16-4408306-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4408306
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4408306
    reference: chr 16
allele count: 2
allele frequency: 1.903094431545693e-5
allele num: 105092
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103426
  ensembl transcript: ENST00000572274
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000572274.1:n.175+62G>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.2403+62G>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.1797+62G>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: ENST00000575714
  gene symbol: CORO7
  hgvsc: ENST00000575714.1:n.2048G>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.2202+62G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460956
  ensembl transcript: ENST00000570779
  gene symbol: CORO7
  hgvsc: ENST00000570779.1:c.84+62G>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.*904+62G>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.2457+62G>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.2457+62G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460177
  ensembl transcript: ENST00000576637
  gene symbol: CORO7
  hgvsc: ENST00000576637.1:c.355+62G>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: ENST00000574849
  gene symbol: CORO7
  hgvsc: ENST00000574849.1:n.150+62G>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.*2393+62G>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: ENST00000575531
  gene symbol: CORO7
  hgvsc: ENST00000575531.1:n.1672+62G>A
  variant of: http://identifiers.org/hgnc/26161
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3990
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22829
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1538
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1272
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4618
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8757
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6281
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10242
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
reference allele: C
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff

16-4408313-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4408313
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4408313
    reference: chr 16
allele count: 1
allele frequency: 9.440196356084207e-6
allele num: 105930
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000575714
  gene symbol: CORO7
  hgvsc: ENST00000575714.1:n.2041G>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.*2393+55G>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.2457+55G>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.2202+55G>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460956
  ensembl transcript: ENST00000570779
  gene symbol: CORO7
  hgvsc: ENST00000570779.1:c.84+55G>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.2403+55G>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.*904+55G>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.2457+55G>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: ENST00000575531
  gene symbol: CORO7
  hgvsc: ENST00000575531.1:n.1672+55G>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103426
  ensembl transcript: ENST00000572274
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000572274.1:n.175+55G>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: ENST00000574849
  gene symbol: CORO7
  hgvsc: ENST00000574849.1:n.150+55G>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.1797+55G>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460177
  ensembl transcript: ENST00000576637
  gene symbol: CORO7
  hgvsc: ENST00000576637.1:c.355+55G>C
  variant of: http://identifiers.org/hgnc/26161
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1451
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5990
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4068
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24044
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10772
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7813
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1289
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4103
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: C
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: QD

16-4408313-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4408313
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4408313
    reference: chr 16
allele count: 1
allele frequency: 9.440196356084207e-6
allele num: 105930
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460956
  ensembl transcript: ENST00000570779
  gene symbol: CORO7
  hgvsc: ENST00000570779.1:c.84+55G>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: ENST00000574849
  gene symbol: CORO7
  hgvsc: ENST00000574849.1:n.150+55G>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: ENST00000575714
  gene symbol: CORO7
  hgvsc: ENST00000575714.1:n.2041G>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.*2393+55G>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.*904+55G>A
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460177
  ensembl transcript: ENST00000576637
  gene symbol: CORO7
  hgvsc: ENST00000576637.1:c.355+55G>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.2202+55G>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.1797+55G>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.2457+55G>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: ENST00000575531
  gene symbol: CORO7
  hgvsc: ENST00000575531.1:n.1672+55G>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.2457+55G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103426
  ensembl transcript: ENST00000572274
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000572274.1:n.175+55G>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.2403+55G>A
  variant of: http://identifiers.org/hgnc/26161
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4103
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4068
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1451
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1289
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7813
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10772
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5990
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24044
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: East Asian
population: Other
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: QD

16-4408317-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4408317
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4408317
    reference: chr 16
allele count: 1
allele frequency: 9.391611412686188e-6
allele num: 106478
alternate allele: G
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.*2393+51G>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103426
  ensembl transcript: ENST00000572274
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000572274.1:n.175+51G>C
  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.2403+51G>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.1797+51G>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: ENST00000575531
  gene symbol: CORO7
  hgvsc: ENST00000575531.1:n.1672+51G>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460956
  ensembl transcript: ENST00000570779
  gene symbol: CORO7
  hgvsc: ENST00000570779.1:c.84+51G>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.2457+51G>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.2202+51G>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: ENST00000574849
  gene symbol: CORO7
  hgvsc: ENST00000574849.1:n.150+51G>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: ENST00000575714
  gene symbol: CORO7
  hgvsc: ENST00000575714.1:n.2037G>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.2457+51G>C
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460177
  ensembl transcript: ENST00000576637
  gene symbol: CORO7
  hgvsc: ENST00000576637.1:c.355+51G>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.*904+51G>C
  variant of: http://identifiers.org/hgnc/44424
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1396
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1309
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24537
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5759
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3921
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4178
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11038
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7389
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum

16-4408317-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4408317
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4408317
    reference: chr 16
allele count: 1
allele frequency: 9.391611412686188e-6
allele num: 106478
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.2202+51G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460956
  ensembl transcript: ENST00000570779
  gene symbol: CORO7
  hgvsc: ENST00000570779.1:c.84+51G>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: ENST00000574849
  gene symbol: CORO7
  hgvsc: ENST00000574849.1:n.150+51G>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.*2393+51G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103426
  ensembl transcript: ENST00000572274
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000572274.1:n.175+51G>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.1797+51G>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: ENST00000575714
  gene symbol: CORO7
  hgvsc: ENST00000575714.1:n.2037G>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.2457+51G>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.2403+51G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460177
  ensembl transcript: ENST00000576637
  gene symbol: CORO7
  hgvsc: ENST00000576637.1:c.355+51G>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.2457+51G>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: ENST00000575531
  gene symbol: CORO7
  hgvsc: ENST00000575531.1:n.1672+51G>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.*904+51G>A
  variant of: http://identifiers.org/hgnc/44424
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1309
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7389
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5759
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3921
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24537
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1396
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4178
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
population: African
population: Latino
population: European (Finnish)
reference allele: C
site quality: MQ
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum

16-4408318-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4408318
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4408318
    reference: chr 16
allele count: 9
allele frequency: 8.428386806765185e-5
allele num: 106782
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.1797+50A>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.*2393+50A>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: ENST00000575531
  gene symbol: CORO7
  hgvsc: ENST00000575531.1:n.1672+50A>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.2202+50A>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: ENST00000575714
  gene symbol: CORO7
  hgvsc: ENST00000575714.1:n.2036A>G
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460177
  ensembl transcript: ENST00000576637
  gene symbol: CORO7
  hgvsc: ENST00000576637.1:c.355+50A>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.2403+50A>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.2457+50A>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: ENST00000574849
  gene symbol: CORO7
  hgvsc: ENST00000574849.1:n.150+50A>G
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460956
  ensembl transcript: ENST00000570779
  gene symbol: CORO7
  hgvsc: ENST00000570779.1:c.84+50A>G
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103426
  ensembl transcript: ENST00000572274
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000572274.1:n.175+50A>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.2457+50A>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.*904+50A>G
  variant of: http://identifiers.org/hgnc/44424
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7206
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4179
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 11097
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5684
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24860
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1309
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1390
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: T
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: DP

16-4408324-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4408324
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4408324
    reference: chr 16
allele count: 1
allele frequency: 9.288500835965075e-6
allele num: 107660
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.1797+44G>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.*904+44G>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: ENST00000575531
  gene symbol: CORO7
  hgvsc: ENST00000575531.1:n.1672+44G>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.2202+44G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460956
  ensembl transcript: ENST00000570779
  gene symbol: CORO7
  hgvsc: ENST00000570779.1:c.84+44G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103426
  ensembl transcript: ENST00000572274
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000572274.1:n.175+44G>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.*2393+44G>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: ENST00000575714
  gene symbol: CORO7
  hgvsc: ENST00000575714.1:n.2030G>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.2403+44G>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.2457+44G>A
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460177
  ensembl transcript: ENST00000576637
  gene symbol: CORO7
  hgvsc: ENST00000576637.1:c.355+44G>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.2457+44G>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: ENST00000574849
  gene symbol: CORO7
  hgvsc: ENST00000574849.1:n.150+44G>A
  variant of: http://identifiers.org/hgnc/26161
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25495
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1320
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11666
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1328
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3611
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6465
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5273
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4375
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: South Asian
population: Latino
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: ClippingRankSum

16-4408325-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4408325
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4408325
    reference: chr 16
allele count: 643
allele frequency: 5.966077790973872e-3
allele num: 107776
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460177
  ensembl transcript: ENST00000576637
  gene symbol: CORO7
  hgvsc: ENST00000576637.1:c.355+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.2457+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.2457+43G>A
  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: ENST00000575714
  gene symbol: CORO7
  hgvsc: ENST00000575714.1:n.2029G>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: ENST00000574849
  gene symbol: CORO7
  hgvsc: ENST00000574849.1:n.150+43G>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.1797+43G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460956
  ensembl transcript: ENST00000570779
  gene symbol: CORO7
  hgvsc: ENST00000570779.1:c.84+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.*2393+43G>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.2202+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.2403+43G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103426
  ensembl transcript: ENST00000572274
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000572274.1:n.175+43G>A
  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.*904+43G>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: ENST00000575531
  gene symbol: CORO7
  hgvsc: ENST00000575531.1:n.1672+43G>A
  variant of: http://identifiers.org/hgnc/26161
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3661
  bin: 1.75e1
  variant carriers: 96
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 4.75e1
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4525
  bin: 3.25e1
  variant carriers: 96
genotype depth: GenotypeDepth
  all individuals: 1386
  bin: 3.75e1
  variant carriers: 53
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 6.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 531
  bin: 4.25e1
  variant carriers: 39
genotype depth: GenotypeDepth
  all individuals: 11832
  bin: 2.75e1
  variant carriers: 104
genotype depth: GenotypeDepth
  all individuals: 5132
  bin: 7.5e0
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6285
  bin: 1.25e1
  variant carriers: 45
genotype depth: GenotypeDepth
  all individuals: 1295
  bin: 2.5e0
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
num of homozygotes: 17
population: South Asian
population: Other
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum

16-4408326-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4408326
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4408326
    reference: chr 16
allele count: 3
allele frequency: 2.770390070921986e-5
allele num: 108288
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000575714
  gene symbol: CORO7
  hgvsc: ENST00000575714.1:n.2028C>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: ENST00000575531
  gene symbol: CORO7
  hgvsc: ENST00000575531.1:n.1672+42C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460177
  ensembl transcript: ENST00000576637
  gene symbol: CORO7
  hgvsc: ENST00000576637.1:c.355+42C>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.1797+42C>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.2457+42C>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: ENST00000574849
  gene symbol: CORO7
  hgvsc: ENST00000574849.1:n.150+42C>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.2457+42C>T
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103426
  ensembl transcript: ENST00000572274
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000572274.1:n.175+42C>T
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460956
  ensembl transcript: ENST00000570779
  gene symbol: CORO7
  hgvsc: ENST00000570779.1:c.84+42C>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.2202+42C>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.*904+42C>T
  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.2403+42C>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.*2393+42C>T
  variant of: http://identifiers.org/hgnc/26161
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6050
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3536
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25686
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1255
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4590
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5021
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1380
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11980
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: QD

16-4408328-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4408328
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4408328
    reference: chr 16
allele count: 1
allele frequency: 9.197601265589934e-6
allele num: 108724
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460956
  ensembl transcript: ENST00000570779
  gene symbol: CORO7
  hgvsc: ENST00000570779.1:c.84+40C>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: ENST00000575531
  gene symbol: CORO7
  hgvsc: ENST00000575531.1:n.1672+40C>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.*2393+40C>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.2457+40C>T
  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.2457+40C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460177
  ensembl transcript: ENST00000576637
  gene symbol: CORO7
  hgvsc: ENST00000576637.1:c.355+40C>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.*904+40C>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: ENST00000574849
  gene symbol: CORO7
  hgvsc: ENST00000574849.1:n.150+40C>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.2202+40C>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: ENST00000575714
  gene symbol: CORO7
  hgvsc: ENST00000575714.1:n.2026C>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.2403+40C>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.1797+40C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103426
  ensembl transcript: ENST00000572274
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000572274.1:n.175+40C>T
  variant of: http://identifiers.org/hgnc/44424
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3521
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5870
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25922
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1211
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1376
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4901
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12101
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff

16-4408333-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4408333
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4408333
    reference: chr 16
allele count: 2
allele frequency: 1.831870889739691e-5
allele num: 109178
alternate allele: T
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.*2393+35G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460177
  ensembl transcript: ENST00000576637
  gene symbol: CORO7
  hgvsc: ENST00000576637.1:c.355+35G>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.2457+35G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460956
  ensembl transcript: ENST00000570779
  gene symbol: CORO7
  hgvsc: ENST00000570779.1:c.84+35G>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.2202+35G>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.*904+35G>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: ENST00000574849
  gene symbol: CORO7
  hgvsc: ENST00000574849.1:n.150+35G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103426
  ensembl transcript: ENST00000572274
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000572274.1:n.175+35G>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.2457+35G>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.2403+35G>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: ENST00000575531
  gene symbol: CORO7
  hgvsc: ENST00000575531.1:n.1672+35G>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.1797+35G>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: ENST00000575714
  gene symbol: CORO7
  hgvsc: ENST00000575714.1:n.2021G>A
  variant of: http://identifiers.org/hgnc/26161
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 25993
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5508
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1148
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4762
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1392
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3626
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4611
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
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: C
site quality: DP
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff

16-4408334-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4408334
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4408334
    reference: chr 16
allele count: 10
allele frequency: 9.129752035934705e-5
allele num: 109532
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000440460
  ensembl transcript: ENST00000537233
  gene symbol: CORO7
  hgvsc: ENST00000537233.2:c.2403+34C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103426
  ensembl transcript: ENST00000572274
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000572274.1:n.175+34C>T
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460177
  ensembl transcript: ENST00000576637
  gene symbol: CORO7
  hgvsc: ENST00000576637.1:c.355+34C>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: ENST00000575531
  gene symbol: CORO7
  hgvsc: ENST00000575531.1:n.1672+34C>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.*2393+34C>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.2457+34C>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.2202+34C>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: ENST00000575714
  gene symbol: CORO7
  hgvsc: ENST00000575714.1:n.2020C>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.*904+34C>T
  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.1797+34C>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.2457+34C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460956
  ensembl transcript: ENST00000570779
  gene symbol: CORO7
  hgvsc: ENST00000570779.1:c.84+34C>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: ENST00000574849
  gene symbol: CORO7
  hgvsc: ENST00000574849.1:n.150+34C>T
  variant of: http://identifiers.org/hgnc/26161
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4544
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1116
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5445
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4800
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3702
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25910
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12587
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: African
reference allele: G
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: DP

16-4408334-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4408334
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4408334
    reference: chr 16
allele count: 1
allele frequency: 9.129752035934704e-6
allele num: 109532
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000574849
  gene symbol: CORO7
  hgvsc: ENST00000574849.1:n.150+34C>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.2457+34C>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: ENST00000575531
  gene symbol: CORO7
  hgvsc: ENST00000575531.1:n.1672+34C>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103426
  ensembl transcript: ENST00000572274
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000572274.1:n.175+34C>A
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460956
  ensembl transcript: ENST00000570779
  gene symbol: CORO7
  hgvsc: ENST00000570779.1:c.84+34C>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.2202+34C>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: ENST00000575714
  gene symbol: CORO7
  hgvsc: ENST00000575714.1:n.2020C>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.2457+34C>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.*904+34C>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.1797+34C>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.2403+34C>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.*2393+34C>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460177
  ensembl transcript: ENST00000576637
  gene symbol: CORO7
  hgvsc: ENST00000576637.1:c.355+34C>A
  variant of: http://identifiers.org/hgnc/26161
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4544
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3702
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12587
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1387
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1116
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4800
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5445
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: ClippingRankSum

16-4408337-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4408337
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4408337
    reference: chr 16
allele count: 1
allele frequency: 9.084467377677646e-6
allele num: 110078
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103426
  ensembl transcript: ENST00000572274
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000572274.1:n.175+31C>T
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460177
  ensembl transcript: ENST00000576637
  gene symbol: CORO7
  hgvsc: ENST00000576637.1:c.355+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.2202+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.*2393+31C>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.2457+31C>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.*904+31C>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: ENST00000574849
  gene symbol: CORO7
  hgvsc: ENST00000574849.1:n.150+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.2457+31C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460956
  ensembl transcript: ENST00000570779
  gene symbol: CORO7
  hgvsc: ENST00000570779.1:c.84+31C>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: ENST00000575714
  gene symbol: CORO7
  hgvsc: ENST00000575714.1:n.2017C>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.1797+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.2403+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: ENST00000575531
  gene symbol: CORO7
  hgvsc: ENST00000575531.1:n.1672+31C>T
  variant of: http://identifiers.org/hgnc/26161
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26263
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1077
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12810
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4338
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5182
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3600
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
reference allele: G
site quality: DP
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum

16-4408345-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4408345
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4408345
    reference: chr 16
allele count: 5
allele frequency: 4.494624429182697e-5
allele num: 111244
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461702
  ensembl transcript: ENST00000574025
  gene symbol: CORO7
  hgvsc: ENST00000574025.1:c.2202+23C>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.2457+23C>T
  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: ENST00000575714
  gene symbol: CORO7
  hgvsc: ENST00000575714.1:n.2009C>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: ENST00000574849
  gene symbol: CORO7
  hgvsc: ENST00000574849.1:n.150+23C>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.1797+23C>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.*904+23C>T
  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.2457+23C>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.*2393+23C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103426
  ensembl transcript: ENST00000572274
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000572274.1:n.175+23C>T
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460956
  ensembl transcript: ENST00000570779
  gene symbol: CORO7
  hgvsc: ENST00000570779.1:c.84+23C>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.2403+23C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460177
  ensembl transcript: ENST00000576637
  gene symbol: CORO7
  hgvsc: ENST00000576637.1:c.355+23C>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: ENST00000575531
  gene symbol: CORO7
  hgvsc: ENST00000575531.1:n.1672+23C>T
  variant of: http://identifiers.org/hgnc/26161
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4587
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26793
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 998
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3366
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3885
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5053
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13404
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQ

http://identifiers.org/exac.variant/16-4408351-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4408351
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4408351
    reference: chr 16
allele count: 3
allele frequency: 2.683123155352831e-5
allele num: 111810
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103426
  ensembl transcript: ENST00000572274
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000572274.1:n.175+17G>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.*904+17G>T
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460956
  ensembl transcript: ENST00000570779
  gene symbol: CORO7
  hgvsc: ENST00000570779.1:c.84+17G>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.2202+17G>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: ENST00000575531
  gene symbol: CORO7
  hgvsc: ENST00000575531.1:n.1672+17G>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.2457+17G>T
  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.*2393+17G>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: ENST00000574849
  gene symbol: CORO7
  hgvsc: ENST00000574849.1:n.150+17G>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: ENST00000575714
  gene symbol: CORO7
  hgvsc: ENST00000575714.1:n.2003G>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.2403+17G>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.2457+17G>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.1797+17G>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460177
  ensembl transcript: ENST00000576637
  gene symbol: CORO7
  hgvsc: ENST00000576637.1:c.355+17G>T
  variant of: http://identifiers.org/hgnc/26161
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1435
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5233
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4255
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26796
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 962
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3643
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3382
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13797
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Other
population: Latino
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD

http://identifiers.org/exac.variant/16-4408361-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4408361
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4408361
    reference: chr 16
allele count: 1
allele frequency: 8.886045354375489e-6
allele num: 112536
alternate allele: A
annotation: 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.*904+7G>T
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460177
  ensembl transcript: ENST00000576637
  gene symbol: CORO7
  hgvsc: ENST00000576637.1:c.355+7G>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.*2393+7G>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: ENST00000575714
  gene symbol: CORO7
  hgvsc: ENST00000575714.1:n.1993G>T
  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: ENSG00000103426
  ensembl transcript: ENST00000572274
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000572274.1:n.175+7G>T
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000574849
  gene symbol: CORO7
  hgvsc: ENST00000574849.1:n.150+7G>T
  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.2457+7G>T
  variant of: http://identifiers.org/hgnc/44424
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.2202+7G>T
  variant of: http://identifiers.org/hgnc/26161
annotation: 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.2403+7G>T
  variant of: http://identifiers.org/hgnc/26161
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.1797+7G>T
  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: ENST00000575531
  gene symbol: CORO7
  hgvsc: ENST00000575531.1:n.1672+7G>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460956
  ensembl transcript: ENST00000570779
  gene symbol: CORO7
  hgvsc: ENST00000570779.1:c.84+7G>T
  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.2457+7G>T
  variant of: http://identifiers.org/hgnc/26161
canonical: true
consequence: splice region
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3185
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14573
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3795
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1474
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 943
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3310
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.2457+7G>T
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: South Asian
population: European (Finnish)
population: Latino
population: African
population: East Asian
reference allele: C
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: DP

http://identifiers.org/exac.variant/16-4408362-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4408362
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4408362
    reference: chr 16
allele count: 1
allele frequency: 8.879259824900996e-6
allele num: 112622
alternate allele: A
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.2457+6G>T
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000574849
  gene symbol: CORO7
  hgvsc: ENST00000574849.1:n.150+6G>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: ENST00000575714
  gene symbol: CORO7
  hgvsc: ENST00000575714.1:n.1992G>T
  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.2202+6G>T
  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: ENSG00000103426
  ensembl transcript: ENST00000572274
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000572274.1:n.175+6G>T
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460177
  ensembl transcript: ENST00000576637
  gene symbol: CORO7
  hgvsc: ENST00000576637.1:c.355+6G>T
  variant of: http://identifiers.org/hgnc/26161
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.1797+6G>T
  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.2457+6G>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: ENSG00000103426
  ensembl protein: ENSP00000458607
  ensembl transcript: ENST00000575334
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000575334.1:c.*904+6G>T
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460956
  ensembl transcript: ENST00000570779
  gene symbol: CORO7
  hgvsc: ENST00000570779.1:c.84+6G>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.*2393+6G>T
  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: ENST00000575531
  gene symbol: CORO7
  hgvsc: ENST00000575531.1:n.1672+6G>T
  variant of: http://identifiers.org/hgnc/26161
annotation: 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.2403+6G>T
  variant of: http://identifiers.org/hgnc/26161
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 26640
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5569
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3182
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1478
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3289
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 936
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3759
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.2457+6G>T
num of homozygotes: 0
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: East Asian
population: African
reference allele: C
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: DP

16-4408362-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4408362
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4408362
    reference: chr 16
allele count: 2
allele frequency: 1.775851964980199e-5
allele num: 112622
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460956
  ensembl transcript: ENST00000570779
  gene symbol: CORO7
  hgvsc: ENST00000570779.1:c.84+6G>A
  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.2202+6G>A
  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: ENSG00000103426
  ensembl transcript: ENST00000572274
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000572274.1:n.175+6G>A
  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: ENST00000575714
  gene symbol: CORO7
  hgvsc: ENST00000575714.1:n.1992G>A
  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.2457+6G>A
  variant of: http://identifiers.org/hgnc/44424
annotation: 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.2403+6G>A
  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: ENST00000574849
  gene symbol: CORO7
  hgvsc: ENST00000574849.1:n.150+6G>A
  variant of: http://identifiers.org/hgnc/26161
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.1797+6G>A
  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.*2393+6G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: 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.*904+6G>A
  variant of: http://identifiers.org/hgnc/44424
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.2457+6G>A
  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: ENSP00000460177
  ensembl transcript: ENST00000576637
  gene symbol: CORO7
  hgvsc: ENST00000576637.1:c.355+6G>A
  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: ENST00000575531
  gene symbol: CORO7
  hgvsc: ENST00000575531.1:n.1672+6G>A
  variant of: http://identifiers.org/hgnc/26161
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3289
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5569
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3182
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 936
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14644
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26640
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.2457+6G>A
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum

16-4408365-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4408365
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4408365
    reference: chr 16
allele count: 1
allele frequency: 8.87154009936125e-6
allele num: 112720
alternate allele: T
annotation: 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.*904+3G>A
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460956
  ensembl transcript: ENST00000570779
  gene symbol: CORO7
  hgvsc: ENST00000570779.1:c.84+3G>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: ENST00000575714
  gene symbol: CORO7
  hgvsc: ENST00000575714.1:n.1989G>A
  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: ENSG00000103426
  ensembl transcript: ENST00000572274
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000572274.1:n.175+3G>A
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000574849
  gene symbol: CORO7
  hgvsc: ENST00000574849.1:n.150+3G>A
  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.2457+3G>A
  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.1797+3G>A
  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.*2393+3G>A
  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.2457+3G>A
  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.2202+3G>A
  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: ENSP00000460177
  ensembl transcript: ENST00000576637
  gene symbol: CORO7
  hgvsc: ENST00000576637.1:c.355+3G>A
  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: ENST00000575531
  gene symbol: CORO7
  hgvsc: ENST00000575531.1:n.1672+3G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: 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.2403+3G>A
  variant of: http://identifiers.org/hgnc/26161
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3257
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3322
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5641
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26259
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1502
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14879
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.2457+3G>A
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: QD

16-4408366-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4408366
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4408366
    reference: chr 16
allele count: 19
allele frequency: 1.685383291642273e-4
allele num: 112734
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: splice_donor_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000460885
  ensembl transcript: ENST00000572467
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000572467.1:c.2457+2T>A
  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: ENST00000575714
  gene symbol: CORO7
  hgvsc: ENST00000575714.1:n.1988T>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460956
  ensembl transcript: ENST00000570779
  gene symbol: CORO7
  hgvsc: ENST00000570779.1:c.84+2T>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: true
  consequence: splice_donor_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000251166
  ensembl transcript: ENST00000251166
  gene symbol: CORO7
  hgvsc: ENST00000251166.4:c.2457+2T>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000458607
  ensembl transcript: ENST00000575334
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000575334.1:c.*904+2T>A
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000103426
  ensembl transcript: ENST00000572274
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000572274.1:n.175+2T>A
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461702
  ensembl transcript: ENST00000574025
  gene symbol: CORO7
  hgvsc: ENST00000574025.1:c.2202+2T>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000446221
  ensembl transcript: ENST00000539968
  gene symbol: CORO7
  hgvsc: ENST00000539968.1:c.1797+2T>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460177
  ensembl transcript: ENST00000576637
  gene symbol: CORO7
  hgvsc: ENST00000576637.1:c.355+2T>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000575531
  gene symbol: CORO7
  hgvsc: ENST00000575531.1:n.1672+2T>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000440460
  ensembl transcript: ENST00000537233
  gene symbol: CORO7
  hgvsc: ENST00000537233.2:c.2403+2T>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458459
  ensembl transcript: ENST00000571227
  gene symbol: CORO7
  hgvsc: ENST00000571227.1:c.*2393+2T>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000574849
  gene symbol: CORO7
  hgvsc: ENST00000574849.1:n.150+2T>A
  variant of: http://identifiers.org/hgnc/26161
canonical: true
consequence: splice donor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3695
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1498
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26213
  bin: 2.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 3240
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 904
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 558
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5642
  bin: 3.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 15001
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: c.2457+2T>A
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: African
population: Other
population: Latino
population: European (Finnish)
population: East Asian
reference allele: A
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/16-4408368-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4408368
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4408368
    reference: chr 16
allele count: 7
allele frequency: 6.203363995675369e-5
allele num: 112842
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000446221
  ensembl transcript: ENST00000539968
  gene symbol: CORO7
  hgvsc: ENST00000539968.1:c.1797G>T
  hgvsp: ENST00000539968.1:c.1797G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458459
  ensembl transcript: ENST00000571227
  gene symbol: CORO7
  hgvsc: ENST00000571227.1:c.*2393G>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000458607
  ensembl transcript: ENST00000575334
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000575334.1:c.*904G>T
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000251166
  ensembl transcript: ENST00000251166
  gene symbol: CORO7
  hgvsc: ENST00000251166.4:c.2457G>T
  hgvsp: ENST00000251166.4:c.2457G>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: ENST00000575714
  gene symbol: CORO7
  hgvsc: ENST00000575714.1:n.1986G>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000103426
  ensembl transcript: ENST00000572274
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000572274.1:n.175G>T
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460177
  ensembl transcript: ENST00000576637
  gene symbol: CORO7
  hgvsc: ENST00000576637.1:c.355G>T
  hgvsp: ENST00000576637.1:c.355G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000460885
  ensembl transcript: ENST00000572467
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000572467.1:c.2457G>T
  hgvsp: ENST00000572467.1:c.2457G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000440460
  ensembl transcript: ENST00000537233
  gene symbol: CORO7
  hgvsc: ENST00000537233.2:c.2403G>T
  hgvsp: ENST00000537233.2:c.2403G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460956
  ensembl transcript: ENST00000570779
  gene symbol: CORO7
  hgvsc: ENST00000570779.1:c.84G>T
  hgvsp: ENST00000570779.1:c.84G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461702
  ensembl transcript: ENST00000574025
  gene symbol: CORO7
  hgvsc: ENST00000574025.1:c.2202G>T
  hgvsp: ENST00000574025.1:c.2202G>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
  consequence: splice_region_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000575531
  gene symbol: CORO7
  hgvsc: ENST00000575531.1:n.1672G>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000574849
  gene symbol: CORO7
  hgvsc: ENST00000574849.1:n.150G>T
  variant of: http://identifiers.org/hgnc/26161
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15124
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1515
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5737
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3167
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3200
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3617
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.2457G>T
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
reference allele: C
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum

16-4408369-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4408369
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4408369
    reference: chr 16
allele count: 18
allele frequency: 1.596282435572267e-4
allele num: 112762
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000574849
  gene symbol: CORO7
  hgvsc: ENST00000574849.1:n.149G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460956
  ensembl transcript: ENST00000570779
  gene symbol: CORO7
  hgvsc: ENST00000570779.1:c.83G>A
  hgvsp: ENSP00000460956.1:p.Arg28Gln
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458459
  ensembl transcript: ENST00000571227
  gene symbol: CORO7
  hgvsc: ENST00000571227.1:c.*2392G>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: ENST00000575714
  gene symbol: CORO7
  hgvsc: ENST00000575714.1:n.1985G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000446221
  ensembl transcript: ENST00000539968
  gene symbol: CORO7
  hgvsc: ENST00000539968.1:c.1796G>A
  hgvsp: ENSP00000446221.1:p.Arg599Gln
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461702
  ensembl transcript: ENST00000574025
  gene symbol: CORO7
  hgvsc: ENST00000574025.1:c.2201G>A
  hgvsp: ENSP00000461702.1:p.Arg734Gln
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460177
  ensembl transcript: ENST00000576637
  gene symbol: CORO7
  hgvsc: ENST00000576637.1:c.354G>A
  hgvsp: ENSP00000460177.1:p.Arg119Gln
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000460885
  ensembl transcript: ENST00000572467
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000572467.1:c.2456G>A
  hgvsp: ENSP00000460885.1:p.Arg819Gln
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000575531
  gene symbol: CORO7
  hgvsc: ENST00000575531.1:n.1671G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000440460
  ensembl transcript: ENST00000537233
  gene symbol: CORO7
  hgvsc: ENST00000537233.2:c.2402G>A
  hgvsp: ENSP00000440460.2:p.Arg801Gln
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000251166
  ensembl transcript: ENST00000251166
  gene symbol: CORO7
  hgvsc: ENST00000251166.4:c.2456G>A
  hgvsp: ENSP00000251166.4:p.Arg819Gln
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000458607
  ensembl transcript: ENST00000575334
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000575334.1:c.*903G>A
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000103426
  ensembl transcript: ENST00000572274
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000572274.1:n.174G>A
  variant of: http://identifiers.org/hgnc/44424
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1531
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 15228
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 905
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3589
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 4.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 3143
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5804
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3155
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg819Gln
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP

16-4408370-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4408370
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4408370
    reference: chr 16
allele count: 4
allele frequency: 3.539760358223748e-5
allele num: 113002
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000251166
  ensembl transcript: ENST00000251166
  gene symbol: CORO7
  hgvsc: ENST00000251166.4:c.2455C>T
  hgvsp: ENSP00000251166.4:p.Arg819Trp
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460956
  ensembl transcript: ENST00000570779
  gene symbol: CORO7
  hgvsc: ENST00000570779.1:c.82C>T
  hgvsp: ENSP00000460956.1:p.Arg28Trp
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000574849
  gene symbol: CORO7
  hgvsc: ENST00000574849.1:n.148C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460177
  ensembl transcript: ENST00000576637
  gene symbol: CORO7
  hgvsc: ENST00000576637.1:c.353C>T
  hgvsp: ENSP00000460177.1:p.Arg119Trp
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000440460
  ensembl transcript: ENST00000537233
  gene symbol: CORO7
  hgvsc: ENST00000537233.2:c.2401C>T
  hgvsp: ENSP00000440460.2:p.Arg801Trp
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461702
  ensembl transcript: ENST00000574025
  gene symbol: CORO7
  hgvsc: ENST00000574025.1:c.2200C>T
  hgvsp: ENSP00000461702.1:p.Arg734Trp
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458459
  ensembl transcript: ENST00000571227
  gene symbol: CORO7
  hgvsc: ENST00000571227.1:c.*2391C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000575531
  gene symbol: CORO7
  hgvsc: ENST00000575531.1:n.1670C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000446221
  ensembl transcript: ENST00000539968
  gene symbol: CORO7
  hgvsc: ENST00000539968.1:c.1795C>T
  hgvsp: ENSP00000446221.1:p.Arg599Trp
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000460885
  ensembl transcript: ENST00000572467
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000572467.1:c.2455C>T
  hgvsp: ENSP00000460885.1:p.Arg819Trp
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000458607
  ensembl transcript: ENST00000575334
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000575334.1:c.*902C>T
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000103426
  ensembl transcript: ENST00000572274
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000572274.1:n.173C>T
  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: ENST00000575714
  gene symbol: CORO7
  hgvsc: ENST00000575714.1:n.1984C>T
  variant of: http://identifiers.org/hgnc/26161
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3042
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26190
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 884
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15297
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1538
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5872
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3526
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg819Trp
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: South Asian
population: Other
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum

16-4408371-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4408371
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4408371
    reference: chr 16
allele count: 2
allele frequency: 1.767846409503942e-5
allele num: 113132
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000440460
  ensembl transcript: ENST00000537233
  gene symbol: CORO7
  hgvsc: ENST00000537233.2:c.2400C>G
  hgvsp: ENST00000537233.2:c.2400C>G(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: ENST00000575531
  gene symbol: CORO7
  hgvsc: ENST00000575531.1:n.1669C>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.*2390C>G
  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.2454C>G
  hgvsp: ENST00000251166.4:c.2454C>G(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: ENSP00000460177
  ensembl transcript: ENST00000576637
  gene symbol: CORO7
  hgvsc: ENST00000576637.1:c.352C>G
  hgvsp: ENST00000576637.1:c.352C>G(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: ENST00000574849
  gene symbol: CORO7
  hgvsc: ENST00000574849.1:n.147C>G
  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.2199C>G
  hgvsp: ENST00000574025.1:c.2199C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000446221
  ensembl transcript: ENST00000539968
  gene symbol: CORO7
  hgvsc: ENST00000539968.1:c.1794C>G
  hgvsp: ENST00000539968.1:c.1794C>G(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: ENSG00000103426
  ensembl transcript: ENST00000572274
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000572274.1:n.172C>G
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460956
  ensembl transcript: ENST00000570779
  gene symbol: CORO7
  hgvsc: ENST00000570779.1:c.81C>G
  hgvsp: ENST00000570779.1:c.81C>G(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.2454C>G
  hgvsp: ENST00000572467.1:c.2454C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000458607
  ensembl transcript: ENST00000575334
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000575334.1:c.*901C>G
  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: ENST00000575714
  gene symbol: CORO7
  hgvsc: ENST00000575714.1:n.1983C>G
  variant of: http://identifiers.org/hgnc/26161
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5849
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15372
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3015
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 878
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26203
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3114
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3506
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val818Val
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
population: African
reference allele: G
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP

16-4408375-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4408375
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4408375
    reference: chr 16
allele count: 3
allele frequency: 2.653552221907727e-5
allele num: 113056
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461702
  ensembl transcript: ENST00000574025
  gene symbol: CORO7
  hgvsc: ENST00000574025.1:c.2195G>A
  hgvsp: ENSP00000461702.1:p.Arg732Gln
  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.2450G>A
  hgvsp: ENSP00000460885.1:p.Arg817Gln
  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.2396G>A
  hgvsp: ENSP00000440460.2:p.Arg799Gln
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000458607
  ensembl transcript: ENST00000575334
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000575334.1:c.*897G>A
  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.*2386G>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: ENST00000575531
  gene symbol: CORO7
  hgvsc: ENST00000575531.1:n.1665G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000446221
  ensembl transcript: ENST00000539968
  gene symbol: CORO7
  hgvsc: ENST00000539968.1:c.1790G>A
  hgvsp: ENSP00000446221.1:p.Arg597Gln
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460956
  ensembl transcript: ENST00000570779
  gene symbol: CORO7
  hgvsc: ENST00000570779.1:c.77G>A
  hgvsp: ENSP00000460956.1:p.Arg26Gln
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103426
  ensembl transcript: ENST00000572274
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000572274.1:n.168G>A
  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.2450G>A
  hgvsp: ENSP00000251166.4:p.Arg817Gln
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460177
  ensembl transcript: ENST00000576637
  gene symbol: CORO7
  hgvsc: ENST00000576637.1:c.348G>A
  hgvsp: ENSP00000460177.1:p.Arg117Gln
  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: ENST00000575714
  gene symbol: CORO7
  hgvsc: ENST00000575714.1:n.1979G>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: ENST00000574849
  gene symbol: CORO7
  hgvsc: ENST00000574849.1:n.143G>A
  variant of: http://identifiers.org/hgnc/26161
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6000
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1571
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3064
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3034
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25929
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 879
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15600
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Arg817Gln
num of homozygotes: 0
population: Latino
population: African
population: Other
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum

16-4408384-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4408384
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4408384
    reference: chr 16
allele count: 6
allele frequency: 5.283178360101437e-5
allele num: 113568
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000460885
  ensembl transcript: ENST00000572467
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000572467.1:c.2441G>A
  hgvsp: ENSP00000460885.1:p.Arg814Gln
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000458607
  ensembl transcript: ENST00000575334
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000575334.1:c.*888G>A
  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.*2377G>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: ENST00000575531
  gene symbol: CORO7
  hgvsc: ENST00000575531.1:n.1656G>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: ENST00000575714
  gene symbol: CORO7
  hgvsc: ENST00000575714.1:n.1970G>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.2186G>A
  hgvsp: ENSP00000461702.1:p.Arg729Gln
  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.2441G>A
  hgvsp: ENSP00000251166.4:p.Arg814Gln
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460177
  ensembl transcript: ENST00000576637
  gene symbol: CORO7
  hgvsc: ENST00000576637.1:c.339G>A
  hgvsp: ENSP00000460177.1:p.Arg114Gln
  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.2387G>A
  hgvsp: ENSP00000440460.2:p.Arg796Gln
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460956
  ensembl transcript: ENST00000570779
  gene symbol: CORO7
  hgvsc: ENST00000570779.1:c.68G>A
  hgvsp: ENSP00000460956.1:p.Arg23Gln
  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: ENST00000574849
  gene symbol: CORO7
  hgvsc: ENST00000574849.1:n.134G>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: ENSG00000103426
  ensembl transcript: ENST00000572274
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000572274.1:n.159G>A
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000446221
  ensembl transcript: ENST00000539968
  gene symbol: CORO7
  hgvsc: ENST00000539968.1:c.1781G>A
  hgvsp: ENSP00000446221.1:p.Arg594Gln
  variant of: http://identifiers.org/hgnc/26161
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2915
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6364
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16160
  bin: 2.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 3036
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 786
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26013
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 586
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1612
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg814Gln
num of homozygotes: 0
population: European (Finnish)
population: Other
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: C
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum

16-4408385-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4408385
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4408385
    reference: chr 16
allele count: 1
allele frequency: 8.798015167778149e-6
allele num: 113662
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460956
  ensembl transcript: ENST00000570779
  gene symbol: CORO7
  hgvsc: ENST00000570779.1:c.67C>T
  hgvsp: ENSP00000460956.1:p.Arg23Trp
  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.2386C>T
  hgvsp: ENSP00000440460.2:p.Arg796Trp
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000446221
  ensembl transcript: ENST00000539968
  gene symbol: CORO7
  hgvsc: ENST00000539968.1:c.1780C>T
  hgvsp: ENSP00000446221.1:p.Arg594Trp
  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: ENST00000575531
  gene symbol: CORO7
  hgvsc: ENST00000575531.1:n.1655C>T
  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.2440C>T
  hgvsp: ENSP00000251166.4:p.Arg814Trp
  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.*2376C>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: ENST00000574849
  gene symbol: CORO7
  hgvsc: ENST00000574849.1:n.133C>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: ENST00000575714
  gene symbol: CORO7
  hgvsc: ENST00000575714.1:n.1969C>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.2440C>T
  hgvsp: ENSP00000460885.1:p.Arg814Trp
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460177
  ensembl transcript: ENST00000576637
  gene symbol: CORO7
  hgvsc: ENST00000576637.1:c.338C>T
  hgvsp: ENSP00000460177.1:p.Arg114Trp
  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.2185C>T
  hgvsp: ENSP00000461702.1:p.Arg729Trp
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103426
  ensembl transcript: ENST00000572274
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000572274.1:n.158C>T
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000458607
  ensembl transcript: ENST00000575334
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000575334.1:c.*887C>T
  variant of: http://identifiers.org/hgnc/44424
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16260
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6440
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2957
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26090
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 596
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2898
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 763
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2405
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg814Trp
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
reference allele: G
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum

16-4408389-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4408389
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4408389
    reference: chr 16
allele count: 1
allele frequency: 8.769775844529415e-6
allele num: 114028
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000575531
  gene symbol: CORO7
  hgvsc: ENST00000575531.1:n.1651C>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.2436C>T
  hgvsp: ENST00000251166.4:c.2436C>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: ENST00000575714
  gene symbol: CORO7
  hgvsc: ENST00000575714.1:n.1965C>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.*2372C>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: ENST00000574849
  gene symbol: CORO7
  hgvsc: ENST00000574849.1:n.129C>T
  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.2382C>T
  hgvsp: ENST00000537233.2:c.2382C>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: ENSP00000460177
  ensembl transcript: ENST00000576637
  gene symbol: CORO7
  hgvsc: ENST00000576637.1:c.334C>T
  hgvsp: ENST00000576637.1:c.334C>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: ENSG00000103426
  ensembl transcript: ENST00000572274
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000572274.1:n.154C>T
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000460885
  ensembl transcript: ENST00000572467
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000572467.1:c.2436C>T
  hgvsp: ENST00000572467.1:c.2436C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000446221
  ensembl transcript: ENST00000539968
  gene symbol: CORO7
  hgvsc: ENST00000539968.1:c.1776C>T
  hgvsp: ENST00000539968.1:c.1776C>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: ENSG00000103426
  ensembl protein: ENSP00000458607
  ensembl transcript: ENST00000575334
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000575334.1:c.*883C>T
  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.2181C>T
  hgvsp: ENST00000574025.1:c.2181C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460956
  ensembl transcript: ENST00000570779
  gene symbol: CORO7
  hgvsc: ENST00000570779.1:c.63C>T
  hgvsp: ENST00000570779.1:c.63C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26161
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2849
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6518
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 735
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26301
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2125
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16526
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala812Ala
num of homozygotes: 0
population: Other
population: East Asian
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum

16-4408405-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4408405
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4408405
    reference: chr 16
allele count: 2
allele frequency: 1.747793410818841e-5
allele num: 114430
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000575714
  gene symbol: CORO7
  hgvsc: ENST00000575714.1:n.1949C>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: ENSG00000103426
  ensembl transcript: ENST00000572274
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000572274.1:n.138C>T
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461702
  ensembl transcript: ENST00000574025
  gene symbol: CORO7
  hgvsc: ENST00000574025.1:c.2165C>T
  hgvsp: ENSP00000461702.1:p.Ser722Phe
  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.2366C>T
  hgvsp: ENSP00000440460.2:p.Ser789Phe
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460177
  ensembl transcript: ENST00000576637
  gene symbol: CORO7
  hgvsc: ENST00000576637.1:c.318C>T
  hgvsp: ENSP00000460177.1:p.Ser107Phe
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000446221
  ensembl transcript: ENST00000539968
  gene symbol: CORO7
  hgvsc: ENST00000539968.1:c.1760C>T
  hgvsp: ENSP00000446221.1:p.Ser587Phe
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460956
  ensembl transcript: ENST00000570779
  gene symbol: CORO7
  hgvsc: ENST00000570779.1:c.47C>T
  hgvsp: ENSP00000460956.1:p.Ser16Phe
  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.*2356C>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.2420C>T
  hgvsp: ENSP00000460885.1:p.Ser807Phe
  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.2420C>T
  hgvsp: ENSP00000251166.4:p.Ser807Phe
  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: ENST00000574849
  gene symbol: CORO7
  hgvsc: ENST00000574849.1:n.113C>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: ENST00000575531
  gene symbol: CORO7
  hgvsc: ENST00000575531.1:n.1635C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000458607
  ensembl transcript: ENST00000575334
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000575334.1:c.*867C>T
  variant of: http://identifiers.org/hgnc/44424
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1850
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25992
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7036
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2692
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2314
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1720
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 676
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser807Phe
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD

16-4408410-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4408410
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4408410
    reference: chr 16
allele count: 4
allele frequency: 3.492595697122101e-5
allele num: 114528
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000575714
  gene symbol: CORO7
  hgvsc: ENST00000575714.1:n.1944G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000458607
  ensembl transcript: ENST00000575334
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000575334.1:c.*862G>A
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460956
  ensembl transcript: ENST00000570779
  gene symbol: CORO7
  hgvsc: ENST00000570779.1:c.42G>A
  hgvsp: ENST00000570779.1:c.42G>A(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.2361G>A
  hgvsp: ENST00000537233.2:c.2361G>A(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: ENSG00000103426
  ensembl transcript: ENST00000572274
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000572274.1:n.133G>A
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000446221
  ensembl transcript: ENST00000539968
  gene symbol: CORO7
  hgvsc: ENST00000539968.1:c.1755G>A
  hgvsp: ENST00000539968.1:c.1755G>A(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.2415G>A
  hgvsp: ENST00000572467.1:c.2415G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000251166
  ensembl transcript: ENST00000251166
  gene symbol: CORO7
  hgvsc: ENST00000251166.4:c.2415G>A
  hgvsp: ENST00000251166.4:c.2415G>A(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.2160G>A
  hgvsp: ENST00000574025.1:c.2160G>A(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: ENST00000574849
  gene symbol: CORO7
  hgvsc: ENST00000574849.1:n.108G>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: ENST00000575531
  gene symbol: CORO7
  hgvsc: ENST00000575531.1:n.1630G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460177
  ensembl transcript: ENST00000576637
  gene symbol: CORO7
  hgvsc: ENST00000576637.1:c.313G>A
  hgvsp: ENST00000576637.1:c.313G>A(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.*2351G>A
  variant of: http://identifiers.org/hgnc/26161
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1739
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25947
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 649
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7187
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2239
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2638
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1730
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln805Gln
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
population: South Asian
population: Latino
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: ClippingRankSum

16-4408410-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4408410
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4408410
    reference: chr 16
allele count: 4
allele frequency: 3.492595697122101e-5
allele num: 114528
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000446221
  ensembl transcript: ENST00000539968
  gene symbol: CORO7
  hgvsc: ENST00000539968.1:c.1755G>C
  hgvsp: ENSP00000446221.1:p.Gln585His
  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: ENST00000575531
  gene symbol: CORO7
  hgvsc: ENST00000575531.1:n.1630G>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.2160G>C
  hgvsp: ENSP00000461702.1:p.Gln720His
  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.2415G>C
  hgvsp: ENSP00000251166.4:p.Gln805His
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460177
  ensembl transcript: ENST00000576637
  gene symbol: CORO7
  hgvsc: ENST00000576637.1:c.313G>C
  hgvsp: ENSP00000460177.1:p.Gln105His
  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.2415G>C
  hgvsp: ENSP00000460885.1:p.Gln805His
  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.*2351G>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.2361G>C
  hgvsp: ENSP00000440460.2:p.Gln787His
  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: ENST00000574849
  gene symbol: CORO7
  hgvsc: ENST00000574849.1:n.108G>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000458607
  ensembl transcript: ENST00000575334
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000575334.1:c.*862G>C
  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: ENST00000575714
  gene symbol: CORO7
  hgvsc: ENST00000575714.1:n.1944G>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460956
  ensembl transcript: ENST00000570779
  gene symbol: CORO7
  hgvsc: ENST00000570779.1:c.42G>C
  hgvsp: ENSP00000460956.1:p.Gln14His
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103426
  ensembl transcript: ENST00000572274
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000572274.1:n.133G>C
  variant of: http://identifiers.org/hgnc/44424
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2638
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1739
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7187
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1730
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 649
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2239
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25947
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Gln805His
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: Other
population: East Asian
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum

16-4408414-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4408414
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4408414
    reference: chr 16
allele count: 7
allele frequency: 6.09979260705136e-5
allele num: 114758
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461702
  ensembl transcript: ENST00000574025
  gene symbol: CORO7
  hgvsc: ENST00000574025.1:c.2156G>A
  hgvsp: ENSP00000461702.1:p.Arg719His
  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.2411G>A
  hgvsp: ENSP00000251166.4:p.Arg804His
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460177
  ensembl transcript: ENST00000576637
  gene symbol: CORO7
  hgvsc: ENST00000576637.1:c.309G>A
  hgvsp: ENSP00000460177.1:p.Arg104His
  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: ENST00000574849
  gene symbol: CORO7
  hgvsc: ENST00000574849.1:n.104G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000458607
  ensembl transcript: ENST00000575334
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000575334.1:c.*858G>A
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460956
  ensembl transcript: ENST00000570779
  gene symbol: CORO7
  hgvsc: ENST00000570779.1:c.38G>A
  hgvsp: ENSP00000460956.1:p.Arg13His
  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.2411G>A
  hgvsp: ENSP00000460885.1:p.Arg804His
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103426
  ensembl transcript: ENST00000572274
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000572274.1:n.129G>A
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000446221
  ensembl transcript: ENST00000539968
  gene symbol: CORO7
  hgvsc: ENST00000539968.1:c.1751G>A
  hgvsp: ENSP00000446221.1:p.Arg584His
  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.*2347G>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: ENST00000575531
  gene symbol: CORO7
  hgvsc: ENST00000575531.1:n.1626G>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.2357G>A
  hgvsp: ENSP00000440460.2:p.Arg786His
  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: ENST00000575714
  gene symbol: CORO7
  hgvsc: ENST00000575714.1:n.1940G>A
  variant of: http://identifiers.org/hgnc/26161
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2182
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2545
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1777
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25806
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1567
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 17564
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg804His
num of homozygotes: 0
population: Other
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: ReadPosRankSum

16-4408415-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4408415
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4408415
    reference: chr 16
allele count: 8
allele frequency: 6.993618323280007e-5
allele num: 114390
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000575714
  gene symbol: CORO7
  hgvsc: ENST00000575714.1:n.1939C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000458607
  ensembl transcript: ENST00000575334
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000575334.1:c.*857C>T
  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: ENST00000574849
  gene symbol: CORO7
  hgvsc: ENST00000574849.1:n.103C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000446221
  ensembl transcript: ENST00000539968
  gene symbol: CORO7
  hgvsc: ENST00000539968.1:c.1750C>T
  hgvsp: ENSP00000446221.1:p.Arg584Cys
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103426
  ensembl transcript: ENST00000572274
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000572274.1:n.128C>T
  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.*2346C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460177
  ensembl transcript: ENST00000576637
  gene symbol: CORO7
  hgvsc: ENST00000576637.1:c.308C>T
  hgvsp: ENSP00000460177.1:p.Arg104Cys
  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.2356C>T
  hgvsp: ENSP00000440460.2:p.Arg786Cys
  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: ENST00000575531
  gene symbol: CORO7
  hgvsc: ENST00000575531.1:n.1625C>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.2410C>T
  hgvsp: ENSP00000460885.1:p.Arg804Cys
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460956
  ensembl transcript: ENST00000570779
  gene symbol: CORO7
  hgvsc: ENST00000570779.1:c.37C>T
  hgvsp: ENSP00000460956.1:p.Arg13Cys
  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.2410C>T
  hgvsp: ENSP00000251166.4:p.Arg804Cys
  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.2155C>T
  hgvsp: ENSP00000461702.1:p.Arg719Cys
  variant of: http://identifiers.org/hgnc/26161
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2439
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2196
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25636
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 611
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7481
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1816
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1598
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 652
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg804Cys
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: South Asian
population: East Asian
population: African
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: DP

16-4408416-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4408416
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4408416
    reference: chr 16
allele count: 3
allele frequency: 2.602224034141179e-5
allele num: 115286
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000446221
  ensembl transcript: ENST00000539968
  gene symbol: CORO7
  hgvsc: ENST00000539968.1:c.1749G>C
  hgvsp: ENST00000539968.1:c.1749G>C(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.2409G>C
  hgvsp: ENST00000251166.4:c.2409G>C(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.2409G>C
  hgvsp: ENST00000572467.1:c.2409G>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.2154G>C
  hgvsp: ENST00000574025.1:c.2154G>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.2355G>C
  hgvsp: ENST00000537233.2:c.2355G>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: ENSG00000103426
  ensembl protein: ENSP00000458607
  ensembl transcript: ENST00000575334
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000575334.1:c.*856G>C
  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: ENST00000575531
  gene symbol: CORO7
  hgvsc: ENST00000575531.1:n.1624G>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460956
  ensembl transcript: ENST00000570779
  gene symbol: CORO7
  hgvsc: ENST00000570779.1:c.36G>C
  hgvsp: ENST00000570779.1:c.36G>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: ENSP00000460177
  ensembl transcript: ENST00000576637
  gene symbol: CORO7
  hgvsc: ENST00000576637.1:c.307G>C
  hgvsp: ENST00000576637.1:c.307G>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: ENST00000575714
  gene symbol: CORO7
  hgvsc: ENST00000575714.1:n.1938G>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: ENSG00000103426
  ensembl transcript: ENST00000572274
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000572274.1:n.127G>C
  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.*2345G>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: ENST00000574849
  gene symbol: CORO7
  hgvsc: ENST00000574849.1:n.102G>C
  variant of: http://identifiers.org/hgnc/26161
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 575
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1424
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7566
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17867
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 658
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2154
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2380
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu803Leu
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD

http://identifiers.org/exac.variant/16-4408419-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4408419
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4408419
    reference: chr 16
allele count: 2
allele frequency: 1.733282490380282e-5
allele num: 115388
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460177
  ensembl transcript: ENST00000576637
  gene symbol: CORO7
  hgvsc: ENST00000576637.1:c.304G>T
  hgvsp: ENST00000576637.1:c.304G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460956
  ensembl transcript: ENST00000570779
  gene symbol: CORO7
  hgvsc: ENST00000570779.1:c.33G>T
  hgvsp: ENST00000570779.1:c.33G>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.*2342G>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: ENST00000574849
  gene symbol: CORO7
  hgvsc: ENST00000574849.1:n.99G>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: ENST00000575714
  gene symbol: CORO7
  hgvsc: ENST00000575714.1:n.1935G>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.2406G>T
  hgvsp: ENST00000251166.4:c.2406G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000446221
  ensembl transcript: ENST00000539968
  gene symbol: CORO7
  hgvsc: ENST00000539968.1:c.1746G>T
  hgvsp: ENST00000539968.1:c.1746G>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.2406G>T
  hgvsp: ENST00000572467.1:c.2406G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103426
  ensembl transcript: ENST00000572274
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000572274.1:n.124G>T
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000440460
  ensembl transcript: ENST00000537233
  gene symbol: CORO7
  hgvsc: ENST00000537233.2:c.2352G>T
  hgvsp: ENST00000537233.2:c.2352G>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.2151G>T
  hgvsp: ENST00000574025.1:c.2151G>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: ENST00000575531
  gene symbol: CORO7
  hgvsc: ENST00000575531.1:n.1621G>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000458607
  ensembl transcript: ENST00000575334
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000575334.1:c.*853G>T
  variant of: http://identifiers.org/hgnc/44424
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2376
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7668
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25525
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 660
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1247
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18145
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2016
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg802Arg
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
population: Other
reference allele: C
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

16-4408420-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4408420
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4408420
    reference: chr 16
allele count: 2
allele frequency: 1.7322316340141e-5
allele num: 115458
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000251166
  ensembl transcript: ENST00000251166
  gene symbol: CORO7
  hgvsc: ENST00000251166.4:c.2405G>A
  hgvsp: ENSP00000251166.4:p.Arg802Gln
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000446221
  ensembl transcript: ENST00000539968
  gene symbol: CORO7
  hgvsc: ENST00000539968.1:c.1745G>A
  hgvsp: ENSP00000446221.1:p.Arg582Gln
  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.2405G>A
  hgvsp: ENSP00000460885.1:p.Arg802Gln
  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: ENST00000574849
  gene symbol: CORO7
  hgvsc: ENST00000574849.1:n.98G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460177
  ensembl transcript: ENST00000576637
  gene symbol: CORO7
  hgvsc: ENST00000576637.1:c.303G>A
  hgvsp: ENSP00000460177.1:p.Arg102Gln
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103426
  ensembl transcript: ENST00000572274
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000572274.1:n.123G>A
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000458607
  ensembl transcript: ENST00000575334
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000575334.1:c.*852G>A
  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.2351G>A
  hgvsp: ENSP00000440460.2:p.Arg784Gln
  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: ENST00000575714
  gene symbol: CORO7
  hgvsc: ENST00000575714.1:n.1934G>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.2150G>A
  hgvsp: ENSP00000461702.1:p.Arg717Gln
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460956
  ensembl transcript: ENST00000570779
  gene symbol: CORO7
  hgvsc: ENST00000570779.1:c.32G>A
  hgvsp: ENSP00000460956.1:p.Arg11Gln
  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: ENST00000575531
  gene symbol: CORO7
  hgvsc: ENST00000575531.1:n.1620G>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.*2341G>A
  variant of: http://identifiers.org/hgnc/26161
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 511
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1995
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2357
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1192
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1886
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 665
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18177
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25537
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7717
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg802Gln
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: African
population: Other
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: DP

16-4408421-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4408421
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4408421
    reference: chr 16
allele count: 12
allele frequency: 1.038943048605219e-4
allele num: 115502
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000458607
  ensembl transcript: ENST00000575334
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000575334.1:c.*851C>T
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460177
  ensembl transcript: ENST00000576637
  gene symbol: CORO7
  hgvsc: ENST00000576637.1:c.302C>T
  hgvsp: ENSP00000460177.1:p.Arg102Trp
  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.2149C>T
  hgvsp: ENSP00000461702.1:p.Arg717Trp
  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.2404C>T
  hgvsp: ENSP00000251166.4:p.Arg802Trp
  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.2350C>T
  hgvsp: ENSP00000440460.2:p.Arg784Trp
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460956
  ensembl transcript: ENST00000570779
  gene symbol: CORO7
  hgvsc: ENST00000570779.1:c.31C>T
  hgvsp: ENSP00000460956.1:p.Arg11Trp
  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: ENST00000574849
  gene symbol: CORO7
  hgvsc: ENST00000574849.1:n.97C>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: ENST00000575714
  gene symbol: CORO7
  hgvsc: ENST00000575714.1:n.1933C>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: ENSG00000103426
  ensembl transcript: ENST00000572274
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000572274.1:n.122C>T
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000446221
  ensembl transcript: ENST00000539968
  gene symbol: CORO7
  hgvsc: ENST00000539968.1:c.1744C>T
  hgvsp: ENSP00000446221.1:p.Arg582Trp
  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.2404C>T
  hgvsp: ENSP00000460885.1:p.Arg802Trp
  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.*2340C>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: ENST00000575531
  gene symbol: CORO7
  hgvsc: ENST00000575531.1:n.1619C>T
  variant of: http://identifiers.org/hgnc/26161
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 499
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7849
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 687
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1947
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2334
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1913
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1122
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg802Trp
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: East Asian
reference allele: G
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD

16-4408421-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4408421
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4408421
    reference: chr 16
allele count: 1
allele frequency: 8.657858738376825e-6
allele num: 115502
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000574849
  gene symbol: CORO7
  hgvsc: ENST00000574849.1:n.97C>A
  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.2350C>A
  hgvsp: ENST00000537233.2:c.2350C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000458607
  ensembl transcript: ENST00000575334
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000575334.1:c.*851C>A
  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: ENST00000575531
  gene symbol: CORO7
  hgvsc: ENST00000575531.1:n.1619C>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.*2340C>A
  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.2404C>A
  hgvsp: ENST00000251166.4:c.2404C>A(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: ENST00000575714
  gene symbol: CORO7
  hgvsc: ENST00000575714.1:n.1933C>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460177
  ensembl transcript: ENST00000576637
  gene symbol: CORO7
  hgvsc: ENST00000576637.1:c.302C>A
  hgvsp: ENST00000576637.1:c.302C>A(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.2149C>A
  hgvsp: ENST00000574025.1:c.2149C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000446221
  ensembl transcript: ENST00000539968
  gene symbol: CORO7
  hgvsc: ENST00000539968.1:c.1744C>A
  hgvsp: ENST00000539968.1:c.1744C>A(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: ENSG00000103426
  ensembl transcript: ENST00000572274
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000572274.1:n.122C>A
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460956
  ensembl transcript: ENST00000570779
  gene symbol: CORO7
  hgvsc: ENST00000570779.1:c.31C>A
  hgvsp: ENST00000570779.1:c.31C>A(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.2404C>A
  hgvsp: ENST00000572467.1:c.2404C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/44424
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2334
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7849
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25411
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 499
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18267
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1947
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1913
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg802Arg
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS

16-4408422-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4408422
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4408422
    reference: chr 16
allele count: 2
allele frequency: 1.729266099467386e-5
allele num: 115656
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460177
  ensembl transcript: ENST00000576637
  gene symbol: CORO7
  hgvsc: ENST00000576637.1:c.301G>A
  hgvsp: ENST00000576637.1:c.301G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000446221
  ensembl transcript: ENST00000539968
  gene symbol: CORO7
  hgvsc: ENST00000539968.1:c.1743G>A
  hgvsp: ENST00000539968.1:c.1743G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460956
  ensembl transcript: ENST00000570779
  gene symbol: CORO7
  hgvsc: ENST00000570779.1:c.30G>A
  hgvsp: ENST00000570779.1:c.30G>A(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.2403G>A
  hgvsp: ENST00000251166.4:c.2403G>A(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: ENST00000575531
  gene symbol: CORO7
  hgvsc: ENST00000575531.1:n.1618G>A
  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.2403G>A
  hgvsp: ENST00000572467.1:c.2403G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000458607
  ensembl transcript: ENST00000575334
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000575334.1:c.*850G>A
  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: ENST00000575714
  gene symbol: CORO7
  hgvsc: ENST00000575714.1:n.1932G>A
  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.2148G>A
  hgvsp: ENST00000574025.1:c.2148G>A(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: ENSG00000103426
  ensembl transcript: ENST00000572274
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000572274.1:n.121G>A
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000440460
  ensembl transcript: ENST00000537233
  gene symbol: CORO7
  hgvsc: ENST00000537233.2:c.2349G>A
  hgvsp: ENST00000537233.2:c.2349G>A(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.*2339G>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: ENST00000574849
  gene symbol: CORO7
  hgvsc: ENST00000574849.1:n.96G>A
  variant of: http://identifiers.org/hgnc/26161
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18359
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25482
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1903
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2326
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1025
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7858
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1908
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu801Leu
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: European (Finnish)
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff

16-4408429-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4408429
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4408429
    reference: chr 16
allele count: 1
allele frequency: 8.633491038436302e-6
allele num: 115828
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000440460
  ensembl transcript: ENST00000537233
  gene symbol: CORO7
  hgvsc: ENST00000537233.2:c.2342G>A
  hgvsp: ENSP00000440460.2:p.Arg781Gln
  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.*2332G>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: ENSG00000103426
  ensembl transcript: ENST00000572274
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000572274.1:n.114G>A
  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: ENST00000575531
  gene symbol: CORO7
  hgvsc: ENST00000575531.1:n.1611G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460956
  ensembl transcript: ENST00000570779
  gene symbol: CORO7
  hgvsc: ENST00000570779.1:c.23G>A
  hgvsp: ENSP00000460956.1:p.Arg8Gln
  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.2141G>A
  hgvsp: ENSP00000461702.1:p.Arg714Gln
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000446221
  ensembl transcript: ENST00000539968
  gene symbol: CORO7
  hgvsc: ENST00000539968.1:c.1736G>A
  hgvsp: ENSP00000446221.1:p.Arg579Gln
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000458607
  ensembl transcript: ENST00000575334
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000575334.1:c.*843G>A
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460177
  ensembl transcript: ENST00000576637
  gene symbol: CORO7
  hgvsc: ENST00000576637.1:c.294G>A
  hgvsp: ENSP00000460177.1:p.Arg99Gln
  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.2396G>A
  hgvsp: ENSP00000251166.4:p.Arg799Gln
  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: ENST00000574849
  gene symbol: CORO7
  hgvsc: ENST00000574849.1:n.89G>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: ENST00000575714
  gene symbol: CORO7
  hgvsc: ENST00000575714.1:n.1925G>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.2396G>A
  hgvsp: ENSP00000460885.1:p.Arg799Gln
  variant of: http://identifiers.org/hgnc/44424
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18606
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 679
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1964
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 693
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1638
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25699
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2281
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8043
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg799Gln
num of homozygotes: 0
population: Latino
population: Other
population: South Asian
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum

16-4408429-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4408429
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4408429
    reference: chr 16
allele count: 1
allele frequency: 8.633491038436302e-6
allele num: 115828
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461702
  ensembl transcript: ENST00000574025
  gene symbol: CORO7
  hgvsc: ENST00000574025.1:c.2141G>C
  hgvsp: ENSP00000461702.1:p.Arg714Pro
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460956
  ensembl transcript: ENST00000570779
  gene symbol: CORO7
  hgvsc: ENST00000570779.1:c.23G>C
  hgvsp: ENSP00000460956.1:p.Arg8Pro
  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: ENST00000574849
  gene symbol: CORO7
  hgvsc: ENST00000574849.1:n.89G>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.2396G>C
  hgvsp: ENSP00000460885.1:p.Arg799Pro
  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.2342G>C
  hgvsp: ENSP00000440460.2:p.Arg781Pro
  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.*2332G>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000446221
  ensembl transcript: ENST00000539968
  gene symbol: CORO7
  hgvsc: ENST00000539968.1:c.1736G>C
  hgvsp: ENSP00000446221.1:p.Arg579Pro
  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: ENST00000575531
  gene symbol: CORO7
  hgvsc: ENST00000575531.1:n.1611G>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000458607
  ensembl transcript: ENST00000575334
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000575334.1:c.*843G>C
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460177
  ensembl transcript: ENST00000576637
  gene symbol: CORO7
  hgvsc: ENST00000576637.1:c.294G>C
  hgvsp: ENSP00000460177.1:p.Arg99Pro
  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: ENST00000575714
  gene symbol: CORO7
  hgvsc: ENST00000575714.1:n.1925G>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.2396G>C
  hgvsp: ENSP00000251166.4:p.Arg799Pro
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103426
  ensembl transcript: ENST00000572274
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000572274.1:n.114G>C
  variant of: http://identifiers.org/hgnc/44424
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18606
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1638
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1964
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2281
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 693
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 679
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25699
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg799Pro
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: African
reference allele: C
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum

16-4408430-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4408430
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4408430
    reference: chr 16
allele count: 1
allele frequency: 8.631702517004453e-6
allele num: 115852
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.2341C>T
  hgvsp: ENSP00000440460.2:p.Arg781Trp
  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.*2331C>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: ENST00000575531
  gene symbol: CORO7
  hgvsc: ENST00000575531.1:n.1610C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460956
  ensembl transcript: ENST00000570779
  gene symbol: CORO7
  hgvsc: ENST00000570779.1:c.22C>T
  hgvsp: ENSP00000460956.1:p.Arg8Trp
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103426
  ensembl transcript: ENST00000572274
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000572274.1:n.113C>T
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460177
  ensembl transcript: ENST00000576637
  gene symbol: CORO7
  hgvsc: ENST00000576637.1:c.293C>T
  hgvsp: ENSP00000460177.1:p.Arg99Trp
  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: ENST00000575714
  gene symbol: CORO7
  hgvsc: ENST00000575714.1:n.1924C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000458607
  ensembl transcript: ENST00000575334
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000575334.1:c.*842C>T
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000460885
  ensembl transcript: ENST00000572467
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000572467.1:c.2395C>T
  hgvsp: ENSP00000460885.1:p.Arg799Trp
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461702
  ensembl transcript: ENST00000574025
  gene symbol: CORO7
  hgvsc: ENST00000574025.1:c.2140C>T
  hgvsp: ENSP00000461702.1:p.Arg714Trp
  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.2395C>T
  hgvsp: ENSP00000251166.4:p.Arg799Trp
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000446221
  ensembl transcript: ENST00000539968
  gene symbol: CORO7
  hgvsc: ENST00000539968.1:c.1735C>T
  hgvsp: ENSP00000446221.1:p.Arg579Trp
  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: ENST00000574849
  gene symbol: CORO7
  hgvsc: ENST00000574849.1:n.88C>T
  variant of: http://identifiers.org/hgnc/26161
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8122
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2246
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1592
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18677
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg799Trp
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: ClippingRankSum

16-4408431-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4408431
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4408431
    reference: chr 16
allele count: 1
allele frequency: 8.62500215625054e-6
allele num: 115942
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000446221
  ensembl transcript: ENST00000539968
  gene symbol: CORO7
  hgvsc: ENST00000539968.1:c.1734G>A
  hgvsp: ENSP00000446221.1:p.Met578Ile
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460177
  ensembl transcript: ENST00000576637
  gene symbol: CORO7
  hgvsc: ENST00000576637.1:c.292G>A
  hgvsp: ENSP00000460177.1:p.Met98Ile
  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.2394G>A
  hgvsp: ENSP00000460885.1:p.Met798Ile
  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.2340G>A
  hgvsp: ENSP00000440460.2:p.Met780Ile
  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: ENST00000574849
  gene symbol: CORO7
  hgvsc: ENST00000574849.1:n.87G>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.2394G>A
  hgvsp: ENSP00000251166.4:p.Met798Ile
  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: ENST00000575714
  gene symbol: CORO7
  hgvsc: ENST00000575714.1:n.1923G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000458607
  ensembl transcript: ENST00000575334
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000575334.1:c.*841G>A
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461702
  ensembl transcript: ENST00000574025
  gene symbol: CORO7
  hgvsc: ENST00000574025.1:c.2139G>A
  hgvsp: ENSP00000461702.1:p.Met713Ile
  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: ENST00000575531
  gene symbol: CORO7
  hgvsc: ENST00000575531.1:n.1609G>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.*2330G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460956
  ensembl transcript: ENST00000570779
  gene symbol: CORO7
  hgvsc: ENST00000570779.1:c.21G>A
  hgvsp: ENSP00000460956.1:p.Met7Ile
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103426
  ensembl transcript: ENST00000572274
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000572274.1:n.112G>A
  variant of: http://identifiers.org/hgnc/44424
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2244
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25645
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18734
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1981
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8096
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Met798Ile
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
population: African
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: DP

16-4408434-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4408434
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4408434
    reference: chr 16
allele count: 4
allele frequency: 3.447562573260704e-5
allele num: 116024
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460956
  ensembl transcript: ENST00000570779
  gene symbol: CORO7
  hgvsc: ENST00000570779.1:c.18G>A
  hgvsp: ENST00000570779.1:c.18G>A(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: ENSG00000103426
  ensembl transcript: ENST00000572274
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000572274.1:n.109G>A
  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.*2327G>A
  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.2337G>A
  hgvsp: ENST00000537233.2:c.2337G>A(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: ENST00000575531
  gene symbol: CORO7
  hgvsc: ENST00000575531.1:n.1606G>A
  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.2136G>A
  hgvsp: ENST00000574025.1:c.2136G>A(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.2391G>A
  hgvsp: ENST00000251166.4:c.2391G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000446221
  ensembl transcript: ENST00000539968
  gene symbol: CORO7
  hgvsc: ENST00000539968.1:c.1731G>A
  hgvsp: ENST00000539968.1:c.1731G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000458607
  ensembl transcript: ENST00000575334
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000575334.1:c.*838G>A
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460177
  ensembl transcript: ENST00000576637
  gene symbol: CORO7
  hgvsc: ENST00000576637.1:c.289G>A
  hgvsp: ENST00000576637.1:c.289G>A(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: ENST00000574849
  gene symbol: CORO7
  hgvsc: ENST00000574849.1:n.84G>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: ENST00000575714
  gene symbol: CORO7
  hgvsc: ENST00000575714.1:n.1920G>A
  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.2391G>A
  hgvsp: ENST00000572467.1:c.2391G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/44424
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1501
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 718
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2217
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25753
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1986
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu797Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: South Asian
population: Other
reference allele: C
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum

16-4408438-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4408438
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4408438
    reference: chr 16
allele count: 2
allele frequency: 1.726102116201194e-5
allele num: 115868
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461702
  ensembl transcript: ENST00000574025
  gene symbol: CORO7
  hgvsc: ENST00000574025.1:c.2132A>G
  hgvsp: ENSP00000461702.1:p.Glu711Gly
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000458607
  ensembl transcript: ENST00000575334
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000575334.1:c.*834A>G
  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.2333A>G
  hgvsp: ENSP00000440460.2:p.Glu778Gly
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000446221
  ensembl transcript: ENST00000539968
  gene symbol: CORO7
  hgvsc: ENST00000539968.1:c.1727A>G
  hgvsp: ENSP00000446221.1:p.Glu576Gly
  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.*2323A>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: ENST00000575714
  gene symbol: CORO7
  hgvsc: ENST00000575714.1:n.1916A>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: ENST00000574849
  gene symbol: CORO7
  hgvsc: ENST00000574849.1:n.80A>G
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460177
  ensembl transcript: ENST00000576637
  gene symbol: CORO7
  hgvsc: ENST00000576637.1:c.285A>G
  hgvsp: ENSP00000460177.1:p.Glu96Gly
  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.2387A>G
  hgvsp: ENSP00000460885.1:p.Glu796Gly
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103426
  ensembl transcript: ENST00000572274
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000572274.1:n.105A>G
  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: ENST00000575531
  gene symbol: CORO7
  hgvsc: ENST00000575531.1:n.1602A>G
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460956
  ensembl transcript: ENST00000570779
  gene symbol: CORO7
  hgvsc: ENST00000570779.1:c.14A>G
  hgvsp: ENSP00000460956.1:p.Glu5Gly
  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.2387A>G
  hgvsp: ENSP00000251166.4:p.Glu796Gly
  variant of: http://identifiers.org/hgnc/26161
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25531
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1542
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 495
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18870
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 717
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2283
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu796Gly
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: T
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQ

http://identifiers.org/exac.variant/16-4408445-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4408445
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4408445
    reference: chr 16
allele count: 1
allele frequency: 8.665511265164645e-6
allele num: 115400
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000574849
  gene symbol: CORO7
  hgvsc: ENST00000574849.1:n.73G>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: ENST00000572666
  gene symbol: CORO7
  hgvsc: ENST00000572666.1:n.1235G>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000251166
  ensembl transcript: ENST00000251166
  gene symbol: CORO7
  hgvsc: ENST00000251166.4:c.2380G>T
  hgvsp: ENSP00000251166.4:p.Glu794Ter
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103426
  ensembl transcript: ENST00000572274
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000572274.1:n.98G>T
  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.*2316G>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: ENST00000575714
  gene symbol: CORO7
  hgvsc: ENST00000575714.1:n.1909G>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000446221
  ensembl transcript: ENST00000539968
  gene symbol: CORO7
  hgvsc: ENST00000539968.1:c.1720G>T
  hgvsp: ENSP00000446221.1:p.Glu574Ter
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000458607
  ensembl transcript: ENST00000575334
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000575334.1:c.*827G>T
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000460885
  ensembl transcript: ENST00000572467
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000572467.1:c.2380G>T
  hgvsp: ENSP00000460885.1:p.Glu794Ter
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460177
  ensembl transcript: ENST00000576637
  gene symbol: CORO7
  hgvsc: ENST00000576637.1:c.278G>T
  hgvsp: ENSP00000460177.1:p.Glu94Ter
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460956
  ensembl transcript: ENST00000570779
  gene symbol: CORO7
  hgvsc: ENST00000570779.1:c.7G>T
  hgvsp: ENSP00000460956.1:p.Glu3Ter
  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: ENST00000575531
  gene symbol: CORO7
  hgvsc: ENST00000575531.1:n.1595G>T
  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.2125G>T
  hgvsp: ENSP00000461702.1:p.Glu709Ter
  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.2326G>T
  hgvsp: ENSP00000440460.2:p.Glu776Ter
  variant of: http://identifiers.org/hgnc/26161
canonical: true
consequence: stop gained
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8232
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 722
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2459
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18818
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1993
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu794Ter
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
population: Other
reference allele: C
site quality: FS
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum

16-4408447-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4408447
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4408447
    reference: chr 16
allele count: 4
allele frequency: 3.475842891901286e-5
allele num: 115080
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000572666
  gene symbol: CORO7
  hgvsc: ENST00000572666.1:n.1233G>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.2378G>A
  hgvsp: ENSP00000251166.4:p.Arg793Gln
  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: ENST00000575714
  gene symbol: CORO7
  hgvsc: ENST00000575714.1:n.1907G>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: ENST00000574849
  gene symbol: CORO7
  hgvsc: ENST00000574849.1:n.71G>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.2324G>A
  hgvsp: ENSP00000440460.2:p.Arg775Gln
  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: ENST00000575531
  gene symbol: CORO7
  hgvsc: ENST00000575531.1:n.1593G>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.2378G>A
  hgvsp: ENSP00000460885.1:p.Arg793Gln
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000446221
  ensembl transcript: ENST00000539968
  gene symbol: CORO7
  hgvsc: ENST00000539968.1:c.1718G>A
  hgvsp: ENSP00000446221.1:p.Arg573Gln
  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.2123G>A
  hgvsp: ENSP00000461702.1:p.Arg708Gln
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460177
  ensembl transcript: ENST00000576637
  gene symbol: CORO7
  hgvsc: ENST00000576637.1:c.276G>A
  hgvsp: ENSP00000460177.1:p.Arg93Gln
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460956
  ensembl transcript: ENST00000570779
  gene symbol: CORO7
  hgvsc: ENST00000570779.1:c.5G>A
  hgvsp: ENSP00000460956.1:p.Arg2Gln
  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.*2314G>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: ENSG00000103426
  ensembl transcript: ENST00000572274
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000572274.1:n.96G>A
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000458607
  ensembl transcript: ENST00000575334
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000575334.1:c.*825G>A
  variant of: http://identifiers.org/hgnc/44424
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 641
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1967
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2571
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8245
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18772
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Arg793Gln
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum

16-4408451-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4408451
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4408451
    reference: chr 16
allele count: 3
allele frequency: 2.61972126165776e-5
allele num: 114516
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000575714
  gene symbol: CORO7
  hgvsc: ENST00000575714.1:n.1903G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460956
  ensembl transcript: ENST00000570779
  gene symbol: CORO7
  hgvsc: ENST00000570779.1:c.1G>A
  hgvsp: ENSP00000460956.1:p.Val1?
  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.2374G>A
  hgvsp: ENSP00000460885.1:p.Val792Met
  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: ENST00000574849
  gene symbol: CORO7
  hgvsc: ENST00000574849.1:n.67G>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: ENSG00000103426
  ensembl transcript: ENST00000572274
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000572274.1:n.92G>A
  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: ENST00000572666
  gene symbol: CORO7
  hgvsc: ENST00000572666.1:n.1229G>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: ENST00000575531
  gene symbol: CORO7
  hgvsc: ENST00000575531.1:n.1589G>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.2119G>A
  hgvsp: ENSP00000461702.1:p.Val707Met
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460177
  ensembl transcript: ENST00000576637
  gene symbol: CORO7
  hgvsc: ENST00000576637.1:c.272G>A
  hgvsp: ENSP00000460177.1:p.Val92Met
  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.2320G>A
  hgvsp: ENSP00000440460.2:p.Val774Met
  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.2374G>A
  hgvsp: ENSP00000251166.4:p.Val792Met
  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.*2310G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000446221
  ensembl transcript: ENST00000539968
  gene symbol: CORO7
  hgvsc: ENST00000539968.1:c.1714G>A
  hgvsp: ENSP00000446221.1:p.Val572Met
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000458607
  ensembl transcript: ENST00000575334
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000575334.1:c.*821G>A
  variant of: http://identifiers.org/hgnc/44424
canonical: false
consequence: start lost
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 535
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23956
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2022
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 733
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2769
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val1?
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: African
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum

16-4408452-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4408452
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4408452
    reference: chr 16
allele count: 1
allele frequency: 8.729507481187912e-6
allele num: 114554
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000251166
  ensembl transcript: ENST00000251166
  gene symbol: CORO7
  hgvsc: ENST00000251166.4:c.2373C>T
  hgvsp: ENST00000251166.4:c.2373C>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: ENST00000572666
  gene symbol: CORO7
  hgvsc: ENST00000572666.1:n.1228C>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.*2309C>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: ENSG00000103426
  ensembl transcript: ENST00000572274
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000572274.1:n.91C>T
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000446221
  ensembl transcript: ENST00000539968
  gene symbol: CORO7
  hgvsc: ENST00000539968.1:c.1713C>T
  hgvsp: ENST00000539968.1:c.1713C>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: ENSP00000460177
  ensembl transcript: ENST00000576637
  gene symbol: CORO7
  hgvsc: ENST00000576637.1:c.271C>T
  hgvsp: ENST00000576637.1:c.271C>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.2319C>T
  hgvsp: ENST00000537233.2:c.2319C>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: ENSG00000103426
  ensembl protein: ENSP00000458607
  ensembl transcript: ENST00000575334
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000575334.1:c.*820C>T
  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.2118C>T
  hgvsp: ENST00000574025.1:c.2118C>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.2373C>T
  hgvsp: ENST00000572467.1:c.2373C>T(p.%3D)
  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: ENST00000574849
  gene symbol: CORO7
  hgvsc: ENST00000574849.1:n.66C>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: ENST00000575531
  gene symbol: CORO7
  hgvsc: ENST00000575531.1:n.1588C>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: ENST00000575714
  gene symbol: CORO7
  hgvsc: ENST00000575714.1:n.1902C>T
  variant of: http://identifiers.org/hgnc/26161
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2332
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2786
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2006
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 684
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 733
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23969
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18697
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp791Asp
num of homozygotes: 0
population: Other
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
population: African
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

16-4408454-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4408454
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4408454
    reference: chr 16
allele count: 1
allele frequency: 8.730422028600862e-6
allele num: 114542
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000440460
  ensembl transcript: ENST00000537233
  gene symbol: CORO7
  hgvsc: ENST00000537233.2:c.2317G>A
  hgvsp: ENSP00000440460.2:p.Asp773Asn
  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: ENST00000574849
  gene symbol: CORO7
  hgvsc: ENST00000574849.1:n.64G>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: ENST00000575714
  gene symbol: CORO7
  hgvsc: ENST00000575714.1:n.1900G>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: ENST00000575531
  gene symbol: CORO7
  hgvsc: ENST00000575531.1:n.1586G>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: ENST00000572666
  gene symbol: CORO7
  hgvsc: ENST00000572666.1:n.1226G>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.2371G>A
  hgvsp: ENSP00000251166.4:p.Asp791Asn
  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.2371G>A
  hgvsp: ENSP00000460885.1:p.Asp791Asn
  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.*2307G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000458607
  ensembl transcript: ENST00000575334
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000575334.1:c.*818G>A
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460177
  ensembl transcript: ENST00000576637
  gene symbol: CORO7
  hgvsc: ENST00000576637.1:c.269G>A
  hgvsp: ENSP00000460177.1:p.Asp91Asn
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000446221
  ensembl transcript: ENST00000539968
  gene symbol: CORO7
  hgvsc: ENST00000539968.1:c.1711G>A
  hgvsp: ENSP00000446221.1:p.Asp571Asn
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103426
  ensembl transcript: ENST00000572274
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000572274.1:n.89G>A
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461702
  ensembl transcript: ENST00000574025
  gene symbol: CORO7
  hgvsc: ENST00000574025.1:c.2116G>A
  hgvsp: ENSP00000461702.1:p.Asp706Asn
  variant of: http://identifiers.org/hgnc/26161
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8262
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 661
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23975
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18719
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2799
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2318
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 734
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp791Asn
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
population: European (Finnish)
population: Other
population: East Asian
reference allele: C
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP

16-4408455-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4408455
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4408455
    reference: chr 16
allele count: 1
allele frequency: 8.734692451478784e-6
allele num: 114486
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000575714
  gene symbol: CORO7
  hgvsc: ENST00000575714.1:n.1899C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000458607
  ensembl transcript: ENST00000575334
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000575334.1:c.*817C>T
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103426
  ensembl transcript: ENST00000572274
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000572274.1:n.88C>T
  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.*2306C>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: ENST00000575531
  gene symbol: CORO7
  hgvsc: ENST00000575531.1:n.1585C>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.2370C>T
  hgvsp: ENST00000572467.1:c.2370C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000251166
  ensembl transcript: ENST00000251166
  gene symbol: CORO7
  hgvsc: ENST00000251166.4:c.2370C>T
  hgvsp: ENST00000251166.4:c.2370C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000446221
  ensembl transcript: ENST00000539968
  gene symbol: CORO7
  hgvsc: ENST00000539968.1:c.1710C>T
  hgvsp: ENST00000539968.1:c.1710C>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: ENSP00000460177
  ensembl transcript: ENST00000576637
  gene symbol: CORO7
  hgvsc: ENST00000576637.1:c.268C>T
  hgvsp: ENST00000576637.1:c.268C>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.2316C>T
  hgvsp: ENST00000537233.2:c.2316C>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.2115C>T
  hgvsp: ENST00000574025.1:c.2115C>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: ENST00000572666
  gene symbol: CORO7
  hgvsc: ENST00000572666.1:n.1225C>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: ENST00000574849
  gene symbol: CORO7
  hgvsc: ENST00000574849.1:n.63C>T
  variant of: http://identifiers.org/hgnc/26161
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2313
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 762
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18737
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2043
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8311
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 654
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23855
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2779
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Cys790Cys
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: ClippingRankSum

16-4408461-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4408461
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4408461
    reference: chr 16
allele count: 4
allele frequency: 3.508279539713725e-5
allele num: 114016
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103426
  ensembl transcript: ENST00000572274
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000572274.1:n.82G>C
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000458607
  ensembl transcript: ENST00000575334
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000575334.1:c.*811G>C
  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: ENST00000575714
  gene symbol: CORO7
  hgvsc: ENST00000575714.1:n.1893G>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.2364G>C
  hgvsp: ENST00000251166.4:c.2364G>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: ENST00000572666
  gene symbol: CORO7
  hgvsc: ENST00000572666.1:n.1219G>C
  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.2109G>C
  hgvsp: ENST00000574025.1:c.2109G>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: ENSP00000460177
  ensembl transcript: ENST00000576637
  gene symbol: CORO7
  hgvsc: ENST00000576637.1:c.262G>C
  hgvsp: ENST00000576637.1:c.262G>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.*2300G>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000446221
  ensembl transcript: ENST00000539968
  gene symbol: CORO7
  hgvsc: ENST00000539968.1:c.1704G>C
  hgvsp: ENST00000539968.1:c.1704G>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.2310G>C
  hgvsp: ENST00000537233.2:c.2310G>C(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.2364G>C
  hgvsp: ENST00000572467.1:c.2364G>C(p.%3D)
  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: ENST00000575531
  gene symbol: CORO7
  hgvsc: ENST00000575531.1:n.1579G>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: ENST00000574849
  gene symbol: CORO7
  hgvsc: ENST00000574849.1:n.57G>C
  variant of: http://identifiers.org/hgnc/26161
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18582
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2039
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 744
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23530
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2566
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2974
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr788Thr
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: QD

16-4408461-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4408461
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4408461
    reference: chr 16
allele count: 1
allele frequency: 8.770698849284312e-6
allele num: 114016
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460177
  ensembl transcript: ENST00000576637
  gene symbol: CORO7
  hgvsc: ENST00000576637.1:c.262G>A
  hgvsp: ENST00000576637.1:c.262G>A(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: ENST00000574849
  gene symbol: CORO7
  hgvsc: ENST00000574849.1:n.57G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000446221
  ensembl transcript: ENST00000539968
  gene symbol: CORO7
  hgvsc: ENST00000539968.1:c.1704G>A
  hgvsp: ENST00000539968.1:c.1704G>A(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.*2300G>A
  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.2364G>A
  hgvsp: ENST00000572467.1:c.2364G>A(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.2109G>A
  hgvsp: ENST00000574025.1:c.2109G>A(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.2364G>A
  hgvsp: ENST00000251166.4:c.2364G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000458607
  ensembl transcript: ENST00000575334
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000575334.1:c.*811G>A
  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: ENST00000572666
  gene symbol: CORO7
  hgvsc: ENST00000572666.1:n.1219G>A
  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.2310G>A
  hgvsp: ENST00000537233.2:c.2310G>A(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: ENST00000575714
  gene symbol: CORO7
  hgvsc: ENST00000575714.1:n.1893G>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: ENST00000575531
  gene symbol: CORO7
  hgvsc: ENST00000575531.1:n.1579G>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: ENSG00000103426
  ensembl transcript: ENST00000572274
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000572274.1:n.82G>A
  variant of: http://identifiers.org/hgnc/44424
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8293
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2039
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2566
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2974
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23530
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18582
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr788Thr
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
population: Latino
population: African
reference allele: C
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQ

16-4408462-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4408462
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4408462
    reference: chr 16
allele count: 7
allele frequency: 6.147792942333702e-5
allele num: 113862
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000574849
  gene symbol: CORO7
  hgvsc: ENST00000574849.1:n.56C>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: ENST00000572666
  gene symbol: CORO7
  hgvsc: ENST00000572666.1:n.1218C>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: ENST00000575714
  gene symbol: CORO7
  hgvsc: ENST00000575714.1:n.1892C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460177
  ensembl transcript: ENST00000576637
  gene symbol: CORO7
  hgvsc: ENST00000576637.1:c.261C>T
  hgvsp: ENSP00000460177.1:p.Thr88Met
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000446221
  ensembl transcript: ENST00000539968
  gene symbol: CORO7
  hgvsc: ENST00000539968.1:c.1703C>T
  hgvsp: ENSP00000446221.1:p.Thr568Met
  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.2309C>T
  hgvsp: ENSP00000440460.2:p.Thr770Met
  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: ENST00000575531
  gene symbol: CORO7
  hgvsc: ENST00000575531.1:n.1578C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000458607
  ensembl transcript: ENST00000575334
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000575334.1:c.*810C>T
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000460885
  ensembl transcript: ENST00000572467
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000572467.1:c.2363C>T
  hgvsp: ENSP00000460885.1:p.Thr788Met
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461702
  ensembl transcript: ENST00000574025
  gene symbol: CORO7
  hgvsc: ENST00000574025.1:c.2108C>T
  hgvsp: ENSP00000461702.1:p.Thr703Met
  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.2363C>T
  hgvsp: ENSP00000251166.4:p.Thr788Met
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103426
  ensembl transcript: ENST00000572274
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000572274.1:n.81C>T
  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.*2299C>T
  variant of: http://identifiers.org/hgnc/26161
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 612
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2649
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 744
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3021
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2029
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8301
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 18527
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23428
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Thr788Met
num of homozygotes: 0
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: African
reference allele: G
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum

16-4408464-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4408464
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4408464
    reference: chr 16
allele count: 0
allele frequency: 0.0e0
allele num: 113788
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000446221
  ensembl transcript: ENST00000539968
  gene symbol: CORO7
  hgvsc: ENST00000539968.1:c.1701G>C
  hgvsp: ENSP00000446221.1:p.Lys567Asn
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103426
  ensembl transcript: ENST00000572274
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000572274.1:n.79G>C
  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.2361G>C
  hgvsp: ENSP00000251166.4:p.Lys787Asn
  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: ENST00000572666
  gene symbol: CORO7
  hgvsc: ENST00000572666.1:n.1216G>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000458607
  ensembl transcript: ENST00000575334
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000575334.1:c.*808G>C
  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.*2297G>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.2307G>C
  hgvsp: ENSP00000440460.2:p.Lys769Asn
  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: ENST00000574849
  gene symbol: CORO7
  hgvsc: ENST00000574849.1:n.54G>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460177
  ensembl transcript: ENST00000576637
  gene symbol: CORO7
  hgvsc: ENST00000576637.1:c.259G>C
  hgvsp: ENSP00000460177.1:p.Lys87Asn
  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: ENST00000575714
  gene symbol: CORO7
  hgvsc: ENST00000575714.1:n.1890G>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.2361G>C
  hgvsp: ENSP00000460885.1:p.Lys787Asn
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461702
  ensembl transcript: ENST00000574025
  gene symbol: CORO7
  hgvsc: ENST00000574025.1:c.2106G>C
  hgvsp: ENSP00000461702.1:p.Lys702Asn
  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: ENST00000575531
  gene symbol: CORO7
  hgvsc: ENST00000575531.1:n.1576G>C
  variant of: http://identifiers.org/hgnc/26161
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 680
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2032
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8288
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3041
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18526
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2698
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23338
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys787Asn
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: East Asian
reference allele: C
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: FS
site quality: DP
site quality: BaseQRankSum

16-4408466-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4408466
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4408466
    reference: chr 16
allele count: 1
allele frequency: 8.798479622721194e-6
allele num: 113656
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000572666
  gene symbol: CORO7
  hgvsc: ENST00000572666.1:n.1214A>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.2305A>G
  hgvsp: ENSP00000440460.2:p.Lys769Glu
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000446221
  ensembl transcript: ENST00000539968
  gene symbol: CORO7
  hgvsc: ENST00000539968.1:c.1699A>G
  hgvsp: ENSP00000446221.1:p.Lys567Glu
  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: ENST00000575714
  gene symbol: CORO7
  hgvsc: ENST00000575714.1:n.1888A>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: ENST00000575531
  gene symbol: CORO7
  hgvsc: ENST00000575531.1:n.1574A>G
  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.2359A>G
  hgvsp: ENSP00000460885.1:p.Lys787Glu
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000458607
  ensembl transcript: ENST00000575334
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000575334.1:c.*806A>G
  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.2359A>G
  hgvsp: ENSP00000251166.4:p.Lys787Glu
  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.2104A>G
  hgvsp: ENSP00000461702.1:p.Lys702Glu
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460177
  ensembl transcript: ENST00000576637
  gene symbol: CORO7
  hgvsc: ENST00000576637.1:c.257A>G
  hgvsp: ENSP00000460177.1:p.Lys87Glu
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103426
  ensembl transcript: ENST00000572274
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000572274.1:n.77A>G
  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: ENST00000574849
  gene symbol: CORO7
  hgvsc: ENST00000574849.1:n.52A>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.*2295A>G
  variant of: http://identifiers.org/hgnc/26161
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 679
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2806
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2029
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8283
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3109
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 748
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 658
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys787Glu
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
reference allele: T
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD

16-4408469-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4408469
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4408469
    reference: chr 16
allele count: 1
allele frequency: 8.843922456487902e-6
allele num: 113072
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.2356C>T
  hgvsp: ENSP00000460885.1:p.Pro786Ser
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461702
  ensembl transcript: ENST00000574025
  gene symbol: CORO7
  hgvsc: ENST00000574025.1:c.2101C>T
  hgvsp: ENSP00000461702.1:p.Pro701Ser
  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.2302C>T
  hgvsp: ENSP00000440460.2:p.Pro768Ser
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000458607
  ensembl transcript: ENST00000575334
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000575334.1:c.*803C>T
  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: ENST00000575531
  gene symbol: CORO7
  hgvsc: ENST00000575531.1:n.1571C>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: ENST00000575714
  gene symbol: CORO7
  hgvsc: ENST00000575714.1:n.1885C>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: ENST00000572666
  gene symbol: CORO7
  hgvsc: ENST00000572666.1:n.1211C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460177
  ensembl transcript: ENST00000576637
  gene symbol: CORO7
  hgvsc: ENST00000576637.1:c.254C>T
  hgvsp: ENSP00000460177.1:p.Pro86Ser
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000446221
  ensembl transcript: ENST00000539968
  gene symbol: CORO7
  hgvsc: ENST00000539968.1:c.1696C>T
  hgvsp: ENSP00000446221.1:p.Pro566Ser
  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.2356C>T
  hgvsp: ENSP00000251166.4:p.Pro786Ser
  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.*2292C>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: ENSG00000103426
  ensembl transcript: ENST00000572274
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000572274.1:n.74C>T
  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: ENST00000574849
  gene symbol: CORO7
  hgvsc: ENST00000574849.1:n.49C>T
  variant of: http://identifiers.org/hgnc/26161
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3103
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 783
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18296
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 747
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 797
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3224
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22708
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2033
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro786Ser
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: South Asian
population: Latino
population: African
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: BaseQRankSum

16-4408473-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4408473
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4408473
    reference: chr 16
allele count: 1
allele frequency: 8.868550346760318e-6
allele num: 112758
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460177
  ensembl transcript: ENST00000576637
  gene symbol: CORO7
  hgvsc: ENST00000576637.1:c.250C>T
  hgvsp: ENST00000576637.1:c.250C>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: ENST00000574849
  gene symbol: CORO7
  hgvsc: ENST00000574849.1:n.45C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000458607
  ensembl transcript: ENST00000575334
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000575334.1:c.*799C>T
  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: ENST00000572666
  gene symbol: CORO7
  hgvsc: ENST00000572666.1:n.1207C>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.2352C>T
  hgvsp: ENST00000251166.4:c.2352C>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.2298C>T
  hgvsp: ENST00000537233.2:c.2298C>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.2352C>T
  hgvsp: ENST00000572467.1:c.2352C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103426
  ensembl transcript: ENST00000572274
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000572274.1:n.70C>T
  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.*2288C>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.2097C>T
  hgvsp: ENST00000574025.1:c.2097C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000446221
  ensembl transcript: ENST00000539968
  gene symbol: CORO7
  hgvsc: ENST00000539968.1:c.1692C>T
  hgvsp: ENST00000539968.1:c.1692C>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: ENST00000575531
  gene symbol: CORO7
  hgvsc: ENST00000575531.1:n.1567C>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: ENST00000575714
  gene symbol: CORO7
  hgvsc: ENST00000575714.1:n.1881C>T
  variant of: http://identifiers.org/hgnc/26161
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 855
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8271
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22515
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18230
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2034
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 780
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3188
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3336
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 747
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu784Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
population: Latino
population: South Asian
population: African
reference allele: G
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD

16-4408476-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4408476
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4408476
    reference: chr 16
allele count: 1
allele frequency: 8.894423196655697e-6
allele num: 112430
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103426
  ensembl transcript: ENST00000572274
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000572274.1:n.67C>T
  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.2094C>T
  hgvsp: ENST00000574025.1:c.2094C>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.2349C>T
  hgvsp: ENST00000572467.1:c.2349C>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.*2285C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460177
  ensembl transcript: ENST00000576637
  gene symbol: CORO7
  hgvsc: ENST00000576637.1:c.247C>T
  hgvsp: ENST00000576637.1:c.247C>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: ENST00000575714
  gene symbol: CORO7
  hgvsc: ENST00000575714.1:n.1878C>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: ENST00000572666
  gene symbol: CORO7
  hgvsc: ENST00000572666.1:n.1204C>T
  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.2295C>T
  hgvsp: ENST00000537233.2:c.2295C>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: ENST00000575531
  gene symbol: CORO7
  hgvsc: ENST00000575531.1:n.1564C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000458607
  ensembl transcript: ENST00000575334
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000575334.1:c.*796C>T
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000446221
  ensembl transcript: ENST00000539968
  gene symbol: CORO7
  hgvsc: ENST00000539968.1:c.1689C>T
  hgvsp: ENST00000539968.1:c.1689C>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.2349C>T
  hgvsp: ENST00000251166.4:c.2349C>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: ENST00000574849
  gene symbol: CORO7
  hgvsc: ENST00000574849.1:n.42C>T
  variant of: http://identifiers.org/hgnc/26161
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 954
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3285
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2033
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3372
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18142
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8245
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 818
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 750
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22351
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val783Val
num of homozygotes: 0
population: European (Finnish)
population: Other
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP

16-4408478-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4408478
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4408478
    reference: chr 16
allele count: 197
allele frequency: 1.758771538255513e-3
allele num: 112010
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000575714
  gene symbol: CORO7
  hgvsc: ENST00000575714.1:n.1876G>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.2347G>A
  hgvsp: ENSP00000251166.4:p.Val783Ile
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000458607
  ensembl transcript: ENST00000575334
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000575334.1:c.*794G>A
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461702
  ensembl transcript: ENST00000574025
  gene symbol: CORO7
  hgvsc: ENST00000574025.1:c.2092G>A
  hgvsp: ENSP00000461702.1:p.Val698Ile
  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.2293G>A
  hgvsp: ENSP00000440460.2:p.Val765Ile
  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.2347G>A
  hgvsp: ENSP00000460885.1:p.Val783Ile
  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: ENST00000575531
  gene symbol: CORO7
  hgvsc: ENST00000575531.1:n.1562G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000446221
  ensembl transcript: ENST00000539968
  gene symbol: CORO7
  hgvsc: ENST00000539968.1:c.1687G>A
  hgvsp: ENSP00000446221.1:p.Val563Ile
  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.*2283G>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: ENST00000572666
  gene symbol: CORO7
  hgvsc: ENST00000572666.1:n.1202G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460177
  ensembl transcript: ENST00000576637
  gene symbol: CORO7
  hgvsc: ENST00000576637.1:c.245G>A
  hgvsp: ENSP00000460177.1:p.Val83Ile
  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: ENST00000574849
  gene symbol: CORO7
  hgvsc: ENST00000574849.1:n.40G>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: ENSG00000103426
  ensembl transcript: ENST00000572274
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000572274.1:n.65G>A
  variant of: http://identifiers.org/hgnc/44424
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3436
  bin: 7.5e0
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 763
  bin: 4.25e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 8229
  bin: 3.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 1003
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2042
  bin: 3.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 22131
  bin: 2.25e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 869
  bin: 1.75e1
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 4.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 6.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 5.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 6.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 18031
  bin: 2.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 7
genotype quality: GenotypeQuality
hgvs: p.Val783Ile
num of homozygotes: 3
population: East Asian
population: South Asian
population: Latino
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum

16-4408479-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4408479
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4408479
    reference: chr 16
allele count: 1
allele frequency: 8.936869950668478e-6
allele num: 111896
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000446221
  ensembl transcript: ENST00000539968
  gene symbol: CORO7
  hgvsc: ENST00000539968.1:c.1686C>T
  hgvsp: ENST00000539968.1:c.1686C>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.2292C>T
  hgvsp: ENST00000537233.2:c.2292C>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.2346C>T
  hgvsp: ENST00000251166.4:c.2346C>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: ENST00000574849
  gene symbol: CORO7
  hgvsc: ENST00000574849.1:n.39C>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: ENST00000575531
  gene symbol: CORO7
  hgvsc: ENST00000575531.1:n.1561C>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: ENSG00000103426
  ensembl transcript: ENST00000572274
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000572274.1:n.64C>T
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000458607
  ensembl transcript: ENST00000575334
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000575334.1:c.*793C>T
  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: ENST00000575714
  gene symbol: CORO7
  hgvsc: ENST00000575714.1:n.1875C>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.2346C>T
  hgvsp: ENST00000572467.1:c.2346C>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.2091C>T
  hgvsp: ENST00000574025.1:c.2091C>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: ENST00000572666
  gene symbol: CORO7
  hgvsc: ENST00000572666.1:n.1201C>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.*2282C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460177
  ensembl transcript: ENST00000576637
  gene symbol: CORO7
  hgvsc: ENST00000576637.1:c.244C>T
  hgvsp: ENST00000576637.1:c.244C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26161
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 843
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1045
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3419
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 763
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22014
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2054
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3515
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8241
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu782Leu
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: G
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP

16-4408481-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4408481
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4408481
    reference: chr 16
allele count: 1
allele frequency: 8.952872081363702e-6
allele num: 111696
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.2344C>T
  hgvsp: ENSP00000251166.4:p.Leu782Phe
  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.*2280C>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.2290C>T
  hgvsp: ENSP00000440460.2:p.Leu764Phe
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460177
  ensembl transcript: ENST00000576637
  gene symbol: CORO7
  hgvsc: ENST00000576637.1:c.242C>T
  hgvsp: ENSP00000460177.1:p.Leu82Phe
  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: ENST00000575531
  gene symbol: CORO7
  hgvsc: ENST00000575531.1:n.1559C>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.2089C>T
  hgvsp: ENSP00000461702.1:p.Leu697Phe
  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: ENST00000574849
  gene symbol: CORO7
  hgvsc: ENST00000574849.1:n.37C>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: ENSG00000103426
  ensembl transcript: ENST00000572274
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000572274.1:n.62C>T
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000458607
  ensembl transcript: ENST00000575334
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000575334.1:c.*791C>T
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000460885
  ensembl transcript: ENST00000572467
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000572467.1:c.2344C>T
  hgvsp: ENSP00000460885.1:p.Leu782Phe
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000446221
  ensembl transcript: ENST00000539968
  gene symbol: CORO7
  hgvsc: ENST00000539968.1:c.1684C>T
  hgvsp: ENSP00000446221.1:p.Leu562Phe
  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: ENST00000572666
  gene symbol: CORO7
  hgvsc: ENST00000572666.1:n.1199C>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: ENST00000575714
  gene symbol: CORO7
  hgvsc: ENST00000575714.1:n.1873C>T
  variant of: http://identifiers.org/hgnc/26161
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3548
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2052
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 901
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3468
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17940
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1112
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21870
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 760
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu782Phe
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
population: African
population: European (Finnish)
population: East Asian
reference allele: G
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD

16-4408483-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4408483
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4408483
    reference: chr 16
allele count: 12
allele frequency: 1.076484202594327e-4
allele num: 111474
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000575714
  gene symbol: CORO7
  hgvsc: ENST00000575714.1:n.1871G>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458459
  ensembl transcript: ENST00000571227
  gene symbol: CORO7
  hgvsc: ENST00000571227.1:c.*2278G>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460177
  ensembl transcript: ENST00000576637
  gene symbol: CORO7
  hgvsc: ENST00000576637.1:c.240G>C
  hgvsp: ENSP00000460177.1:p.Gly81Ala
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000446221
  ensembl transcript: ENST00000539968
  gene symbol: CORO7
  hgvsc: ENST00000539968.1:c.1682G>C
  hgvsp: ENSP00000446221.1:p.Gly561Ala
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000103426
  ensembl transcript: ENST00000572274
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000572274.1:n.60G>C
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000440460
  ensembl transcript: ENST00000537233
  gene symbol: CORO7
  hgvsc: ENST00000537233.2:c.2288G>C
  hgvsp: ENSP00000440460.2:p.Gly763Ala
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461702
  ensembl transcript: ENST00000574025
  gene symbol: CORO7
  hgvsc: ENST00000574025.1:c.2087G>C
  hgvsp: ENSP00000461702.1:p.Gly696Ala
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000251166
  ensembl transcript: ENST00000251166
  gene symbol: CORO7
  hgvsc: ENST00000251166.4:c.2342G>C
  hgvsp: ENSP00000251166.4:p.Gly781Ala
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000460885
  ensembl transcript: ENST00000572467
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000572467.1:c.2342G>C
  hgvsp: ENSP00000460885.1:p.Gly781Ala
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000572666
  gene symbol: CORO7
  hgvsc: ENST00000572666.1:n.1197G>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000575531
  gene symbol: CORO7
  hgvsc: ENST00000575531.1:n.1557G>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000574849
  gene symbol: CORO7
  hgvsc: ENST00000574849.1:n.35G>C
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000458607
  ensembl transcript: ENST00000575334
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000575334.1:c.*789G>C
  variant of: http://identifiers.org/hgnc/44424
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17930
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3494
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3581
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1137
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21792
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 889
  bin: 1.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
hgvs: p.Gly781Ala
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
reference allele: C
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD

16-4408484-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4408484
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4408484
    reference: chr 16
allele count: 1
allele frequency: 8.98375736668104e-6
allele num: 111312
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000458459
  ensembl transcript: ENST00000571227
  gene symbol: CORO7
  hgvsc: ENST00000571227.1:c.*2277G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000458607
  ensembl transcript: ENST00000575334
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000575334.1:c.*788G>A
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000446221
  ensembl transcript: ENST00000539968
  gene symbol: CORO7
  hgvsc: ENST00000539968.1:c.1681G>A
  hgvsp: ENSP00000446221.1:p.Gly561Ser
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000574849
  gene symbol: CORO7
  hgvsc: ENST00000574849.1:n.34G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000103426
  ensembl protein: ENSP00000460885
  ensembl transcript: ENST00000572467
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000572467.1:c.2341G>A
  hgvsp: ENSP00000460885.1:p.Gly781Ser
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000572666
  gene symbol: CORO7
  hgvsc: ENST00000572666.1:n.1196G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000461702
  ensembl transcript: ENST00000574025
  gene symbol: CORO7
  hgvsc: ENST00000574025.1:c.2086G>A
  hgvsp: ENSP00000461702.1:p.Gly696Ser
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460177
  ensembl transcript: ENST00000576637
  gene symbol: CORO7
  hgvsc: ENST00000576637.1:c.239G>A
  hgvsp: ENSP00000460177.1:p.Gly81Ser
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000103426
  ensembl transcript: ENST00000572274
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000572274.1:n.59G>A
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000251166
  ensembl transcript: ENST00000251166
  gene symbol: CORO7
  hgvsc: ENST00000251166.4:c.2341G>A
  hgvsp: ENSP00000251166.4:p.Gly781Ser
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000440460
  ensembl transcript: ENST00000537233
  gene symbol: CORO7
  hgvsc: ENST00000537233.2:c.2287G>A
  hgvsp: ENSP00000440460.2:p.Gly763Ser
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000575714
  gene symbol: CORO7
  hgvsc: ENST00000575714.1:n.1870G>A
  variant of: http://identifiers.org/hgnc/26161
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000575531
  gene symbol: CORO7
  hgvsc: ENST00000575531.1:n.1556G>A
  variant of: http://identifiers.org/hgnc/26161
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21659
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3659
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3515
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1178
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 761
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17899
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly781Ser
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: QD

16-4408488-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4408488
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4408488
    reference: chr 16
allele count: 1
allele frequency: 9.014856483484784e-6
allele num: 110928
alternate allele: A
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.2086-4C>T
  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: ENST00000574849
  gene symbol: CORO7
  hgvsc: ENST00000574849.1:n.34-4C>T
  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: ENST00000575531
  gene symbol: CORO7
  hgvsc: ENST00000575531.1:n.1556-4C>T
  variant of: http://identifiers.org/hgnc/26161
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.1681-4C>T
  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.2341-4C>T
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000262246
  ensembl protein: ENSP00000460177
  ensembl transcript: ENST00000576637
  gene symbol: CORO7
  hgvsc: ENST00000576637.1:c.239-4C>T
  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: ENSG00000103426
  ensembl transcript: ENST00000572274
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000572274.1:n.59-4C>T
  variant of: http://identifiers.org/hgnc/44424
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.*2277-4C>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: ENSG00000103426
  ensembl protein: ENSP00000458607
  ensembl transcript: ENST00000575334
  gene symbol: CORO7-PAM16
  hgvsc: ENST00000575334.1:c.*788-4C>T
  variant of: http://identifiers.org/hgnc/44424
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262246
  ensembl transcript: ENST00000572666
  gene symbol: CORO7
  hgvsc: ENST00000572666.1:n.1196-4C>T
  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: ENST00000575714
  gene symbol: CORO7
  hgvsc: ENST00000575714.1:n.1870-4C>T
  variant of: http://identifiers.org/hgnc/26161
annotation: 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.2287-4C>T
  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.2341-4C>T
  variant of: http://identifiers.org/hgnc/26161
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2060
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8236
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3679
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 763
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3629
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.2341-4C>T
num of homozygotes: 0
reference allele: G

GenotypeDepth
all individuals: 29
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 29
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 229
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24556
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2794
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 367
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1516
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 957
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1200
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2551
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8330
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3638
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1217
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 2058
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1298
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 294
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 147
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2018
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5174
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 408
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 953
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 548
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 541
bin: 8.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5774
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12254
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10898
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.409827121764926e-5
allele num: 58654
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8514
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8250
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 748
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.233872e6

VQSLOD
type: SiteQuality
SIO_000300: -1.185e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.271e0

MQRankSum
type: SiteQuality
SIO_000300: 1.22e0

MQ
type: SiteQuality
SIO_000300: 5.54e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.27e0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.1e-2

QD
type: SiteQuality
SIO_000300: 1.136e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.9e-3

GenotypeDepth
all individuals: 7
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7
bin: 7.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 5
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2108
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25843
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2131
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 278
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 335
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 133
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2552
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3177
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7972
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1104
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1435
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5423
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 425
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 563
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1221
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1071
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1326
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2099
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 827
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 548
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8582
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8268
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10948
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5776
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.695720002713152e-5
allele num: 58972
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12636
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 748
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.0049e1

MQRankSum
type: SiteQuality
SIO_000300: 4.5e-1

VQSLOD
type: SiteQuality
SIO_000300: -7.785e-1

DP
type: SiteQuality
SIO_000300: 1.255992e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.2e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.81e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.96e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.26e-1

QD
type: SiteQuality
SIO_000300: 1.194e1

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

GenotypeDepth
all individuals: 52
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 127
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1221
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1071
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2131
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 133
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1104
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 278
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 425
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 335
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1435
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5423
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25843
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 827
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2108
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7972
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 563
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 548
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1326
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2552
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2099
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3177
bin: 3.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12636
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8268
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 748
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 9.134088417975886e-5
allele num: 10948
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8582
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5776
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 58972
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.0049e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.81e-1

VQSLOD
type: SiteQuality
SIO_000300: -7.785e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.26e-1

DP
type: SiteQuality
SIO_000300: 1.255992e6

MQRankSum
type: SiteQuality
SIO_000300: 4.5e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.2e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.96e-1

QD
type: SiteQuality
SIO_000300: 1.194e1

GenotypeDepth
all individuals: 7
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 230
bin: 4.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 51
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 272
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7720
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1224
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 780
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2148
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5477
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 134
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1033
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 337
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1382
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 26359
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1994
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2399
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 541
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1349
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 568
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1129
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2175
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2996
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 556
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8624
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.208021261174197e-4
allele num: 8278
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 752
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5794
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12914
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 59148
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10968
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 8.53e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.6e-2

DP
type: SiteQuality
SIO_000300: 1.268626e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.2e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.43e-1

QD
type: SiteQuality
SIO_000300: 1.312e1

VQSLOD
type: SiteQuality
SIO_000300: 6.57e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.11e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.54e0

GenotypeDepth
all individuals: 7
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 51
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 11038
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5
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variant carriers: 0

GenotypeQuality
all individuals: 541
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 134
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1382
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 26359
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1224
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 272
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2148
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7720
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2175
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1033
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2399
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 337
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1129
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2996
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1994
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 780
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 556
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1349
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5477
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 568
bin: 9.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8278
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.690674240887266e-5
allele num: 59148
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12914
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 752
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8624
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10968
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5794
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.268626e6

FS
type: SiteQuality
SIO_000300: 8.53e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.54e0

VQSLOD
type: SiteQuality
SIO_000300: 6.57e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.2e-3

MQRankSum
type: SiteQuality
SIO_000300: 1.11e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.6e-2

QD
type: SiteQuality
SIO_000300: 1.312e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.43e-1

GenotypeDepth
all individuals: 229
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 482
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3805
bin: 1.75e1
variant carriers: 2

GenotypeQuality
all individuals: 2201
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 466
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variant carriers: 0

GenotypeQuality
all individuals: 256
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1010
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1357
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1232
bin: 9.75e1
variant carriers: 9

GenotypeQuality
all individuals: 1925
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 570
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variant carriers: 0

GenotypeQuality
all individuals: 983
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 563
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2346
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1362
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 286
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2917
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 109
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variant carriers: 0

GenotypeQuality
all individuals: 26911
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 724
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2172
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variant carriers: 0

GenotypeQuality
all individuals: 7652
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5532
bin: 6.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8292
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 2.730251183108846e-4
allele num: 10988
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 2.298146162095909e-4
allele num: 13054
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8642
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 5.062436719541006e-5
allele num: 59260
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5794
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 752
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 3.5e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.78e-1

QD
type: SiteQuality
SIO_000300: 1.317e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.82e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.7e-3

MQ
type: SiteQuality
SIO_000300: 5.945e1

FS
type: SiteQuality
SIO_000300: 2.674e0

VQSLOD
type: SiteQuality
SIO_000300: 1.0e0

DP
type: SiteQuality
SIO_000300: 1.272557e6

GenotypeDepth
all individuals: 5
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 69
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variant carriers: 0

GenotypeDepth
all individuals: 7
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7
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variant carriers: 0

GenotypeQuality
all individuals: 1071
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 678
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variant carriers: 0

GenotypeQuality
all individuals: 577
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variant carriers: 0

GenotypeQuality
all individuals: 2138
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 579
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variant carriers: 0

GenotypeQuality
all individuals: 122
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 306
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2614
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5744
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 238
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7152
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2233
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1723
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1312
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 955
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1404
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variant carriers: 0

GenotypeQuality
all individuals: 656
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variant carriers: 0

GenotypeQuality
all individuals: 27561
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variant carriers: 0

GenotypeQuality
all individuals: 1229
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2295
bin: 7.75e1
variant carriers: 0

Other
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allele count: 0
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South Asian
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allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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African
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East Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 1.678810059429876e-5
allele num: 59566
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VQSLOD
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InbreedingCoeff
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FS
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BaseQRankSum
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MQ
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MQRankSum
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ReadPosRankSum
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QD
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DP
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ClippingRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele frequency: 1.478415138971023e-4
allele num: 13528
num of homozygotes: 0

Other
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African
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allele frequency: 6.524694154961486e-2
allele num: 8828
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Latino
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allele frequency: 3.454545454545454e-3
allele num: 11000
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European (Finnish)
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East Asian
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allele frequency: 4.807692307692308e-4
allele num: 8320
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European (Non-Finnish)
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allele frequency: 3.358522250209908e-4
allele num: 59550
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VQSLOD
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ReadPosRankSum
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BaseQRankSum
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DP
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FS
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QD
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InbreedingCoeff
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ClippingRankSum
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MQ
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MQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11028
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 59732
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European (Finnish)
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allele frequency: 0.0e0
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East Asian
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allele num: 8318
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African
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allele num: 8858
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South Asian
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allele frequency: 7.259001161440186e-5
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Other
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BaseQRankSum
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VQSLOD
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ReadPosRankSum
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MQ
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InbreedingCoeff
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MQRankSum
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ClippingRankSum
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FS
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DP
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele frequency: 7.136739937196689e-5
allele num: 14012
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
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Other
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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MQ
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ReadPosRankSum
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BaseQRankSum
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MQRankSum
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DP
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QD
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ClippingRankSum
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VQSLOD
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FS
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InbreedingCoeff
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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European (Finnish)
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African
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East Asian
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South Asian
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Other
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DP
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FS
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MQ
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MQRankSum
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ReadPosRankSum
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VQSLOD
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ClippingRankSum
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QD
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BaseQRankSum
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InbreedingCoeff
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele num: 11072
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South Asian
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East Asian
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European (Non-Finnish)
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Other
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European (Finnish)
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African
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BaseQRankSum
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VQSLOD
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MQRankSum
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ReadPosRankSum
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FS
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ClippingRankSum
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InbreedingCoeff
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QD
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MQ
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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num of homozygotes: 0

European (Non-Finnish)
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num of homozygotes: 0

Latino
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African
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East Asian
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European (Finnish)
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Other
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VQSLOD
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FS
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BaseQRankSum
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MQRankSum
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DP
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ReadPosRankSum
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InbreedingCoeff
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MQ
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QD
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ClippingRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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European (Finnish)
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Latino
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European (Non-Finnish)
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Other
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East Asian
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QD
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MQ
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MQRankSum
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InbreedingCoeff
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ClippingRankSum
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FS
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VQSLOD
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ReadPosRankSum
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BaseQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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European (Finnish)
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Other
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European (Non-Finnish)
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East Asian
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Latino
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South Asian
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DP
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FS
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VQSLOD
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InbreedingCoeff
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MQRankSum
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ReadPosRankSum
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QD
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ClippingRankSum
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MQ
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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Other
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Latino
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European (Finnish)
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African
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East Asian
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European (Non-Finnish)
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allele frequency: 4.914165902240859e-5
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ReadPosRankSum
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VQSLOD
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DP
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FS
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ClippingRankSum
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BaseQRankSum
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MQ
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MQRankSum
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InbreedingCoeff
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QD
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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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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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allele num: 61344
num of homozygotes: 0

Other
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South Asian
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European (Finnish)
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Latino
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African
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East Asian
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ClippingRankSum
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FS
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InbreedingCoeff
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VQSLOD
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MQRankSum
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MQ
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ReadPosRankSum
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QD
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BaseQRankSum
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DP
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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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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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European (Non-Finnish)
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South Asian
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European (Finnish)
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East Asian
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African
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ReadPosRankSum
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ClippingRankSum
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FS
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MQRankSum
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InbreedingCoeff
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BaseQRankSum
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MQ
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QD
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VQSLOD
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DP
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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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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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East Asian
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African
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European (Finnish)
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European (Non-Finnish)
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FS
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DP
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BaseQRankSum
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MQ
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QD
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VQSLOD
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InbreedingCoeff
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ClippingRankSum
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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East Asian
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African
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European (Non-Finnish)
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Other
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South Asian
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ReadPosRankSum
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MQRankSum
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VQSLOD
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BaseQRankSum
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InbreedingCoeff
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FS
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ClippingRankSum
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DP
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MQ
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 61446
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele frequency: 2.062975027144408e-3
allele num: 9210
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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MQRankSum
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FS
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BaseQRankSum
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ReadPosRankSum
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DP
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MQ
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ClippingRankSum
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QD
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VQSLOD
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InbreedingCoeff
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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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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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African
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allele frequency: 1.085540599218411e-4
allele num: 9212
num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 1.626280696048138e-5
allele num: 61490
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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East Asian
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allele num: 8436
num of homozygotes: 0

Latino
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South Asian
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MQ
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MQRankSum
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VQSLOD
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BaseQRankSum
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QD
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InbreedingCoeff
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FS
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ReadPosRankSum
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DP
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ClippingRankSum
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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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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele count: 1
allele frequency: 1.085776330076004e-4
allele num: 9210
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5818
num of homozygotes: 0

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

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

Latino
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allele count: 7
allele frequency: 6.256703611011798e-4
allele num: 11188
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.627816121890871e-5
allele num: 61432
num of homozygotes: 0

East Asian
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allele frequency: 1.067869008068344e-3
allele num: 8428
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QD
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InbreedingCoeff
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MQ
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MQRankSum
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FS
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BaseQRankSum
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ClippingRankSum
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VQSLOD
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ReadPosRankSum
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DP
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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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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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South Asian
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Other
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European (Non-Finnish)
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East Asian
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ClippingRankSum
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ReadPosRankSum
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InbreedingCoeff
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DP
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QD
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VQSLOD
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MQ
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FS
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BaseQRankSum
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MQRankSum
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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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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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East Asian
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European (Finnish)
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Other
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Latino
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European (Non-Finnish)
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African
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QD
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ClippingRankSum
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InbreedingCoeff
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MQRankSum
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BaseQRankSum
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MQ
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FS
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ReadPosRankSum
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VQSLOD
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DP
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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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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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num of homozygotes: 0

African
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Other
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European (Finnish)
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East Asian
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European (Non-Finnish)
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South Asian
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FS
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ClippingRankSum
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BaseQRankSum
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InbreedingCoeff
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VQSLOD
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MQ
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QD
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MQRankSum
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DP
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ReadPosRankSum
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5836
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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African
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

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

East Asian
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allele frequency: 0.0e0
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South Asian
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allele frequency: 3.746721618583739e-4
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FS
type: SiteQuality
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DP
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MQRankSum
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BaseQRankSum
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ReadPosRankSum
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InbreedingCoeff
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MQ
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VQSLOD
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QD
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ClippingRankSum
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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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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11252
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5848
num of homozygotes: 0

East Asian
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allele num: 8462
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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South Asian
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Other
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num of homozygotes: 0

DP
type: SiteQuality
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FS
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VQSLOD
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QD
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InbreedingCoeff
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ClippingRankSum
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ReadPosRankSum
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MQ
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BaseQRankSum
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MQRankSum
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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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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
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Latino
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.609632038116087e-5
allele num: 62126
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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MQRankSum
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ReadPosRankSum
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VQSLOD
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FS
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DP
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QD
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InbreedingCoeff
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MQ
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SIO_000300: 6.0e1

BaseQRankSum
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SIO_000300: -1.013e0

ClippingRankSum
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GenotypeDepth
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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allele frequency: 0.0e0
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African
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South Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Finnish)
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Latino
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European (Non-Finnish)
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East Asian
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BaseQRankSum
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DP
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ClippingRankSum
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MQ
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InbreedingCoeff
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FS
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MQRankSum
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ReadPosRankSum
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VQSLOD
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QD
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GenotypeDepth
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variant carriers: 0

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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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num of homozygotes: 0

African
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European (Finnish)
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East Asian
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South Asian
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Latino
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Other
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ReadPosRankSum
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BaseQRankSum
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FS
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VQSLOD
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DP
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InbreedingCoeff
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MQRankSum
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MQ
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QD
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ClippingRankSum
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GenotypeDepth
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variant carriers: 0

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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele num: 62418
num of homozygotes: 0

European (Finnish)
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African
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Latino
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Other
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East Asian
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South Asian
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MQRankSum
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VQSLOD
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QD
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ClippingRankSum
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MQ
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BaseQRankSum
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DP
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FS
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InbreedingCoeff
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ReadPosRankSum
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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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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.75e1
variant carriers: 0

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 814
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16156
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62582
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8482
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11316
num of homozygotes: 0

African
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allele count: 6
allele frequency: 6.335797254487857e-4
allele num: 9470
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.684068710003368e-4
allele num: 5938
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.4e-3

QD
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SIO_000300: 1.297e1

FS
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MQRankSum
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SIO_000300: -4.3e-2

VQSLOD
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BaseQRankSum
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SIO_000300: -1.169e0

ClippingRankSum
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SIO_000300: -2.99e-1

MQ
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SIO_000300: 5.966e1

DP
type: SiteQuality
SIO_000300: 1.474678e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.64e-1

GenotypeDepth
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variant carriers: 0

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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 8

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 8000
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variant carriers: 0

Latino
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allele count: 2
allele frequency: 1.769911504424779e-4
allele num: 11300
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5904
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.20728695596395e-5
allele num: 62358
num of homozygotes: 0

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 812
num of homozygotes: 0

South Asian
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allele frequency: 6.195786864931847e-5
allele num: 16140
num of homozygotes: 0

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

African
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allele count: 3
allele frequency: 3.186743148502231e-4
allele num: 9414
num of homozygotes: 0

MQRankSum
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SIO_000300: 4.88e-1

VQSLOD
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FS
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InbreedingCoeff
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SIO_000300: -1.0e-3

ClippingRankSum
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MQ
type: SiteQuality
SIO_000300: 5.953e1

ReadPosRankSum
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SIO_000300: 1.5e-2

QD
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SIO_000300: 1.296e1

BaseQRankSum
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SIO_000300: 1.11e0

DP
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SIO_000300: 1.479333e6

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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11352
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62914
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9562
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16158
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5972
num of homozygotes: 0

East Asian
type: Population
allele count: 3
allele frequency: 3.529411764705883e-4
allele num: 8500
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -7.89e-1

FS
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MQRankSum
type: SiteQuality
SIO_000300: 6.68e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.14e-1

DP
type: SiteQuality
SIO_000300: 1.485029e6

InbreedingCoeff
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SIO_000300: -1.5e-3

VQSLOD
type: SiteQuality
SIO_000300: 7.73e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.068e0

QD
type: SiteQuality
SIO_000300: 1.07e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 32321
bin: 6.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5990
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11350
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.173394262503174e-5
allele num: 63024
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9558
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16140
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8504
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 822
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.491407e6

MQRankSum
type: SiteQuality
SIO_000300: 1.77e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 5.246e0

QD
type: SiteQuality
SIO_000300: 1.049e1

VQSLOD
type: SiteQuality
SIO_000300: 8.28e-1

BaseQRankSum
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SIO_000300: -9.66e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.9e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.5e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.8e-1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11346
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.17067757379752e-5
allele num: 63078
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8504
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South Asian
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele frequency: 0.0e0
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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VQSLOD
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SIO_000300: 1.1e0

BaseQRankSum
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MQRankSum
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FS
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ClippingRankSum
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InbreedingCoeff
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ReadPosRankSum
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MQ
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QD
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DP
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GenotypeDepth
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variant carriers: 3

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele count: 0
allele frequency: 0.0e0
allele num: 9576
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
allele num: 6006
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South Asian
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allele frequency: 6.196554715578138e-5
allele num: 16138
num of homozygotes: 0

European (Non-Finnish)
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allele count: 4
allele frequency: 6.339345145646455e-5
allele num: 63098
num of homozygotes: 0

Latino
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num of homozygotes: 0

Other
type: Population
allele count: 1
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East Asian
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allele count: 6
allele frequency: 7.057163020465773e-4
allele num: 8502
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ReadPosRankSum
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SIO_000300: 3.29e-1

InbreedingCoeff
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BaseQRankSum
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MQRankSum
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MQ
type: SiteQuality
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FS
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DP
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ClippingRankSum
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VQSLOD
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QD
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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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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8502
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6006
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9576
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.584836286411614e-5
allele num: 63098
num of homozygotes: 0

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

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

South Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

InbreedingCoeff
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VQSLOD
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MQRankSum
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ClippingRankSum
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DP
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MQ
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QD
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BaseQRankSum
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ReadPosRankSum
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FS
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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allele frequency: 0.0e0
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Latino
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East Asian
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European (Finnish)
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Other
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South Asian
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European (Non-Finnish)
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FS
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MQ
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ClippingRankSum
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ReadPosRankSum
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VQSLOD
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QD
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DP
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MQRankSum
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InbreedingCoeff
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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African
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East Asian
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European (Finnish)
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European (Non-Finnish)
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ReadPosRankSum
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MQ
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MQRankSum
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QD
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VQSLOD
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ClippingRankSum
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DP
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InbreedingCoeff
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FS
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BaseQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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South Asian
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Latino
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European (Non-Finnish)
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Other
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African
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MQRankSum
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MQ
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ReadPosRankSum
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InbreedingCoeff
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FS
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QD
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DP
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VQSLOD
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BaseQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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African
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South Asian
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European (Non-Finnish)
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Latino
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ReadPosRankSum
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InbreedingCoeff
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QD
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VQSLOD
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FS
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BaseQRankSum
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MQRankSum
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DP
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MQ
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ClippingRankSum
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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East Asian
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South Asian
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European (Finnish)
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African
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FS
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VQSLOD
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InbreedingCoeff
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QD
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MQ
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BaseQRankSum
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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African
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Latino
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East Asian
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South Asian
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ReadPosRankSum
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DP
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FS
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MQ
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VQSLOD
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InbreedingCoeff
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QD
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ClippingRankSum
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BaseQRankSum
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GenotypeQuality
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African
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European (Non-Finnish)
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Latino
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East Asian
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European (Finnish)
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South Asian
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DP
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MQRankSum
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FS
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InbreedingCoeff
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VQSLOD
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ReadPosRankSum
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BaseQRankSum
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QD
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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European (Finnish)
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European (Non-Finnish)
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Latino
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African
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Other
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FS
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QD
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MQ
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MQRankSum
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ClippingRankSum
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VQSLOD
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BaseQRankSum
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InbreedingCoeff
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DP
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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Latino
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European (Finnish)
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East Asian
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African
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Other
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European (Non-Finnish)
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QD
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DP
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MQ
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InbreedingCoeff
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BaseQRankSum
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MQRankSum
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FS
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VQSLOD
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ClippingRankSum
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ReadPosRankSum
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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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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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num of homozygotes: 0

Latino
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East Asian
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South Asian
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African
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Other
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European (Non-Finnish)
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FS
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VQSLOD
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MQ
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QD
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ReadPosRankSum
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DP
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InbreedingCoeff
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MQRankSum
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ClippingRankSum
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BaseQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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European (Non-Finnish)
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East Asian
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South Asian
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European (Finnish)
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African
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VQSLOD
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FS
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DP
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BaseQRankSum
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MQ
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QD
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ClippingRankSum
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InbreedingCoeff
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ReadPosRankSum
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GenotypeDepth
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Latino
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South Asian
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African
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European (Finnish)
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East Asian
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FS
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InbreedingCoeff
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ReadPosRankSum
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VQSLOD
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MQ
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MQRankSum
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ClippingRankSum
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DP
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European (Finnish)
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Latino
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African
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East Asian
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VQSLOD
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FS
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MQRankSum
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MQ
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BaseQRankSum
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ReadPosRankSum
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InbreedingCoeff
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QD
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DP
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ClippingRankSum
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SIO_000300: 1.58e-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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

African
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allele frequency: 4.142502071251035e-4
allele num: 9656
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
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Latino
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Other
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ClippingRankSum
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BaseQRankSum
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MQRankSum
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InbreedingCoeff
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MQ
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ReadPosRankSum
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FS
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VQSLOD
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DP
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QD
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

East Asian
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allele frequency: 0.0e0
allele num: 8522
num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 0.0e0
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South Asian
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allele num: 14548
num of homozygotes: 0

Other
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Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

African
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QD
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VQSLOD
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ClippingRankSum
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MQRankSum
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InbreedingCoeff
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FS
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BaseQRankSum
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DP
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SIO_000300: 1.493407e6

ReadPosRankSum
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MQ
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SIO_000300: 5.972e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8520
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 7
allele frequency: 1.11358574610245e-4
allele num: 62860
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European (Finnish)
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allele frequency: 0.0e0
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South Asian
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allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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VQSLOD
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DP
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InbreedingCoeff
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FS
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MQ
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BaseQRankSum
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MQRankSum
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QD
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ReadPosRankSum
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ClippingRankSum
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 62848
num of homozygotes: 0

Other
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European (Finnish)
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South Asian
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Latino
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African
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East Asian
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InbreedingCoeff
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ClippingRankSum
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MQRankSum
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ReadPosRankSum
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VQSLOD
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MQ
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QD
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FS
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DP
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BaseQRankSum
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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num of homozygotes: 0

Other
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East Asian
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European (Non-Finnish)
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Latino
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European (Finnish)
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South Asian
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DP
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BaseQRankSum
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VQSLOD
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FS
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ReadPosRankSum
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MQRankSum
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ClippingRankSum
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InbreedingCoeff
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MQ
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QD
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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East Asian
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South Asian
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Latino
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African
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Other
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European (Non-Finnish)
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FS
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DP
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VQSLOD
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ClippingRankSum
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MQRankSum
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ReadPosRankSum
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InbreedingCoeff
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MQ
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QD
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BaseQRankSum
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GenotypeDepth
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 62496
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6160
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
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allele frequency: 0.0e0
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Latino
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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African
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allele frequency: 1.042752867570386e-4
allele num: 9590
num of homozygotes: 0

VQSLOD
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DP
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MQ
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FS
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InbreedingCoeff
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ReadPosRankSum
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ClippingRankSum
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MQRankSum
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BaseQRankSum
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QD
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6154
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 792
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9562
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Latino
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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allele frequency: 7.311010381634741e-5
allele num: 13678
num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 62336
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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VQSLOD
type: SiteQuality
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MQ
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SIO_000300: 6.0e1

MQRankSum
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InbreedingCoeff
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QD
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ClippingRankSum
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ReadPosRankSum
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FS
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SIO_000300: 0.0e0

BaseQRankSum
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DP
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GenotypeDepth
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variant carriers: 23

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

South Asian
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allele count: 193
allele frequency: 1.433026433026433e-2
allele num: 13468
num of homozygotes: 3

Latino
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allele frequency: 1.755001755001755e-4
allele num: 11396
num of homozygotes: 0

Other
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 2
allele frequency: 3.216054544285071e-5
allele num: 62188
num of homozygotes: 0

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

InbreedingCoeff
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DP
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MQRankSum
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QD
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FS
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MQ
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ClippingRankSum
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ReadPosRankSum
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VQSLOD
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BaseQRankSum
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SIO_000300: 8.129999999999999e-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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6170
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.608906908646266e-5
allele num: 62154
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

Other
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allele count: 0
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InbreedingCoeff
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VQSLOD
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ReadPosRankSum
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MQ
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BaseQRankSum
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QD
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MQRankSum
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FS
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SIO_000300: 0.0e0

ClippingRankSum
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SIO_000300: 7.78e-1

DP
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SIO_000300: 1.464263e6

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 62098
num of homozygotes: 0

South Asian
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allele num: 13284
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Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
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allele count: 0
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African
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allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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East Asian
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MQRankSum
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FS
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InbreedingCoeff
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BaseQRankSum
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MQ
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DP
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ReadPosRankSum
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ClippingRankSum
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VQSLOD
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QD
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GenotypeDepth
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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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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

African
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allele frequency: 1.055297593921486e-4
allele num: 9476
num of homozygotes: 0

European (Finnish)
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allele count: 0
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Other
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East Asian
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European (Non-Finnish)
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South Asian
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allele frequency: 8.354853410299256e-4
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Latino
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FS
type: SiteQuality
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MQ
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BaseQRankSum
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MQRankSum
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DP
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ClippingRankSum
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VQSLOD
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ReadPosRankSum
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InbreedingCoeff
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QD
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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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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele count: 0
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European (Finnish)
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allele count: 1
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allele num: 6166
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South Asian
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Latino
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num of homozygotes: 0

African
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European (Non-Finnish)
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Other
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FS
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InbreedingCoeff
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BaseQRankSum
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ReadPosRankSum
type: SiteQuality
SIO_000300: 6.53e-1

MQ
type: SiteQuality
SIO_000300: 5.89e1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.6e-1

VQSLOD
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SIO_000300: -3.737e-1

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.457487e6

QD
type: SiteQuality
SIO_000300: 9.83e0

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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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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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