000571059
  gene symbol: CORO7
  hgvsc: ENST00000571059.1:c.157+31C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461797
  ensembl transcript: ENST00000575038
  gene symbol: CORO7
  hgvsc: ENST00000575038.1:c.157+31C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458459
  ensembl transcript: ENST00000571227
  gene symbol: CORO7
  hgvsc: ENST00000571227.1:c.*154+31C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459286
  ensembl transcript: ENST00000572549
  gene symbol: CORO7
  hgvsc: ENST00000572549.1:c.99+3508C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460199
  ensembl transcript: ENST00000570928
  gene symbol: CORO7
  hgvsc: ENST00000570928.1:c.157+31C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461051
  ensembl transcript: ENST00000572153
  gene symbol: CORO7
  hgvsc: ENST00000572153.1:c.61-847C>T
  variant of: http://identifiers.org/hgnc/26161
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: South Asian
population: Other
reference allele: G
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: BaseQRankSum

http://identifiers.org/exac.variant/16-4463281-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4463281
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4463281
    reference: chr 16
allele count: 5
allele frequency: 2.153501593591179e-4
allele num: 23218
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461702
  ensembl transcript: ENST00000574025
  gene symbol: CORO7
  hgvsc: ENST00000574025.1:c.157+28T>G
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000458607
  ensembl transcript: ENST00000575334
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000575334.1:c.157+28T>G
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458828
  ensembl transcript: ENST00000571756
  gene symbol: CORO7
  hgvsc: ENST00000571756.1:c.157+28T>G
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460036
  ensembl transcript: ENST00000571059
  gene symbol: CORO7
  hgvsc: ENST00000571059.1:c.157+28T>G
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000577144
  gene symbol: CORO7
  hgvsc: ENST00000577144.1:n.265+28T>G
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000440460
  ensembl transcript: ENST00000537233
  gene symbol: CORO7
  hgvsc: ENST00000537233.2:c.157+28T>G
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459085
  ensembl transcript: ENST00000571052
  gene symbol: CORO7
  hgvsc: ENST00000571052.1:c.-268+3179T>G
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000391530
  ensembl transcript: ENST00000423908
  gene symbol: CORO7
  hgvsc: ENST00000423908.2:c.60+3179T>G
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460910
  ensembl transcript: ENST00000575850
  gene symbol: CORO7
  hgvsc: ENST00000575850.1:c.196+28T>G
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000460885
  ensembl transcript: ENST00000572467
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000572467.1:c.157+28T>G
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460901
  ensembl transcript: ENST00000570645
  gene symbol: CORO7
  hgvsc: ENST00000570645.1:c.-214+3200T>G
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000572026
  gene symbol: CORO7
  hgvsc: ENST00000572026.1:n.280+28T>G
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461797
  ensembl transcript: ENST00000575038
  gene symbol: CORO7
  hgvsc: ENST00000575038.1:c.157+28T>G
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461187
  ensembl transcript: ENST00000574311
  gene symbol: CORO7
  hgvsc: ENST00000574311.1:c.60+3179T>G
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000446221
  ensembl transcript: ENST00000539968
  gene symbol: CORO7
  hgvsc: ENST00000539968.1:c.-443+28T>G
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458411
  ensembl transcript: ENST00000572044
  gene symbol: CORO7
  hgvsc: ENST00000572044.1:c.60+3179T>G
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459228
  ensembl transcript: ENST00000576437
  gene symbol: CORO7
  hgvsc: ENST00000576437.1:c.-214+3200T>G
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461051
  ensembl transcript: ENST00000572153
  gene symbol: CORO7
  hgvsc: ENST00000572153.1:c.61-850T>G
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000251166
  ensembl transcript: ENST00000251166
  gene symbol: CORO7
  hgvsc: ENST00000251166.4:c.157+28T>G
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000576457
  gene symbol: CORO7
  hgvsc: ENST00000576457.1:n.217+28T>G
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460199
  ensembl transcript: ENST00000570928
  gene symbol: CORO7
  hgvsc: ENST00000570928.1:c.157+28T>G
  variant of: http://identifiers.org/hgnc/26161
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: Other
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: A
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/16-4463284-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4463284
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4463284
    reference: chr 16
allele count: 33
allele frequency: 1.410497520943751e-3
allele num: 23396
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460901
  ensembl transcript: ENST00000570645
  gene symbol: CORO7
  hgvsc: ENST00000570645.1:c.-214+3197T>G
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459888
  ensembl transcript: ENST00000576051
  gene symbol: CORO7
  hgvsc: ENST00000576051.1:c.-343+25T>G
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461797
  ensembl transcript: ENST00000575038
  gene symbol: CORO7
  hgvsc: ENST00000575038.1:c.157+25T>G
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000446221
  ensembl transcript: ENST00000539968
  gene symbol: CORO7
  hgvsc: ENST00000539968.1:c.-443+25T>G
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460199
  ensembl transcript: ENST00000570928
  gene symbol: CORO7
  hgvsc: ENST00000570928.1:c.157+25T>G
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461187
  ensembl transcript: ENST00000574311
  gene symbol: CORO7
  hgvsc: ENST00000574311.1:c.60+3176T>G
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000458607
  ensembl transcript: ENST00000575334
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000575334.1:c.157+25T>G
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460910
  ensembl transcript: ENST00000575850
  gene symbol: CORO7
  hgvsc: ENST00000575850.1:c.196+25T>G
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459228
  ensembl transcript: ENST00000576437
  gene symbol: CORO7
  hgvsc: ENST00000576437.1:c.-214+3197T>G
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000391530
  ensembl transcript: ENST00000423908
  gene symbol: CORO7
  hgvsc: ENST00000423908.2:c.60+3176T>G
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000577144
  gene symbol: CORO7
  hgvsc: ENST00000577144.1:n.265+25T>G
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000460885
  ensembl transcript: ENST00000572467
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000572467.1:c.157+25T>G
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459085
  ensembl transcript: ENST00000571052
  gene symbol: CORO7
  hgvsc: ENST00000571052.1:c.-268+3176T>G
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460036
  ensembl transcript: ENST00000571059
  gene symbol: CORO7
  hgvsc: ENST00000571059.1:c.157+25T>G
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461051
  ensembl transcript: ENST00000572153
  gene symbol: CORO7
  hgvsc: ENST00000572153.1:c.61-853T>G
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458459
  ensembl transcript: ENST00000571227
  gene symbol: CORO7
  hgvsc: ENST00000571227.1:c.*154+25T>G
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461702
  ensembl transcript: ENST00000574025
  gene symbol: CORO7
  hgvsc: ENST00000574025.1:c.157+25T>G
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459286
  ensembl transcript: ENST00000572549
  gene symbol: CORO7
  hgvsc: ENST00000572549.1:c.99+3502T>G
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000440460
  ensembl transcript: ENST00000537233
  gene symbol: CORO7
  hgvsc: ENST00000537233.2:c.157+25T>G
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000572026
  gene symbol: CORO7
  hgvsc: ENST00000572026.1:n.280+25T>G
  variant of: http://identifiers.org/hgnc/26161
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
reference allele: A
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP

16-4463290-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4463290
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4463290
    reference: chr 16
allele count: 0
allele frequency: 0.0e0
allele num: 24282
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460036
  ensembl transcript: ENST00000571059
  gene symbol: CORO7
  hgvsc: ENST00000571059.1:c.157+19T>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461051
  ensembl transcript: ENST00000572153
  gene symbol: CORO7
  hgvsc: ENST00000572153.1:c.61-859T>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459228
  ensembl transcript: ENST00000576437
  gene symbol: CORO7
  hgvsc: ENST00000576437.1:c.-214+3191T>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458411
  ensembl transcript: ENST00000572044
  gene symbol: CORO7
  hgvsc: ENST00000572044.1:c.60+3170T>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459888
  ensembl transcript: ENST00000576051
  gene symbol: CORO7
  hgvsc: ENST00000576051.1:c.-343+19T>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000458607
  ensembl transcript: ENST00000575334
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000575334.1:c.157+19T>C
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461702
  ensembl transcript: ENST00000574025
  gene symbol: CORO7
  hgvsc: ENST00000574025.1:c.157+19T>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458828
  ensembl transcript: ENST00000571756
  gene symbol: CORO7
  hgvsc: ENST00000571756.1:c.157+19T>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461187
  ensembl transcript: ENST00000574311
  gene symbol: CORO7
  hgvsc: ENST00000574311.1:c.60+3170T>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460910
  ensembl transcript: ENST00000575850
  gene symbol: CORO7
  hgvsc: ENST00000575850.1:c.196+19T>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000391530
  ensembl transcript: ENST00000423908
  gene symbol: CORO7
  hgvsc: ENST00000423908.2:c.60+3170T>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460901
  ensembl transcript: ENST00000570645
  gene symbol: CORO7
  hgvsc: ENST00000570645.1:c.-214+3191T>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000572026
  gene symbol: CORO7
  hgvsc: ENST00000572026.1:n.280+19T>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000251166
  ensembl transcript: ENST00000251166
  gene symbol: CORO7
  hgvsc: ENST00000251166.4:c.157+19T>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458459
  ensembl transcript: ENST00000571227
  gene symbol: CORO7
  hgvsc: ENST00000571227.1:c.*154+19T>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000577144
  gene symbol: CORO7
  hgvsc: ENST00000577144.1:n.265+19T>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000446221
  ensembl transcript: ENST00000539968
  gene symbol: CORO7
  hgvsc: ENST00000539968.1:c.-443+19T>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000460885
  ensembl transcript: ENST00000572467
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000572467.1:c.157+19T>C
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459286
  ensembl transcript: ENST00000572549
  gene symbol: CORO7
  hgvsc: ENST00000572549.1:c.99+3496T>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000440460
  ensembl transcript: ENST00000537233
  gene symbol: CORO7
  hgvsc: ENST00000537233.2:c.157+19T>C
  variant of: http://identifiers.org/hgnc/26161
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: Other
reference allele: A
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum

16-4463291-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4463291
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4463291
    reference: chr 16
allele count: 7
allele frequency: 2.871677059402691e-4
allele num: 24376
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460910
  ensembl transcript: ENST00000575850
  gene symbol: CORO7
  hgvsc: ENST00000575850.1:c.196+18G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000572026
  gene symbol: CORO7
  hgvsc: ENST00000572026.1:n.280+18G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461187
  ensembl transcript: ENST00000574311
  gene symbol: CORO7
  hgvsc: ENST00000574311.1:c.60+3169G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000446221
  ensembl transcript: ENST00000539968
  gene symbol: CORO7
  hgvsc: ENST00000539968.1:c.-443+18G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460036
  ensembl transcript: ENST00000571059
  gene symbol: CORO7
  hgvsc: ENST00000571059.1:c.157+18G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459228
  ensembl transcript: ENST00000576437
  gene symbol: CORO7
  hgvsc: ENST00000576437.1:c.-214+3190G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461702
  ensembl transcript: ENST00000574025
  gene symbol: CORO7
  hgvsc: ENST00000574025.1:c.157+18G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000458607
  ensembl transcript: ENST00000575334
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000575334.1:c.157+18G>A
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000251166
  ensembl transcript: ENST00000251166
  gene symbol: CORO7
  hgvsc: ENST00000251166.4:c.157+18G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458411
  ensembl transcript: ENST00000572044
  gene symbol: CORO7
  hgvsc: ENST00000572044.1:c.60+3169G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458935
  ensembl transcript: ENST00000572898
  gene symbol: CORO7
  hgvsc: ENST00000572898.1:c.157+18G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000460885
  ensembl transcript: ENST00000572467
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000572467.1:c.157+18G>A
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458459
  ensembl transcript: ENST00000571227
  gene symbol: CORO7
  hgvsc: ENST00000571227.1:c.*154+18G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458828
  ensembl transcript: ENST00000571756
  gene symbol: CORO7
  hgvsc: ENST00000571756.1:c.157+18G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460901
  ensembl transcript: ENST00000570645
  gene symbol: CORO7
  hgvsc: ENST00000570645.1:c.-214+3190G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459888
  ensembl transcript: ENST00000576051
  gene symbol: CORO7
  hgvsc: ENST00000576051.1:c.-343+18G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460199
  ensembl transcript: ENST00000570928
  gene symbol: CORO7
  hgvsc: ENST00000570928.1:c.157+18G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459085
  ensembl transcript: ENST00000571052
  gene symbol: CORO7
  hgvsc: ENST00000571052.1:c.-268+3169G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000576457
  gene symbol: CORO7
  hgvsc: ENST00000576457.1:n.217+18G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000440460
  ensembl transcript: ENST00000537233
  gene symbol: CORO7
  hgvsc: ENST00000537233.2:c.157+18G>A
  variant of: http://identifiers.org/hgnc/26161
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
population: Other
reference allele: C
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ

16-4463294-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4463294
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4463294
    reference: chr 16
allele count: 0
allele frequency: 0.0e0
allele num: 24998
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000458607
  ensembl transcript: ENST00000575334
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000575334.1:c.157+15T>C
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000576457
  gene symbol: CORO7
  hgvsc: ENST00000576457.1:n.217+15T>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000572026
  gene symbol: CORO7
  hgvsc: ENST00000572026.1:n.280+15T>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000460885
  ensembl transcript: ENST00000572467
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000572467.1:c.157+15T>C
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000251166
  ensembl transcript: ENST00000251166
  gene symbol: CORO7
  hgvsc: ENST00000251166.4:c.157+15T>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458828
  ensembl transcript: ENST00000571756
  gene symbol: CORO7
  hgvsc: ENST00000571756.1:c.157+15T>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461051
  ensembl transcript: ENST00000572153
  gene symbol: CORO7
  hgvsc: ENST00000572153.1:c.61-863T>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460901
  ensembl transcript: ENST00000570645
  gene symbol: CORO7
  hgvsc: ENST00000570645.1:c.-214+3187T>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458411
  ensembl transcript: ENST00000572044
  gene symbol: CORO7
  hgvsc: ENST00000572044.1:c.60+3166T>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460036
  ensembl transcript: ENST00000571059
  gene symbol: CORO7
  hgvsc: ENST00000571059.1:c.157+15T>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461187
  ensembl transcript: ENST00000574311
  gene symbol: CORO7
  hgvsc: ENST00000574311.1:c.60+3166T>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461797
  ensembl transcript: ENST00000575038
  gene symbol: CORO7
  hgvsc: ENST00000575038.1:c.157+15T>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458935
  ensembl transcript: ENST00000572898
  gene symbol: CORO7
  hgvsc: ENST00000572898.1:c.157+15T>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000577144
  gene symbol: CORO7
  hgvsc: ENST00000577144.1:n.265+15T>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460910
  ensembl transcript: ENST00000575850
  gene symbol: CORO7
  hgvsc: ENST00000575850.1:c.196+15T>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000446221
  ensembl transcript: ENST00000539968
  gene symbol: CORO7
  hgvsc: ENST00000539968.1:c.-443+15T>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459286
  ensembl transcript: ENST00000572549
  gene symbol: CORO7
  hgvsc: ENST00000572549.1:c.99+3492T>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459888
  ensembl transcript: ENST00000576051
  gene symbol: CORO7
  hgvsc: ENST00000576051.1:c.-343+15T>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000391530
  ensembl transcript: ENST00000423908
  gene symbol: CORO7
  hgvsc: ENST00000423908.2:c.60+3166T>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458459
  ensembl transcript: ENST00000571227
  gene symbol: CORO7
  hgvsc: ENST00000571227.1:c.*154+15T>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000440460
  ensembl transcript: ENST00000537233
  gene symbol: CORO7
  hgvsc: ENST00000537233.2:c.157+15T>C
  variant of: http://identifiers.org/hgnc/26161
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
population: Latino
population: African
population: European (Finnish)
reference allele: A
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD

16-4463295-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4463295
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4463295
    reference: chr 16
allele count: 1
allele frequency: 3.985016338566988e-5
allele num: 25094
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000446221
  ensembl transcript: ENST00000539968
  gene symbol: CORO7
  hgvsc: ENST00000539968.1:c.-443+14A>G
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458411
  ensembl transcript: ENST00000572044
  gene symbol: CORO7
  hgvsc: ENST00000572044.1:c.60+3165A>G
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460910
  ensembl transcript: ENST00000575850
  gene symbol: CORO7
  hgvsc: ENST00000575850.1:c.196+14A>G
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000460885
  ensembl transcript: ENST00000572467
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000572467.1:c.157+14A>G
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000577144
  gene symbol: CORO7
  hgvsc: ENST00000577144.1:n.265+14A>G
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000391530
  ensembl transcript: ENST00000423908
  gene symbol: CORO7
  hgvsc: ENST00000423908.2:c.60+3165A>G
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459085
  ensembl transcript: ENST00000571052
  gene symbol: CORO7
  hgvsc: ENST00000571052.1:c.-268+3165A>G
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461797
  ensembl transcript: ENST00000575038
  gene symbol: CORO7
  hgvsc: ENST00000575038.1:c.157+14A>G
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460036
  ensembl transcript: ENST00000571059
  gene symbol: CORO7
  hgvsc: ENST00000571059.1:c.157+14A>G
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000458607
  ensembl transcript: ENST00000575334
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000575334.1:c.157+14A>G
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459286
  ensembl transcript: ENST00000572549
  gene symbol: CORO7
  hgvsc: ENST00000572549.1:c.99+3491A>G
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458828
  ensembl transcript: ENST00000571756
  gene symbol: CORO7
  hgvsc: ENST00000571756.1:c.157+14A>G
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459228
  ensembl transcript: ENST00000576437
  gene symbol: CORO7
  hgvsc: ENST00000576437.1:c.-214+3186A>G
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458459
  ensembl transcript: ENST00000571227
  gene symbol: CORO7
  hgvsc: ENST00000571227.1:c.*154+14A>G
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460199
  ensembl transcript: ENST00000570928
  gene symbol: CORO7
  hgvsc: ENST00000570928.1:c.157+14A>G
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460901
  ensembl transcript: ENST00000570645
  gene symbol: CORO7
  hgvsc: ENST00000570645.1:c.-214+3186A>G
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000572026
  gene symbol: CORO7
  hgvsc: ENST00000572026.1:n.280+14A>G
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459888
  ensembl transcript: ENST00000576051
  gene symbol: CORO7
  hgvsc: ENST00000576051.1:c.-343+14A>G
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461702
  ensembl transcript: ENST00000574025
  gene symbol: CORO7
  hgvsc: ENST00000574025.1:c.157+14A>G
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000576457
  gene symbol: CORO7
  hgvsc: ENST00000576457.1:n.217+14A>G
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458935
  ensembl transcript: ENST00000572898
  gene symbol: CORO7
  hgvsc: ENST00000572898.1:c.157+14A>G
  variant of: http://identifiers.org/hgnc/26161
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD

16-4463300-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4463300
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4463300
    reference: chr 16
allele count: 0
allele frequency: 0.0e0
allele num: 26266
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000576457
  gene symbol: CORO7
  hgvsc: ENST00000576457.1:n.217+9T>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458459
  ensembl transcript: ENST00000571227
  gene symbol: CORO7
  hgvsc: ENST00000571227.1:c.*154+9T>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000251166
  ensembl transcript: ENST00000251166
  gene symbol: CORO7
  hgvsc: ENST00000251166.4:c.157+9T>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461187
  ensembl transcript: ENST00000574311
  gene symbol: CORO7
  hgvsc: ENST00000574311.1:c.60+3160T>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461051
  ensembl transcript: ENST00000572153
  gene symbol: CORO7
  hgvsc: ENST00000572153.1:c.61-869T>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000440460
  ensembl transcript: ENST00000537233
  gene symbol: CORO7
  hgvsc: ENST00000537233.2:c.157+9T>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459085
  ensembl transcript: ENST00000571052
  gene symbol: CORO7
  hgvsc: ENST00000571052.1:c.-268+3160T>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460910
  ensembl transcript: ENST00000575850
  gene symbol: CORO7
  hgvsc: ENST00000575850.1:c.196+9T>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460036
  ensembl transcript: ENST00000571059
  gene symbol: CORO7
  hgvsc: ENST00000571059.1:c.157+9T>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000572026
  gene symbol: CORO7
  hgvsc: ENST00000572026.1:n.280+9T>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458828
  ensembl transcript: ENST00000571756
  gene symbol: CORO7
  hgvsc: ENST00000571756.1:c.157+9T>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459888
  ensembl transcript: ENST00000576051
  gene symbol: CORO7
  hgvsc: ENST00000576051.1:c.-343+9T>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000458607
  ensembl transcript: ENST00000575334
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000575334.1:c.157+9T>C
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459286
  ensembl transcript: ENST00000572549
  gene symbol: CORO7
  hgvsc: ENST00000572549.1:c.99+3486T>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000577144
  gene symbol: CORO7
  hgvsc: ENST00000577144.1:n.265+9T>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461797
  ensembl transcript: ENST00000575038
  gene symbol: CORO7
  hgvsc: ENST00000575038.1:c.157+9T>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458935
  ensembl transcript: ENST00000572898
  gene symbol: CORO7
  hgvsc: ENST00000572898.1:c.157+9T>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000446221
  ensembl transcript: ENST00000539968
  gene symbol: CORO7
  hgvsc: ENST00000539968.1:c.-443+9T>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460901
  ensembl transcript: ENST00000570645
  gene symbol: CORO7
  hgvsc: ENST00000570645.1:c.-214+3181T>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000460885
  ensembl transcript: ENST00000572467
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000572467.1:c.157+9T>C
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459228
  ensembl transcript: ENST00000576437
  gene symbol: CORO7
  hgvsc: ENST00000576437.1:c.-214+3181T>C
  variant of: http://identifiers.org/hgnc/26161
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
reference allele: A
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum

16-4463301-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4463301
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4463301
    reference: chr 16
allele count: 12
allele frequency: 4.536518977771057e-4
allele num: 26452
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000572026
  gene symbol: CORO7
  hgvsc: ENST00000572026.1:n.280+8A>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458828
  ensembl transcript: ENST00000571756
  gene symbol: CORO7
  hgvsc: ENST00000571756.1:c.157+8A>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460199
  ensembl transcript: ENST00000570928
  gene symbol: CORO7
  hgvsc: ENST00000570928.1:c.157+8A>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461051
  ensembl transcript: ENST00000572153
  gene symbol: CORO7
  hgvsc: ENST00000572153.1:c.61-870A>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459888
  ensembl transcript: ENST00000576051
  gene symbol: CORO7
  hgvsc: ENST00000576051.1:c.-343+8A>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000460885
  ensembl transcript: ENST00000572467
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000572467.1:c.157+8A>C
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000446221
  ensembl transcript: ENST00000539968
  gene symbol: CORO7
  hgvsc: ENST00000539968.1:c.-443+8A>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461702
  ensembl transcript: ENST00000574025
  gene symbol: CORO7
  hgvsc: ENST00000574025.1:c.157+8A>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461797
  ensembl transcript: ENST00000575038
  gene symbol: CORO7
  hgvsc: ENST00000575038.1:c.157+8A>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458459
  ensembl transcript: ENST00000571227
  gene symbol: CORO7
  hgvsc: ENST00000571227.1:c.*154+8A>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460901
  ensembl transcript: ENST00000570645
  gene symbol: CORO7
  hgvsc: ENST00000570645.1:c.-214+3180A>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000577144
  gene symbol: CORO7
  hgvsc: ENST00000577144.1:n.265+8A>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458935
  ensembl transcript: ENST00000572898
  gene symbol: CORO7
  hgvsc: ENST00000572898.1:c.157+8A>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000391530
  ensembl transcript: ENST00000423908
  gene symbol: CORO7
  hgvsc: ENST00000423908.2:c.60+3159A>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460910
  ensembl transcript: ENST00000575850
  gene symbol: CORO7
  hgvsc: ENST00000575850.1:c.196+8A>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460036
  ensembl transcript: ENST00000571059
  gene symbol: CORO7
  hgvsc: ENST00000571059.1:c.157+8A>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000576457
  gene symbol: CORO7
  hgvsc: ENST00000576457.1:n.217+8A>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000251166
  ensembl transcript: ENST00000251166
  gene symbol: CORO7
  hgvsc: ENST00000251166.4:c.157+8A>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459085
  ensembl transcript: ENST00000571052
  gene symbol: CORO7
  hgvsc: ENST00000571052.1:c.-268+3159A>C
  variant of: http://identifiers.org/hgnc/26161
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: c.157+8A>C
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: DP

http://identifiers.org/exac.variant/16-4463314-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4463314
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4463314
    reference: chr 16
allele count: 1
allele frequency: 3.431237990667032e-5
allele num: 29144
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000572026
  gene symbol: CORO7
  hgvsc: ENST00000572026.1:n.275G>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000577144
  gene symbol: CORO7
  hgvsc: ENST00000577144.1:n.260G>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460901
  ensembl transcript: ENST00000570645
  gene symbol: CORO7
  hgvsc: ENST00000570645.1:c.-214+3167G>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000440460
  ensembl transcript: ENST00000537233
  gene symbol: CORO7
  hgvsc: ENST00000537233.2:c.152G>T
  hgvsp: ENSP00000440460.2:p.Arg51Leu
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461187
  ensembl transcript: ENST00000574311
  gene symbol: CORO7
  hgvsc: ENST00000574311.1:c.60+3146G>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000446221
  ensembl transcript: ENST00000539968
  gene symbol: CORO7
  hgvsc: ENST00000539968.1:c.-448G>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459888
  ensembl transcript: ENST00000576051
  gene symbol: CORO7
  hgvsc: ENST00000576051.1:c.-348G>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000460885
  ensembl transcript: ENST00000572467
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000572467.1:c.152G>T
  hgvsp: ENSP00000460885.1:p.Arg51Leu
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000251166
  ensembl transcript: ENST00000251166
  gene symbol: CORO7
  hgvsc: ENST00000251166.4:c.152G>T
  hgvsp: ENSP00000251166.4:p.Arg51Leu
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458828
  ensembl transcript: ENST00000571756
  gene symbol: CORO7
  hgvsc: ENST00000571756.1:c.152G>T
  hgvsp: ENSP00000458828.1:p.Arg51Leu
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459286
  ensembl transcript: ENST00000572549
  gene symbol: CORO7
  hgvsc: ENST00000572549.1:c.99+3472G>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460036
  ensembl transcript: ENST00000571059
  gene symbol: CORO7
  hgvsc: ENST00000571059.1:c.152G>T
  hgvsp: ENSP00000460036.1:p.Arg51Leu
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461702
  ensembl transcript: ENST00000574025
  gene symbol: CORO7
  hgvsc: ENST00000574025.1:c.152G>T
  hgvsp: ENSP00000461702.1:p.Arg51Leu
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460910
  ensembl transcript: ENST00000575850
  gene symbol: CORO7
  hgvsc: ENST00000575850.1:c.191G>T
  hgvsp: ENSP00000460910.1:p.Arg64Leu
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461797
  ensembl transcript: ENST00000575038
  gene symbol: CORO7
  hgvsc: ENST00000575038.1:c.152G>T
  hgvsp: ENSP00000461797.1:p.Arg51Leu
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000458607
  ensembl transcript: ENST00000575334
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000575334.1:c.152G>T
  hgvsp: ENSP00000458607.1:p.Arg51Leu
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459085
  ensembl transcript: ENST00000571052
  gene symbol: CORO7
  hgvsc: ENST00000571052.1:c.-268+3146G>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458411
  ensembl transcript: ENST00000572044
  gene symbol: CORO7
  hgvsc: ENST00000572044.1:c.60+3146G>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000576457
  gene symbol: CORO7
  hgvsc: ENST00000576457.1:n.212G>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459228
  ensembl transcript: ENST00000576437
  gene symbol: CORO7
  hgvsc: ENST00000576437.1:c.-214+3167G>T
  variant of: http://identifiers.org/hgnc/26161
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Arg51Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Other
population: European (Finnish)
population: African
population: Latino
population: East Asian
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum

16-4463314-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4463314
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4463314
    reference: chr 16
allele count: 1
allele frequency: 3.431237990667032e-5
allele num: 29144
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459888
  ensembl transcript: ENST00000576051
  gene symbol: CORO7
  hgvsc: ENST00000576051.1:c.-348G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000391530
  ensembl transcript: ENST00000423908
  gene symbol: CORO7
  hgvsc: ENST00000423908.2:c.60+3146G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000446221
  ensembl transcript: ENST00000539968
  gene symbol: CORO7
  hgvsc: ENST00000539968.1:c.-448G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000576457
  gene symbol: CORO7
  hgvsc: ENST00000576457.1:n.212G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459228
  ensembl transcript: ENST00000576437
  gene symbol: CORO7
  hgvsc: ENST00000576437.1:c.-214+3167G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460901
  ensembl transcript: ENST00000570645
  gene symbol: CORO7
  hgvsc: ENST00000570645.1:c.-214+3167G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461702
  ensembl transcript: ENST00000574025
  gene symbol: CORO7
  hgvsc: ENST00000574025.1:c.152G>A
  hgvsp: ENSP00000461702.1:p.Arg51His
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460199
  ensembl transcript: ENST00000570928
  gene symbol: CORO7
  hgvsc: ENST00000570928.1:c.152G>A
  hgvsp: ENSP00000460199.1:p.Arg51His
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461797
  ensembl transcript: ENST00000575038
  gene symbol: CORO7
  hgvsc: ENST00000575038.1:c.152G>A
  hgvsp: ENSP00000461797.1:p.Arg51His
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460910
  ensembl transcript: ENST00000575850
  gene symbol: CORO7
  hgvsc: ENST00000575850.1:c.191G>A
  hgvsp: ENSP00000460910.1:p.Arg64His
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460036
  ensembl transcript: ENST00000571059
  gene symbol: CORO7
  hgvsc: ENST00000571059.1:c.152G>A
  hgvsp: ENSP00000460036.1:p.Arg51His
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000577144
  gene symbol: CORO7
  hgvsc: ENST00000577144.1:n.260G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000458607
  ensembl transcript: ENST00000575334
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000575334.1:c.152G>A
  hgvsp: ENSP00000458607.1:p.Arg51His
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459085
  ensembl transcript: ENST00000571052
  gene symbol: CORO7
  hgvsc: ENST00000571052.1:c.-268+3146G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458411
  ensembl transcript: ENST00000572044
  gene symbol: CORO7
  hgvsc: ENST00000572044.1:c.60+3146G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000251166
  ensembl transcript: ENST00000251166
  gene symbol: CORO7
  hgvsc: ENST00000251166.4:c.152G>A
  hgvsp: ENSP00000251166.4:p.Arg51His
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000460885
  ensembl transcript: ENST00000572467
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000572467.1:c.152G>A
  hgvsp: ENSP00000460885.1:p.Arg51His
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458828
  ensembl transcript: ENST00000571756
  gene symbol: CORO7
  hgvsc: ENST00000571756.1:c.152G>A
  hgvsp: ENSP00000458828.1:p.Arg51His
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000572026
  gene symbol: CORO7
  hgvsc: ENST00000572026.1:n.275G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461187
  ensembl transcript: ENST00000574311
  gene symbol: CORO7
  hgvsc: ENST00000574311.1:c.60+3146G>A
  variant of: http://identifiers.org/hgnc/26161
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Arg51His
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP

16-4463315-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4463315
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4463315
    reference: chr 16
allele count: 3
allele frequency: 1.018952516812716e-4
allele num: 29442
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000251166
  ensembl transcript: ENST00000251166
  gene symbol: CORO7
  hgvsc: ENST00000251166.4:c.151C>T
  hgvsp: ENSP00000251166.4:p.Arg51Cys
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000460885
  ensembl transcript: ENST00000572467
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000572467.1:c.151C>T
  hgvsp: ENSP00000460885.1:p.Arg51Cys
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458935
  ensembl transcript: ENST00000572898
  gene symbol: CORO7
  hgvsc: ENST00000572898.1:c.151C>T
  hgvsp: ENSP00000458935.1:p.Arg51Cys
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000446221
  ensembl transcript: ENST00000539968
  gene symbol: CORO7
  hgvsc: ENST00000539968.1:c.-449C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000572026
  gene symbol: CORO7
  hgvsc: ENST00000572026.1:n.274C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000577144
  gene symbol: CORO7
  hgvsc: ENST00000577144.1:n.259C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461797
  ensembl transcript: ENST00000575038
  gene symbol: CORO7
  hgvsc: ENST00000575038.1:c.151C>T
  hgvsp: ENSP00000461797.1:p.Arg51Cys
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461702
  ensembl transcript: ENST00000574025
  gene symbol: CORO7
  hgvsc: ENST00000574025.1:c.151C>T
  hgvsp: ENSP00000461702.1:p.Arg51Cys
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460199
  ensembl transcript: ENST00000570928
  gene symbol: CORO7
  hgvsc: ENST00000570928.1:c.151C>T
  hgvsp: ENSP00000460199.1:p.Arg51Cys
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460910
  ensembl transcript: ENST00000575850
  gene symbol: CORO7
  hgvsc: ENST00000575850.1:c.190C>T
  hgvsp: ENSP00000460910.1:p.Arg64Cys
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000576457
  gene symbol: CORO7
  hgvsc: ENST00000576457.1:n.211C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460036
  ensembl transcript: ENST00000571059
  gene symbol: CORO7
  hgvsc: ENST00000571059.1:c.151C>T
  hgvsp: ENSP00000460036.1:p.Arg51Cys
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458828
  ensembl transcript: ENST00000571756
  gene symbol: CORO7
  hgvsc: ENST00000571756.1:c.151C>T
  hgvsp: ENSP00000458828.1:p.Arg51Cys
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461187
  ensembl transcript: ENST00000574311
  gene symbol: CORO7
  hgvsc: ENST00000574311.1:c.60+3145C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458411
  ensembl transcript: ENST00000572044
  gene symbol: CORO7
  hgvsc: ENST00000572044.1:c.60+3145C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000458607
  ensembl transcript: ENST00000575334
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000575334.1:c.151C>T
  hgvsp: ENSP00000458607.1:p.Arg51Cys
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000440460
  ensembl transcript: ENST00000537233
  gene symbol: CORO7
  hgvsc: ENST00000537233.2:c.151C>T
  hgvsp: ENSP00000440460.2:p.Arg51Cys
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461051
  ensembl transcript: ENST00000572153
  gene symbol: CORO7
  hgvsc: ENST00000572153.1:c.61-884C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460901
  ensembl transcript: ENST00000570645
  gene symbol: CORO7
  hgvsc: ENST00000570645.1:c.-214+3166C>T
  variant of: http://identifiers.org/hgnc/26161
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Arg51Cys
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum

16-4463319-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4463319
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4463319
    reference: chr 16
allele count: 20
allele frequency: 6.593696426216537e-4
allele num: 30332
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459228
  ensembl transcript: ENST00000576437
  gene symbol: CORO7
  hgvsc: ENST00000576437.1:c.-214+3162C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000251166
  ensembl transcript: ENST00000251166
  gene symbol: CORO7
  hgvsc: ENST00000251166.4:c.147C>T
  hgvsp: ENST00000251166.4:c.147C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000446221
  ensembl transcript: ENST00000539968
  gene symbol: CORO7
  hgvsc: ENST00000539968.1:c.-453C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000576457
  gene symbol: CORO7
  hgvsc: ENST00000576457.1:n.207C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460036
  ensembl transcript: ENST00000571059
  gene symbol: CORO7
  hgvsc: ENST00000571059.1:c.147C>T
  hgvsp: ENST00000571059.1:c.147C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000572026
  gene symbol: CORO7
  hgvsc: ENST00000572026.1:n.270C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000458607
  ensembl transcript: ENST00000575334
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000575334.1:c.147C>T
  hgvsp: ENST00000575334.1:c.147C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458935
  ensembl transcript: ENST00000572898
  gene symbol: CORO7
  hgvsc: ENST00000572898.1:c.147C>T
  hgvsp: ENST00000572898.1:c.147C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461702
  ensembl transcript: ENST00000574025
  gene symbol: CORO7
  hgvsc: ENST00000574025.1:c.147C>T
  hgvsp: ENST00000574025.1:c.147C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461797
  ensembl transcript: ENST00000575038
  gene symbol: CORO7
  hgvsc: ENST00000575038.1:c.147C>T
  hgvsp: ENST00000575038.1:c.147C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000440460
  ensembl transcript: ENST00000537233
  gene symbol: CORO7
  hgvsc: ENST00000537233.2:c.147C>T
  hgvsp: ENST00000537233.2:c.147C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000391530
  ensembl transcript: ENST00000423908
  gene symbol: CORO7
  hgvsc: ENST00000423908.2:c.60+3141C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460910
  ensembl transcript: ENST00000575850
  gene symbol: CORO7
  hgvsc: ENST00000575850.1:c.186C>T
  hgvsp: ENST00000575850.1:c.186C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461051
  ensembl transcript: ENST00000572153
  gene symbol: CORO7
  hgvsc: ENST00000572153.1:c.61-888C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458459
  ensembl transcript: ENST00000571227
  gene symbol: CORO7
  hgvsc: ENST00000571227.1:c.*144C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000460885
  ensembl transcript: ENST00000572467
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000572467.1:c.147C>T
  hgvsp: ENST00000572467.1:c.147C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458411
  ensembl transcript: ENST00000572044
  gene symbol: CORO7
  hgvsc: ENST00000572044.1:c.60+3141C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458828
  ensembl transcript: ENST00000571756
  gene symbol: CORO7
  hgvsc: ENST00000571756.1:c.147C>T
  hgvsp: ENST00000571756.1:c.147C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461187
  ensembl transcript: ENST00000574311
  gene symbol: CORO7
  hgvsc: ENST00000574311.1:c.60+3141C>T
  variant of: http://identifiers.org/hgnc/26161
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Ser49Ser
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
population: South Asian
population: Other
reference allele: G
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff

16-4463322-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4463322
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4463322
    reference: chr 16
allele count: 1
allele frequency: 3.223518793114564e-5
allele num: 31022
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000577144
  gene symbol: CORO7
  hgvsc: ENST00000577144.1:n.252C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461702
  ensembl transcript: ENST00000574025
  gene symbol: CORO7
  hgvsc: ENST00000574025.1:c.144C>T
  hgvsp: ENST00000574025.1:c.144C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461797
  ensembl transcript: ENST00000575038
  gene symbol: CORO7
  hgvsc: ENST00000575038.1:c.144C>T
  hgvsp: ENST00000575038.1:c.144C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458828
  ensembl transcript: ENST00000571756
  gene symbol: CORO7
  hgvsc: ENST00000571756.1:c.144C>T
  hgvsp: ENST00000571756.1:c.144C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000440460
  ensembl transcript: ENST00000537233
  gene symbol: CORO7
  hgvsc: ENST00000537233.2:c.144C>T
  hgvsp: ENST00000537233.2:c.144C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460910
  ensembl transcript: ENST00000575850
  gene symbol: CORO7
  hgvsc: ENST00000575850.1:c.183C>T
  hgvsp: ENST00000575850.1:c.183C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460901
  ensembl transcript: ENST00000570645
  gene symbol: CORO7
  hgvsc: ENST00000570645.1:c.-214+3159C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000458607
  ensembl transcript: ENST00000575334
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000575334.1:c.144C>T
  hgvsp: ENST00000575334.1:c.144C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458459
  ensembl transcript: ENST00000571227
  gene symbol: CORO7
  hgvsc: ENST00000571227.1:c.*141C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458411
  ensembl transcript: ENST00000572044
  gene symbol: CORO7
  hgvsc: ENST00000572044.1:c.60+3138C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460036
  ensembl transcript: ENST00000571059
  gene symbol: CORO7
  hgvsc: ENST00000571059.1:c.144C>T
  hgvsp: ENST00000571059.1:c.144C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461187
  ensembl transcript: ENST00000574311
  gene symbol: CORO7
  hgvsc: ENST00000574311.1:c.60+3138C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461051
  ensembl transcript: ENST00000572153
  gene symbol: CORO7
  hgvsc: ENST00000572153.1:c.61-891C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000251166
  ensembl transcript: ENST00000251166
  gene symbol: CORO7
  hgvsc: ENST00000251166.4:c.144C>T
  hgvsp: ENST00000251166.4:c.144C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000446221
  ensembl transcript: ENST00000539968
  gene symbol: CORO7
  hgvsc: ENST00000539968.1:c.-456C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000576457
  gene symbol: CORO7
  hgvsc: ENST00000576457.1:n.204C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459228
  ensembl transcript: ENST00000576437
  gene symbol: CORO7
  hgvsc: ENST00000576437.1:c.-214+3159C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000460885
  ensembl transcript: ENST00000572467
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000572467.1:c.144C>T
  hgvsp: ENST00000572467.1:c.144C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459888
  ensembl transcript: ENST00000576051
  gene symbol: CORO7
  hgvsc: ENST00000576051.1:c.-356C>T
  variant of: http://identifiers.org/hgnc/26161
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Asn48Asn
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: South Asian
population: East Asian
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum

http://identifiers.org/exac.variant/16-4463330-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4463330
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4463330
    reference: chr 16
allele count: 6
allele frequency: 1.865555624650208e-4
allele num: 32162
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000440460
  ensembl transcript: ENST00000537233
  gene symbol: CORO7
  hgvsc: ENST00000537233.2:c.136G>T
  hgvsp: ENSP00000440460.2:p.Ala46Ser
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460036
  ensembl transcript: ENST00000571059
  gene symbol: CORO7
  hgvsc: ENST00000571059.1:c.136G>T
  hgvsp: ENSP00000460036.1:p.Ala46Ser
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460901
  ensembl transcript: ENST00000570645
  gene symbol: CORO7
  hgvsc: ENST00000570645.1:c.-214+3151G>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459228
  ensembl transcript: ENST00000576437
  gene symbol: CORO7
  hgvsc: ENST00000576437.1:c.-214+3151G>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000458607
  ensembl transcript: ENST00000575334
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000575334.1:c.136G>T
  hgvsp: ENSP00000458607.1:p.Ala46Ser
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461797
  ensembl transcript: ENST00000575038
  gene symbol: CORO7
  hgvsc: ENST00000575038.1:c.136G>T
  hgvsp: ENSP00000461797.1:p.Ala46Ser
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000460885
  ensembl transcript: ENST00000572467
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000572467.1:c.136G>T
  hgvsp: ENSP00000460885.1:p.Ala46Ser
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000391530
  ensembl transcript: ENST00000423908
  gene symbol: CORO7
  hgvsc: ENST00000423908.2:c.60+3130G>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000576457
  gene symbol: CORO7
  hgvsc: ENST00000576457.1:n.196G>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461702
  ensembl transcript: ENST00000574025
  gene symbol: CORO7
  hgvsc: ENST00000574025.1:c.136G>T
  hgvsp: ENSP00000461702.1:p.Ala46Ser
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460199
  ensembl transcript: ENST00000570928
  gene symbol: CORO7
  hgvsc: ENST00000570928.1:c.136G>T
  hgvsp: ENSP00000460199.1:p.Ala46Ser
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458935
  ensembl transcript: ENST00000572898
  gene symbol: CORO7
  hgvsc: ENST00000572898.1:c.136G>T
  hgvsp: ENSP00000458935.1:p.Ala46Ser
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461051
  ensembl transcript: ENST00000572153
  gene symbol: CORO7
  hgvsc: ENST00000572153.1:c.61-899G>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459085
  ensembl transcript: ENST00000571052
  gene symbol: CORO7
  hgvsc: ENST00000571052.1:c.-268+3130G>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460910
  ensembl transcript: ENST00000575850
  gene symbol: CORO7
  hgvsc: ENST00000575850.1:c.175G>T
  hgvsp: ENSP00000460910.1:p.Ala59Ser
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000251166
  ensembl transcript: ENST00000251166
  gene symbol: CORO7
  hgvsc: ENST00000251166.4:c.136G>T
  hgvsp: ENSP00000251166.4:p.Ala46Ser
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000577144
  gene symbol: CORO7
  hgvsc: ENST00000577144.1:n.244G>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458828
  ensembl transcript: ENST00000571756
  gene symbol: CORO7
  hgvsc: ENST00000571756.1:c.136G>T
  hgvsp: ENSP00000458828.1:p.Ala46Ser
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459888
  ensembl transcript: ENST00000576051
  gene symbol: CORO7
  hgvsc: ENST00000576051.1:c.-364G>T
  variant of: http://identifiers.org/hgnc/26161
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Ala46Ser
num of homozygotes: 1
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
population: Latino
population: East Asian
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

16-4463331-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4463331
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4463331
    reference: chr 16
allele count: 1
allele frequency: 3.090807937194783e-5
allele num: 32354
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458411
  ensembl transcript: ENST00000572044
  gene symbol: CORO7
  hgvsc: ENST00000572044.1:c.60+3129C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000572026
  gene symbol: CORO7
  hgvsc: ENST00000572026.1:n.258C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461797
  ensembl transcript: ENST00000575038
  gene symbol: CORO7
  hgvsc: ENST00000575038.1:c.135C>T
  hgvsp: ENST00000575038.1:c.135C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459286
  ensembl transcript: ENST00000572549
  gene symbol: CORO7
  hgvsc: ENST00000572549.1:c.99+3455C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460199
  ensembl transcript: ENST00000570928
  gene symbol: CORO7
  hgvsc: ENST00000570928.1:c.135C>T
  hgvsp: ENST00000570928.1:c.135C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460901
  ensembl transcript: ENST00000570645
  gene symbol: CORO7
  hgvsc: ENST00000570645.1:c.-214+3150C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458828
  ensembl transcript: ENST00000571756
  gene symbol: CORO7
  hgvsc: ENST00000571756.1:c.135C>T
  hgvsp: ENST00000571756.1:c.135C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000460885
  ensembl transcript: ENST00000572467
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000572467.1:c.135C>T
  hgvsp: ENST00000572467.1:c.135C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461702
  ensembl transcript: ENST00000574025
  gene symbol: CORO7
  hgvsc: ENST00000574025.1:c.135C>T
  hgvsp: ENST00000574025.1:c.135C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000576457
  gene symbol: CORO7
  hgvsc: ENST00000576457.1:n.195C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459085
  ensembl transcript: ENST00000571052
  gene symbol: CORO7
  hgvsc: ENST00000571052.1:c.-268+3129C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459888
  ensembl transcript: ENST00000576051
  gene symbol: CORO7
  hgvsc: ENST00000576051.1:c.-365C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460910
  ensembl transcript: ENST00000575850
  gene symbol: CORO7
  hgvsc: ENST00000575850.1:c.174C>T
  hgvsp: ENST00000575850.1:c.174C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460036
  ensembl transcript: ENST00000571059
  gene symbol: CORO7
  hgvsc: ENST00000571059.1:c.135C>T
  hgvsp: ENST00000571059.1:c.135C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000251166
  ensembl transcript: ENST00000251166
  gene symbol: CORO7
  hgvsc: ENST00000251166.4:c.135C>T
  hgvsp: ENST00000251166.4:c.135C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000391530
  ensembl transcript: ENST00000423908
  gene symbol: CORO7
  hgvsc: ENST00000423908.2:c.60+3129C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461051
  ensembl transcript: ENST00000572153
  gene symbol: CORO7
  hgvsc: ENST00000572153.1:c.61-900C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000458607
  ensembl transcript: ENST00000575334
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000575334.1:c.135C>T
  hgvsp: ENST00000575334.1:c.135C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458935
  ensembl transcript: ENST00000572898
  gene symbol: CORO7
  hgvsc: ENST00000572898.1:c.135C>T
  hgvsp: ENST00000572898.1:c.135C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461187
  ensembl transcript: ENST00000574311
  gene symbol: CORO7
  hgvsc: ENST00000574311.1:c.60+3129C>T
  variant of: http://identifiers.org/hgnc/26161
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Ile45Ile
num of homozygotes: 0
population: European (Finnish)
population: Other
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
reference allele: G
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: MQ

16-4463333-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4463333
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4463333
    reference: chr 16
allele count: 1
allele frequency: 3.034717164360282e-5
allele num: 32952
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000458607
  ensembl transcript: ENST00000575334
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000575334.1:c.133A>G
  hgvsp: ENSP00000458607.1:p.Ile45Val
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461187
  ensembl transcript: ENST00000574311
  gene symbol: CORO7
  hgvsc: ENST00000574311.1:c.60+3127A>G
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000251166
  ensembl transcript: ENST00000251166
  gene symbol: CORO7
  hgvsc: ENST00000251166.4:c.133A>G
  hgvsp: ENSP00000251166.4:p.Ile45Val
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461702
  ensembl transcript: ENST00000574025
  gene symbol: CORO7
  hgvsc: ENST00000574025.1:c.133A>G
  hgvsp: ENSP00000461702.1:p.Ile45Val
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460036
  ensembl transcript: ENST00000571059
  gene symbol: CORO7
  hgvsc: ENST00000571059.1:c.133A>G
  hgvsp: ENSP00000460036.1:p.Ile45Val
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459286
  ensembl transcript: ENST00000572549
  gene symbol: CORO7
  hgvsc: ENST00000572549.1:c.99+3453A>G
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459085
  ensembl transcript: ENST00000571052
  gene symbol: CORO7
  hgvsc: ENST00000571052.1:c.-268+3127A>G
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459228
  ensembl transcript: ENST00000576437
  gene symbol: CORO7
  hgvsc: ENST00000576437.1:c.-214+3148A>G
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460910
  ensembl transcript: ENST00000575850
  gene symbol: CORO7
  hgvsc: ENST00000575850.1:c.172A>G
  hgvsp: ENSP00000460910.1:p.Ile58Val
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000576457
  gene symbol: CORO7
  hgvsc: ENST00000576457.1:n.193A>G
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000391530
  ensembl transcript: ENST00000423908
  gene symbol: CORO7
  hgvsc: ENST00000423908.2:c.60+3127A>G
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458935
  ensembl transcript: ENST00000572898
  gene symbol: CORO7
  hgvsc: ENST00000572898.1:c.133A>G
  hgvsp: ENSP00000458935.1:p.Ile45Val
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458411
  ensembl transcript: ENST00000572044
  gene symbol: CORO7
  hgvsc: ENST00000572044.1:c.60+3127A>G
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000572026
  gene symbol: CORO7
  hgvsc: ENST00000572026.1:n.256A>G
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460199
  ensembl transcript: ENST00000570928
  gene symbol: CORO7
  hgvsc: ENST00000570928.1:c.133A>G
  hgvsp: ENSP00000460199.1:p.Ile45Val
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461797
  ensembl transcript: ENST00000575038
  gene symbol: CORO7
  hgvsc: ENST00000575038.1:c.133A>G
  hgvsp: ENSP00000461797.1:p.Ile45Val
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000460885
  ensembl transcript: ENST00000572467
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000572467.1:c.133A>G
  hgvsp: ENSP00000460885.1:p.Ile45Val
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000446221
  ensembl transcript: ENST00000539968
  gene symbol: CORO7
  hgvsc: ENST00000539968.1:c.-467A>G
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458459
  ensembl transcript: ENST00000571227
  gene symbol: CORO7
  hgvsc: ENST00000571227.1:c.*130A>G
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461051
  ensembl transcript: ENST00000572153
  gene symbol: CORO7
  hgvsc: ENST00000572153.1:c.61-902A>G
  variant of: http://identifiers.org/hgnc/26161
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Ile45Val
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Other
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
reference allele: T
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: QD

16-4463339-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4463339
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4463339
    reference: chr 16
allele count: 3
allele frequency: 8.955223880597016e-5
allele num: 33500
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459085
  ensembl transcript: ENST00000571052
  gene symbol: CORO7
  hgvsc: ENST00000571052.1:c.-268+3121A>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459888
  ensembl transcript: ENST00000576051
  gene symbol: CORO7
  hgvsc: ENST00000576051.1:c.-373A>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458935
  ensembl transcript: ENST00000572898
  gene symbol: CORO7
  hgvsc: ENST00000572898.1:c.127A>T
  hgvsp: ENSP00000458935.1:p.Ser43Cys
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000440460
  ensembl transcript: ENST00000537233
  gene symbol: CORO7
  hgvsc: ENST00000537233.2:c.127A>T
  hgvsp: ENSP00000440460.2:p.Ser43Cys
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459228
  ensembl transcript: ENST00000576437
  gene symbol: CORO7
  hgvsc: ENST00000576437.1:c.-214+3142A>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459286
  ensembl transcript: ENST00000572549
  gene symbol: CORO7
  hgvsc: ENST00000572549.1:c.99+3447A>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461797
  ensembl transcript: ENST00000575038
  gene symbol: CORO7
  hgvsc: ENST00000575038.1:c.127A>T
  hgvsp: ENSP00000461797.1:p.Ser43Cys
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458828
  ensembl transcript: ENST00000571756
  gene symbol: CORO7
  hgvsc: ENST00000571756.1:c.127A>T
  hgvsp: ENSP00000458828.1:p.Ser43Cys
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460910
  ensembl transcript: ENST00000575850
  gene symbol: CORO7
  hgvsc: ENST00000575850.1:c.166A>T
  hgvsp: ENSP00000460910.1:p.Ser56Cys
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000251166
  ensembl transcript: ENST00000251166
  gene symbol: CORO7
  hgvsc: ENST00000251166.4:c.127A>T
  hgvsp: ENSP00000251166.4:p.Ser43Cys
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000460885
  ensembl transcript: ENST00000572467
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000572467.1:c.127A>T
  hgvsp: ENSP00000460885.1:p.Ser43Cys
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458411
  ensembl transcript: ENST00000572044
  gene symbol: CORO7
  hgvsc: ENST00000572044.1:c.60+3121A>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460199
  ensembl transcript: ENST00000570928
  gene symbol: CORO7
  hgvsc: ENST00000570928.1:c.127A>T
  hgvsp: ENSP00000460199.1:p.Ser43Cys
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461702
  ensembl transcript: ENST00000574025
  gene symbol: CORO7
  hgvsc: ENST00000574025.1:c.127A>T
  hgvsp: ENSP00000461702.1:p.Ser43Cys
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460036
  ensembl transcript: ENST00000571059
  gene symbol: CORO7
  hgvsc: ENST00000571059.1:c.127A>T
  hgvsp: ENSP00000460036.1:p.Ser43Cys
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461051
  ensembl transcript: ENST00000572153
  gene symbol: CORO7
  hgvsc: ENST00000572153.1:c.61-908A>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000572026
  gene symbol: CORO7
  hgvsc: ENST00000572026.1:n.250A>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000576457
  gene symbol: CORO7
  hgvsc: ENST00000576457.1:n.187A>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458459
  ensembl transcript: ENST00000571227
  gene symbol: CORO7
  hgvsc: ENST00000571227.1:c.*124A>T
  variant of: http://identifiers.org/hgnc/26161
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Ser43Cys
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
reference allele: T
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff

16-4463352-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4463352
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4463352
    reference: chr 16
allele count: 0
allele frequency: 0.0e0
allele num: 34332
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000440460
  ensembl transcript: ENST00000537233
  gene symbol: CORO7
  hgvsc: ENST00000537233.2:c.114C>T
  hgvsp: ENST00000537233.2:c.114C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461187
  ensembl transcript: ENST00000574311
  gene symbol: CORO7
  hgvsc: ENST00000574311.1:c.60+3108C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000391530
  ensembl transcript: ENST00000423908
  gene symbol: CORO7
  hgvsc: ENST00000423908.2:c.60+3108C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000460885
  ensembl transcript: ENST00000572467
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000572467.1:c.114C>T
  hgvsp: ENST00000572467.1:c.114C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458828
  ensembl transcript: ENST00000571756
  gene symbol: CORO7
  hgvsc: ENST00000571756.1:c.114C>T
  hgvsp: ENST00000571756.1:c.114C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000572026
  gene symbol: CORO7
  hgvsc: ENST00000572026.1:n.237C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000446221
  ensembl transcript: ENST00000539968
  gene symbol: CORO7
  hgvsc: ENST00000539968.1:c.-486C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460910
  ensembl transcript: ENST00000575850
  gene symbol: CORO7
  hgvsc: ENST00000575850.1:c.153C>T
  hgvsp: ENST00000575850.1:c.153C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460036
  ensembl transcript: ENST00000571059
  gene symbol: CORO7
  hgvsc: ENST00000571059.1:c.114C>T
  hgvsp: ENST00000571059.1:c.114C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461702
  ensembl transcript: ENST00000574025
  gene symbol: CORO7
  hgvsc: ENST00000574025.1:c.114C>T
  hgvsp: ENST00000574025.1:c.114C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461797
  ensembl transcript: ENST00000575038
  gene symbol: CORO7
  hgvsc: ENST00000575038.1:c.114C>T
  hgvsp: ENST00000575038.1:c.114C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459286
  ensembl transcript: ENST00000572549
  gene symbol: CORO7
  hgvsc: ENST00000572549.1:c.99+3434C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459228
  ensembl transcript: ENST00000576437
  gene symbol: CORO7
  hgvsc: ENST00000576437.1:c.-214+3129C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000576457
  gene symbol: CORO7
  hgvsc: ENST00000576457.1:n.174C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000251166
  ensembl transcript: ENST00000251166
  gene symbol: CORO7
  hgvsc: ENST00000251166.4:c.114C>T
  hgvsp: ENST00000251166.4:c.114C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460199
  ensembl transcript: ENST00000570928
  gene symbol: CORO7
  hgvsc: ENST00000570928.1:c.114C>T
  hgvsp: ENST00000570928.1:c.114C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458935
  ensembl transcript: ENST00000572898
  gene symbol: CORO7
  hgvsc: ENST00000572898.1:c.114C>T
  hgvsp: ENST00000572898.1:c.114C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458459
  ensembl transcript: ENST00000571227
  gene symbol: CORO7
  hgvsc: ENST00000571227.1:c.*111C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458411
  ensembl transcript: ENST00000572044
  gene symbol: CORO7
  hgvsc: ENST00000572044.1:c.60+3108C>T
  variant of: http://identifiers.org/hgnc/26161
canonical: true
consequence: synonymous
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Ile38Ile
num of homozygotes: 0
population: South Asian
population: African
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD

16-4463353-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4463353
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4463353
    reference: chr 16
allele count: 1
allele frequency: 2.90985276145027e-5
allele num: 34366
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000251166
  ensembl transcript: ENST00000251166
  gene symbol: CORO7
  hgvsc: ENST00000251166.4:c.113T>C
  hgvsp: ENSP00000251166.4:p.Ile38Thr
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459286
  ensembl transcript: ENST00000572549
  gene symbol: CORO7
  hgvsc: ENST00000572549.1:c.99+3433T>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000572026
  gene symbol: CORO7
  hgvsc: ENST00000572026.1:n.236T>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461702
  ensembl transcript: ENST00000574025
  gene symbol: CORO7
  hgvsc: ENST00000574025.1:c.113T>C
  hgvsp: ENSP00000461702.1:p.Ile38Thr
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000391530
  ensembl transcript: ENST00000423908
  gene symbol: CORO7
  hgvsc: ENST00000423908.2:c.60+3107T>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460910
  ensembl transcript: ENST00000575850
  gene symbol: CORO7
  hgvsc: ENST00000575850.1:c.152T>C
  hgvsp: ENSP00000460910.1:p.Ile51Thr
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458459
  ensembl transcript: ENST00000571227
  gene symbol: CORO7
  hgvsc: ENST00000571227.1:c.*110T>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460901
  ensembl transcript: ENST00000570645
  gene symbol: CORO7
  hgvsc: ENST00000570645.1:c.-214+3128T>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000440460
  ensembl transcript: ENST00000537233
  gene symbol: CORO7
  hgvsc: ENST00000537233.2:c.113T>C
  hgvsp: ENSP00000440460.2:p.Ile38Thr
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461797
  ensembl transcript: ENST00000575038
  gene symbol: CORO7
  hgvsc: ENST00000575038.1:c.113T>C
  hgvsp: ENSP00000461797.1:p.Ile38Thr
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459085
  ensembl transcript: ENST00000571052
  gene symbol: CORO7
  hgvsc: ENST00000571052.1:c.-268+3107T>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000458607
  ensembl transcript: ENST00000575334
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000575334.1:c.113T>C
  hgvsp: ENSP00000458607.1:p.Ile38Thr
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458411
  ensembl transcript: ENST00000572044
  gene symbol: CORO7
  hgvsc: ENST00000572044.1:c.60+3107T>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458935
  ensembl transcript: ENST00000572898
  gene symbol: CORO7
  hgvsc: ENST00000572898.1:c.113T>C
  hgvsp: ENSP00000458935.1:p.Ile38Thr
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458828
  ensembl transcript: ENST00000571756
  gene symbol: CORO7
  hgvsc: ENST00000571756.1:c.113T>C
  hgvsp: ENSP00000458828.1:p.Ile38Thr
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459888
  ensembl transcript: ENST00000576051
  gene symbol: CORO7
  hgvsc: ENST00000576051.1:c.-387T>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000460885
  ensembl transcript: ENST00000572467
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000572467.1:c.113T>C
  hgvsp: ENSP00000460885.1:p.Ile38Thr
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460036
  ensembl transcript: ENST00000571059
  gene symbol: CORO7
  hgvsc: ENST00000571059.1:c.113T>C
  hgvsp: ENSP00000460036.1:p.Ile38Thr
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000446221
  ensembl transcript: ENST00000539968
  gene symbol: CORO7
  hgvsc: ENST00000539968.1:c.-487T>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000576457
  gene symbol: CORO7
  hgvsc: ENST00000576457.1:n.173T>C
  variant of: http://identifiers.org/hgnc/26161
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Ile38Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: South Asian
population: East Asian
population: Other
reference allele: A
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: DP

16-4463362-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4463362
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4463362
    reference: chr 16
allele count: 1
allele frequency: 2.902589109485661e-5
allele num: 34452
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460901
  ensembl transcript: ENST00000570645
  gene symbol: CORO7
  hgvsc: ENST00000570645.1:c.-214+3119G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000440460
  ensembl transcript: ENST00000537233
  gene symbol: CORO7
  hgvsc: ENST00000537233.2:c.104G>A
  hgvsp: ENSP00000440460.2:p.Arg35Lys
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460199
  ensembl transcript: ENST00000570928
  gene symbol: CORO7
  hgvsc: ENST00000570928.1:c.104G>A
  hgvsp: ENSP00000460199.1:p.Arg35Lys
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461702
  ensembl transcript: ENST00000574025
  gene symbol: CORO7
  hgvsc: ENST00000574025.1:c.104G>A
  hgvsp: ENSP00000461702.1:p.Arg35Lys
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000458607
  ensembl transcript: ENST00000575334
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000575334.1:c.104G>A
  hgvsp: ENSP00000458607.1:p.Arg35Lys
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460036
  ensembl transcript: ENST00000571059
  gene symbol: CORO7
  hgvsc: ENST00000571059.1:c.104G>A
  hgvsp: ENSP00000460036.1:p.Arg35Lys
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459286
  ensembl transcript: ENST00000572549
  gene symbol: CORO7
  hgvsc: ENST00000572549.1:c.99+3424G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000577144
  gene symbol: CORO7
  hgvsc: ENST00000577144.1:n.212G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458935
  ensembl transcript: ENST00000572898
  gene symbol: CORO7
  hgvsc: ENST00000572898.1:c.104G>A
  hgvsp: ENSP00000458935.1:p.Arg35Lys
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461797
  ensembl transcript: ENST00000575038
  gene symbol: CORO7
  hgvsc: ENST00000575038.1:c.104G>A
  hgvsp: ENSP00000461797.1:p.Arg35Lys
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460910
  ensembl transcript: ENST00000575850
  gene symbol: CORO7
  hgvsc: ENST00000575850.1:c.143G>A
  hgvsp: ENSP00000460910.1:p.Arg48Lys
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458411
  ensembl transcript: ENST00000572044
  gene symbol: CORO7
  hgvsc: ENST00000572044.1:c.60+3098G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458828
  ensembl transcript: ENST00000571756
  gene symbol: CORO7
  hgvsc: ENST00000571756.1:c.104G>A
  hgvsp: ENSP00000458828.1:p.Arg35Lys
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000391530
  ensembl transcript: ENST00000423908
  gene symbol: CORO7
  hgvsc: ENST00000423908.2:c.60+3098G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000460885
  ensembl transcript: ENST00000572467
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000572467.1:c.104G>A
  hgvsp: ENSP00000460885.1:p.Arg35Lys
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000576457
  gene symbol: CORO7
  hgvsc: ENST00000576457.1:n.164G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000446221
  ensembl transcript: ENST00000539968
  gene symbol: CORO7
  hgvsc: ENST00000539968.1:c.-496G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459228
  ensembl transcript: ENST00000576437
  gene symbol: CORO7
  hgvsc: ENST00000576437.1:c.-214+3119G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459888
  ensembl transcript: ENST00000576051
  gene symbol: CORO7
  hgvsc: ENST00000576051.1:c.-396G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000251166
  ensembl transcript: ENST00000251166
  gene symbol: CORO7
  hgvsc: ENST00000251166.4:c.104G>A
  hgvsp: ENSP00000251166.4:p.Arg35Lys
  variant of: http://identifiers.org/hgnc/26161
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Arg35Lys
num of homozygotes: 0
population: European (Finnish)
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: DP

16-4463370-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4463370
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4463370
    reference: chr 16
allele count: 2
allele frequency: 5.914709883480215e-5
allele num: 33814
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461187
  ensembl transcript: ENST00000574311
  gene symbol: CORO7
  hgvsc: ENST00000574311.1:c.60+3090T>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458411
  ensembl transcript: ENST00000572044
  gene symbol: CORO7
  hgvsc: ENST00000572044.1:c.60+3090T>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000576457
  gene symbol: CORO7
  hgvsc: ENST00000576457.1:n.156T>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458935
  ensembl transcript: ENST00000572898
  gene symbol: CORO7
  hgvsc: ENST00000572898.1:c.96T>C
  hgvsp: ENST00000572898.1:c.96T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460910
  ensembl transcript: ENST00000575850
  gene symbol: CORO7
  hgvsc: ENST00000575850.1:c.135T>C
  hgvsp: ENST00000575850.1:c.135T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460901
  ensembl transcript: ENST00000570645
  gene symbol: CORO7
  hgvsc: ENST00000570645.1:c.-214+3111T>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000391530
  ensembl transcript: ENST00000423908
  gene symbol: CORO7
  hgvsc: ENST00000423908.2:c.60+3090T>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460036
  ensembl transcript: ENST00000571059
  gene symbol: CORO7
  hgvsc: ENST00000571059.1:c.96T>C
  hgvsp: ENST00000571059.1:c.96T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458828
  ensembl transcript: ENST00000571756
  gene symbol: CORO7
  hgvsc: ENST00000571756.1:c.96T>C
  hgvsp: ENST00000571756.1:c.96T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000572026
  gene symbol: CORO7
  hgvsc: ENST00000572026.1:n.219T>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000577144
  gene symbol: CORO7
  hgvsc: ENST00000577144.1:n.204T>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459085
  ensembl transcript: ENST00000571052
  gene symbol: CORO7
  hgvsc: ENST00000571052.1:c.-268+3090T>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461797
  ensembl transcript: ENST00000575038
  gene symbol: CORO7
  hgvsc: ENST00000575038.1:c.96T>C
  hgvsp: ENST00000575038.1:c.96T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458459
  ensembl transcript: ENST00000571227
  gene symbol: CORO7
  hgvsc: ENST00000571227.1:c.*93T>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000460885
  ensembl transcript: ENST00000572467
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000572467.1:c.96T>C
  hgvsp: ENST00000572467.1:c.96T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461702
  ensembl transcript: ENST00000574025
  gene symbol: CORO7
  hgvsc: ENST00000574025.1:c.96T>C
  hgvsp: ENST00000574025.1:c.96T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000440460
  ensembl transcript: ENST00000537233
  gene symbol: CORO7
  hgvsc: ENST00000537233.2:c.96T>C
  hgvsp: ENST00000537233.2:c.96T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459228
  ensembl transcript: ENST00000576437
  gene symbol: CORO7
  hgvsc: ENST00000576437.1:c.-214+3111T>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000251166
  ensembl transcript: ENST00000251166
  gene symbol: CORO7
  hgvsc: ENST00000251166.4:c.96T>C
  hgvsp: ENST00000251166.4:c.96T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461051
  ensembl transcript: ENST00000572153
  gene symbol: CORO7
  hgvsc: ENST00000572153.1:c.61-939T>C
  variant of: http://identifiers.org/hgnc/26161
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Pro32Pro
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: FS
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum

16-4463375-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4463375
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4463375
    reference: chr 16
allele count: 2
allele frequency: 6.048874909266876e-5
allele num: 33064
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000577144
  gene symbol: CORO7
  hgvsc: ENST00000577144.1:n.199G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458935
  ensembl transcript: ENST00000572898
  gene symbol: CORO7
  hgvsc: ENST00000572898.1:c.91G>A
  hgvsp: ENSP00000458935.1:p.Ala31Thr
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458828
  ensembl transcript: ENST00000571756
  gene symbol: CORO7
  hgvsc: ENST00000571756.1:c.91G>A
  hgvsp: ENSP00000458828.1:p.Ala31Thr
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461702
  ensembl transcript: ENST00000574025
  gene symbol: CORO7
  hgvsc: ENST00000574025.1:c.91G>A
  hgvsp: ENSP00000461702.1:p.Ala31Thr
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000458607
  ensembl transcript: ENST00000575334
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000575334.1:c.91G>A
  hgvsp: ENSP00000458607.1:p.Ala31Thr
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000446221
  ensembl transcript: ENST00000539968
  gene symbol: CORO7
  hgvsc: ENST00000539968.1:c.-509G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460901
  ensembl transcript: ENST00000570645
  gene symbol: CORO7
  hgvsc: ENST00000570645.1:c.-214+3106G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461187
  ensembl transcript: ENST00000574311
  gene symbol: CORO7
  hgvsc: ENST00000574311.1:c.60+3085G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000572026
  gene symbol: CORO7
  hgvsc: ENST00000572026.1:n.214G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461797
  ensembl transcript: ENST00000575038
  gene symbol: CORO7
  hgvsc: ENST00000575038.1:c.91G>A
  hgvsp: ENSP00000461797.1:p.Ala31Thr
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000460885
  ensembl transcript: ENST00000572467
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000572467.1:c.91G>A
  hgvsp: ENSP00000460885.1:p.Ala31Thr
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000576457
  gene symbol: CORO7
  hgvsc: ENST00000576457.1:n.151G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458459
  ensembl transcript: ENST00000571227
  gene symbol: CORO7
  hgvsc: ENST00000571227.1:c.*88G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460199
  ensembl transcript: ENST00000570928
  gene symbol: CORO7
  hgvsc: ENST00000570928.1:c.91G>A
  hgvsp: ENSP00000460199.1:p.Ala31Thr
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459228
  ensembl transcript: ENST00000576437
  gene symbol: CORO7
  hgvsc: ENST00000576437.1:c.-214+3106G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460910
  ensembl transcript: ENST00000575850
  gene symbol: CORO7
  hgvsc: ENST00000575850.1:c.130G>A
  hgvsp: ENSP00000460910.1:p.Ala44Thr
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460036
  ensembl transcript: ENST00000571059
  gene symbol: CORO7
  hgvsc: ENST00000571059.1:c.91G>A
  hgvsp: ENSP00000460036.1:p.Ala31Thr
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459286
  ensembl transcript: ENST00000572549
  gene symbol: CORO7
  hgvsc: ENST00000572549.1:c.99+3411G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461051
  ensembl transcript: ENST00000572153
  gene symbol: CORO7
  hgvsc: ENST00000572153.1:c.61-944G>A
  variant of: http://identifiers.org/hgnc/26161
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Ala31Thr
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: DP

16-4463376-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4463376
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4463376
    reference: chr 16
allele count: 2
allele frequency: 6.051071039574004e-5
allele num: 33052
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000577144
  gene symbol: CORO7
  hgvsc: ENST00000577144.1:n.198C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000576457
  gene symbol: CORO7
  hgvsc: ENST00000576457.1:n.150C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000572026
  gene symbol: CORO7
  hgvsc: ENST00000572026.1:n.213C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000391530
  ensembl transcript: ENST00000423908
  gene symbol: CORO7
  hgvsc: ENST00000423908.2:c.60+3084C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459888
  ensembl transcript: ENST00000576051
  gene symbol: CORO7
  hgvsc: ENST00000576051.1:c.-410C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000446221
  ensembl transcript: ENST00000539968
  gene symbol: CORO7
  hgvsc: ENST00000539968.1:c.-510C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000460885
  ensembl transcript: ENST00000572467
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000572467.1:c.90C>T
  hgvsp: ENST00000572467.1:c.90C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459085
  ensembl transcript: ENST00000571052
  gene symbol: CORO7
  hgvsc: ENST00000571052.1:c.-268+3084C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458459
  ensembl transcript: ENST00000571227
  gene symbol: CORO7
  hgvsc: ENST00000571227.1:c.*87C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460036
  ensembl transcript: ENST00000571059
  gene symbol: CORO7
  hgvsc: ENST00000571059.1:c.90C>T
  hgvsp: ENST00000571059.1:c.90C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461702
  ensembl transcript: ENST00000574025
  gene symbol: CORO7
  hgvsc: ENST00000574025.1:c.90C>T
  hgvsp: ENST00000574025.1:c.90C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460199
  ensembl transcript: ENST00000570928
  gene symbol: CORO7
  hgvsc: ENST00000570928.1:c.90C>T
  hgvsp: ENST00000570928.1:c.90C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460910
  ensembl transcript: ENST00000575850
  gene symbol: CORO7
  hgvsc: ENST00000575850.1:c.129C>T
  hgvsp: ENST00000575850.1:c.129C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000440460
  ensembl transcript: ENST00000537233
  gene symbol: CORO7
  hgvsc: ENST00000537233.2:c.90C>T
  hgvsp: ENST00000537233.2:c.90C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458935
  ensembl transcript: ENST00000572898
  gene symbol: CORO7
  hgvsc: ENST00000572898.1:c.90C>T
  hgvsp: ENST00000572898.1:c.90C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461797
  ensembl transcript: ENST00000575038
  gene symbol: CORO7
  hgvsc: ENST00000575038.1:c.90C>T
  hgvsp: ENST00000575038.1:c.90C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458828
  ensembl transcript: ENST00000571756
  gene symbol: CORO7
  hgvsc: ENST00000571756.1:c.90C>T
  hgvsp: ENST00000571756.1:c.90C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460901
  ensembl transcript: ENST00000570645
  gene symbol: CORO7
  hgvsc: ENST00000570645.1:c.-214+3105C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461187
  ensembl transcript: ENST00000574311
  gene symbol: CORO7
  hgvsc: ENST00000574311.1:c.60+3084C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459286
  ensembl transcript: ENST00000572549
  gene symbol: CORO7
  hgvsc: ENST00000572549.1:c.99+3410C>T
  variant of: http://identifiers.org/hgnc/26161
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Thr30Thr
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
population: East Asian
reference allele: G
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP

16-4463383-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4463383
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4463383
    reference: chr 16
allele count: 4
allele frequency: 1.237930180737806e-4
allele num: 32312
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000460885
  ensembl transcript: ENST00000572467
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000572467.1:c.83C>T
  hgvsp: ENSP00000460885.1:p.Ala28Val
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461797
  ensembl transcript: ENST00000575038
  gene symbol: CORO7
  hgvsc: ENST00000575038.1:c.83C>T
  hgvsp: ENSP00000461797.1:p.Ala28Val
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459286
  ensembl transcript: ENST00000572549
  gene symbol: CORO7
  hgvsc: ENST00000572549.1:c.99+3403C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459228
  ensembl transcript: ENST00000576437
  gene symbol: CORO7
  hgvsc: ENST00000576437.1:c.-214+3098C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460901
  ensembl transcript: ENST00000570645
  gene symbol: CORO7
  hgvsc: ENST00000570645.1:c.-214+3098C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000458607
  ensembl transcript: ENST00000575334
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000575334.1:c.83C>T
  hgvsp: ENSP00000458607.1:p.Ala28Val
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460036
  ensembl transcript: ENST00000571059
  gene symbol: CORO7
  hgvsc: ENST00000571059.1:c.83C>T
  hgvsp: ENSP00000460036.1:p.Ala28Val
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459888
  ensembl transcript: ENST00000576051
  gene symbol: CORO7
  hgvsc: ENST00000576051.1:c.-417C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460199
  ensembl transcript: ENST00000570928
  gene symbol: CORO7
  hgvsc: ENST00000570928.1:c.83C>T
  hgvsp: ENSP00000460199.1:p.Ala28Val
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000440460
  ensembl transcript: ENST00000537233
  gene symbol: CORO7
  hgvsc: ENST00000537233.2:c.83C>T
  hgvsp: ENSP00000440460.2:p.Ala28Val
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459085
  ensembl transcript: ENST00000571052
  gene symbol: CORO7
  hgvsc: ENST00000571052.1:c.-268+3077C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000577144
  gene symbol: CORO7
  hgvsc: ENST00000577144.1:n.191C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000391530
  ensembl transcript: ENST00000423908
  gene symbol: CORO7
  hgvsc: ENST00000423908.2:c.60+3077C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461702
  ensembl transcript: ENST00000574025
  gene symbol: CORO7
  hgvsc: ENST00000574025.1:c.83C>T
  hgvsp: ENSP00000461702.1:p.Ala28Val
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458411
  ensembl transcript: ENST00000572044
  gene symbol: CORO7
  hgvsc: ENST00000572044.1:c.60+3077C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458935
  ensembl transcript: ENST00000572898
  gene symbol: CORO7
  hgvsc: ENST00000572898.1:c.83C>T
  hgvsp: ENSP00000458935.1:p.Ala28Val
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000251166
  ensembl transcript: ENST00000251166
  gene symbol: CORO7
  hgvsc: ENST00000251166.4:c.83C>T
  hgvsp: ENSP00000251166.4:p.Ala28Val
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460910
  ensembl transcript: ENST00000575850
  gene symbol: CORO7
  hgvsc: ENST00000575850.1:c.122C>T
  hgvsp: ENSP00000460910.1:p.Ala41Val
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461187
  ensembl transcript: ENST00000574311
  gene symbol: CORO7
  hgvsc: ENST00000574311.1:c.60+3077C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458459
  ensembl transcript: ENST00000571227
  gene symbol: CORO7
  hgvsc: ENST00000571227.1:c.*80C>T
  variant of: http://identifiers.org/hgnc/26161
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Ala28Val
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
population: East Asian
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: BaseQRankSum

16-4463386-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4463386
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4463386
    reference: chr 16
allele count: 1
allele frequency: 3.133224714876551e-5
allele num: 31916
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000391530
  ensembl transcript: ENST00000423908
  gene symbol: CORO7
  hgvsc: ENST00000423908.2:c.60+3074G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459888
  ensembl transcript: ENST00000576051
  gene symbol: CORO7
  hgvsc: ENST00000576051.1:c.-420G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000460885
  ensembl transcript: ENST00000572467
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000572467.1:c.80G>A
  hgvsp: ENSP00000460885.1:p.Arg27Gln
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000251166
  ensembl transcript: ENST00000251166
  gene symbol: CORO7
  hgvsc: ENST00000251166.4:c.80G>A
  hgvsp: ENSP00000251166.4:p.Arg27Gln
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461702
  ensembl transcript: ENST00000574025
  gene symbol: CORO7
  hgvsc: ENST00000574025.1:c.80G>A
  hgvsp: ENSP00000461702.1:p.Arg27Gln
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000576457
  gene symbol: CORO7
  hgvsc: ENST00000576457.1:n.140G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460910
  ensembl transcript: ENST00000575850
  gene symbol: CORO7
  hgvsc: ENST00000575850.1:c.119G>A
  hgvsp: ENSP00000460910.1:p.Arg40Gln
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000440460
  ensembl transcript: ENST00000537233
  gene symbol: CORO7
  hgvsc: ENST00000537233.2:c.80G>A
  hgvsp: ENSP00000440460.2:p.Arg27Gln
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458459
  ensembl transcript: ENST00000571227
  gene symbol: CORO7
  hgvsc: ENST00000571227.1:c.*77G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458828
  ensembl transcript: ENST00000571756
  gene symbol: CORO7
  hgvsc: ENST00000571756.1:c.80G>A
  hgvsp: ENSP00000458828.1:p.Arg27Gln
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458411
  ensembl transcript: ENST00000572044
  gene symbol: CORO7
  hgvsc: ENST00000572044.1:c.60+3074G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459085
  ensembl transcript: ENST00000571052
  gene symbol: CORO7
  hgvsc: ENST00000571052.1:c.-268+3074G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460036
  ensembl transcript: ENST00000571059
  gene symbol: CORO7
  hgvsc: ENST00000571059.1:c.80G>A
  hgvsp: ENSP00000460036.1:p.Arg27Gln
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000458607
  ensembl transcript: ENST00000575334
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000575334.1:c.80G>A
  hgvsp: ENSP00000458607.1:p.Arg27Gln
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461187
  ensembl transcript: ENST00000574311
  gene symbol: CORO7
  hgvsc: ENST00000574311.1:c.60+3074G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000446221
  ensembl transcript: ENST00000539968
  gene symbol: CORO7
  hgvsc: ENST00000539968.1:c.-520G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000572026
  gene symbol: CORO7
  hgvsc: ENST00000572026.1:n.203G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000577144
  gene symbol: CORO7
  hgvsc: ENST00000577144.1:n.188G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460199
  ensembl transcript: ENST00000570928
  gene symbol: CORO7
  hgvsc: ENST00000570928.1:c.80G>A
  hgvsp: ENSP00000460199.1:p.Arg27Gln
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461051
  ensembl transcript: ENST00000572153
  gene symbol: CORO7
  hgvsc: ENST00000572153.1:c.61-955G>A
  variant of: http://identifiers.org/hgnc/26161
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Arg27Gln
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
reference allele: C
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP

16-4463387-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4463387
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4463387
    reference: chr 16
allele count: 2
allele frequency: 6.357279084551812e-5
allele num: 31460
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458828
  ensembl transcript: ENST00000571756
  gene symbol: CORO7
  hgvsc: ENST00000571756.1:c.79C>T
  hgvsp: ENSP00000458828.1:p.Arg27Ter
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460910
  ensembl transcript: ENST00000575850
  gene symbol: CORO7
  hgvsc: ENST00000575850.1:c.118C>T
  hgvsp: ENSP00000460910.1:p.Arg40Ter
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461702
  ensembl transcript: ENST00000574025
  gene symbol: CORO7
  hgvsc: ENST00000574025.1:c.79C>T
  hgvsp: ENSP00000461702.1:p.Arg27Ter
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000576457
  gene symbol: CORO7
  hgvsc: ENST00000576457.1:n.139C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458459
  ensembl transcript: ENST00000571227
  gene symbol: CORO7
  hgvsc: ENST00000571227.1:c.*76C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000572026
  gene symbol: CORO7
  hgvsc: ENST00000572026.1:n.202C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458411
  ensembl transcript: ENST00000572044
  gene symbol: CORO7
  hgvsc: ENST00000572044.1:c.60+3073C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000446221
  ensembl transcript: ENST00000539968
  gene symbol: CORO7
  hgvsc: ENST00000539968.1:c.-521C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458935
  ensembl transcript: ENST00000572898
  gene symbol: CORO7
  hgvsc: ENST00000572898.1:c.79C>T
  hgvsp: ENSP00000458935.1:p.Arg27Ter
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460036
  ensembl transcript: ENST00000571059
  gene symbol: CORO7
  hgvsc: ENST00000571059.1:c.79C>T
  hgvsp: ENSP00000460036.1:p.Arg27Ter
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460901
  ensembl transcript: ENST00000570645
  gene symbol: CORO7
  hgvsc: ENST00000570645.1:c.-214+3094C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461187
  ensembl transcript: ENST00000574311
  gene symbol: CORO7
  hgvsc: ENST00000574311.1:c.60+3073C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000458607
  ensembl transcript: ENST00000575334
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000575334.1:c.79C>T
  hgvsp: ENSP00000458607.1:p.Arg27Ter
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459228
  ensembl transcript: ENST00000576437
  gene symbol: CORO7
  hgvsc: ENST00000576437.1:c.-214+3094C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460199
  ensembl transcript: ENST00000570928
  gene symbol: CORO7
  hgvsc: ENST00000570928.1:c.79C>T
  hgvsp: ENSP00000460199.1:p.Arg27Ter
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461797
  ensembl transcript: ENST00000575038
  gene symbol: CORO7
  hgvsc: ENST00000575038.1:c.79C>T
  hgvsp: ENSP00000461797.1:p.Arg27Ter
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000460885
  ensembl transcript: ENST00000572467
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000572467.1:c.79C>T
  hgvsp: ENSP00000460885.1:p.Arg27Ter
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459888
  ensembl transcript: ENST00000576051
  gene symbol: CORO7
  hgvsc: ENST00000576051.1:c.-421C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000440460
  ensembl transcript: ENST00000537233
  gene symbol: CORO7
  hgvsc: ENST00000537233.2:c.79C>T
  hgvsp: ENSP00000440460.2:p.Arg27Ter
  variant of: http://identifiers.org/hgnc/26161
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Arg27Ter
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum

16-4463392-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4463392
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4463392
    reference: chr 16
allele count: 1
allele frequency: 3.206361421059382e-5
allele num: 31188
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458935
  ensembl transcript: ENST00000572898
  gene symbol: CORO7
  hgvsc: ENST00000572898.1:c.74A>G
  hgvsp: ENSP00000458935.1:p.Asp25Gly
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000460885
  ensembl transcript: ENST00000572467
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000572467.1:c.74A>G
  hgvsp: ENSP00000460885.1:p.Asp25Gly
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459888
  ensembl transcript: ENST00000576051
  gene symbol: CORO7
  hgvsc: ENST00000576051.1:c.-426A>G
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460036
  ensembl transcript: ENST00000571059
  gene symbol: CORO7
  hgvsc: ENST00000571059.1:c.74A>G
  hgvsp: ENSP00000460036.1:p.Asp25Gly
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459085
  ensembl transcript: ENST00000571052
  gene symbol: CORO7
  hgvsc: ENST00000571052.1:c.-268+3068A>G
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000440460
  ensembl transcript: ENST00000537233
  gene symbol: CORO7
  hgvsc: ENST00000537233.2:c.74A>G
  hgvsp: ENSP00000440460.2:p.Asp25Gly
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461702
  ensembl transcript: ENST00000574025
  gene symbol: CORO7
  hgvsc: ENST00000574025.1:c.74A>G
  hgvsp: ENSP00000461702.1:p.Asp25Gly
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000572026
  gene symbol: CORO7
  hgvsc: ENST00000572026.1:n.197A>G
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000458607
  ensembl transcript: ENST00000575334
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000575334.1:c.74A>G
  hgvsp: ENSP00000458607.1:p.Asp25Gly
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461797
  ensembl transcript: ENST00000575038
  gene symbol: CORO7
  hgvsc: ENST00000575038.1:c.74A>G
  hgvsp: ENSP00000461797.1:p.Asp25Gly
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460910
  ensembl transcript: ENST00000575850
  gene symbol: CORO7
  hgvsc: ENST00000575850.1:c.113A>G
  hgvsp: ENSP00000460910.1:p.Asp38Gly
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000446221
  ensembl transcript: ENST00000539968
  gene symbol: CORO7
  hgvsc: ENST00000539968.1:c.-526A>G
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459286
  ensembl transcript: ENST00000572549
  gene symbol: CORO7
  hgvsc: ENST00000572549.1:c.99+3394A>G
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000251166
  ensembl transcript: ENST00000251166
  gene symbol: CORO7
  hgvsc: ENST00000251166.4:c.74A>G
  hgvsp: ENSP00000251166.4:p.Asp25Gly
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459228
  ensembl transcript: ENST00000576437
  gene symbol: CORO7
  hgvsc: ENST00000576437.1:c.-214+3089A>G
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460901
  ensembl transcript: ENST00000570645
  gene symbol: CORO7
  hgvsc: ENST00000570645.1:c.-214+3089A>G
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000391530
  ensembl transcript: ENST00000423908
  gene symbol: CORO7
  hgvsc: ENST00000423908.2:c.60+3068A>G
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458828
  ensembl transcript: ENST00000571756
  gene symbol: CORO7
  hgvsc: ENST00000571756.1:c.74A>G
  hgvsp: ENSP00000458828.1:p.Asp25Gly
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000577144
  gene symbol: CORO7
  hgvsc: ENST00000577144.1:n.182A>G
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458459
  ensembl transcript: ENST00000571227
  gene symbol: CORO7
  hgvsc: ENST00000571227.1:c.*71A>G
  variant of: http://identifiers.org/hgnc/26161
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Asp25Gly
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
reference allele: T
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: MQ

16-4463399-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4463399
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4463399
    reference: chr 16
allele count: 2
allele frequency: 6.635259770420012e-5
allele num: 30142
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000576457
  gene symbol: CORO7
  hgvsc: ENST00000576457.1:n.127A>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459286
  ensembl transcript: ENST00000572549
  gene symbol: CORO7
  hgvsc: ENST00000572549.1:c.99+3387A>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460910
  ensembl transcript: ENST00000575850
  gene symbol: CORO7
  hgvsc: ENST00000575850.1:c.106A>T
  hgvsp: ENSP00000460910.1:p.Ile36Phe
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458411
  ensembl transcript: ENST00000572044
  gene symbol: CORO7
  hgvsc: ENST00000572044.1:c.60+3061A>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000460885
  ensembl transcript: ENST00000572467
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000572467.1:c.67A>T
  hgvsp: ENSP00000460885.1:p.Ile23Phe
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458935
  ensembl transcript: ENST00000572898
  gene symbol: CORO7
  hgvsc: ENST00000572898.1:c.67A>T
  hgvsp: ENSP00000458935.1:p.Ile23Phe
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000577144
  gene symbol: CORO7
  hgvsc: ENST00000577144.1:n.175A>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460199
  ensembl transcript: ENST00000570928
  gene symbol: CORO7
  hgvsc: ENST00000570928.1:c.67A>T
  hgvsp: ENSP00000460199.1:p.Ile23Phe
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458459
  ensembl transcript: ENST00000571227
  gene symbol: CORO7
  hgvsc: ENST00000571227.1:c.*64A>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461702
  ensembl transcript: ENST00000574025
  gene symbol: CORO7
  hgvsc: ENST00000574025.1:c.67A>T
  hgvsp: ENSP00000461702.1:p.Ile23Phe
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000458607
  ensembl transcript: ENST00000575334
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000575334.1:c.67A>T
  hgvsp: ENSP00000458607.1:p.Ile23Phe
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461797
  ensembl transcript: ENST00000575038
  gene symbol: CORO7
  hgvsc: ENST00000575038.1:c.67A>T
  hgvsp: ENSP00000461797.1:p.Ile23Phe
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458828
  ensembl transcript: ENST00000571756
  gene symbol: CORO7
  hgvsc: ENST00000571756.1:c.67A>T
  hgvsp: ENSP00000458828.1:p.Ile23Phe
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000251166
  ensembl transcript: ENST00000251166
  gene symbol: CORO7
  hgvsc: ENST00000251166.4:c.67A>T
  hgvsp: ENSP00000251166.4:p.Ile23Phe
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459085
  ensembl transcript: ENST00000571052
  gene symbol: CORO7
  hgvsc: ENST00000571052.1:c.-268+3061A>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460036
  ensembl transcript: ENST00000571059
  gene symbol: CORO7
  hgvsc: ENST00000571059.1:c.67A>T
  hgvsp: ENSP00000460036.1:p.Ile23Phe
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461051
  ensembl transcript: ENST00000572153
  gene symbol: CORO7
  hgvsc: ENST00000572153.1:c.61-968A>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000572026
  gene symbol: CORO7
  hgvsc: ENST00000572026.1:n.190A>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000440460
  ensembl transcript: ENST00000537233
  gene symbol: CORO7
  hgvsc: ENST00000537233.2:c.67A>T
  hgvsp: ENSP00000440460.2:p.Ile23Phe
  variant of: http://identifiers.org/hgnc/26161
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Ile23Phe
num of homozygotes: 0
population: Other
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: T
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum

16-4463401-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4463401
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4463401
    reference: chr 16
allele count: 0
allele frequency: 0.0e0
allele num: 29662
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458459
  ensembl transcript: ENST00000571227
  gene symbol: CORO7
  hgvsc: ENST00000571227.1:c.*62G>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460036
  ensembl transcript: ENST00000571059
  gene symbol: CORO7
  hgvsc: ENST00000571059.1:c.65G>C
  hgvsp: ENSP00000460036.1:p.Trp22Ser
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459888
  ensembl transcript: ENST00000576051
  gene symbol: CORO7
  hgvsc: ENST00000576051.1:c.-435G>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000251166
  ensembl transcript: ENST00000251166
  gene symbol: CORO7
  hgvsc: ENST00000251166.4:c.65G>C
  hgvsp: ENSP00000251166.4:p.Trp22Ser
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000458607
  ensembl transcript: ENST00000575334
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000575334.1:c.65G>C
  hgvsp: ENSP00000458607.1:p.Trp22Ser
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000576457
  gene symbol: CORO7
  hgvsc: ENST00000576457.1:n.125G>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000572026
  gene symbol: CORO7
  hgvsc: ENST00000572026.1:n.188G>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458828
  ensembl transcript: ENST00000571756
  gene symbol: CORO7
  hgvsc: ENST00000571756.1:c.65G>C
  hgvsp: ENSP00000458828.1:p.Trp22Ser
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461702
  ensembl transcript: ENST00000574025
  gene symbol: CORO7
  hgvsc: ENST00000574025.1:c.65G>C
  hgvsp: ENSP00000461702.1:p.Trp22Ser
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458935
  ensembl transcript: ENST00000572898
  gene symbol: CORO7
  hgvsc: ENST00000572898.1:c.65G>C
  hgvsp: ENSP00000458935.1:p.Trp22Ser
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459286
  ensembl transcript: ENST00000572549
  gene symbol: CORO7
  hgvsc: ENST00000572549.1:c.99+3385G>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461797
  ensembl transcript: ENST00000575038
  gene symbol: CORO7
  hgvsc: ENST00000575038.1:c.65G>C
  hgvsp: ENSP00000461797.1:p.Trp22Ser
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000391530
  ensembl transcript: ENST00000423908
  gene symbol: CORO7
  hgvsc: ENST00000423908.2:c.60+3059G>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460910
  ensembl transcript: ENST00000575850
  gene symbol: CORO7
  hgvsc: ENST00000575850.1:c.104G>C
  hgvsp: ENSP00000460910.1:p.Trp35Ser
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000460885
  ensembl transcript: ENST00000572467
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000572467.1:c.65G>C
  hgvsp: ENSP00000460885.1:p.Trp22Ser
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000440460
  ensembl transcript: ENST00000537233
  gene symbol: CORO7
  hgvsc: ENST00000537233.2:c.65G>C
  hgvsp: ENSP00000440460.2:p.Trp22Ser
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460901
  ensembl transcript: ENST00000570645
  gene symbol: CORO7
  hgvsc: ENST00000570645.1:c.-214+3080G>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459228
  ensembl transcript: ENST00000576437
  gene symbol: CORO7
  hgvsc: ENST00000576437.1:c.-214+3080G>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461187
  ensembl transcript: ENST00000574311
  gene symbol: CORO7
  hgvsc: ENST00000574311.1:c.60+3059G>C
  variant of: http://identifiers.org/hgnc/26161
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Trp22Ser
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
population: South Asian
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: QD

16-4463417-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4463417
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4463417
    reference: chr 16
allele count: 1
allele frequency: 3.991060025542784e-5
allele num: 25056
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461702
  ensembl transcript: ENST00000574025
  gene symbol: CORO7
  hgvsc: ENST00000574025.1:c.61-12C>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000446221
  ensembl transcript: ENST00000539968
  gene symbol: CORO7
  hgvsc: ENST00000539968.1:c.-539-12C>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461797
  ensembl transcript: ENST00000575038
  gene symbol: CORO7
  hgvsc: ENST00000575038.1:c.61-12C>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459286
  ensembl transcript: ENST00000572549
  gene symbol: CORO7
  hgvsc: ENST00000572549.1:c.99+3369C>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000460885
  ensembl transcript: ENST00000572467
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000572467.1:c.61-12C>A
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459888
  ensembl transcript: ENST00000576051
  gene symbol: CORO7
  hgvsc: ENST00000576051.1:c.-451C>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000572026
  gene symbol: CORO7
  hgvsc: ENST00000572026.1:n.184-12C>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460199
  ensembl transcript: ENST00000570928
  gene symbol: CORO7
  hgvsc: ENST00000570928.1:c.61-12C>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459228
  ensembl transcript: ENST00000576437
  gene symbol: CORO7
  hgvsc: ENST00000576437.1:c.-214+3064C>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459085
  ensembl transcript: ENST00000571052
  gene symbol: CORO7
  hgvsc: ENST00000571052.1:c.-268+3043C>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000577144
  gene symbol: CORO7
  hgvsc: ENST00000577144.1:n.169-12C>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460910
  ensembl transcript: ENST00000575850
  gene symbol: CORO7
  hgvsc: ENST00000575850.1:c.100-12C>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458411
  ensembl transcript: ENST00000572044
  gene symbol: CORO7
  hgvsc: ENST00000572044.1:c.60+3043C>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000458607
  ensembl transcript: ENST00000575334
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000575334.1:c.61-12C>A
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460901
  ensembl transcript: ENST00000570645
  gene symbol: CORO7
  hgvsc: ENST00000570645.1:c.-214+3064C>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458935
  ensembl transcript: ENST00000572898
  gene symbol: CORO7
  hgvsc: ENST00000572898.1:c.61-12C>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000576457
  gene symbol: CORO7
  hgvsc: ENST00000576457.1:n.121-12C>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458828
  ensembl transcript: ENST00000571756
  gene symbol: CORO7
  hgvsc: ENST00000571756.1:c.61-12C>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461187
  ensembl transcript: ENST00000574311
  gene symbol: CORO7
  hgvsc: ENST00000574311.1:c.60+3043C>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000440460
  ensembl transcript: ENST00000537233
  gene symbol: CORO7
  hgvsc: ENST00000537233.2:c.61-12C>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000251166
  ensembl transcript: ENST00000251166
  gene symbol: CORO7
  hgvsc: ENST00000251166.4:c.61-12C>A
  variant of: http://identifiers.org/hgnc/26161
canonical: false
consequence: 5' UTR
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
population: European (Finnish)
population: East Asian
population: Latino
reference allele: G
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum

16-4463421-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4463421
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4463421
    reference: chr 16
allele count: 1
allele frequency: 4.123371268349002e-5
allele num: 24252
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000460885
  ensembl transcript: ENST00000572467
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000572467.1:c.61-16T>A
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000440460
  ensembl transcript: ENST00000537233
  gene symbol: CORO7
  hgvsc: ENST00000537233.2:c.61-16T>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460910
  ensembl transcript: ENST00000575850
  gene symbol: CORO7
  hgvsc: ENST00000575850.1:c.100-16T>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000391530
  ensembl transcript: ENST00000423908
  gene symbol: CORO7
  hgvsc: ENST00000423908.2:c.60+3039T>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458459
  ensembl transcript: ENST00000571227
  gene symbol: CORO7
  hgvsc: ENST00000571227.1:c.*58-16T>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000458607
  ensembl transcript: ENST00000575334
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000575334.1:c.61-16T>A
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461702
  ensembl transcript: ENST00000574025
  gene symbol: CORO7
  hgvsc: ENST00000574025.1:c.61-16T>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459888
  ensembl transcript: ENST00000576051
  gene symbol: CORO7
  hgvsc: ENST00000576051.1:c.-455T>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461051
  ensembl transcript: ENST00000572153
  gene symbol: CORO7
  hgvsc: ENST00000572153.1:c.61-990T>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459228
  ensembl transcript: ENST00000576437
  gene symbol: CORO7
  hgvsc: ENST00000576437.1:c.-214+3060T>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459085
  ensembl transcript: ENST00000571052
  gene symbol: CORO7
  hgvsc: ENST00000571052.1:c.-268+3039T>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000577144
  gene symbol: CORO7
  hgvsc: ENST00000577144.1:n.169-16T>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458411
  ensembl transcript: ENST00000572044
  gene symbol: CORO7
  hgvsc: ENST00000572044.1:c.60+3039T>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000446221
  ensembl transcript: ENST00000539968
  gene symbol: CORO7
  hgvsc: ENST00000539968.1:c.-539-16T>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000251166
  ensembl transcript: ENST00000251166
  gene symbol: CORO7
  hgvsc: ENST00000251166.4:c.61-16T>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458828
  ensembl transcript: ENST00000571756
  gene symbol: CORO7
  hgvsc: ENST00000571756.1:c.61-16T>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460036
  ensembl transcript: ENST00000571059
  gene symbol: CORO7
  hgvsc: ENST00000571059.1:c.61-16T>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461797
  ensembl transcript: ENST00000575038
  gene symbol: CORO7
  hgvsc: ENST00000575038.1:c.61-16T>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458935
  ensembl transcript: ENST00000572898
  gene symbol: CORO7
  hgvsc: ENST00000572898.1:c.61-16T>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000576457
  gene symbol: CORO7
  hgvsc: ENST00000576457.1:n.121-16T>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459286
  ensembl transcript: ENST00000572549
  gene symbol: CORO7
  hgvsc: ENST00000572549.1:c.99+3365T>A
  variant of: http://identifiers.org/hgnc/26161
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
population: East Asian
reference allele: A
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: MQ
site quality: ClippingRankSum

16-4463423-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4463423
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4463423
    reference: chr 16
allele count: 0
allele frequency: 0.0e0
allele num: 23816
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458828
  ensembl transcript: ENST00000571756
  gene symbol: CORO7
  hgvsc: ENST00000571756.1:c.61-18T>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000458607
  ensembl transcript: ENST00000575334
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000575334.1:c.61-18T>C
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460036
  ensembl transcript: ENST00000571059
  gene symbol: CORO7
  hgvsc: ENST00000571059.1:c.61-18T>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000460885
  ensembl transcript: ENST00000572467
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000572467.1:c.61-18T>C
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000446221
  ensembl transcript: ENST00000539968
  gene symbol: CORO7
  hgvsc: ENST00000539968.1:c.-539-18T>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459286
  ensembl transcript: ENST00000572549
  gene symbol: CORO7
  hgvsc: ENST00000572549.1:c.99+3363T>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461702
  ensembl transcript: ENST00000574025
  gene symbol: CORO7
  hgvsc: ENST00000574025.1:c.61-18T>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459888
  ensembl transcript: ENST00000576051
  gene symbol: CORO7
  hgvsc: ENST00000576051.1:c.-457T>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000577144
  gene symbol: CORO7
  hgvsc: ENST00000577144.1:n.169-18T>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458935
  ensembl transcript: ENST00000572898
  gene symbol: CORO7
  hgvsc: ENST00000572898.1:c.61-18T>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000576457
  gene symbol: CORO7
  hgvsc: ENST00000576457.1:n.121-18T>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461797
  ensembl transcript: ENST00000575038
  gene symbol: CORO7
  hgvsc: ENST00000575038.1:c.61-18T>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458411
  ensembl transcript: ENST00000572044
  gene symbol: CORO7
  hgvsc: ENST00000572044.1:c.60+3037T>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000440460
  ensembl transcript: ENST00000537233
  gene symbol: CORO7
  hgvsc: ENST00000537233.2:c.61-18T>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459228
  ensembl transcript: ENST00000576437
  gene symbol: CORO7
  hgvsc: ENST00000576437.1:c.-214+3058T>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460901
  ensembl transcript: ENST00000570645
  gene symbol: CORO7
  hgvsc: ENST00000570645.1:c.-214+3058T>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460910
  ensembl transcript: ENST00000575850
  gene symbol: CORO7
  hgvsc: ENST00000575850.1:c.100-18T>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000251166
  ensembl transcript: ENST00000251166
  gene symbol: CORO7
  hgvsc: ENST00000251166.4:c.61-18T>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459085
  ensembl transcript: ENST00000571052
  gene symbol: CORO7
  hgvsc: ENST00000571052.1:c.-268+3037T>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461187
  ensembl transcript: ENST00000574311
  gene symbol: CORO7
  hgvsc: ENST00000574311.1:c.60+3037T>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458459
  ensembl transcript: ENST00000571227
  gene symbol: CORO7
  hgvsc: ENST00000571227.1:c.*58-18T>C
  variant of: http://identifiers.org/hgnc/26161
canonical: false
consequence: 5' UTR
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: Other
population: South Asian
reference allele: A
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum

http://identifiers.org/exac.variant/16-4463426-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4463426
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4463426
    reference: chr 16
allele count: 115
allele frequency: 4.974478761138506e-3
allele num: 23118
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000572026
  gene symbol: CORO7
  hgvsc: ENST00000572026.1:n.184-21T>G
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000577144
  gene symbol: CORO7
  hgvsc: ENST00000577144.1:n.169-21T>G
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458828
  ensembl transcript: ENST00000571756
  gene symbol: CORO7
  hgvsc: ENST00000571756.1:c.61-21T>G
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459228
  ensembl transcript: ENST00000576437
  gene symbol: CORO7
  hgvsc: ENST00000576437.1:c.-214+3055T>G
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000576457
  gene symbol: CORO7
  hgvsc: ENST00000576457.1:n.121-21T>G
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458411
  ensembl transcript: ENST00000572044
  gene symbol: CORO7
  hgvsc: ENST00000572044.1:c.60+3034T>G
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459888
  ensembl transcript: ENST00000576051
  gene symbol: CORO7
  hgvsc: ENST00000576051.1:c.-460T>G
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458459
  ensembl transcript: ENST00000571227
  gene symbol: CORO7
  hgvsc: ENST00000571227.1:c.*58-21T>G
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460910
  ensembl transcript: ENST00000575850
  gene symbol: CORO7
  hgvsc: ENST00000575850.1:c.100-21T>G
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461051
  ensembl transcript: ENST00000572153
  gene symbol: CORO7
  hgvsc: ENST00000572153.1:c.61-995T>G
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461702
  ensembl transcript: ENST00000574025
  gene symbol: CORO7
  hgvsc: ENST00000574025.1:c.61-21T>G
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000458607
  ensembl transcript: ENST00000575334
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000575334.1:c.61-21T>G
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000440460
  ensembl transcript: ENST00000537233
  gene symbol: CORO7
  hgvsc: ENST00000537233.2:c.61-21T>G
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460901
  ensembl transcript: ENST00000570645
  gene symbol: CORO7
  hgvsc: ENST00000570645.1:c.-214+3055T>G
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000251166
  ensembl transcript: ENST00000251166
  gene symbol: CORO7
  hgvsc: ENST00000251166.4:c.61-21T>G
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460199
  ensembl transcript: ENST00000570928
  gene symbol: CORO7
  hgvsc: ENST00000570928.1:c.61-21T>G
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000446221
  ensembl transcript: ENST00000539968
  gene symbol: CORO7
  hgvsc: ENST00000539968.1:c.-539-21T>G
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000391530
  ensembl transcript: ENST00000423908
  gene symbol: CORO7
  hgvsc: ENST00000423908.2:c.60+3034T>G
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000460885
  ensembl transcript: ENST00000572467
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000572467.1:c.61-21T>G
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458935
  ensembl transcript: ENST00000572898
  gene symbol: CORO7
  hgvsc: ENST00000572898.1:c.61-21T>G
  variant of: http://identifiers.org/hgnc/26161
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 2
population: South Asian
population: Other
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: A
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff

16-4463436-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4463436
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4463436
    reference: chr 16
allele count: 1
allele frequency: 4.79570305006714e-5
allele num: 20852
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458828
  ensembl transcript: ENST00000571756
  gene symbol: CORO7
  hgvsc: ENST00000571756.1:c.61-31C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460901
  ensembl transcript: ENST00000570645
  gene symbol: CORO7
  hgvsc: ENST00000570645.1:c.-214+3045C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000446221
  ensembl transcript: ENST00000539968
  gene symbol: CORO7
  hgvsc: ENST00000539968.1:c.-539-31C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460199
  ensembl transcript: ENST00000570928
  gene symbol: CORO7
  hgvsc: ENST00000570928.1:c.61-31C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459228
  ensembl transcript: ENST00000576437
  gene symbol: CORO7
  hgvsc: ENST00000576437.1:c.-214+3045C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459888
  ensembl transcript: ENST00000576051
  gene symbol: CORO7
  hgvsc: ENST00000576051.1:c.-470C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000577144
  gene symbol: CORO7
  hgvsc: ENST00000577144.1:n.169-31C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461797
  ensembl transcript: ENST00000575038
  gene symbol: CORO7
  hgvsc: ENST00000575038.1:c.61-31C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461187
  ensembl transcript: ENST00000574311
  gene symbol: CORO7
  hgvsc: ENST00000574311.1:c.60+3024C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459286
  ensembl transcript: ENST00000572549
  gene symbol: CORO7
  hgvsc: ENST00000572549.1:c.99+3350C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461702
  ensembl transcript: ENST00000574025
  gene symbol: CORO7
  hgvsc: ENST00000574025.1:c.61-31C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000572026
  gene symbol: CORO7
  hgvsc: ENST00000572026.1:n.184-31C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000251166
  ensembl transcript: ENST00000251166
  gene symbol: CORO7
  hgvsc: ENST00000251166.4:c.61-31C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458459
  ensembl transcript: ENST00000571227
  gene symbol: CORO7
  hgvsc: ENST00000571227.1:c.*58-31C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000440460
  ensembl transcript: ENST00000537233
  gene symbol: CORO7
  hgvsc: ENST00000537233.2:c.61-31C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000391530
  ensembl transcript: ENST00000423908
  gene symbol: CORO7
  hgvsc: ENST00000423908.2:c.60+3024C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460910
  ensembl transcript: ENST00000575850
  gene symbol: CORO7
  hgvsc: ENST00000575850.1:c.100-31C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459085
  ensembl transcript: ENST00000571052
  gene symbol: CORO7
  hgvsc: ENST00000571052.1:c.-268+3024C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000576457
  gene symbol: CORO7
  hgvsc: ENST00000576457.1:n.121-31C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000458607
  ensembl transcript: ENST00000575334
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000575334.1:c.61-31C>T
  variant of: http://identifiers.org/hgnc/44424
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: East Asian
population: African
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD

16-4463440-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4463440
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4463440
    reference: chr 16
allele count: 0
allele frequency: 0.0e0
allele num: 20518
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458935
  ensembl transcript: ENST00000572898
  gene symbol: CORO7
  hgvsc: ENST00000572898.1:c.61-35C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458411
  ensembl transcript: ENST00000572044
  gene symbol: CORO7
  hgvsc: ENST00000572044.1:c.60+3020C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000572026
  gene symbol: CORO7
  hgvsc: ENST00000572026.1:n.184-35C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000458607
  ensembl transcript: ENST00000575334
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000575334.1:c.61-35C>T
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459888
  ensembl transcript: ENST00000576051
  gene symbol: CORO7
  hgvsc: ENST00000576051.1:c.-474C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461187
  ensembl transcript: ENST00000574311
  gene symbol: CORO7
  hgvsc: ENST00000574311.1:c.60+3020C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460910
  ensembl transcript: ENST00000575850
  gene symbol: CORO7
  hgvsc: ENST00000575850.1:c.100-35C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000446221
  ensembl transcript: ENST00000539968
  gene symbol: CORO7
  hgvsc: ENST00000539968.1:c.-539-35C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460901
  ensembl transcript: ENST00000570645
  gene symbol: CORO7
  hgvsc: ENST00000570645.1:c.-214+3041C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460036
  ensembl transcript: ENST00000571059
  gene symbol: CORO7
  hgvsc: ENST00000571059.1:c.61-35C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458828
  ensembl transcript: ENST00000571756
  gene symbol: CORO7
  hgvsc: ENST00000571756.1:c.61-35C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461702
  ensembl transcript: ENST00000574025
  gene symbol: CORO7
  hgvsc: ENST00000574025.1:c.61-35C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000251166
  ensembl transcript: ENST00000251166
  gene symbol: CORO7
  hgvsc: ENST00000251166.4:c.61-35C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000391530
  ensembl transcript: ENST00000423908
  gene symbol: CORO7
  hgvsc: ENST00000423908.2:c.60+3020C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000577144
  gene symbol: CORO7
  hgvsc: ENST00000577144.1:n.169-35C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459085
  ensembl transcript: ENST00000571052
  gene symbol: CORO7
  hgvsc: ENST00000571052.1:c.-268+3020C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000460885
  ensembl transcript: ENST00000572467
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000572467.1:c.61-35C>T
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461797
  ensembl transcript: ENST00000575038
  gene symbol: CORO7
  hgvsc: ENST00000575038.1:c.61-35C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460199
  ensembl transcript: ENST00000570928
  gene symbol: CORO7
  hgvsc: ENST00000570928.1:c.61-35C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461051
  ensembl transcript: ENST00000572153
  gene symbol: CORO7
  hgvsc: ENST00000572153.1:c.61-1009C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000440460
  ensembl transcript: ENST00000537233
  gene symbol: CORO7
  hgvsc: ENST00000537233.2:c.61-35C>T
  variant of: http://identifiers.org/hgnc/26161
canonical: false
consequence: 5' UTR
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
reference allele: G
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP

16-4465792-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4465792
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4465792
    reference: chr 16
allele count: 0
allele frequency: 0.0e0
allele num: 8
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000446221
  ensembl transcript: ENST00000539968
  gene symbol: CORO7
  hgvsc: ENST00000539968.1:c.-616C>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000458607
  ensembl transcript: ENST00000575334
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000575334.1:c.60+668C>A
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000251166
  ensembl transcript: ENST00000251166
  gene symbol: CORO7
  hgvsc: ENST00000251166.4:c.60+668C>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458828
  ensembl transcript: ENST00000571756
  gene symbol: CORO7
  hgvsc: ENST00000571756.1:c.60+668C>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460901
  ensembl transcript: ENST00000570645
  gene symbol: CORO7
  hgvsc: ENST00000570645.1:c.-214+689C>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000577144
  gene symbol: CORO7
  hgvsc: ENST00000577144.1:n.143C>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459286
  ensembl transcript: ENST00000572549
  gene symbol: CORO7
  hgvsc: ENST00000572549.1:c.99+994C>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000440460
  ensembl transcript: ENST00000537233
  gene symbol: CORO7
  hgvsc: ENST00000537233.2:c.60+668C>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000572026
  gene symbol: CORO7
  hgvsc: ENST00000572026.1:n.107C>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460036
  ensembl transcript: ENST00000571059
  gene symbol: CORO7
  hgvsc: ENST00000571059.1:c.60+668C>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461051
  ensembl transcript: ENST00000572153
  gene symbol: CORO7
  hgvsc: ENST00000572153.1:c.60+668C>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458411
  ensembl transcript: ENST00000572044
  gene symbol: CORO7
  hgvsc: ENST00000572044.1:c.60+668C>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461187
  ensembl transcript: ENST00000574311
  gene symbol: CORO7
  hgvsc: ENST00000574311.1:c.60+668C>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458935
  ensembl transcript: ENST00000572898
  gene symbol: CORO7
  hgvsc: ENST00000572898.1:c.60+668C>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460910
  ensembl transcript: ENST00000575850
  gene symbol: CORO7
  hgvsc: ENST00000575850.1:c.99+994C>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458459
  ensembl transcript: ENST00000571227
  gene symbol: CORO7
  hgvsc: ENST00000571227.1:c.122C>A
  hgvsp: ENSP00000458459.1:p.Pro41Gln
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459228
  ensembl transcript: ENST00000576437
  gene symbol: CORO7
  hgvsc: ENST00000576437.1:c.-214+689C>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461797
  ensembl transcript: ENST00000575038
  gene symbol: CORO7
  hgvsc: ENST00000575038.1:c.60+668C>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459085
  ensembl transcript: ENST00000571052
  gene symbol: CORO7
  hgvsc: ENST00000571052.1:c.-268+668C>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000460885
  ensembl transcript: ENST00000572467
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000572467.1:c.60+668C>A
  variant of: http://identifiers.org/hgnc/44424
canonical: false
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Pro41Gln
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: Other
reference allele: G
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: FS

16-4465850-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4465850
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4465850
    reference: chr 16
allele count: 0
allele frequency: 0.0e0
allele num: 8
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000446221
  ensembl transcript: ENST00000539968
  gene symbol: CORO7
  hgvsc: ENST00000539968.1:c.-674G>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461051
  ensembl transcript: ENST00000572153
  gene symbol: CORO7
  hgvsc: ENST00000572153.1:c.60+610G>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000572026
  gene symbol: CORO7
  hgvsc: ENST00000572026.1:n.49G>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000440460
  ensembl transcript: ENST00000537233
  gene symbol: CORO7
  hgvsc: ENST00000537233.2:c.60+610G>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000458607
  ensembl transcript: ENST00000575334
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000575334.1:c.60+610G>C
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460910
  ensembl transcript: ENST00000575850
  gene symbol: CORO7
  hgvsc: ENST00000575850.1:c.99+936G>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000577144
  gene symbol: CORO7
  hgvsc: ENST00000577144.1:n.85G>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458459
  ensembl transcript: ENST00000571227
  gene symbol: CORO7
  hgvsc: ENST00000571227.1:c.64G>C
  hgvsp: ENSP00000458459.1:p.Glu22Gln
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458828
  ensembl transcript: ENST00000571756
  gene symbol: CORO7
  hgvsc: ENST00000571756.1:c.60+610G>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458935
  ensembl transcript: ENST00000572898
  gene symbol: CORO7
  hgvsc: ENST00000572898.1:c.60+610G>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000251166
  ensembl transcript: ENST00000251166
  gene symbol: CORO7
  hgvsc: ENST00000251166.4:c.60+610G>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460036
  ensembl transcript: ENST00000571059
  gene symbol: CORO7
  hgvsc: ENST00000571059.1:c.60+610G>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460901
  ensembl transcript: ENST00000570645
  gene symbol: CORO7
  hgvsc: ENST00000570645.1:c.-214+631G>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459286
  ensembl transcript: ENST00000572549
  gene symbol: CORO7
  hgvsc: ENST00000572549.1:c.99+936G>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461187
  ensembl transcript: ENST00000574311
  gene symbol: CORO7
  hgvsc: ENST00000574311.1:c.60+610G>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461797
  ensembl transcript: ENST00000575038
  gene symbol: CORO7
  hgvsc: ENST00000575038.1:c.60+610G>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459085
  ensembl transcript: ENST00000571052
  gene symbol: CORO7
  hgvsc: ENST00000571052.1:c.-268+610G>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461702
  ensembl transcript: ENST00000574025
  gene symbol: CORO7
  hgvsc: ENST00000574025.1:c.60+610G>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459228
  ensembl transcript: ENST00000576437
  gene symbol: CORO7
  hgvsc: ENST00000576437.1:c.-214+631G>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000391530
  ensembl transcript: ENST00000423908
  gene symbol: CORO7
  hgvsc: ENST00000423908.2:c.60+610G>C
  variant of: http://identifiers.org/hgnc/26161
canonical: false
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Glu22Gln
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: Other
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD

http://identifiers.org/exac.variant/16-4465857-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4465857
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4465857
    reference: chr 16
allele count: 0
allele frequency: 0.0e0
allele num: 8
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000251166
  ensembl transcript: ENST00000251166
  gene symbol: CORO7
  hgvsc: ENST00000251166.4:c.60+603G>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000577144
  gene symbol: CORO7
  hgvsc: ENST00000577144.1:n.78G>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461797
  ensembl transcript: ENST00000575038
  gene symbol: CORO7
  hgvsc: ENST00000575038.1:c.60+603G>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461051
  ensembl transcript: ENST00000572153
  gene symbol: CORO7
  hgvsc: ENST00000572153.1:c.60+603G>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460036
  ensembl transcript: ENST00000571059
  gene symbol: CORO7
  hgvsc: ENST00000571059.1:c.60+603G>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458411
  ensembl transcript: ENST00000572044
  gene symbol: CORO7
  hgvsc: ENST00000572044.1:c.60+603G>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459228
  ensembl transcript: ENST00000576437
  gene symbol: CORO7
  hgvsc: ENST00000576437.1:c.-214+624G>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000572026
  gene symbol: CORO7
  hgvsc: ENST00000572026.1:n.42G>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000446221
  ensembl transcript: ENST00000539968
  gene symbol: CORO7
  hgvsc: ENST00000539968.1:c.-681G>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000440460
  ensembl transcript: ENST00000537233
  gene symbol: CORO7
  hgvsc: ENST00000537233.2:c.60+603G>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460901
  ensembl transcript: ENST00000570645
  gene symbol: CORO7
  hgvsc: ENST00000570645.1:c.-214+624G>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000458607
  ensembl transcript: ENST00000575334
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000575334.1:c.60+603G>T
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460199
  ensembl transcript: ENST00000570928
  gene symbol: CORO7
  hgvsc: ENST00000570928.1:c.60+603G>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458459
  ensembl transcript: ENST00000571227
  gene symbol: CORO7
  hgvsc: ENST00000571227.1:c.61-4G>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000391530
  ensembl transcript: ENST00000423908
  gene symbol: CORO7
  hgvsc: ENST00000423908.2:c.60+603G>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458935
  ensembl transcript: ENST00000572898
  gene symbol: CORO7
  hgvsc: ENST00000572898.1:c.60+603G>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461702
  ensembl transcript: ENST00000574025
  gene symbol: CORO7
  hgvsc: ENST00000574025.1:c.60+603G>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461187
  ensembl transcript: ENST00000574311
  gene symbol: CORO7
  hgvsc: ENST00000574311.1:c.60+603G>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459085
  ensembl transcript: ENST00000571052
  gene symbol: CORO7
  hgvsc: ENST00000571052.1:c.-268+603G>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000460885
  ensembl transcript: ENST00000572467
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000572467.1:c.60+603G>T
  variant of: http://identifiers.org/hgnc/44424
canonical: false
consequence: splice region
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: c.61-4G>T
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: DP

16-4465870-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4465870
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4465870
    reference: chr 16
allele count: 0
allele frequency: 0.0e0
allele num: 12
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461797
  ensembl transcript: ENST00000575038
  gene symbol: CORO7
  hgvsc: ENST00000575038.1:c.60+590G>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461702
  ensembl transcript: ENST00000574025
  gene symbol: CORO7
  hgvsc: ENST00000574025.1:c.60+590G>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458459
  ensembl transcript: ENST00000571227
  gene symbol: CORO7
  hgvsc: ENST00000571227.1:c.61-17G>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000577144
  gene symbol: CORO7
  hgvsc: ENST00000577144.1:n.65G>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461187
  ensembl transcript: ENST00000574311
  gene symbol: CORO7
  hgvsc: ENST00000574311.1:c.60+590G>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458935
  ensembl transcript: ENST00000572898
  gene symbol: CORO7
  hgvsc: ENST00000572898.1:c.60+590G>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458828
  ensembl transcript: ENST00000571756
  gene symbol: CORO7
  hgvsc: ENST00000571756.1:c.60+590G>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459085
  ensembl transcript: ENST00000571052
  gene symbol: CORO7
  hgvsc: ENST00000571052.1:c.-268+590G>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460910
  ensembl transcript: ENST00000575850
  gene symbol: CORO7
  hgvsc: ENST00000575850.1:c.99+916G>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459286
  ensembl transcript: ENST00000572549
  gene symbol: CORO7
  hgvsc: ENST00000572549.1:c.99+916G>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000460885
  ensembl transcript: ENST00000572467
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000572467.1:c.60+590G>C
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000446221
  ensembl transcript: ENST00000539968
  gene symbol: CORO7
  hgvsc: ENST00000539968.1:c.-694G>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000572026
  gene symbol: CORO7
  hgvsc: ENST00000572026.1:n.29G>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000458607
  ensembl transcript: ENST00000575334
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000575334.1:c.60+590G>C
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460199
  ensembl transcript: ENST00000570928
  gene symbol: CORO7
  hgvsc: ENST00000570928.1:c.60+590G>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459228
  ensembl transcript: ENST00000576437
  gene symbol: CORO7
  hgvsc: ENST00000576437.1:c.-214+611G>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460901
  ensembl transcript: ENST00000570645
  gene symbol: CORO7
  hgvsc: ENST00000570645.1:c.-214+611G>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000440460
  ensembl transcript: ENST00000537233
  gene symbol: CORO7
  hgvsc: ENST00000537233.2:c.60+590G>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000251166
  ensembl transcript: ENST00000251166
  gene symbol: CORO7
  hgvsc: ENST00000251166.4:c.60+590G>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460036
  ensembl transcript: ENST00000571059
  gene symbol: CORO7
  hgvsc: ENST00000571059.1:c.60+590G>C
  variant of: http://identifiers.org/hgnc/26161
canonical: false
consequence: 5' UTR
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: C
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: DP

16-4466412-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4466412
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4466412
    reference: chr 16
allele count: 0
allele frequency: 0.0e0
allele num: 72062
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460199
  ensembl transcript: ENST00000570928
  gene symbol: CORO7
  hgvsc: ENST00000570928.1:c.60+48G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460036
  ensembl transcript: ENST00000571059
  gene symbol: CORO7
  hgvsc: ENST00000571059.1:c.60+48G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461702
  ensembl transcript: ENST00000574025
  gene symbol: CORO7
  hgvsc: ENST00000574025.1:c.60+48G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000460885
  ensembl transcript: ENST00000572467
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000572467.1:c.60+48G>A
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460901
  ensembl transcript: ENST00000570645
  gene symbol: CORO7
  hgvsc: ENST00000570645.1:c.-214+69G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461051
  ensembl transcript: ENST00000572153
  gene symbol: CORO7
  hgvsc: ENST00000572153.1:c.60+48G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459286
  ensembl transcript: ENST00000572549
  gene symbol: CORO7
  hgvsc: ENST00000572549.1:c.99+374G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458459
  ensembl transcript: ENST00000571227
  gene symbol: CORO7
  hgvsc: ENST00000571227.1:c.60+48G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458411
  ensembl transcript: ENST00000572044
  gene symbol: CORO7
  hgvsc: ENST00000572044.1:c.60+48G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000440460
  ensembl transcript: ENST00000537233
  gene symbol: CORO7
  hgvsc: ENST00000537233.2:c.60+48G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000458607
  ensembl transcript: ENST00000575334
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000575334.1:c.60+48G>A
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461797
  ensembl transcript: ENST00000575038
  gene symbol: CORO7
  hgvsc: ENST00000575038.1:c.60+48G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459085
  ensembl transcript: ENST00000571052
  gene symbol: CORO7
  hgvsc: ENST00000571052.1:c.-268+48G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461187
  ensembl transcript: ENST00000574311
  gene symbol: CORO7
  hgvsc: ENST00000574311.1:c.60+48G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458935
  ensembl transcript: ENST00000572898
  gene symbol: CORO7
  hgvsc: ENST00000572898.1:c.60+48G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460910
  ensembl transcript: ENST00000575850
  gene symbol: CORO7
  hgvsc: ENST00000575850.1:c.99+374G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459228
  ensembl transcript: ENST00000576437
  gene symbol: CORO7
  hgvsc: ENST00000576437.1:c.-214+69G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458828
  ensembl transcript: ENST00000571756
  gene symbol: CORO7
  hgvsc: ENST00000571756.1:c.60+48G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000391530
  ensembl transcript: ENST00000423908
  gene symbol: CORO7
  hgvsc: ENST00000423908.2:c.60+48G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000251166
  ensembl transcript: ENST00000251166
  gene symbol: CORO7
  hgvsc: ENST00000251166.4:c.60+48G>A
  variant of: http://identifiers.org/hgnc/26161
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
population: African
population: Other
reference allele: C
site quality: FS
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum

http://identifiers.org/exac.variant/16-4466413-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4466413
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4466413
    reference: chr 16
allele count: 1
allele frequency: 1.382399292211562e-5
allele num: 72338
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461187
  ensembl transcript: ENST00000574311
  gene symbol: CORO7
  hgvsc: ENST00000574311.1:c.60+47G>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460910
  ensembl transcript: ENST00000575850
  gene symbol: CORO7
  hgvsc: ENST00000575850.1:c.99+373G>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458459
  ensembl transcript: ENST00000571227
  gene symbol: CORO7
  hgvsc: ENST00000571227.1:c.60+47G>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461702
  ensembl transcript: ENST00000574025
  gene symbol: CORO7
  hgvsc: ENST00000574025.1:c.60+47G>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460036
  ensembl transcript: ENST00000571059
  gene symbol: CORO7
  hgvsc: ENST00000571059.1:c.60+47G>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000458607
  ensembl transcript: ENST00000575334
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000575334.1:c.60+47G>T
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460901
  ensembl transcript: ENST00000570645
  gene symbol: CORO7
  hgvsc: ENST00000570645.1:c.-214+68G>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000460885
  ensembl transcript: ENST00000572467
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000572467.1:c.60+47G>T
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459228
  ensembl transcript: ENST00000576437
  gene symbol: CORO7
  hgvsc: ENST00000576437.1:c.-214+68G>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459085
  ensembl transcript: ENST00000571052
  gene symbol: CORO7
  hgvsc: ENST00000571052.1:c.-268+47G>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000440460
  ensembl transcript: ENST00000537233
  gene symbol: CORO7
  hgvsc: ENST00000537233.2:c.60+47G>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459286
  ensembl transcript: ENST00000572549
  gene symbol: CORO7
  hgvsc: ENST00000572549.1:c.99+373G>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458935
  ensembl transcript: ENST00000572898
  gene symbol: CORO7
  hgvsc: ENST00000572898.1:c.60+47G>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458411
  ensembl transcript: ENST00000572044
  gene symbol: CORO7
  hgvsc: ENST00000572044.1:c.60+47G>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460199
  ensembl transcript: ENST00000570928
  gene symbol: CORO7
  hgvsc: ENST00000570928.1:c.60+47G>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461797
  ensembl transcript: ENST00000575038
  gene symbol: CORO7
  hgvsc: ENST00000575038.1:c.60+47G>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458828
  ensembl transcript: ENST00000571756
  gene symbol: CORO7
  hgvsc: ENST00000571756.1:c.60+47G>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461051
  ensembl transcript: ENST00000572153
  gene symbol: CORO7
  hgvsc: ENST00000572153.1:c.60+47G>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000391530
  ensembl transcript: ENST00000423908
  gene symbol: CORO7
  hgvsc: ENST00000423908.2:c.60+47G>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000251166
  ensembl transcript: ENST00000251166
  gene symbol: CORO7
  hgvsc: ENST00000251166.4:c.60+47G>T
  variant of: http://identifiers.org/hgnc/26161
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: South Asian
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff

16-4466414-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4466414
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4466414
    reference: chr 16
allele count: 2
allele frequency: 2.758696791635631e-5
allele num: 72498
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461797
  ensembl transcript: ENST00000575038
  gene symbol: CORO7
  hgvsc: ENST00000575038.1:c.60+46C>G
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000391530
  ensembl transcript: ENST00000423908
  gene symbol: CORO7
  hgvsc: ENST00000423908.2:c.60+46C>G
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458828
  ensembl transcript: ENST00000571756
  gene symbol: CORO7
  hgvsc: ENST00000571756.1:c.60+46C>G
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459286
  ensembl transcript: ENST00000572549
  gene symbol: CORO7
  hgvsc: ENST00000572549.1:c.99+372C>G
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000460885
  ensembl transcript: ENST00000572467
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000572467.1:c.60+46C>G
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459085
  ensembl transcript: ENST00000571052
  gene symbol: CORO7
  hgvsc: ENST00000571052.1:c.-268+46C>G
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460036
  ensembl transcript: ENST00000571059
  gene symbol: CORO7
  hgvsc: ENST00000571059.1:c.60+46C>G
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460199
  ensembl transcript: ENST00000570928
  gene symbol: CORO7
  hgvsc: ENST00000570928.1:c.60+46C>G
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460910
  ensembl transcript: ENST00000575850
  gene symbol: CORO7
  hgvsc: ENST00000575850.1:c.99+372C>G
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460901
  ensembl transcript: ENST00000570645
  gene symbol: CORO7
  hgvsc: ENST00000570645.1:c.-214+67C>G
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461702
  ensembl transcript: ENST00000574025
  gene symbol: CORO7
  hgvsc: ENST00000574025.1:c.60+46C>G
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458459
  ensembl transcript: ENST00000571227
  gene symbol: CORO7
  hgvsc: ENST00000571227.1:c.60+46C>G
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000458607
  ensembl transcript: ENST00000575334
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000575334.1:c.60+46C>G
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000251166
  ensembl transcript: ENST00000251166
  gene symbol: CORO7
  hgvsc: ENST00000251166.4:c.60+46C>G
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458411
  ensembl transcript: ENST00000572044
  gene symbol: CORO7
  hgvsc: ENST00000572044.1:c.60+46C>G
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461051
  ensembl transcript: ENST00000572153
  gene symbol: CORO7
  hgvsc: ENST00000572153.1:c.60+46C>G
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461187
  ensembl transcript: ENST00000574311
  gene symbol: CORO7
  hgvsc: ENST00000574311.1:c.60+46C>G
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459228
  ensembl transcript: ENST00000576437
  gene symbol: CORO7
  hgvsc: ENST00000576437.1:c.-214+67C>G
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458935
  ensembl transcript: ENST00000572898
  gene symbol: CORO7
  hgvsc: ENST00000572898.1:c.60+46C>G
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000440460
  ensembl transcript: ENST00000537233
  gene symbol: CORO7
  hgvsc: ENST00000537233.2:c.60+46C>G
  variant of: http://identifiers.org/hgnc/26161
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: African
population: Other
population: East Asian
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD

16-4466417-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4466417
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4466417
    reference: chr 16
allele count: 4
allele frequency: 5.503123022315164e-5
allele num: 72686
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458411
  ensembl transcript: ENST00000572044
  gene symbol: CORO7
  hgvsc: ENST00000572044.1:c.60+43G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460199
  ensembl transcript: ENST00000570928
  gene symbol: CORO7
  hgvsc: ENST00000570928.1:c.60+43G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461187
  ensembl transcript: ENST00000574311
  gene symbol: CORO7
  hgvsc: ENST00000574311.1:c.60+43G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461051
  ensembl transcript: ENST00000572153
  gene symbol: CORO7
  hgvsc: ENST00000572153.1:c.60+43G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458459
  ensembl transcript: ENST00000571227
  gene symbol: CORO7
  hgvsc: ENST00000571227.1:c.60+43G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458828
  ensembl transcript: ENST00000571756
  gene symbol: CORO7
  hgvsc: ENST00000571756.1:c.60+43G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458935
  ensembl transcript: ENST00000572898
  gene symbol: CORO7
  hgvsc: ENST00000572898.1:c.60+43G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000251166
  ensembl transcript: ENST00000251166
  gene symbol: CORO7
  hgvsc: ENST00000251166.4:c.60+43G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000458607
  ensembl transcript: ENST00000575334
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000575334.1:c.60+43G>A
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461702
  ensembl transcript: ENST00000574025
  gene symbol: CORO7
  hgvsc: ENST00000574025.1:c.60+43G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000460885
  ensembl transcript: ENST00000572467
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000572467.1:c.60+43G>A
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459228
  ensembl transcript: ENST00000576437
  gene symbol: CORO7
  hgvsc: ENST00000576437.1:c.-214+64G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461797
  ensembl transcript: ENST00000575038
  gene symbol: CORO7
  hgvsc: ENST00000575038.1:c.60+43G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460901
  ensembl transcript: ENST00000570645
  gene symbol: CORO7
  hgvsc: ENST00000570645.1:c.-214+64G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460036
  ensembl transcript: ENST00000571059
  gene symbol: CORO7
  hgvsc: ENST00000571059.1:c.60+43G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459286
  ensembl transcript: ENST00000572549
  gene symbol: CORO7
  hgvsc: ENST00000572549.1:c.99+369G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000391530
  ensembl transcript: ENST00000423908
  gene symbol: CORO7
  hgvsc: ENST00000423908.2:c.60+43G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459085
  ensembl transcript: ENST00000571052
  gene symbol: CORO7
  hgvsc: ENST00000571052.1:c.-268+43G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000440460
  ensembl transcript: ENST00000537233
  gene symbol: CORO7
  hgvsc: ENST00000537233.2:c.60+43G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460910
  ensembl transcript: ENST00000575850
  gene symbol: CORO7
  hgvsc: ENST00000575850.1:c.99+369G>A
  variant of: http://identifiers.org/hgnc/26161
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum

16-4466421-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4466421
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4466421
    reference: chr 16
allele count: 1
allele frequency: 1.34665625252498e-5
allele num: 74258
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000459286
  ensembl transcript: ENST00000572549
  gene symbol: CORO7
  hgvsc: ENST00000572549.1:c.99+365C>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460036
  ensembl transcript: ENST00000571059
  gene symbol: CORO7
  hgvsc: ENST00000571059.1:c.60+39C>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000440460
  ensembl transcript: ENST00000537233
  gene symbol: CORO7
  hgvsc: ENST00000537233.2:c.60+39C>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458828
  ensembl transcript: ENST00000571756
  gene symbol: CORO7
  hgvsc: ENST00000571756.1:c.60+39C>A
  variant of: http://identifiers.org/hgnc/26161
canonical: true
consequence: intron
filter: PASS
num of homozygotes: 0
reference allele: G

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000458935
ensembl transcript: ENST00000572898
gene symbol: CORO7
hgvsc: ENST00000572898.1:c.158-16C>T
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl transcript: ENST00000572026
gene symbol: CORO7
hgvsc: ENST00000572026.1:n.281-16C>T
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000461702
ensembl transcript: ENST00000574025
gene symbol: CORO7
hgvsc: ENST00000574025.1:c.158-16C>T
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000459228
ensembl transcript: ENST00000576437
gene symbol: CORO7
hgvsc: ENST00000576437.1:c.-214+4034C>T
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000459888
ensembl transcript: ENST00000576051
gene symbol: CORO7
hgvsc: ENST00000576051.1:c.-342-16C>T
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000459085
ensembl transcript: ENST00000571052
gene symbol: CORO7
hgvsc: ENST00000571052.1:c.-268+4013C>T
variant of: http://identifiers.org/hgnc/26161

GenotypeDepth
all individuals: 359
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 316
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 142
bin: 8.75e1
variant carriers: 1

GenotypeDepth
all individuals: 1085
bin: 6.25e1
variant carriers: 3

GenotypeDepth
all individuals: 834
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1700
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 481
bin: 7.25e1
variant carriers: 2

GenotypeDepth
all individuals: 2684
bin: 5.25e1
variant carriers: 2

GenotypeDepth
all individuals: 4585
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 13558
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 320
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 9337
bin: 3.75e1
variant carriers: 1

GenotypeDepth
all individuals: 4240
bin: 4.75e1
variant carriers: 3

GenotypeDepth
all individuals: 6538
bin: 4.25e1
variant carriers: 1

GenotypeDepth
all individuals: 19
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 13087
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 301
bin: 7.75e1
variant carriers: 1

GenotypeDepth
all individuals: 222
bin: 8.25e1
variant carriers: 1

GenotypeDepth
all individuals: 105
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 793
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4762
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 237
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15851
bin: 9.75e1
variant carriers: 16

GenotypeQuality
all individuals: 4209
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 170
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 17698
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 326
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 697
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7672
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3380
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 63
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2113
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3255
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 89
bin: 5.25e1
variant carriers: 0

East Asian
type: Population
allele count: 5
allele frequency: 5.795085767269356e-4
allele num: 8628
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.1020258725897e-5
allele num: 16388
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6608
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.673026886383348e-5
allele num: 11530
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10292
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 9
allele frequency: 1.356524884695385e-4
allele num: 66346
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.215412e6

ClippingRankSum
type: SiteQuality
SIO_000300: 5.9e-2

VQSLOD
type: SiteQuality
SIO_000300: 3.85e0

MQRankSum
type: SiteQuality
SIO_000300: 1.5e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.4e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -4.61e-1

QD
type: SiteQuality
SIO_000300: 1.471e1

MQ
type: SiteQuality
SIO_000300: 5.968e1

Annotation
canonical: true
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000251166
ensembl transcript: ENST00000251166
gene symbol: CORO7
hgvsc: ENST00000251166.4:c.158-17C>G
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000458828
ensembl transcript: ENST00000571756
gene symbol: CORO7
hgvsc: ENST00000571756.1:c.158-17C>G
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000459085
ensembl transcript: ENST00000571052
gene symbol: CORO7
hgvsc: ENST00000571052.1:c.-268+4012C>G
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl transcript: ENST00000572026
gene symbol: CORO7
hgvsc: ENST00000572026.1:n.281-17C>G
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000391530
ensembl transcript: ENST00000423908
gene symbol: CORO7
hgvsc: ENST00000423908.2:c.60+4012C>G
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl transcript: ENST00000572518
gene symbol: CORO7
hgvsc: ENST00000572518.1:n.406-17C>G
variant of: http://identifiers.org/hgnc/26161

GenotypeDepth
all individuals: 13080
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 792
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2682
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 326
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 316
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1082
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6532
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 22
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1700
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 222
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4549
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 391
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 479
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 877
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9328
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4237
bin: 4.75e1
variant carriers: 1

GenotypeDepth
all individuals: 141
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 300
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 13545
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 105
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2110
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7668
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17655
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 86
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15837
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 343
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3255
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 246
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4761
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 725
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 186
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3381
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4207
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11526
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.507249871883761e-5
allele num: 66346
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16388
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10290
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8626
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6610
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 4.75e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.29e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.79e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.19e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.984e0

QD
type: SiteQuality
SIO_000300: 1.232e1

DP
type: SiteQuality
SIO_000300: 2.213676e6

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000459888
ensembl transcript: ENST00000576051
gene symbol: CORO7
hgvsc: ENST00000576051.1:c.-342-19C>T
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000461797
ensembl transcript: ENST00000575038
gene symbol: CORO7
hgvsc: ENST00000575038.1:c.158-19C>T
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl transcript: ENST00000572518
gene symbol: CORO7
hgvsc: ENST00000572518.1:n.406-19C>T
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000461187
ensembl transcript: ENST00000574311
gene symbol: CORO7
hgvsc: ENST00000574311.1:c.60+4010C>T
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl transcript: ENST00000572026
gene symbol: CORO7
hgvsc: ENST00000572026.1:n.281-19C>T
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000440460
ensembl transcript: ENST00000537233
gene symbol: CORO7
hgvsc: ENST00000537233.2:c.158-19C>T
variant of: http://identifiers.org/hgnc/26161

GenotypeDepth
all individuals: 24
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 6518
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 105
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9305
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 316
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4233
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 221
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 12999
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 479
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1700
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1082
bin: 6.25e1
variant carriers: 2

GenotypeDepth
all individuals: 141
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 353
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 301
bin: 7.75e1
variant carriers: 1

GenotypeDepth
all individuals: 1000
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 489
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2682
bin: 5.25e1
variant carriers: 1

GenotypeDepth
all individuals: 4455
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 792
bin: 6.75e1
variant carriers: 1

GenotypeDepth
all individuals: 13511
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 228
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4759
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 92
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 802
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 296
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3379
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15832
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 4206
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2108
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17456
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7649
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3252
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 394
bin: 3.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.032090722644468e-5
allele num: 66312
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8618
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6608
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11524
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10282
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.104260774020266e-5
allele num: 16382
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.33e-1

FS
type: SiteQuality
SIO_000300: 1.236e0

DP
type: SiteQuality
SIO_000300: 2.210014e6

VQSLOD
type: SiteQuality
SIO_000300: 3.05e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.39e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.802e0

MQRankSum
type: SiteQuality
SIO_000300: -4.17e-1

QD
type: SiteQuality
SIO_000300: 1.638e1

Annotation
canonical: true
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000251166
ensembl transcript: ENST00000251166
gene symbol: CORO7
hgvsc: ENST00000251166.4:c.158-26T>C
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000458935
ensembl transcript: ENST00000572898
gene symbol: CORO7
hgvsc: ENST00000572898.1:c.158-26T>C
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl transcript: ENST00000572026
gene symbol: CORO7
hgvsc: ENST00000572026.1:n.281-26T>C
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000460199
ensembl transcript: ENST00000570928
gene symbol: CORO7
hgvsc: ENST00000570928.1:c.158-26T>C
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000440460
ensembl transcript: ENST00000537233
gene symbol: CORO7
hgvsc: ENST00000537233.2:c.158-26T>C
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000459888
ensembl transcript: ENST00000576051
gene symbol: CORO7
hgvsc: ENST00000576051.1:c.-342-26T>C
variant of: http://identifiers.org/hgnc/26161

GenotypeDepth
all individuals: 40
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 9199
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 12563
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 142
bin: 8.75e1
variant carriers: 1

GenotypeDepth
all individuals: 1079
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4105
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 479
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2680
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 429
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1564
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6483
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1091
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 791
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 13192
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1698
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 316
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 221
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 104
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 300
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4230
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 173
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 135
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3231
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2103
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7561
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 94
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1152
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15820
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 454
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4197
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4749
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3377
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16265
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 508
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 709
bin: 3.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16356
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 894
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.735202492211838e-5
allele num: 10272
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11514
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8590
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66220
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6606
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.09e-1

QD
type: SiteQuality
SIO_000300: 8.51e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.6e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -4.57e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -4.48e-1

FS
type: SiteQuality
SIO_000300: 4.981e0

MQRankSum
type: SiteQuality
SIO_000300: 1.02e0

DP
type: SiteQuality
SIO_000300: 2.191927e6

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000460901
ensembl transcript: ENST00000570645
gene symbol: CORO7
hgvsc: ENST00000570645.1:c.-214+4022delA
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000459228
ensembl transcript: ENST00000576437
gene symbol: CORO7
hgvsc: ENST00000576437.1:c.-214+4022delA
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl transcript: ENST00000576457
gene symbol: CORO7
hgvsc: ENST00000576457.1:n.218-28delA
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl transcript: ENST00000572026
gene symbol: CORO7
hgvsc: ENST00000572026.1:n.281-28delA
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000461702
ensembl transcript: ENST00000574025
gene symbol: CORO7
hgvsc: ENST00000574025.1:c.158-28delA
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000459085
ensembl transcript: ENST00000571052
gene symbol: CORO7
hgvsc: ENST00000571052.1:c.-268+4001delA
variant of: http://identifiers.org/hgnc/26161

GenotypeDepth
all individuals: 221
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 479
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3987
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 440
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 42
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1079
bin: 6.25e1
variant carriers: 1

GenotypeDepth
all individuals: 13093
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4229
bin: 4.75e1
variant carriers: 3

GenotypeDepth
all individuals: 9152
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2680
bin: 5.25e1
variant carriers: 1

GenotypeDepth
all individuals: 791
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1734
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6473
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 12411
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 141
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1336
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 300
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1698
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 104
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 316
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 542
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 152
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1233
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 585
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3376
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 821
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 15771
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 215
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 132
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4195
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4746
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 186
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7483
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2102
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3218
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15824
bin: 9.75e1
variant carriers: 5

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8590
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6606
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11512
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16322
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10272
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 894
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.553554702843159e-5
allele num: 66194
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -2.036e0

VQSLOD
type: SiteQuality
SIO_000300: 3.26e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.23e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.1e-2

MQ
type: SiteQuality
SIO_000300: 5.495e1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

DP
type: SiteQuality
SIO_000300: 2.186077e6

BaseQRankSum
type: SiteQuality
SIO_000300: -4.2e-2

QD
type: SiteQuality
SIO_000300: 1.873e1

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000461051
ensembl transcript: ENST00000572153
gene symbol: CORO7
hgvsc: ENST00000572153.1:c.61-31T>A
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000459228
ensembl transcript: ENST00000576437
gene symbol: CORO7
hgvsc: ENST00000576437.1:c.-214+4019T>A
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000459286
ensembl transcript: ENST00000572549
gene symbol: CORO7
hgvsc: ENST00000572549.1:c.99+4324T>A
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000391530
ensembl transcript: ENST00000423908
gene symbol: CORO7
hgvsc: ENST00000423908.2:c.60+3998T>A
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000458459
ensembl transcript: ENST00000571227
gene symbol: CORO7
hgvsc: ENST00000571227.1:c.*155-31T>A
variant of: http://identifiers.org/hgnc/26161

GenotypeDepth
all individuals: 6418
bin: 4.25e1
variant carriers: 1

GenotypeDepth
all individuals: 1079
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 790
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 487
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 2679
bin: 5.25e1
variant carriers: 1

GenotypeDepth
all individuals: 8837
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2175
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 104
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1697
bin: 5.75e1
variant carriers: 1

GenotypeDepth
all individuals: 61
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 11872
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3841
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2623
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4220
bin: 4.75e1
variant carriers: 2

GenotypeDepth
all individuals: 12366
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 221
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 316
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 300
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 479
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 141
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1233
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 162
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3369
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 441
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1507
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2096
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6927
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 355
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 807
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 990
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3071
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14445
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 473
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4172
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4650
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15819
bin: 9.75e1
variant carriers: 5

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6598
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10256
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16318
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8572
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.56132232404803e-5
allele num: 66126
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11494
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 894
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.966e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.71e-1

DP
type: SiteQuality
SIO_000300: 2.158492e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

FS
type: SiteQuality
SIO_000300: 9.69e-1

VQSLOD
type: SiteQuality
SIO_000300: -7.423999999999999e-1

QD
type: SiteQuality
SIO_000300: 2.027e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.316e0

MQ
type: SiteQuality
SIO_000300: 5.448e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.2e-2

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000459085
ensembl transcript: ENST00000571052
gene symbol: CORO7
hgvsc: ENST00000571052.1:c.-268+3996C>T
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000460901
ensembl transcript: ENST00000570645
gene symbol: CORO7
hgvsc: ENST00000570645.1:c.-214+4017C>T
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000458935
ensembl transcript: ENST00000572898
gene symbol: CORO7
hgvsc: ENST00000572898.1:c.158-33C>T
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl transcript: ENST00000572026
gene symbol: CORO7
hgvsc: ENST00000572026.1:n.281-33C>T
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl transcript: ENST00000577144
gene symbol: CORO7
hgvsc: ENST00000577144.1:n.266-33C>T
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000458459
ensembl transcript: ENST00000571227
gene symbol: CORO7
hgvsc: ENST00000571227.1:c.*155-33C>T
variant of: http://identifiers.org/hgnc/26161

GenotypeDepth
all individuals: 516
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 70
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 221
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 11927
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1079
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1697
bin: 5.75e1
variant carriers: 1

GenotypeDepth
all individuals: 141
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 790
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 104
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 11769
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3961
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 300
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 479
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8541
bin: 3.75e1
variant carriers: 1

GenotypeDepth
all individuals: 2257
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4202
bin: 4.75e1
variant carriers: 2

GenotypeDepth
all individuals: 3321
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6340
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2675
bin: 5.25e1
variant carriers: 1

GenotypeDepth
all individuals: 316
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6602
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1249
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 904
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4621
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13492
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 619
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 82
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 80
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1564
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15819
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 3014
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3365
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1412
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4174
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 412
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 533
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 608
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2095
bin: 8.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6592
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16304
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8568
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11496
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.567960283344433e-5
allele num: 66068
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 894
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10246
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.868e0

FS
type: SiteQuality
SIO_000300: 1.106e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.71e-1

VQSLOD
type: SiteQuality
SIO_000300: -6.775e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

DP
type: SiteQuality
SIO_000300: 2.142306e6

QD
type: SiteQuality
SIO_000300: 2.122e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.412e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.0e-2

MQ
type: SiteQuality
SIO_000300: 5.432e1

Annotation
canonical: true
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000251166
ensembl transcript: ENST00000251166
gene symbol: CORO7
hgvsc: ENST00000251166.4:c.158-39G>A
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000459228
ensembl transcript: ENST00000576437
gene symbol: CORO7
hgvsc: ENST00000576437.1:c.-214+4011G>A
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000440460
ensembl transcript: ENST00000537233
gene symbol: CORO7
hgvsc: ENST00000537233.2:c.158-39G>A
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl transcript: ENST00000576457
gene symbol: CORO7
hgvsc: ENST00000576457.1:n.218-39G>A
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000461051
ensembl transcript: ENST00000572153
gene symbol: CORO7
hgvsc: ENST00000572153.1:c.61-39G>A
variant of: http://identifiers.org/hgnc/26161

GenotypeDepth
all individuals: 1078
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 791
bin: 6.75e1
variant carriers: 1

GenotypeDepth
all individuals: 2674
bin: 5.25e1
variant carriers: 1

GenotypeDepth
all individuals: 316
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 4579
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 73
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1694
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4453
bin: 2.25e1
variant carriers: 1

GenotypeDepth
all individuals: 2272
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 10989
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8334
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 104
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 594
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 6304
bin: 4.25e1
variant carriers: 1

GenotypeDepth
all individuals: 140
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 11125
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 222
bin: 8.25e1
variant carriers: 1

GenotypeDepth
all individuals: 299
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 479
bin: 7.25e1
variant carriers: 1

GenotypeDepth
all individuals: 4185
bin: 4.75e1
variant carriers: 3

GenotypeQuality
all individuals: 1715
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3360
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12191
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15805
bin: 9.75e1
variant carriers: 10

GenotypeQuality
all individuals: 2960
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 109
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 870
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 513
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 127
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1621
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4147
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 527
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1034
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6282
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2091
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1049
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1667
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4552
bin: 7.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6586
num of homozygotes: 0

East Asian
type: Population
allele count: 10
allele frequency: 1.170138076293003e-3
allele num: 8546
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16234
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65958
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10238
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11490
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 890
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.949e1

QD
type: SiteQuality
SIO_000300: 1.169e1

VQSLOD
type: SiteQuality
SIO_000300: 2.04e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 3.97e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.433e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.62e-1

DP
type: SiteQuality
SIO_000300: 2.118716e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.59e-1

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000461797
ensembl transcript: ENST00000575038
gene symbol: CORO7
hgvsc: ENST00000575038.1:c.158-47G>A
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl transcript: ENST00000572518
gene symbol: CORO7
hgvsc: ENST00000572518.1:n.406-47G>A
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000459085
ensembl transcript: ENST00000571052
gene symbol: CORO7
hgvsc: ENST00000571052.1:c.-268+3982G>A
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000460199
ensembl transcript: ENST00000570928
gene symbol: CORO7
hgvsc: ENST00000570928.1:c.158-47G>A
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl transcript: ENST00000572026
gene symbol: CORO7
hgvsc: ENST00000572026.1:n.281-47G>A
variant of: http://identifiers.org/hgnc/26161

GenotypeDepth
all individuals: 140
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 477
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 77
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 683
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 4158
bin: 4.75e1
variant carriers: 2

GenotypeDepth
all individuals: 2296
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2664
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 105
bin: 9.25e1
variant carriers: 1

GenotypeDepth
all individuals: 9810
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 10016
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 222
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1688
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6712
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 297
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1077
bin: 6.25e1
variant carriers: 1

GenotypeDepth
all individuals: 8183
bin: 3.75e1
variant carriers: 1

GenotypeDepth
all individuals: 4733
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 790
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6262
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 314
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 131
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2146
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 181
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15740
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 1315
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1593
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2851
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5737
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4059
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4374
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 116
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2242
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1149
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1887
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 280
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3336
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1358
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10112
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2076
bin: 8.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8524
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6580
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16210
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.07921213410742e-5
allele num: 65798
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.716875871687587e-5
allele num: 11472
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 886
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10220
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.18e0

VQSLOD
type: SiteQuality
SIO_000300: 1.34e0

QD
type: SiteQuality
SIO_000300: 1.156e1

MQRankSum
type: SiteQuality
SIO_000300: 7.15e-1

FS
type: SiteQuality
SIO_000300: 3.801e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.968e0

DP
type: SiteQuality
SIO_000300: 2.093863e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

MQ
type: SiteQuality
SIO_000300: 5.96e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.42e0

Annotation
canonical: true
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000251166
ensembl transcript: ENST00000251166
gene symbol: CORO7
hgvsc: ENST00000251166.4:c.158-49G>A
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000459888
ensembl transcript: ENST00000576051
gene symbol: CORO7
hgvsc: ENST00000576051.1:c.-342-49G>A
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000461187
ensembl transcript: ENST00000574311
gene symbol: CORO7
hgvsc: ENST00000574311.1:c.60+3980G>A
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000459228
ensembl transcript: ENST00000576437
gene symbol: CORO7
hgvsc: ENST00000576437.1:c.-214+4001G>A
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000458828
ensembl transcript: ENST00000571756
gene symbol: CORO7
hgvsc: ENST00000571756.1:c.158-49G>A
variant of: http://identifiers.org/hgnc/26161

GenotypeDepth
all individuals: 104
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6246
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 141
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 77
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 4157
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 314
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1079
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2662
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 475
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8136
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7570
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2278
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 222
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 724
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1687
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 9484
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 297
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 791
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 9539
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4721
bin: 1.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1925
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7348
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4348
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2239
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2823
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 135
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2077
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1486
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1027
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15732
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 348
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4051
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1147
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1431
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 142
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2911
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2790
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3338
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5372
bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65630
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 884
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10194
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.185056902523504e-5
allele num: 16168
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6572
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11456
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8490
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 5.19e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -2.172e0

DP
type: SiteQuality
SIO_000300: 2.086328e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.27e0

MQRankSum
type: SiteQuality
SIO_000300: 1.09e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.898e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.087e0

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000461051
ensembl transcript: ENST00000572153
gene symbol: CORO7
hgvsc: ENST00000572153.1:c.61-830C>T
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000458459
ensembl transcript: ENST00000571227
gene symbol: CORO7
hgvsc: ENST00000571227.1:c.*154+48C>T
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000459228
ensembl transcript: ENST00000576437
gene symbol: CORO7
hgvsc: ENST00000576437.1:c.-214+3220C>T
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000458935
ensembl transcript: ENST00000572898
gene symbol: CORO7
hgvsc: ENST00000572898.1:c.157+48C>T
variant of: http://identifiers.org/hgnc/26161

GenotypeDepth
all individuals: 560
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 15761
bin: 7.5e0
variant carriers: 1

GenotypeDepth
all individuals: 374
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 30938
bin: 2.5e0
variant carriers: 1

GenotypeDepth
all individuals: 275
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3448
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 92
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1048
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 430
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 397
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 719
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1725
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 235
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 510
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 316
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 174
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 130
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 369
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 105
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 152
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1195
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5939
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6783
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22892
bin: 7.5e0
variant carriers: 1

GenotypeQuality
all individuals: 418
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 166
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7228
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1334
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1017
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 255
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4321
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 634
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2987
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 188
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 288
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 336
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1098
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 405
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 233
bin: 9.25e1
variant carriers: 1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 934
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 222
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 190
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10352
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3160
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6578
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 488
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.22e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.36e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.36e-1

DP
type: SiteQuality
SIO_000300: 5.35078e5

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.98e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.2e-1

QD
type: SiteQuality
SIO_000300: 1.272e1

VQSLOD
type: SiteQuality
SIO_000300: 2.27e0

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000460199
ensembl transcript: ENST00000570928
gene symbol: CORO7
hgvsc: ENST00000570928.1:c.157+42G>A
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000391530
ensembl transcript: ENST00000423908
gene symbol: CORO7
hgvsc: ENST00000423908.2:c.60+3193G>A
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000459286
ensembl transcript: ENST00000572549
gene symbol: CORO7
hgvsc: ENST00000572549.1:c.99+3519G>A
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000459085
ensembl transcript: ENST00000571052
gene symbol: CORO7
hgvsc: ENST00000571052.1:c.-268+3193G>A
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: true
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000251166
ensembl transcript: ENST00000251166
gene symbol: CORO7
hgvsc: ENST00000251166.4:c.157+42G>A
variant of: http://identifiers.org/hgnc/26161

GenotypeDepth
all individuals: 316
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 772
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 568
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 30433
bin: 2.5e0
variant carriers: 1

GenotypeDepth
all individuals: 3401
bin: 1.25e1
variant carriers: 2

GenotypeDepth
all individuals: 1262
bin: 1.75e1
variant carriers: 1

GenotypeDepth
all individuals: 92
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 374
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 105
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 174
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 398
bin: 4.75e1
variant carriers: 1

GenotypeDepth
all individuals: 1618
bin: 2.25e1
variant carriers: 1

GenotypeDepth
all individuals: 275
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 16481
bin: 7.5e0
variant carriers: 3

GenotypeDepth
all individuals: 235
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 152
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 511
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 130
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 429
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 369
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1820
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 44
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1280
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 254
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3862
bin: 1.75e1
variant carriers: 1

GenotypeQuality
all individuals: 432
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6138
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24414
bin: 7.5e0
variant carriers: 1

GenotypeQuality
all individuals: 120
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2851
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 10229
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 284
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 232
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 937
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 427
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1074
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 185
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2993
bin: 9.75e1
variant carriers: 7

GenotypeQuality
all individuals: 353
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 166
bin: 8.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 214
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 944
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.526717557251908e-4
allele num: 6550
num of homozygotes: 0

African
type: Population
allele count: 5
allele frequency: 1.578282828282828e-3
allele num: 3168
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 184
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10436
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 486
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 4.83e-1

FS
type: SiteQuality
SIO_000300: 5.057e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.58e-1

DP
type: SiteQuality
SIO_000300: 5.48891e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.76e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 3.58e-1

MQRankSum
type: SiteQuality
SIO_000300: -6.840000000000001e-1

QD
type: SiteQuality
SIO_000300: 1.368e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.97e-1

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl transcript: ENST00000577144
gene symbol: CORO7
hgvsc: ENST00000577144.1:n.265+41C>T
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000461051
ensembl transcript: ENST00000572153
gene symbol: CORO7
hgvsc: ENST00000572153.1:c.61-837C>T
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000460199
ensembl transcript: ENST00000570928
gene symbol: CORO7
hgvsc: ENST00000570928.1:c.157+41C>T
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl transcript: ENST00000572026
gene symbol: CORO7
hgvsc: ENST00000572026.1:n.280+41C>T
variant of: http://identifiers.org/hgnc/26161

GenotypeDepth
all individuals: 794
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 397
bin: 4.75e1
variant carriers: 1

GenotypeDepth
all individuals: 152
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 373
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 174
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 235
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 30098
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 571
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1172
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 318
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 428
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 16842
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 512
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1759
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3372
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 275
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 92
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 106
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 130
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 368
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 331
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 188
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3760
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24411
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 10682
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 234
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 167
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 453
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 908
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2986
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 5834
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1090
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 253
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2779
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 284
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1922
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1277
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 136
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 405
bin: 4.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 220
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 956
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 3.15059861373661e-4
allele num: 3174
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 186
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 486
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10502
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6636
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.424e0

VQSLOD
type: SiteQuality
SIO_000300: -8.962e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 5.53102e5

QD
type: SiteQuality
SIO_000300: 1.057e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.46e0

MQRankSum
type: SiteQuality
SIO_000300: -3.36e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.7e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.79e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.76e-2

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000459888
ensembl transcript: ENST00000576051
gene symbol: CORO7
hgvsc: ENST00000576051.1:c.-343+31C>T
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000103426
ensembl protein: ENSP00000458607
ensembl transcript: ENST00000575334
gene symbol: CORO7-PAM16
hgvsc: ENST00000575334.1:c.157+31C>T
variant of: http://identifiers.org/hgnc/44424

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl transcript: ENST00000572026
gene symbol: CORO7
hgvsc: ENST00000572026.1:n.280+31C>T
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: true
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000251166
ensembl transcript: ENST00000251166
gene symbol: CORO7
hgvsc: ENST00000251166.4:c.157+31C>T
variant of: http://identifiers.org/hgnc/26161

GenotypeDepth
all individuals: 2718
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 130
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 106
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 429
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 673
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3115
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 235
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 574
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 27375
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 276
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 317
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 19907
bin: 7.5e0
variant carriers: 1

GenotypeDepth
all individuals: 512
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 152
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 937
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 396
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 368
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 92
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 373
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 174
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2542
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 107
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24031
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 501
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 259
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1596
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1150
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15591
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2987
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 643
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 233
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 290
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4103
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 207
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1079
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 192
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 188
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2926
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 166
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10828
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 522
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1038
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3224
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 190
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6816
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 222
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -7.2e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.32e-2

VQSLOD
type: SiteQuality
SIO_000300: -9.46e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.2e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 5.83053e5

ClippingRankSum
type: SiteQuality
SIO_000300: 7.2e-1

QD
type: SiteQuality
SIO_000300: 1.06e1

MQ
type: SiteQuality
SIO_000300: 5.604e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.38e0

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000458459
ensembl transcript: ENST00000571227
gene symbol: CORO7
hgvsc: ENST00000571227.1:c.*154+28T>G
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000458935
ensembl transcript: ENST00000572898
gene symbol: CORO7
hgvsc: ENST00000572898.1:c.157+28T>G
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000459286
ensembl transcript: ENST00000572549
gene symbol: CORO7
hgvsc: ENST00000572549.1:c.99+3505T>G
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000459888
ensembl transcript: ENST00000576051
gene symbol: CORO7
hgvsc: ENST00000576051.1:c.-343+28T>G
variant of: http://identifiers.org/hgnc/26161

GenotypeDepth
all individuals: 2941
bin: 1.25e1
variant carriers: 2

GenotypeDepth
all individuals: 317
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 512
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 92
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 581
bin: 3.25e1
variant carriers: 1

GenotypeDepth
all individuals: 428
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 26386
bin: 2.5e0
variant carriers: 2

GenotypeDepth
all individuals: 21013
bin: 7.5e0
variant carriers: 1

GenotypeDepth
all individuals: 1006
bin: 2.75e1
variant carriers: 1

GenotypeDepth
all individuals: 174
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 373
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 235
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 396
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2979
bin: 2.25e1
variant carriers: 1

GenotypeDepth
all individuals: 130
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 368
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 106
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 276
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 602
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 152
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23524
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 173
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 568
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 187
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 234
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 3263
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17117
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 294
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2375
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1179
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 166
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3689
bin: 1.25e1
variant carriers: 1

GenotypeQuality
all individuals: 195
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 529
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1099
bin: 3.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1066
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 114
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2991
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 258
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 5.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 2.727272727272727e-4
allele num: 11000
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 3.082614056720099e-4
allele num: 3244
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.872659176029963e-3
allele num: 534
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 228
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6938
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1082
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 192
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 8.31e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.6e-1

DP
type: SiteQuality
SIO_000300: 5.93007e5

BaseQRankSum
type: SiteQuality
SIO_000300: 9.45e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.7e-1

QD
type: SiteQuality
SIO_000300: 1.554e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.2e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.82e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.07e-2

Annotation
canonical: true
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000251166
ensembl transcript: ENST00000251166
gene symbol: CORO7
hgvsc: ENST00000251166.4:c.157+25T>G
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000458935
ensembl transcript: ENST00000572898
gene symbol: CORO7
hgvsc: ENST00000572898.1:c.157+25T>G
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000458828
ensembl transcript: ENST00000571756
gene symbol: CORO7
hgvsc: ENST00000571756.1:c.157+25T>G
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl transcript: ENST00000576457
gene symbol: CORO7
hgvsc: ENST00000576457.1:n.217+25T>G
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000458411
ensembl transcript: ENST00000572044
gene symbol: CORO7
hgvsc: ENST00000572044.1:c.60+3176T>G
variant of: http://identifiers.org/hgnc/26161

GenotypeDepth
all individuals: 378
bin: 9.75e1
variant carriers: 10

GenotypeDepth
all individuals: 150
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 316
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 130
bin: 8.25e1
variant carriers: 1

GenotypeDepth
all individuals: 585
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 512
bin: 3.75e1
variant carriers: 3

GenotypeDepth
all individuals: 529
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2798
bin: 1.25e1
variant carriers: 7

GenotypeDepth
all individuals: 428
bin: 4.25e1
variant carriers: 1

GenotypeDepth
all individuals: 177
bin: 7.25e1
variant carriers: 3

GenotypeDepth
all individuals: 106
bin: 9.25e1
variant carriers: 1

GenotypeDepth
all individuals: 275
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 369
bin: 5.25e1
variant carriers: 2

GenotypeDepth
all individuals: 397
bin: 4.75e1
variant carriers: 3

GenotypeDepth
all individuals: 1037
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 25295
bin: 2.5e0
variant carriers: 5

GenotypeDepth
all individuals: 22141
bin: 7.5e0
variant carriers: 19

GenotypeDepth
all individuals: 91
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 236
bin: 6.75e1
variant carriers: 1

GenotypeDepth
all individuals: 3271
bin: 2.25e1
variant carriers: 1

GenotypeQuality
all individuals: 165
bin: 4.25e1
variant carriers: 4

GenotypeQuality
all individuals: 232
bin: 9.25e1
variant carriers: 2

GenotypeQuality
all individuals: 3343
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 292
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1021
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 131
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17885
bin: 2.25e1
variant carriers: 1

GenotypeQuality
all individuals: 492
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1155
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 541
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3005
bin: 9.75e1
variant carriers: 36

GenotypeQuality
all individuals: 2804
bin: 1.75e1
variant carriers: 1

GenotypeQuality
all individuals: 151
bin: 4.75e1
variant carriers: 3

GenotypeQuality
all individuals: 3479
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 22757
bin: 7.5e0
variant carriers: 2

GenotypeQuality
all individuals: 125
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1019
bin: 2.75e1
variant carriers: 1

GenotypeQuality
all individuals: 259
bin: 8.25e1
variant carriers: 2

GenotypeQuality
all individuals: 196
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 169
bin: 8.75e1
variant carriers: 3

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 544
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 230
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1092
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11074
num of homozygotes: 0

African
type: Population
allele count: 33
allele frequency: 1.012269938650307e-2
allele num: 3260
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 204
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6992
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 3.12e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.83e-1

FS
type: SiteQuality
SIO_000300: 6.96e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.97e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -2.14e-1

QD
type: SiteQuality
SIO_000300: 1.565e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.17e0

MQRankSum
type: SiteQuality
SIO_000300: 1.98e-1

DP
type: SiteQuality
SIO_000300: 6.03489e5

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl transcript: ENST00000576457
gene symbol: CORO7
hgvsc: ENST00000576457.1:n.217+19T>C
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000459085
ensembl transcript: ENST00000571052
gene symbol: CORO7
hgvsc: ENST00000571052.1:c.-268+3170T>C
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000460199
ensembl transcript: ENST00000570928
gene symbol: CORO7
hgvsc: ENST00000570928.1:c.157+19T>C
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000461797
ensembl transcript: ENST00000575038
gene symbol: CORO7
hgvsc: ENST00000575038.1:c.157+19T>C
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000458935
ensembl transcript: ENST00000572898
gene symbol: CORO7
hgvsc: ENST00000572898.1:c.157+19T>C
variant of: http://identifiers.org/hgnc/26161

GenotypeDepth
all individuals: 22738
bin: 2.5e0
variant carriers: 1

GenotypeDepth
all individuals: 2630
bin: 1.25e1
variant carriers: 1

GenotypeDepth
all individuals: 372
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 129
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 616
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 174
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 105
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 430
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 24584
bin: 7.5e0
variant carriers: 2

GenotypeDepth
all individuals: 235
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 151
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3794
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 396
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 275
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 91
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 508
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1226
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 372
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 319
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 427
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 872
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 142
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20862
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 884
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 172
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2979
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2580
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 956
bin: 2.75e1
variant carriers: 1

GenotypeQuality
all individuals: 117
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 261
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 20995
bin: 7.5e0
variant carriers: 1

GenotypeQuality
all individuals: 114
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 399
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 606
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 231
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 294
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 203
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2622
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4202
bin: 6.25e1
variant carriers: 1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1162
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7202
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11566
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 232
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3326
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 558
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 236
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.271e1

MQRankSum
type: SiteQuality
SIO_000300: 7.27e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 6.27228e5

FS
type: SiteQuality
SIO_000300: 3.332e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.840000000000001e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.67e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 3.58e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.01e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.231e0

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl transcript: ENST00000577144
gene symbol: CORO7
hgvsc: ENST00000577144.1:n.265+18G>A
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000459286
ensembl transcript: ENST00000572549
gene symbol: CORO7
hgvsc: ENST00000572549.1:c.99+3495G>A
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000391530
ensembl transcript: ENST00000423908
gene symbol: CORO7
hgvsc: ENST00000423908.2:c.60+3169G>A
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000461797
ensembl transcript: ENST00000575038
gene symbol: CORO7
hgvsc: ENST00000575038.1:c.157+18G>A
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000461051
ensembl transcript: ENST00000572153
gene symbol: CORO7
hgvsc: ENST00000572153.1:c.61-860G>A
variant of: http://identifiers.org/hgnc/26161

GenotypeDepth
all individuals: 151
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 22286
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 632
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 373
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 3857
bin: 2.25e1
variant carriers: 1

GenotypeDepth
all individuals: 1282
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 373
bin: 5.25e1
variant carriers: 1

GenotypeDepth
all individuals: 319
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 174
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 25018
bin: 7.5e0
variant carriers: 2

GenotypeDepth
all individuals: 274
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 91
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 421
bin: 1.75e1
variant carriers: 1

GenotypeDepth
all individuals: 396
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 105
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2568
bin: 1.25e1
variant carriers: 3

GenotypeDepth
all individuals: 427
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 509
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 129
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 235
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2257
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 200
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 812
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 171
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2986
bin: 9.75e1
variant carriers: 8

GenotypeQuality
all individuals: 21699
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 145
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 109
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 105
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20694
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 396
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 293
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 957
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 599
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4334
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2481
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 837
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 261
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 229
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3332
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7222
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 7
allele frequency: 6.028246641405443e-4
allele num: 11612
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 242
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 562
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1172
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 234
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 3.63e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.303e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.35e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.94e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 6.32154e5

MQRankSum
type: SiteQuality
SIO_000300: -2.12e-1

QD
type: SiteQuality
SIO_000300: 1.398e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.62e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000461702
ensembl transcript: ENST00000574025
gene symbol: CORO7
hgvsc: ENST00000574025.1:c.157+15T>C
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000459228
ensembl transcript: ENST00000576437
gene symbol: CORO7
hgvsc: ENST00000576437.1:c.-214+3187T>C
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000460199
ensembl transcript: ENST00000570928
gene symbol: CORO7
hgvsc: ENST00000570928.1:c.157+15T>C
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000459085
ensembl transcript: ENST00000571052
gene symbol: CORO7
hgvsc: ENST00000571052.1:c.-268+3166T>C
variant of: http://identifiers.org/hgnc/26161

GenotypeDepth
all individuals: 91
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 642
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2454
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 20748
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 396
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 175
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 508
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 26435
bin: 7.5e0
variant carriers: 1

GenotypeDepth
all individuals: 105
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 274
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 427
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4181
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 319
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 383
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 129
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 151
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1370
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 372
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 372
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 235
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 100
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 906
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 90
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 753
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19469
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 631
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23552
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 174
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 619
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2061
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 205
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2139
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 232
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 346
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 110
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4781
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2981
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 307
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 262
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11898
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 234
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1234
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7404
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 590
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3390
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 248
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.06e-1

DP
type: SiteQuality
SIO_000300: 6.46415e5

MQRankSum
type: SiteQuality
SIO_000300: -1.17e-1

FS
type: SiteQuality
SIO_000300: 8.61e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.38e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 8.799999999999999e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.537e0

QD
type: SiteQuality
SIO_000300: 1.405e1

VQSLOD
type: SiteQuality
SIO_000300: 1.48e0

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000461051
ensembl transcript: ENST00000572153
gene symbol: CORO7
hgvsc: ENST00000572153.1:c.61-864A>G
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000461187
ensembl transcript: ENST00000574311
gene symbol: CORO7
hgvsc: ENST00000574311.1:c.60+3165A>G
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000440460
ensembl transcript: ENST00000537233
gene symbol: CORO7
hgvsc: ENST00000537233.2:c.157+14A>G
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: true
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000251166
ensembl transcript: ENST00000251166
gene symbol: CORO7
hgvsc: ENST00000251166.4:c.157+14A>G
variant of: http://identifiers.org/hgnc/26161

GenotypeDepth
all individuals: 235
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1396
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 395
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 372
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 427
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 274
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 20328
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 26819
bin: 7.5e0
variant carriers: 2

GenotypeDepth
all individuals: 92
bin: 8.75e1
variant carriers: 1

GenotypeDepth
all individuals: 4246
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2437
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 129
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 375
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 151
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 175
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 105
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 372
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 509
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 642
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 319
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 340
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 742
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 173
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 230
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 655
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 106
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 203
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 891
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4819
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2203
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23776
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2086
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19105
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 631
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 107
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 308
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2981
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 106
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 266
bin: 8.25e1
variant carriers: 1

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 592
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3402
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1242
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 250
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 234
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7448
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 8.385041086701326e-5
allele num: 11926
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 7.39e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.26e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.29e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.35e-2

DP
type: SiteQuality
SIO_000300: 6.49991e5

FS
type: SiteQuality
SIO_000300: 3.757e0

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.73e-1

QD
type: SiteQuality
SIO_000300: 8.470000000000001e0

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000461702
ensembl transcript: ENST00000574025
gene symbol: CORO7
hgvsc: ENST00000574025.1:c.157+9T>C
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000460199
ensembl transcript: ENST00000570928
gene symbol: CORO7
hgvsc: ENST00000570928.1:c.157+9T>C
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000458411
ensembl transcript: ENST00000572044
gene symbol: CORO7
hgvsc: ENST00000572044.1:c.60+3160T>C
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000391530
ensembl transcript: ENST00000423908
gene symbol: CORO7
hgvsc: ENST00000423908.2:c.60+3160T>C
variant of: http://identifiers.org/hgnc/26161

GenotypeDepth
all individuals: 175
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 105
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 129
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1651
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2463
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 428
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 274
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 672
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 362
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 319
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 17918
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 395
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 511
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4558
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 28826
bin: 7.5e0
variant carriers: 2

GenotypeDepth
all individuals: 372
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 91
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 236
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 151
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 372
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 172
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 115
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 709
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5348
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1747
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 574
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 862
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2983
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 25793
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17026
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2390
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 232
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 105
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 263
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 308
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 705
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 305
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 212
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 114
bin: 4.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 300
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 656
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7668
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12550
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3496
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 246
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1350
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.61e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.219e0

VQSLOD
type: SiteQuality
SIO_000300: -6.829e-1

QD
type: SiteQuality
SIO_000300: 7.11e0

FS
type: SiteQuality
SIO_000300: 5.035e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.04e-2

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 6.73898e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.61e-1

Annotation
canonical: false
consequence: splice_region_variant
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000440460
ensembl transcript: ENST00000537233
gene symbol: CORO7
hgvsc: ENST00000537233.2:c.157+8A>C
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000459228
ensembl transcript: ENST00000576437
gene symbol: CORO7
hgvsc: ENST00000576437.1:c.-214+3180A>C
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000458411
ensembl transcript: ENST00000572044
gene symbol: CORO7
hgvsc: ENST00000572044.1:c.60+3159A>C
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000459286
ensembl transcript: ENST00000572549
gene symbol: CORO7
hgvsc: ENST00000572549.1:c.99+3485A>C
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: splice_region_variant
consequence: intron_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000103426
ensembl protein: ENSP00000458607
ensembl transcript: ENST00000575334
gene symbol: CORO7-PAM16
hgvsc: ENST00000575334.1:c.157+8A>C
variant of: http://identifiers.org/hgnc/44424

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000461187
ensembl transcript: ENST00000574311
gene symbol: CORO7
hgvsc: ENST00000574311.1:c.60+3159A>C
variant of: http://identifiers.org/hgnc/26161

GenotypeDepth
all individuals: 174
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 90
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 29244
bin: 7.5e0
variant carriers: 2

GenotypeDepth
all individuals: 376
bin: 9.75e1
variant carriers: 6

GenotypeDepth
all individuals: 347
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4647
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 106
bin: 9.25e1
variant carriers: 1

GenotypeDepth
all individuals: 1661
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 17486
bin: 2.5e0
variant carriers: 2

GenotypeDepth
all individuals: 319
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 370
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 511
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 236
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 395
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2424
bin: 1.25e1
variant carriers: 3

GenotypeDepth
all individuals: 130
bin: 8.25e1
variant carriers: 1

GenotypeDepth
all individuals: 428
bin: 4.25e1
variant carriers: 1

GenotypeDepth
all individuals: 672
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 274
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 150
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1658
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2985
bin: 9.75e1
variant carriers: 12

GenotypeQuality
all individuals: 16647
bin: 7.5e0
variant carriers: 1

GenotypeQuality
all individuals: 27
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26607
bin: 2.25e1
variant carriers: 1

GenotypeQuality
all individuals: 264
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 89
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 308
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 307
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5489
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2085
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 104
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 496
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 717
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 697
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 107
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 215
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 173
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 230
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 835
bin: 2.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 658
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 304
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1366
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7710
num of homozygotes: 0

African
type: Population
allele count: 12
allele frequency: 3.412969283276451e-3
allele num: 3516
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12650
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 248
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 3.75e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.94e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 2.71e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.372e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.07e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.65e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.4e0

FS
type: SiteQuality
SIO_000300: 2.4e0

DP
type: SiteQuality
SIO_000300: 6.78084e5

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000391530
ensembl transcript: ENST00000423908
gene symbol: CORO7
hgvsc: ENST00000423908.2:c.60+3146G>T
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000458459
ensembl transcript: ENST00000571227
gene symbol: CORO7
hgvsc: ENST00000571227.1:c.*149G>T
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000461051
ensembl transcript: ENST00000572153
gene symbol: CORO7
hgvsc: ENST00000572153.1:c.61-883G>T
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000458935
ensembl transcript: ENST00000572898
gene symbol: CORO7
hgvsc: ENST00000572898.1:c.152G>T
hgvsp: ENSP00000458935.1:p.Arg51Leu
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000460199
ensembl transcript: ENST00000570928
gene symbol: CORO7
hgvsc: ENST00000570928.1:c.152G>T
hgvsp: ENSP00000460199.1:p.Arg51Leu
variant of: http://identifiers.org/hgnc/26161

GenotypeDepth
all individuals: 32607
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 90
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 12894
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 237
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 518
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2592
bin: 1.25e1
variant carriers: 1

GenotypeDepth
all individuals: 430
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 174
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 751
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 274
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 373
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1987
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5518
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 370
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 396
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 373
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 129
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 320
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 150
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 106
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 173
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 95
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 114
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 766
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 764
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12496
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 472
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 267
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 303
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 643
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1092
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 123
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30596
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2979
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 298
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1955
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 215
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 105
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 232
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6601
bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 7.117437722419929e-5
allele num: 14050
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8146
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 268
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 404
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3742
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 838
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1696
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 7.608e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.98e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -6.728e-1

DP
type: SiteQuality
SIO_000300: 7.24007e5

MQRankSum
type: SiteQuality
SIO_000300: 2.78e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.89e-1

QD
type: SiteQuality
SIO_000300: 8.359999999999999e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.36e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.66e-1

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000440460
ensembl transcript: ENST00000537233
gene symbol: CORO7
hgvsc: ENST00000537233.2:c.152G>A
hgvsp: ENSP00000440460.2:p.Arg51His
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000459286
ensembl transcript: ENST00000572549
gene symbol: CORO7
hgvsc: ENST00000572549.1:c.99+3472G>A
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000461051
ensembl transcript: ENST00000572153
gene symbol: CORO7
hgvsc: ENST00000572153.1:c.61-883G>A
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000458459
ensembl transcript: ENST00000571227
gene symbol: CORO7
hgvsc: ENST00000571227.1:c.*149G>A
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000458935
ensembl transcript: ENST00000572898
gene symbol: CORO7
hgvsc: ENST00000572898.1:c.152G>A
hgvsp: ENSP00000458935.1:p.Arg51His
variant of: http://identifiers.org/hgnc/26161

GenotypeDepth
all individuals: 12894
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 518
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 751
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 129
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5518
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 373
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 90
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 237
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 150
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 274
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 373
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 430
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 370
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 320
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2592
bin: 1.25e1
variant carriers: 1

GenotypeDepth
all individuals: 32607
bin: 7.5e0
variant carriers: 1

GenotypeDepth
all individuals: 174
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 396
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 106
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1987
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 267
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1092
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 173
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30596
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 114
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 123
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 215
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 472
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 764
bin: 2.75e1
variant carriers: 1

GenotypeQuality
all individuals: 303
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 298
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1955
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 643
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 105
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12496
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 95
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6601
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 232
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2979
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 766
bin: 6.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 404
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 838
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1696
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8146
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 2.672367717797969e-4
allele num: 3742
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14050
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 268
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 8.359999999999999e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.98e-2

VQSLOD
type: SiteQuality
SIO_000300: -6.728e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.66e-1

FS
type: SiteQuality
SIO_000300: 7.608e0

MQRankSum
type: SiteQuality
SIO_000300: 2.78e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.89e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.36e-1

DP
type: SiteQuality
SIO_000300: 7.24007e5

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000459228
ensembl transcript: ENST00000576437
gene symbol: CORO7
hgvsc: ENST00000576437.1:c.-214+3166C>T
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: 5_prime_UTR_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000459888
ensembl transcript: ENST00000576051
gene symbol: CORO7
hgvsc: ENST00000576051.1:c.-349C>T
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000459286
ensembl transcript: ENST00000572549
gene symbol: CORO7
hgvsc: ENST00000572549.1:c.99+3471C>T
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000458459
ensembl transcript: ENST00000571227
gene symbol: CORO7
hgvsc: ENST00000571227.1:c.*148C>T
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000391530
ensembl transcript: ENST00000423908
gene symbol: CORO7
hgvsc: ENST00000423908.2:c.60+3145C>T
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000459085
ensembl transcript: ENST00000571052
gene symbol: CORO7
hgvsc: ENST00000571052.1:c.-268+3145C>T
variant of: http://identifiers.org/hgnc/26161

GenotypeDepth
all individuals: 106
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 512
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 12401
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 237
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 32909
bin: 7.5e0
variant carriers: 4

GenotypeDepth
all individuals: 428
bin: 4.25e1
variant carriers: 1

GenotypeDepth
all individuals: 150
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 274
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 174
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 370
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 373
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2624
bin: 1.25e1
variant carriers: 2

GenotypeDepth
all individuals: 5645
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 396
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2023
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 745
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 396
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 90
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 129
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 320
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 121
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 744
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 629
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 267
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 783
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 99
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1079
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12021
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6786
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1963
bin: 1.75e1
variant carriers: 1

GenotypeQuality
all individuals: 30925
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 288
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 304
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 219
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 504
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 172
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 232
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2980
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 105
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 5.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 418
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.157407407407407e-3
allele num: 864
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3754
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 1.407855835562438e-4
allele num: 14206
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1744
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 268
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8188
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 2.48e0

FS
type: SiteQuality
SIO_000300: 1.157e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.29e-2

DP
type: SiteQuality
SIO_000300: 7.29039e5

QD
type: SiteQuality
SIO_000300: 1.352e1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.36e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.36e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.8e-2

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000459085
ensembl transcript: ENST00000571052
gene symbol: CORO7
hgvsc: ENST00000571052.1:c.-268+3141C>T
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000459286
ensembl transcript: ENST00000572549
gene symbol: CORO7
hgvsc: ENST00000572549.1:c.99+3467C>T
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: 5_prime_UTR_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000459888
ensembl transcript: ENST00000576051
gene symbol: CORO7
hgvsc: ENST00000576051.1:c.-353C>T
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000460901
ensembl transcript: ENST00000570645
gene symbol: CORO7
hgvsc: ENST00000570645.1:c.-214+3162C>T
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000262246
ensembl transcript: ENST00000577144
gene symbol: CORO7
hgvsc: ENST00000577144.1:n.255C>T
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: synonymous_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000460199
ensembl transcript: ENST00000570928
gene symbol: CORO7
hgvsc: ENST00000570928.1:c.147C>T
hgvsp: ENST00000570928.1:c.147C>T(p.%3D)
variant of: http://identifiers.org/hgnc/26161

GenotypeDepth
all individuals: 174
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 106
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 370
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 373
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 427
bin: 4.25e1
variant carriers: 1

GenotypeDepth
all individuals: 11372
bin: 2.5e0
variant carriers: 4

GenotypeDepth
all individuals: 439
bin: 1.75e1
variant carriers: 3

GenotypeDepth
all individuals: 512
bin: 3.75e1
variant carriers: 1

GenotypeDepth
all individuals: 33541
bin: 7.5e0
variant carriers: 8

GenotypeDepth
all individuals: 274
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5818
bin: 2.25e1
variant carriers: 2

GenotypeDepth
all individuals: 90
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2774
bin: 1.25e1
variant carriers: 10

GenotypeDepth
all individuals: 237
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 151
bin: 7.75e1
variant carriers: 1

GenotypeDepth
all individuals: 397
bin: 4.75e1
variant carriers: 1

GenotypeDepth
all individuals: 129
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 320
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 749
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2113
bin: 2.75e1
variant carriers: 1

GenotypeQuality
all individuals: 304
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 798
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 107
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1073
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11077
bin: 7.5e0
variant carriers: 1

GenotypeQuality
all individuals: 7009
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 302
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 234
bin: 9.25e1
variant carriers: 2

GenotypeQuality
all individuals: 117
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 263
bin: 8.25e1
variant carriers: 2

GenotypeQuality
all individuals: 455
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2000
bin: 1.75e1
variant carriers: 2

GenotypeQuality
all individuals: 173
bin: 8.75e1
variant carriers: 2

GenotypeQuality
all individuals: 658
bin: 3.25e1
variant carriers: 1

GenotypeQuality
all individuals: 119
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 224
bin: 7.25e1
variant carriers: 1

GenotypeQuality
all individuals: 2992
bin: 9.75e1
variant carriers: 16

GenotypeQuality
all individuals: 104
bin: 5.75e1
variant carriers: 3

GenotypeQuality
all individuals: 739
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31618
bin: 2.25e1
variant carriers: 1

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 920
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 6.820351930159596e-5
allele num: 14662
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 466
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3822
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1864
num of homozygotes: 0

South Asian
type: Population
allele count: 19
allele frequency: 2.28310502283105e-3
allele num: 8322
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 276
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.053e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.48e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.06e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 1.939e0

VQSLOD
type: SiteQuality
SIO_000300: 8.3e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.06e-1

DP
type: SiteQuality
SIO_000300: 7.40123e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.11e-2

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000458935
ensembl transcript: ENST00000572898
gene symbol: CORO7
hgvsc: ENST00000572898.1:c.144C>T
hgvsp: ENST00000572898.1:c.144C>T(p.%3D)
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000262246
ensembl transcript: ENST00000572026
gene symbol: CORO7
hgvsc: ENST00000572026.1:n.267C>T
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000459286
ensembl transcript: ENST00000572549
gene symbol: CORO7
hgvsc: ENST00000572549.1:c.99+3464C>T
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: synonymous_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000460199
ensembl transcript: ENST00000570928
gene symbol: CORO7
hgvsc: ENST00000570928.1:c.144C>T
hgvsp: ENST00000570928.1:c.144C>T(p.%3D)
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000459085
ensembl transcript: ENST00000571052
gene symbol: CORO7
hgvsc: ENST00000571052.1:c.-268+3138C>T
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000391530
ensembl transcript: ENST00000423908
gene symbol: CORO7
hgvsc: ENST00000423908.2:c.60+3138C>T
variant of: http://identifiers.org/hgnc/26161

GenotypeDepth
all individuals: 425
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 150
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 237
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 396
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2136
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 33933
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 373
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 10796
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 6048
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 370
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 174
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2763
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 426
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 107
bin: 9.25e1
variant carriers: 1

GenotypeDepth
all individuals: 512
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 129
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 274
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 747
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 90
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 320
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 302
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 10521
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 658
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 231
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 171
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1003
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7294
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 94
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1786
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 122
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 753
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 304
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 225
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32411
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 297
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 62
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 807
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 127
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2977
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 261
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 6.638343069569835e-5
allele num: 15064
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 492
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 968
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3874
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8384
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1962
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 278
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.03e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -4.162e0

DP
type: SiteQuality
SIO_000300: 7.46799e5

FS
type: SiteQuality
SIO_000300: 8.59e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.2e-2

MQRankSum
type: SiteQuality
SIO_000300: -2.075e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -2.513e-1

QD
type: SiteQuality
SIO_000300: 1.305e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.79e-1

Annotation
canonical: false
consequence: 5_prime_UTR_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000446221
ensembl transcript: ENST00000539968
gene symbol: CORO7
hgvsc: ENST00000539968.1:c.-464G>T
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000458411
ensembl transcript: ENST00000572044
gene symbol: CORO7
hgvsc: ENST00000572044.1:c.60+3130G>T
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000459286
ensembl transcript: ENST00000572549
gene symbol: CORO7
hgvsc: ENST00000572549.1:c.99+3456G>T
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000458459
ensembl transcript: ENST00000571227
gene symbol: CORO7
hgvsc: ENST00000571227.1:c.*133G>T
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000262246
ensembl transcript: ENST00000572026
gene symbol: CORO7
hgvsc: ENST00000572026.1:n.259G>T
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000461187
ensembl transcript: ENST00000574311
gene symbol: CORO7
hgvsc: ENST00000574311.1:c.60+3130G>T
variant of: http://identifiers.org/hgnc/26161

GenotypeDepth
all individuals: 3140
bin: 1.25e1
variant carriers: 1

GenotypeDepth
all individuals: 150
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2202
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6244
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 397
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 34231
bin: 7.5e0
variant carriers: 1

GenotypeDepth
all individuals: 430
bin: 4.25e1
variant carriers: 1

GenotypeDepth
all individuals: 762
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 371
bin: 5.25e1
variant carriers: 1

GenotypeDepth
all individuals: 275
bin: 6.25e1
variant carriers: 1

GenotypeDepth
all individuals: 515
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 319
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 511
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 9756
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 174
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 237
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 106
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 129
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 90
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 374
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 260
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32353
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 104
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 758
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 641
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 222
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 471
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 163
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 230
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1067
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2291
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9567
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 112
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 820
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 172
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 231
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 301
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 301
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2981
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 7368
bin: 6.25e1
variant carriers: 0

South Asian
type: Population
allele count: 6
allele frequency: 7.078810759792355e-4
allele num: 8476
num of homozygotes: 1

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15706
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4000
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 542
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 282
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1052
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2104
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.463e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.91e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 7.59377e5

MQRankSum
type: SiteQuality
SIO_000300: -2.8e-2

QD
type: SiteQuality
SIO_000300: 1.969e1

FS
type: SiteQuality
SIO_000300: 5.545e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.44e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.4e-1

Annotation
canonical: false
consequence: 5_prime_UTR_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000446221
ensembl transcript: ENST00000539968
gene symbol: CORO7
hgvsc: ENST00000539968.1:c.-465C>T
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000262246
ensembl transcript: ENST00000577144
gene symbol: CORO7
hgvsc: ENST00000577144.1:n.243C>T
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000440460
ensembl transcript: ENST00000537233
gene symbol: CORO7
hgvsc: ENST00000537233.2:c.135C>T
hgvsp: ENST00000537233.2:c.135C>T(p.%3D)
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000458459
ensembl transcript: ENST00000571227
gene symbol: CORO7
hgvsc: ENST00000571227.1:c.*132C>T
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000459228
ensembl transcript: ENST00000576437
gene symbol: CORO7
hgvsc: ENST00000576437.1:c.-214+3150C>T
variant of: http://identifiers.org/hgnc/26161

GenotypeDepth
all individuals: 6290
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 766
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 514
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2227
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 9563
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 90
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 175
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3224
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 577
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 428
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 370
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 319
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 397
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 34213
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 373
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 106
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 129
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 238
bin: 6.75e1
variant carriers: 1

GenotypeDepth
all individuals: 150
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 274
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7464
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 172
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 154
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1052
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 96
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 627
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 300
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 303
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 826
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2135
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9415
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 222
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 734
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32511
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2978
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 261
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 629
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 216
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 97
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 231
bin: 9.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 544
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 280
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.180637544273908e-4
allele num: 8470
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1072
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2122
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15852
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4014
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.98e-2

DP
type: SiteQuality
SIO_000300: 7.62569e5

VQSLOD
type: SiteQuality
SIO_000300: -1.105e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.15e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.82e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.14e-1

FS
type: SiteQuality
SIO_000300: 2.612e0

MQRankSum
type: SiteQuality
SIO_000300: -1.18e-1

QD
type: SiteQuality
SIO_000300: 7.68e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

Annotation
canonical: false
consequence: 5_prime_UTR_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000459888
ensembl transcript: ENST00000576051
gene symbol: CORO7
hgvsc: ENST00000576051.1:c.-367A>G
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000262246
ensembl transcript: ENST00000577144
gene symbol: CORO7
hgvsc: ENST00000577144.1:n.241A>G
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000458828
ensembl transcript: ENST00000571756
gene symbol: CORO7
hgvsc: ENST00000571756.1:c.133A>G
hgvsp: ENSP00000458828.1:p.Ile45Val
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000460901
ensembl transcript: ENST00000570645
gene symbol: CORO7
hgvsc: ENST00000570645.1:c.-214+3148A>G
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000440460
ensembl transcript: ENST00000537233
gene symbol: CORO7
hgvsc: ENST00000537233.2:c.133A>G
hgvsp: ENSP00000440460.2:p.Ile45Val
variant of: http://identifiers.org/hgnc/26161

GenotypeDepth
all individuals: 9414
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 2245
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 175
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6361
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 129
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 150
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 762
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 90
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 319
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 274
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 370
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 427
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 509
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 237
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 397
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 34383
bin: 7.5e0
variant carriers: 1

GenotypeDepth
all individuals: 3202
bin: 1.25e1
variant carriers: 1

GenotypeDepth
all individuals: 373
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 106
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 511
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 172
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 836
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 314
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 215
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 645
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 729
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9247
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 302
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2138
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1036
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 231
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 220
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 282
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 100
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7612
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2979
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 165
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32885
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 262
bin: 8.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 570
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8514
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 282
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 2.452182442373713e-4
allele num: 4078
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16192
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1114
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2202
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 9.370000000000001e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.58e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.17e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.85e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.034e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 8.786e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.199999999999999e-2

DP
type: SiteQuality
SIO_000300: 7.64026e5

QD
type: SiteQuality
SIO_000300: 1.157e1

Annotation
canonical: false
consequence: 5_prime_UTR_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000446221
ensembl transcript: ENST00000539968
gene symbol: CORO7
hgvsc: ENST00000539968.1:c.-473A>T
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000461187
ensembl transcript: ENST00000574311
gene symbol: CORO7
hgvsc: ENST00000574311.1:c.60+3121A>T
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000262246
ensembl transcript: ENST00000577144
gene symbol: CORO7
hgvsc: ENST00000577144.1:n.235A>T
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000391530
ensembl transcript: ENST00000423908
gene symbol: CORO7
hgvsc: ENST00000423908.2:c.60+3121A>T
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000460901
ensembl transcript: ENST00000570645
gene symbol: CORO7
hgvsc: ENST00000570645.1:c.-214+3142A>T
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000103426
ensembl protein: ENSP00000458607
ensembl transcript: ENST00000575334
gene symbol: CORO7-PAM16
hgvsc: ENST00000575334.1:c.127A>T
hgvsp: ENSP00000458607.1:p.Ser43Cys
variant of: http://identifiers.org/hgnc/44424

GenotypeDepth
all individuals: 373
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 274
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 90
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2267
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 175
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3319
bin: 1.25e1
variant carriers: 1

GenotypeDepth
all individuals: 34369
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 511
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 760
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 319
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6459
bin: 2.25e1
variant carriers: 1

GenotypeDepth
all individuals: 535
bin: 1.75e1
variant carriers: 1

GenotypeDepth
all individuals: 237
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 397
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 427
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 150
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 9176
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 370
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 106
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 129
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 655
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 147
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1021
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2536
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 231
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9017
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2980
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 303
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 171
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 90
bin: 4.25e1
variant carriers: 1

GenotypeQuality
all individuals: 836
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 286
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 221
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 704
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 299
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7625
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 262
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 174
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32630
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 255
bin: 5.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4144
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1160
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 1.816420440784694e-4
allele num: 16516
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 588
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2248
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 286
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8558
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -2.051e0

MQ
type: SiteQuality
SIO_000300: 5.787e1

QD
type: SiteQuality
SIO_000300: 6.84e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.227e0

FS
type: SiteQuality
SIO_000300: 1.241e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.199999999999999e-2

VQSLOD
type: SiteQuality
SIO_000300: -2.465e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.5e-1

DP
type: SiteQuality
SIO_000300: 7.68439e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.82e-2

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000459085
ensembl transcript: ENST00000571052
gene symbol: CORO7
hgvsc: ENST00000571052.1:c.-268+3108C>T
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: 5_prime_UTR_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000459888
ensembl transcript: ENST00000576051
gene symbol: CORO7
hgvsc: ENST00000576051.1:c.-386C>T
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: synonymous_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000103426
ensembl protein: ENSP00000458607
ensembl transcript: ENST00000575334
gene symbol: CORO7-PAM16
hgvsc: ENST00000575334.1:c.114C>T
hgvsp: ENST00000575334.1:c.114C>T(p.%3D)
variant of: http://identifiers.org/hgnc/44424

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000460901
ensembl transcript: ENST00000570645
gene symbol: CORO7
hgvsc: ENST00000570645.1:c.-214+3129C>T
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000461051
ensembl transcript: ENST00000572153
gene symbol: CORO7
hgvsc: ENST00000572153.1:c.61-921C>T
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000262246
ensembl transcript: ENST00000577144
gene symbol: CORO7
hgvsc: ENST00000577144.1:n.222C>T
variant of: http://identifiers.org/hgnc/26161

GenotypeDepth
all individuals: 370
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 471
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 513
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 319
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2310
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8868
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 397
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 237
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3572
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 763
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 175
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 427
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 34235
bin: 7.5e0
variant carriers: 1

GenotypeDepth
all individuals: 373
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 106
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 90
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 129
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 150
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 274
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6692
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 598
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8782
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 275
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1894
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2979
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 297
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 265
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 913
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 231
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33510
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 671
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 835
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 346
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 171
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 175
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8030
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 219
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 132
bin: 4.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8640
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4212
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 286
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2342
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1214
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16976
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 662
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.83e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 7.75762e5

BaseQRankSum
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.22e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.21e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.22e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.055e0

QD
type: SiteQuality
SIO_000300: 7.11e0

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000461187
ensembl transcript: ENST00000574311
gene symbol: CORO7
hgvsc: ENST00000574311.1:c.60+3107T>C
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000459228
ensembl transcript: ENST00000576437
gene symbol: CORO7
hgvsc: ENST00000576437.1:c.-214+3128T>C
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000262246
ensembl transcript: ENST00000577144
gene symbol: CORO7
hgvsc: ENST00000577144.1:n.221T>C
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000461051
ensembl transcript: ENST00000572153
gene symbol: CORO7
hgvsc: ENST00000572153.1:c.61-922T>C
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000460199
ensembl transcript: ENST00000570928
gene symbol: CORO7
hgvsc: ENST00000570928.1:c.113T>C
hgvsp: ENSP00000460199.1:p.Ile38Thr
variant of: http://identifiers.org/hgnc/26161

GenotypeDepth
all individuals: 6681
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2308
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 106
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 175
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 511
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 428
bin: 4.25e1
variant carriers: 1

GenotypeDepth
all individuals: 34177
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 3586
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 129
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8927
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 763
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 373
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 397
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 274
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 470
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 90
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 150
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 237
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 370
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 319
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 171
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2979
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 96
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8011
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 300
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 128
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8843
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 283
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 597
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1904
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 177
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 920
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33510
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 220
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 250
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 682
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 836
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 265
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 231
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 5.882352941176471e-5
allele num: 17000
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4198
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 650
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1238
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8646
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2346
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 288
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.81e-2

QD
type: SiteQuality
SIO_000300: 1.04e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.87e0

MQ
type: SiteQuality
SIO_000300: 4.97e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.28e0

VQSLOD
type: SiteQuality
SIO_000300: -1.935e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.98e0

MQRankSum
type: SiteQuality
SIO_000300: -2.63e-1

FS
type: SiteQuality
SIO_000300: 4.199e0

DP
type: SiteQuality
SIO_000300: 7.75398e5

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000461187
ensembl transcript: ENST00000574311
gene symbol: CORO7
hgvsc: ENST00000574311.1:c.60+3098G>A
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000459085
ensembl transcript: ENST00000571052
gene symbol: CORO7
hgvsc: ENST00000571052.1:c.-268+3098G>A
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000461051
ensembl transcript: ENST00000572153
gene symbol: CORO7
hgvsc: ENST00000572153.1:c.61-931G>A
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000458459
ensembl transcript: ENST00000571227
gene symbol: CORO7
hgvsc: ENST00000571227.1:c.*101G>A
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000262246
ensembl transcript: ENST00000572026
gene symbol: CORO7
hgvsc: ENST00000572026.1:n.227G>A
variant of: http://identifiers.org/hgnc/26161

GenotypeDepth
all individuals: 2355
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 397
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 467
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 370
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 237
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6354
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9652
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 106
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 514
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 761
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 373
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 319
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 428
bin: 4.25e1
variant carriers: 1

GenotypeDepth
all individuals: 33301
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 3966
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 175
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 90
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 274
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 150
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 129
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 264
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 94
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 231
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 846
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 123
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 309
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2979
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 9655
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 222
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 846
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 246
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 560
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 680
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33180
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1784
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7787
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 302
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 171
bin: 8.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 622
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 298
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2360
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1234
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 17064
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4198
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.152604887044721e-4
allele num: 8676
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 4.5e-1

QD
type: SiteQuality
SIO_000300: 4.7e0

FS
type: SiteQuality
SIO_000300: 2.285e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.5e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.94e-2

VQSLOD
type: SiteQuality
SIO_000300: -1.668e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.92e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.0e-2

DP
type: SiteQuality
SIO_000300: 7.70536e5

Annotation
canonical: false
consequence: 5_prime_UTR_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000459888
ensembl transcript: ENST00000576051
gene symbol: CORO7
hgvsc: ENST00000576051.1:c.-404T>C
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: synonymous_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000103426
ensembl protein: ENSP00000458607
ensembl transcript: ENST00000575334
gene symbol: CORO7-PAM16
hgvsc: ENST00000575334.1:c.96T>C
hgvsp: ENST00000575334.1:c.96T>C(p.%3D)
variant of: http://identifiers.org/hgnc/44424

Annotation
canonical: false
consequence: synonymous_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000460199
ensembl transcript: ENST00000570928
gene symbol: CORO7
hgvsc: ENST00000570928.1:c.96T>C
hgvsp: ENST00000570928.1:c.96T>C(p.%3D)
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000459286
ensembl transcript: ENST00000572549
gene symbol: CORO7
hgvsc: ENST00000572549.1:c.99+3416T>C
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: 5_prime_UTR_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000446221
ensembl transcript: ENST00000539968
gene symbol: CORO7
hgvsc: ENST00000539968.1:c.-504T>C
variant of: http://identifiers.org/hgnc/26161

GenotypeDepth
all individuals: 5567
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 31816
bin: 7.5e0
variant carriers: 1

GenotypeDepth
all individuals: 2334
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 427
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 129
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 764
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 150
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 90
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4460
bin: 1.25e1
variant carriers: 2

GenotypeDepth
all individuals: 175
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 11386
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 451
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 319
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 370
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 397
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 514
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 106
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 274
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 237
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 373
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 573
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11403
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 348
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 263
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7056
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 682
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31852
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 218
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 232
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 910
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 262
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 78
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 101
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 806
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1976
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 172
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2981
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 300
bin: 7.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 570
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8670
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4120
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2326
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1176
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 1.200624324648817e-4
allele num: 16658
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 294
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.3594e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 7.52609e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.21e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.677e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.21e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.21e-2

QD
type: SiteQuality
SIO_000300: 1.06e1

MQRankSum
type: SiteQuality
SIO_000300: -4.21e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.07e0

Annotation
canonical: false
consequence: 5_prime_UTR_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000459888
ensembl transcript: ENST00000576051
gene symbol: CORO7
hgvsc: ENST00000576051.1:c.-409G>A
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000458411
ensembl transcript: ENST00000572044
gene symbol: CORO7
hgvsc: ENST00000572044.1:c.60+3085G>A
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000391530
ensembl transcript: ENST00000423908
gene symbol: CORO7
hgvsc: ENST00000423908.2:c.60+3085G>A
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000440460
ensembl transcript: ENST00000537233
gene symbol: CORO7
hgvsc: ENST00000537233.2:c.91G>A
hgvsp: ENSP00000440460.2:p.Ala31Thr
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: true
consequence: missense_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000251166
ensembl transcript: ENST00000251166
gene symbol: CORO7
hgvsc: ENST00000251166.4:c.91G>A
hgvsp: ENSP00000251166.4:p.Ala31Thr
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000459085
ensembl transcript: ENST00000571052
gene symbol: CORO7
hgvsc: ENST00000571052.1:c.-268+3085G>A
variant of: http://identifiers.org/hgnc/26161

GenotypeDepth
all individuals: 105
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5248
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 176
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 30505
bin: 7.5e0
variant carriers: 4

GenotypeDepth
all individuals: 427
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 519
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 12761
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 237
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 90
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 319
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 767
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4627
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 514
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2280
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 374
bin: 9.75e1
variant carriers: 2

GenotypeDepth
all individuals: 274
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 397
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 150
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 370
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 129
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 634
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 12824
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 30233
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 794
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2175
bin: 1.75e1
variant carriers: 1

GenotypeQuality
all individuals: 58
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 671
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1015
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 520
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 251
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 98
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 76
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 295
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 232
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2979
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 6705
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 262
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 173
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 216
bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 2
allele frequency: 4.965243296921549e-4
allele num: 4028
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2276
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 282
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 532
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16190
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1132
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8624
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.88e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.06e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.53e-2

VQSLOD
type: SiteQuality
SIO_000300: 2.11e0

FS
type: SiteQuality
SIO_000300: 6.46e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.06e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.5e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.388e1

DP
type: SiteQuality
SIO_000300: 7.41361e5

Annotation
canonical: false
consequence: synonymous_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000103426
ensembl protein: ENSP00000458607
ensembl transcript: ENST00000575334
gene symbol: CORO7-PAM16
hgvsc: ENST00000575334.1:c.90C>T
hgvsp: ENST00000575334.1:c.90C>T(p.%3D)
variant of: http://identifiers.org/hgnc/44424

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000461051
ensembl transcript: ENST00000572153
gene symbol: CORO7
hgvsc: ENST00000572153.1:c.61-945C>T
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: true
consequence: synonymous_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000251166
ensembl transcript: ENST00000251166
gene symbol: CORO7
hgvsc: ENST00000251166.4:c.90C>T
hgvsp: ENST00000251166.4:c.90C>T(p.%3D)
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000458411
ensembl transcript: ENST00000572044
gene symbol: CORO7
hgvsc: ENST00000572044.1:c.60+3084C>T
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000459228
ensembl transcript: ENST00000576437
gene symbol: CORO7
hgvsc: ENST00000576437.1:c.-214+3105C>T
variant of: http://identifiers.org/hgnc/26161

GenotypeDepth
all individuals: 513
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 372
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 13119
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 237
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 150
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 370
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2278
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5177
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 30261
bin: 7.5e0
variant carriers: 4

GenotypeDepth
all individuals: 4628
bin: 1.25e1
variant carriers: 1

GenotypeDepth
all individuals: 397
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 767
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 105
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 90
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 428
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 468
bin: 1.75e1
variant carriers: 1

GenotypeDepth
all individuals: 319
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 275
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 176
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 129
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 293
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2982
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 13195
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 89
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 664
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 797
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 172
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2168
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 512
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1010
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 558
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 262
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 73
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30016
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 233
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 46
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 215
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 244
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6672
bin: 6.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1134
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 2.481389578163772e-4
allele num: 4030
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 6.179705846001731e-5
allele num: 16182
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8624
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 536
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 278
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2268
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.83e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -9.22e-1

FS
type: SiteQuality
SIO_000300: 4.43e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.06e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.56e-2

QD
type: SiteQuality
SIO_000300: 1.185e1

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.85e-1

DP
type: SiteQuality
SIO_000300: 7.37729e5

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000461051
ensembl transcript: ENST00000572153
gene symbol: CORO7
hgvsc: ENST00000572153.1:c.61-952C>T
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: 5_prime_UTR_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000446221
ensembl transcript: ENST00000539968
gene symbol: CORO7
hgvsc: ENST00000539968.1:c.-517C>T
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000262246
ensembl transcript: ENST00000572026
gene symbol: CORO7
hgvsc: ENST00000572026.1:n.206C>T
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000458828
ensembl transcript: ENST00000571756
gene symbol: CORO7
hgvsc: ENST00000571756.1:c.83C>T
hgvsp: ENSP00000458828.1:p.Ala28Val
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000262246
ensembl transcript: ENST00000576457
gene symbol: CORO7
hgvsc: ENST00000576457.1:n.143C>T
variant of: http://identifiers.org/hgnc/26161

GenotypeDepth
all individuals: 28433
bin: 7.5e0
variant carriers: 2

GenotypeDepth
all individuals: 370
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 428
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4844
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4631
bin: 1.25e1
variant carriers: 1

GenotypeDepth
all individuals: 129
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 15266
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 90
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 754
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 275
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 405
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 512
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2234
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 372
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 105
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 398
bin: 4.75e1
variant carriers: 1

GenotypeDepth
all individuals: 150
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 319
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 237
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 177
bin: 7.25e1
variant carriers: 1

GenotypeQuality
all individuals: 186
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28173
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 215
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15374
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1035
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 232
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 556
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 615
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 457
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 262
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2250
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 60
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 170
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6330
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 784
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 295
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2981
bin: 9.75e1
variant carriers: 4

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 506
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 2.523977788995457e-4
allele num: 3962
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 1.903553299492386e-4
allele num: 15760
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1094
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8568
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 274
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2148
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.33e-1

FS
type: SiteQuality
SIO_000300: 1.1851e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.43e-1

VQSLOD
type: SiteQuality
SIO_000300: -4.816e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.85e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 2.48e-1

DP
type: SiteQuality
SIO_000300: 7.19913e5

QD
type: SiteQuality
SIO_000300: 1.159e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.054e0

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000458935
ensembl transcript: ENST00000572898
gene symbol: CORO7
hgvsc: ENST00000572898.1:c.80G>A
hgvsp: ENSP00000458935.1:p.Arg27Gln
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000459286
ensembl transcript: ENST00000572549
gene symbol: CORO7
hgvsc: ENST00000572549.1:c.99+3400G>A
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000461797
ensembl transcript: ENST00000575038
gene symbol: CORO7
hgvsc: ENST00000575038.1:c.80G>A
hgvsp: ENSP00000461797.1:p.Arg27Gln
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000460901
ensembl transcript: ENST00000570645
gene symbol: CORO7
hgvsc: ENST00000570645.1:c.-214+3095G>A
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000459228
ensembl transcript: ENST00000576437
gene symbol: CORO7
hgvsc: ENST00000576437.1:c.-214+3095G>A
variant of: http://identifiers.org/hgnc/26161

GenotypeDepth
all individuals: 27522
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 237
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 515
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 370
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 150
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 395
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 427
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 275
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 16257
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 399
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 129
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 176
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4657
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4670
bin: 1.25e1
variant carriers: 1

GenotypeDepth
all individuals: 758
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2228
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 319
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 90
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 372
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 105
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 634
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 16406
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2230
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 593
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 261
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1033
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27287
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 168
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 163
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 232
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 217
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 294
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6170
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 426
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 778
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2978
bin: 9.75e1
variant carriers: 1

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 502
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3936
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8528
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 6.446621970087674e-5
allele num: 15512
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1066
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2094
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 278
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 3.68e0

FS
type: SiteQuality
SIO_000300: 1.455e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.110000000000001e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.86e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.04e-2

QD
type: SiteQuality
SIO_000300: 1.23e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.96e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.81e-1

DP
type: SiteQuality
SIO_000300: 7.11867e5

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000459286
ensembl transcript: ENST00000572549
gene symbol: CORO7
hgvsc: ENST00000572549.1:c.99+3399C>T
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000459085
ensembl transcript: ENST00000571052
gene symbol: CORO7
hgvsc: ENST00000571052.1:c.-268+3073C>T
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000461051
ensembl transcript: ENST00000572153
gene symbol: CORO7
hgvsc: ENST00000572153.1:c.61-956C>T
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000262246
ensembl transcript: ENST00000577144
gene symbol: CORO7
hgvsc: ENST00000577144.1:n.187C>T
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: true
consequence: stop_gained
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000251166
ensembl transcript: ENST00000251166
gene symbol: CORO7
hgvsc: ENST00000251166.4:c.79C>T
hgvsp: ENSP00000251166.4:p.Arg27Ter
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000391530
ensembl transcript: ENST00000423908
gene symbol: CORO7
hgvsc: ENST00000423908.2:c.60+3073C>T
variant of: http://identifiers.org/hgnc/26161

GenotypeDepth
all individuals: 17230
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 275
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 105
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 237
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2220
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4494
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 428
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 26641
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 176
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 90
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4681
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 756
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 515
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 360
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 372
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 399
bin: 4.75e1
variant carriers: 1

GenotypeDepth
all individuals: 129
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 150
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 320
bin: 5.75e1
variant carriers: 1

GenotypeDepth
all individuals: 370
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 582
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 169
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 767
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2688
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17360
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 259
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 232
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 295
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25887
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1068
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2979
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 708
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 216
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 162
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5955
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 401
bin: 3.25e1
variant carriers: 0

South Asian
type: Population
allele count: 2
allele frequency: 2.355712603062426e-4
allele num: 8490
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1026
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2050
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3902
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15242
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 272
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 478
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.326e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.65e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.209e0

FS
type: SiteQuality
SIO_000300: 1.1791e1

QD
type: SiteQuality
SIO_000300: 1.003e1

MQ
type: SiteQuality
SIO_000300: 5.95e1

DP
type: SiteQuality
SIO_000300: 7.03603e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.23e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.09e-1

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000262246
ensembl transcript: ENST00000576457
gene symbol: CORO7
hgvsc: ENST00000576457.1:n.134A>G
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000460199
ensembl transcript: ENST00000570928
gene symbol: CORO7
hgvsc: ENST00000570928.1:c.74A>G
hgvsp: ENSP00000460199.1:p.Asp25Gly
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000458411
ensembl transcript: ENST00000572044
gene symbol: CORO7
hgvsc: ENST00000572044.1:c.60+3068A>G
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000461187
ensembl transcript: ENST00000574311
gene symbol: CORO7
hgvsc: ENST00000574311.1:c.60+3068A>G
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000461051
ensembl transcript: ENST00000572153
gene symbol: CORO7
hgvsc: ENST00000572153.1:c.61-961A>G
variant of: http://identifiers.org/hgnc/26161

GenotypeDepth
all individuals: 4380
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2210
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 25830
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 370
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 294
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 275
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 427
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 398
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4559
bin: 1.25e1
variant carriers: 1

GenotypeDepth
all individuals: 129
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 18291
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 511
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 90
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 237
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 749
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 150
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 176
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 372
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 105
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 319
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5913
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18487
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2009
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 168
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 496
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 259
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 295
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 147
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 232
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 376
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2977
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 28
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1049
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 215
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 551
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 767
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25814
bin: 2.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3878
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 6.616382162233691e-5
allele num: 15114
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1016
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 472
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2014
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 262
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8432
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.55e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.452e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.42e-1

DP
type: SiteQuality
SIO_000300: 6.95228e5

MQRankSum
type: SiteQuality
SIO_000300: 8.45e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.3e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.78e0

QD
type: SiteQuality
SIO_000300: 1.036e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

Annotation
canonical: false
consequence: 5_prime_UTR_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000459888
ensembl transcript: ENST00000576051
gene symbol: CORO7
hgvsc: ENST00000576051.1:c.-433A>T
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000460901
ensembl transcript: ENST00000570645
gene symbol: CORO7
hgvsc: ENST00000570645.1:c.-214+3082A>T
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: 5_prime_UTR_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000446221
ensembl transcript: ENST00000539968
gene symbol: CORO7
hgvsc: ENST00000539968.1:c.-533A>T
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000459228
ensembl transcript: ENST00000576437
gene symbol: CORO7
hgvsc: ENST00000576437.1:c.-214+3082A>T
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000391530
ensembl transcript: ENST00000423908
gene symbol: CORO7
hgvsc: ENST00000423908.2:c.60+3061A>T
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000461187
ensembl transcript: ENST00000574311
gene symbol: CORO7
hgvsc: ENST00000574311.1:c.60+3061A>T
variant of: http://identifiers.org/hgnc/26161

GenotypeDepth
all individuals: 426
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 90
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 22723
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 105
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 176
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 372
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 21555
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 275
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 281
bin: 1.75e1
variant carriers: 1

GenotypeDepth
all individuals: 237
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 319
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4530
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 150
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 398
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 511
bin: 3.75e1
variant carriers: 1

GenotypeDepth
all individuals: 749
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3968
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2140
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 129
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 370
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 231
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 204
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1786
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 349
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 289
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 522
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21853
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 644
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5464
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 255
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 748
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 124
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22695
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2978
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1090
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 168
bin: 8.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 258
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8292
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1900
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 948
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 424
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3790
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 1.37646249139711e-4
allele num: 14530
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.341e-1

QD
type: SiteQuality
SIO_000300: 1.273e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.98e-1

FS
type: SiteQuality
SIO_000300: 5.285e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.88e-2

MQ
type: SiteQuality
SIO_000300: 5.909e1

DP
type: SiteQuality
SIO_000300: 6.69712e5

ClippingRankSum
type: SiteQuality
SIO_000300: 3.69e-1

MQRankSum
type: SiteQuality
SIO_000300: -5.3e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 1.21e0

Annotation
canonical: false
consequence: 5_prime_UTR_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000446221
ensembl transcript: ENST00000539968
gene symbol: CORO7
hgvsc: ENST00000539968.1:c.-535G>C
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000460199
ensembl transcript: ENST00000570928
gene symbol: CORO7
hgvsc: ENST00000570928.1:c.65G>C
hgvsp: ENSP00000460199.1:p.Trp22Ser
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000461051
ensembl transcript: ENST00000572153
gene symbol: CORO7
hgvsc: ENST00000572153.1:c.61-970G>C
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000458411
ensembl transcript: ENST00000572044
gene symbol: CORO7
hgvsc: ENST00000572044.1:c.60+3059G>C
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000459085
ensembl transcript: ENST00000571052
gene symbol: CORO7
hgvsc: ENST00000571052.1:c.-268+3059G>C
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000262246
ensembl transcript: ENST00000577144
gene symbol: CORO7
hgvsc: ENST00000577144.1:n.173G>C
variant of: http://identifiers.org/hgnc/26161

GenotypeDepth
all individuals: 2123
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 319
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 275
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 150
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 21721
bin: 7.5e0
variant carriers: 1

GenotypeDepth
all individuals: 129
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 22586
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 370
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 176
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4540
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 290
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 90
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 372
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 428
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 105
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 516
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 747
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3808
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 237
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 398
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 199
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 168
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1691
bin: 1.75e1
variant carriers: 1

GenotypeQuality
all individuals: 231
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1131
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 784
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 106
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 510
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 335
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22923
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 21640
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 288
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2975
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5293
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 254
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 730
bin: 6.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3754
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14280
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1832
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 250
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 924
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8214
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 408
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.42e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.1e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -7.42e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.42e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.42e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.695e0

DP
type: SiteQuality
SIO_000300: 6.61624e5

QD
type: SiteQuality
SIO_000300: 1.836e1

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000461051
ensembl transcript: ENST00000572153
gene symbol: CORO7
hgvsc: ENST00000572153.1:c.61-986C>A
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000458459
ensembl transcript: ENST00000571227
gene symbol: CORO7
hgvsc: ENST00000571227.1:c.*58-12C>A
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000460036
ensembl transcript: ENST00000571059
gene symbol: CORO7
hgvsc: ENST00000571059.1:c.61-12C>A
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000391530
ensembl transcript: ENST00000423908
gene symbol: CORO7
hgvsc: ENST00000423908.2:c.60+3043C>A
variant of: http://identifiers.org/hgnc/26161

GenotypeDepth
all individuals: 30629
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 176
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2458
bin: 2.25e1
variant carriers: 1

GenotypeDepth
all individuals: 1649
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 14274
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 150
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 105
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 370
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 398
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 319
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 515
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 129
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 490
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 426
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 372
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3845
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 237
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 275
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 673
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 90
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1588
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1527
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 556
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2976
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 53
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 273
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 231
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 251
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 533
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30525
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 93
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 167
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12459
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 183
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1798
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 500
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 226
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3551
bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11640
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 2.9708853238265e-4
allele num: 3366
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7604
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 226
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 252
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1326
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 642
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.06e-1

DP
type: SiteQuality
SIO_000300: 5.77437e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.95e-1

MQRankSum
type: SiteQuality
SIO_000300: -4.06e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.805e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.62e-2

QD
type: SiteQuality
SIO_000300: 3.199e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.537e0

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl transcript: ENST00000572026
gene symbol: CORO7
hgvsc: ENST00000572026.1:n.184-16T>A
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000460901
ensembl transcript: ENST00000570645
gene symbol: CORO7
hgvsc: ENST00000570645.1:c.-214+3060T>A
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000461187
ensembl transcript: ENST00000574311
gene symbol: CORO7
hgvsc: ENST00000574311.1:c.60+3039T>A
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000460199
ensembl transcript: ENST00000570928
gene symbol: CORO7
hgvsc: ENST00000570928.1:c.61-16T>A
variant of: http://identifiers.org/hgnc/26161

GenotypeDepth
all individuals: 633
bin: 3.25e1
variant carriers: 1

GenotypeDepth
all individuals: 129
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 319
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 105
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 237
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 13216
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 564
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 426
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 150
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 398
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 510
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 275
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 370
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2257
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 31688
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 90
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 372
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 176
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3688
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1508
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3228
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 71
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 564
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 181
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1382
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1589
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 600
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 269
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31386
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 230
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2976
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 11376
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 249
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1909
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 273
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 507
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 167
bin: 8.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 218
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 226
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11172
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.332977872567315e-4
allele num: 7502
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 580
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3310
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1244
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.99e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.842e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.79e-2

DP
type: SiteQuality
SIO_000300: 5.62276e5

MQRankSum
type: SiteQuality
SIO_000300: -1.956e0

VQSLOD
type: SiteQuality
SIO_000300: -2.281e0

QD
type: SiteQuality
SIO_000300: 1.325e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.37e-1

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000460199
ensembl transcript: ENST00000570928
gene symbol: CORO7
hgvsc: ENST00000570928.1:c.61-18T>C
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl transcript: ENST00000572026
gene symbol: CORO7
hgvsc: ENST00000572026.1:n.184-18T>C
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000461051
ensembl transcript: ENST00000572153
gene symbol: CORO7
hgvsc: ENST00000572153.1:c.61-992T>C
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000391530
ensembl transcript: ENST00000423908
gene symbol: CORO7
hgvsc: ENST00000423908.2:c.60+3037T>C
variant of: http://identifiers.org/hgnc/26161

GenotypeDepth
all individuals: 3656
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 679
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 12606
bin: 7.5e0
variant carriers: 1

GenotypeDepth
all individuals: 370
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 275
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 32181
bin: 2.5e0
variant carriers: 1

GenotypeDepth
all individuals: 426
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 105
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 372
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 625
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 398
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2079
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 509
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 237
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1385
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 176
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 129
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 90
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 150
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 319
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1758
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31733
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 230
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 647
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2067
bin: 1.25e1
variant carriers: 1

GenotypeQuality
all individuals: 181
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10510
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 167
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 62
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2975
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 323
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1344
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 272
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 633
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 498
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2940
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 249
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10960
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 192
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1174
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3270
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 548
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 222
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7450
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.728e1

DP
type: SiteQuality
SIO_000300: 5.52736e5

BaseQRankSum
type: SiteQuality
SIO_000300: 1.23e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.58e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -1.729e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.89e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.23e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.58e-1

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000459286
ensembl transcript: ENST00000572549
gene symbol: CORO7
hgvsc: ENST00000572549.1:c.99+3360T>G
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000461187
ensembl transcript: ENST00000574311
gene symbol: CORO7
hgvsc: ENST00000574311.1:c.60+3034T>G
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000459085
ensembl transcript: ENST00000571052
gene symbol: CORO7
hgvsc: ENST00000571052.1:c.-268+3034T>G
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000460036
ensembl transcript: ENST00000571059
gene symbol: CORO7
hgvsc: ENST00000571059.1:c.61-21T>G
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000461797
ensembl transcript: ENST00000575038
gene symbol: CORO7
hgvsc: ENST00000575038.1:c.61-21T>G
variant of: http://identifiers.org/hgnc/26161

GenotypeDepth
all individuals: 3569
bin: 1.25e1
variant carriers: 26

GenotypeDepth
all individuals: 513
bin: 3.75e1
variant carriers: 5

GenotypeDepth
all individuals: 375
bin: 9.75e1
variant carriers: 4

GenotypeDepth
all individuals: 176
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 370
bin: 5.25e1
variant carriers: 1

GenotypeDepth
all individuals: 876
bin: 1.75e1
variant carriers: 12

GenotypeDepth
all individuals: 275
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 32891
bin: 2.5e0
variant carriers: 15

GenotypeDepth
all individuals: 426
bin: 4.25e1
variant carriers: 3

GenotypeDepth
all individuals: 604
bin: 3.25e1
variant carriers: 12

GenotypeDepth
all individuals: 11610
bin: 7.5e0
variant carriers: 75

GenotypeDepth
all individuals: 149
bin: 7.75e1
variant carriers: 1

GenotypeDepth
all individuals: 1249
bin: 2.75e1
variant carriers: 17

GenotypeDepth
all individuals: 106
bin: 9.25e1
variant carriers: 1

GenotypeDepth
all individuals: 239
bin: 6.75e1
variant carriers: 2

GenotypeDepth
all individuals: 1760
bin: 2.25e1
variant carriers: 22

GenotypeDepth
all individuals: 129
bin: 8.25e1
variant carriers: 2

GenotypeDepth
all individuals: 320
bin: 5.75e1
variant carriers: 3

GenotypeDepth
all individuals: 93
bin: 8.75e1
variant carriers: 3

GenotypeDepth
all individuals: 397
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 696
bin: 2.75e1
variant carriers: 7

GenotypeQuality
all individuals: 1336
bin: 1.75e1
variant carriers: 2

GenotypeQuality
all individuals: 32020
bin: 7.5e0
variant carriers: 3

GenotypeQuality
all individuals: 78
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 177
bin: 8.75e1
variant carriers: 10

GenotypeQuality
all individuals: 258
bin: 8.25e1
variant carriers: 9

GenotypeQuality
all individuals: 2464
bin: 6.25e1
variant carriers: 11

GenotypeQuality
all individuals: 416
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2336
bin: 1.25e1
variant carriers: 5

GenotypeQuality
all individuals: 88
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 472
bin: 6.75e1
variant carriers: 5

GenotypeQuality
all individuals: 65
bin: 5.25e1
variant carriers: 4

GenotypeQuality
all individuals: 2179
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 743
bin: 3.25e1
variant carriers: 3

GenotypeQuality
all individuals: 51
bin: 5.75e1
variant carriers: 7

GenotypeQuality
all individuals: 239
bin: 9.25e1
variant carriers: 11

GenotypeQuality
all individuals: 3082
bin: 9.75e1
variant carriers: 119

GenotypeQuality
all individuals: 8978
bin: 2.25e1
variant carriers: 4

GenotypeQuality
all individuals: 272
bin: 7.75e1
variant carriers: 2

GenotypeQuality
all individuals: 177
bin: 7.25e1
variant carriers: 2

South Asian
type: Population
allele count: 64
allele frequency: 8.698015765153574e-3
allele num: 7358
num of homozygotes: 2

Other
type: Population
allele count: 2
allele frequency: 9.09090909090909e-3
allele num: 220
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3172
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1100
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 174
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 3.846153846153846e-3
allele num: 520
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 47
allele frequency: 4.444864762625307e-3
allele num: 10574
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 7.02e-1

DP
type: SiteQuality
SIO_000300: 5.38653e5

BaseQRankSum
type: SiteQuality
SIO_000300: -1.537e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.58e-1

QD
type: SiteQuality
SIO_000300: 1.332e1

MQRankSum
type: SiteQuality
SIO_000300: 3.58e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.58e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.87e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.07e-2

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000458411
ensembl transcript: ENST00000572044
gene symbol: CORO7
hgvsc: ENST00000572044.1:c.60+3024C>T
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: true
consequence: intron_variant
ensembl gene: ENSG00000103426
ensembl protein: ENSP00000460885
ensembl transcript: ENST00000572467
gene symbol: CORO7-PAM16
hgvsc: ENST00000572467.1:c.61-31C>T
variant of: http://identifiers.org/hgnc/44424

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000458935
ensembl transcript: ENST00000572898
gene symbol: CORO7
hgvsc: ENST00000572898.1:c.61-31C>T
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000460036
ensembl transcript: ENST00000571059
gene symbol: CORO7
hgvsc: ENST00000571059.1:c.61-31C>T
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000461051
ensembl transcript: ENST00000572153
gene symbol: CORO7
hgvsc: ENST00000572153.1:c.61-1005C>T
variant of: http://identifiers.org/hgnc/26161

GenotypeDepth
all individuals: 105
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 239
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 33752
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 92
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 318
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 425
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2918
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 148
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 276
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9645
bin: 7.5e0
variant carriers: 3

GenotypeDepth
all individuals: 803
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 399
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 127
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 505
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1084
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 370
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 546
bin: 3.25e1
variant carriers: 1

GenotypeDepth
all individuals: 1623
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 373
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 177
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 115
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1670
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 188
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5264
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 673
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4402
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 228
bin: 9.25e1
variant carriers: 2

GenotypeQuality
all individuals: 997
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30520
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3285
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 268
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 232
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 391
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2975
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 782
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 168
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 166
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 254
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1288
bin: 6.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 430
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 108
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9396
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 194
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 840
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 3.367003367003367e-4
allele num: 2970
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6914
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 6.022e0

DP
type: SiteQuality
SIO_000300: 4.97633e5

VQSLOD
type: SiteQuality
SIO_000300: -7.137e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.93e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.26e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.221e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.73e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.137e1

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000458459
ensembl transcript: ENST00000571227
gene symbol: CORO7
hgvsc: ENST00000571227.1:c.*58-35C>T
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000459228
ensembl transcript: ENST00000576437
gene symbol: CORO7
hgvsc: ENST00000576437.1:c.-214+3041C>T
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl transcript: ENST00000576457
gene symbol: CORO7
hgvsc: ENST00000576457.1:n.121-35C>T
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000459286
ensembl transcript: ENST00000572549
gene symbol: CORO7
hgvsc: ENST00000572549.1:c.99+3346C>T
variant of: http://identifiers.org/hgnc/26161

GenotypeDepth
all individuals: 370
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 505
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 534
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 399
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 105
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1709
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 728
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 177
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 127
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 318
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 33711
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 92
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 239
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2784
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9438
bin: 7.5e0
variant carriers: 2

GenotypeDepth
all individuals: 425
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 148
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 276
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1041
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 373
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1159
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 167
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3405
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 113
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 793
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 708
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 227
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1019
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 254
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4896
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4829
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 379
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2974
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 265
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1685
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 168
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29942
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 264
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 213
bin: 4.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 186
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9224
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2950
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6836
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 94
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 804
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 424
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.809999999999999e-2

MQRankSum
type: SiteQuality
SIO_000300: 3.22e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.23e0

VQSLOD
type: SiteQuality
SIO_000300: 3.57e-1

QD
type: SiteQuality
SIO_000300: 6.26e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.22e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.22e-1

DP
type: SiteQuality
SIO_000300: 4.9151e5

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000391530
ensembl transcript: ENST00000423908
gene symbol: CORO7
hgvsc: ENST00000423908.2:c.60+668C>A
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000460199
ensembl transcript: ENST00000570928
gene symbol: CORO7
hgvsc: ENST00000570928.1:c.60+668C>A
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000461702
ensembl transcript: ENST00000574025
gene symbol: CORO7
hgvsc: ENST00000574025.1:c.60+668C>A
variant of: http://identifiers.org/hgnc/26161

GenotypeDepth
all individuals: 0
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 100
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3249
bin: 2.5e0
variant carriers: 1

GenotypeDepth
all individuals: 0
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2898
bin: 7.5e0
variant carriers: 1

GenotypeQuality
all individuals: 0
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 353
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 8.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.8e-1

QD
type: SiteQuality
SIO_000300: 1.914e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.109e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 7.55e3

FS
type: SiteQuality
SIO_000300: 0.0e0

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000458411
ensembl transcript: ENST00000572044
gene symbol: CORO7
hgvsc: ENST00000572044.1:c.60+610G>C
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: true
consequence: intron_variant
ensembl gene: ENSG00000103426
ensembl protein: ENSP00000460885
ensembl transcript: ENST00000572467
gene symbol: CORO7-PAM16
hgvsc: ENST00000572467.1:c.60+610G>C
variant of: http://identifiers.org/hgnc/44424

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000460199
ensembl transcript: ENST00000570928
gene symbol: CORO7
hgvsc: ENST00000570928.1:c.60+610G>C
variant of: http://identifiers.org/hgnc/26161

GenotypeDepth
all individuals: 0
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4224
bin: 2.5e0
variant carriers: 3

GenotypeDepth
all individuals: 1
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 87
bin: 7.5e0
variant carriers: 1

GenotypeDepth
all individuals: 0
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3612
bin: 7.5e0
variant carriers: 1

GenotypeQuality
all individuals: 0
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 609
bin: 2.5e0
variant carriers: 1

GenotypeQuality
all individuals: 0
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 2.75e1
variant carriers: 1

GenotypeQuality
all individuals: 35
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 0
bin: 8.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.06e-1

DP
type: SiteQuality
SIO_000300: 9.515e3

MQRankSum
type: SiteQuality
SIO_000300: 7.27e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.06e-1

FS
type: SiteQuality
SIO_000300: 2.632e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.23e0

QD
type: SiteQuality
SIO_000300: 1.37e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.11e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.029e-1

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000458828
ensembl transcript: ENST00000571756
gene symbol: CORO7
hgvsc: ENST00000571756.1:c.60+603G>T
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000459286
ensembl transcript: ENST00000572549
gene symbol: CORO7
hgvsc: ENST00000572549.1:c.99+929G>T
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000460910
ensembl transcript: ENST00000575850
gene symbol: CORO7
hgvsc: ENST00000575850.1:c.99+929G>T
variant of: http://identifiers.org/hgnc/26161

GenotypeDepth
all individuals: 0
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4490
bin: 2.5e0
variant carriers: 1

GenotypeDepth
all individuals: 0
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 88
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 536
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3947
bin: 7.5e0
variant carriers: 1

GenotypeQuality
all individuals: 0
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 6.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.543e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.138e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 1.88e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.0068e4

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000458411
ensembl transcript: ENST00000572044
gene symbol: CORO7
hgvsc: ENST00000572044.1:c.60+590G>C
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000391530
ensembl transcript: ENST00000423908
gene symbol: CORO7
hgvsc: ENST00000423908.2:c.60+590G>C
variant of: http://identifiers.org/hgnc/26161

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000262246
ensembl protein: ENSP00000461051
ensembl transcript: ENST00000572153
gene symbol: CORO7
hgvsc: ENST00000572153.1:c.60+590G>C
variant of: http://identifiers.org/hgnc/26161

GenotypeDepth
all individuals: 0
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4619
bin: 2.5e0
variant carriers: 2

GenotypeDepth
all individuals: 6
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 104
bin: 7.5e0
variant carriers: 1

GenotypeDepth
all individuals: 0
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 2.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3952
bin: 7.5e0
variant carriers: 1

GenotypeQuality
all individuals: 0
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 0
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 664
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 9.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 1.43e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.27e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.123e-1

FS
type: SiteQuality
SIO_000300: 1.74e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.27e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.06e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.06e-1

QD
type: SiteQuality
SIO_000300: 1.101e1

DP
type: SiteQuality
SIO_000300: 1.0693e4

GenotypeDepth
all individuals: 1288
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 314
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 10109
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9176
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 63
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7981
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 10141
bin: 7.5e0
variant carriers: 1

GenotypeDepth
all individuals: 13
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 168
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 602
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7974
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 38
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2705
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4980
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 29
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 15
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 93
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2200
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2975
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1562
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 522
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3933
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6456
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4537
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1231
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1970
bin: 1.25e1
variant carriers: 1

GenotypeQuality
all individuals: 3240
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 679
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1083
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7726
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1877
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2771
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6249
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2257
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1887
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 592
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1960
bin: 9.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 38528
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6256
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7688
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11202
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3186
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4706
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 496
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 8.60753e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.04e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 8.04e-1

QD
type: SiteQuality
SIO_000300: 1.875e1

VQSLOD
type: SiteQuality
SIO_000300: -7.464e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.45e-2

MQRankSum
type: SiteQuality
SIO_000300: 8.04e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.04e-1

GenotypeDepth
all individuals: 5
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8556
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 29
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9013
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 169
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 93
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 63
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 10355
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 10115
bin: 1.25e1
variant carriers: 1

GenotypeDepth
all individuals: 38
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7337
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 314
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5110
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 13
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 15
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2729
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 601
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1289
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1600
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1868
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4530
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1245
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1645
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2858
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2955
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1764
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8606
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3913
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1502
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 684
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6774
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 527
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1095
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2997
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 277
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1578
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7475
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1964
bin: 9.75e1
variant carriers: 1

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 500
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11270
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7700
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 2.107037505267594e-4
allele num: 4746
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3210
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6274
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 38638
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.03e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.76e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.66e0

QD
type: SiteQuality
SIO_000300: 8.84e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 4.7e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.268e0

DP
type: SiteQuality
SIO_000300: 8.68635e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.49e-2

GenotypeDepth
all individuals: 93
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 314
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 10760
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 2797
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 603
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 8.75e1
variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
all individuals: 8710
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variant carriers: 1

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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bin: 1.75e1
variant carriers: 1

GenotypeDepth
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bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 63
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3840
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6971
bin: 7.5e0
variant carriers: 1

GenotypeQuality
all individuals: 1104
bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9591
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1966
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variant carriers: 2

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2500
bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 690
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1107
bin: 8.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3232
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4748
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 504
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 3.184713375796178e-4
allele num: 6280
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11324
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7698
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 38712
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 8.79992e5

BaseQRankSum
type: SiteQuality
SIO_000300: 2.87e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.99e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.67e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 9.58e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.4e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.39e-2

VQSLOD
type: SiteQuality
SIO_000300: -4.832e-1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 2

GenotypeDepth
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variant carriers: 0

GenotypeDepth
all individuals: 13
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variant carriers: 0

GenotypeDepth
all individuals: 29
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variant carriers: 0

GenotypeDepth
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bin: 5.25e1
variant carriers: 0

GenotypeDepth
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6750
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2947
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 919
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 699
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9869
bin: 6.25e1
variant carriers: 1

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 3

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 886
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 3617
bin: 3.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11324
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7728
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6296
num of homozygotes: 0

African
type: Population
allele count: 4
allele frequency: 8.375209380234506e-4
allele num: 4776
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 38840
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3220
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 502
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.17e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.46e-2

VQSLOD
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SIO_000300: -2.027e0

QD
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SIO_000300: 9.19e0

DP
type: SiteQuality
SIO_000300: 8.98744e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
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SIO_000300: -2.166e0

FS
type: SiteQuality
SIO_000300: 1.5311e1

MQRankSum
type: SiteQuality
SIO_000300: -7.199999999999999e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.46e-1