16-30134505-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30134505
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30134505
    reference: chr 16
allele count: 2
allele frequency: 2.891008962127783e-4
allele num: 6918
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000102882
  ensembl protein: ENSP00000263025
  ensembl transcript: ENST00000263025
  gene symbol: MAPK3
  hgvsc: ENST00000263025.4:c.26G>A
  hgvsp: ENSP00000263025.4:p.Gly9Asp
  variant of: http://identifiers.org/hgnc/6877
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102882
  ensembl protein: ENSP00000378628
  ensembl transcript: ENST00000395202
  gene symbol: MAPK3
  hgvsc: ENST00000395202.1:c.26G>A
  hgvsp: ENSP00000378628.1:p.Gly9Asp
  variant of: http://identifiers.org/hgnc/6877
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000102882
  ensembl protein: ENSP00000433746
  ensembl transcript: ENST00000466521
  gene symbol: MAPK3
  hgvsc: ENST00000466521.1:c.26G>A
  hgvsp: ENSP00000433746.1:p.Gly9Asp
  variant of: http://identifiers.org/hgnc/6877
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102882
  ensembl protein: ENSP00000384895
  ensembl transcript: ENST00000403394
  gene symbol: MAPK3
  hgvsc: ENST00000403394.1:c.26G>A
  hgvsp: ENSP00000384895.1:p.Gly9Asp
  variant of: http://identifiers.org/hgnc/6877
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102882
  ensembl protein: ENSP00000327293
  ensembl transcript: ENST00000322266
  gene symbol: MAPK3
  hgvsc: ENST00000322266.5:c.26G>A
  hgvsp: ENSP00000327293.5:p.Gly9Asp
  variant of: http://identifiers.org/hgnc/6877
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102882
  ensembl protein: ENSP00000378625
  ensembl transcript: ENST00000395199
  gene symbol: MAPK3
  hgvsc: ENST00000395199.3:c.26G>A
  hgvsp: ENSP00000378625.3:p.Gly9Asp
  variant of: http://identifiers.org/hgnc/6877
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000102882
  ensembl protein: ENSP00000432479
  ensembl transcript: ENST00000490298
  gene symbol: MAPK3
  hgvsc: ENST00000490298.1:c.26G>A
  hgvsp: ENSP00000432479.1:p.Gly9Asp
  variant of: http://identifiers.org/hgnc/6877
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102882
  ensembl protein: ENSP00000433639
  ensembl transcript: ENST00000481230
  gene symbol: MAPK3
  hgvsc: ENST00000481230.1:c.-173+292G>A
  variant of: http://identifiers.org/hgnc/6877
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30702
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11257
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3381
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 31343
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 156
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 8.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1498
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Gly9Asp
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: Latino
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff

16-30134513-A-AGCC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30134513
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30134516
    reference: chr 16
allele count: 1
allele frequency: 2.600104004160167e-4
allele num: 3846
alternate allele: AGCC
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000102882
  ensembl protein: ENSP00000432479
  ensembl transcript: ENST00000490298
  gene symbol: MAPK3
  hgvsc: ENST00000490298.1:c.15_17dupGGC
  hgvsp: ENSP00000432479.1:p.Ala6dup
  variant of: http://identifiers.org/hgnc/6877
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102882
  ensembl protein: ENSP00000433639
  ensembl transcript: ENST00000481230
  gene symbol: MAPK3
  hgvsc: ENST00000481230.1:c.-173+281_-173+283dupGGC
  variant of: http://identifiers.org/hgnc/6877
annotation: Annotation
  canonical: true
  consequence: inframe_insertion
  ensembl gene: ENSG00000102882
  ensembl protein: ENSP00000263025
  ensembl transcript: ENST00000263025
  gene symbol: MAPK3
  hgvsc: ENST00000263025.4:c.15_17dupGGC
  hgvsp: ENSP00000263025.4:p.Ala6dup
  variant of: http://identifiers.org/hgnc/6877
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000102882
  ensembl protein: ENSP00000378628
  ensembl transcript: ENST00000395202
  gene symbol: MAPK3
  hgvsc: ENST00000395202.1:c.15_17dupGGC
  hgvsp: ENSP00000378628.1:p.Ala6dup
  variant of: http://identifiers.org/hgnc/6877
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000102882
  ensembl protein: ENSP00000327293
  ensembl transcript: ENST00000322266
  gene symbol: MAPK3
  hgvsc: ENST00000322266.5:c.15_17dupGGC
  hgvsp: ENSP00000327293.5:p.Ala6dup
  variant of: http://identifiers.org/hgnc/6877
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000102882
  ensembl protein: ENSP00000384895
  ensembl transcript: ENST00000403394
  gene symbol: MAPK3
  hgvsc: ENST00000403394.1:c.15_17dupGGC
  hgvsp: ENSP00000384895.1:p.Ala6dup
  variant of: http://identifiers.org/hgnc/6877
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000102882
  ensembl protein: ENSP00000433746
  ensembl transcript: ENST00000466521
  gene symbol: MAPK3
  hgvsc: ENST00000466521.1:c.15_17dupGGC
  hgvsp: ENSP00000433746.1:p.Ala6dup
  variant of: http://identifiers.org/hgnc/6877
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000102882
  ensembl protein: ENSP00000378625
  ensembl transcript: ENST00000395199
  gene symbol: MAPK3
  hgvsc: ENST00000395199.3:c.15_17dupGGC
  hgvsp: ENSP00000378625.3:p.Ala6dup
  variant of: http://identifiers.org/hgnc/6877
canonical: true
consequence: inframe insertion
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8398
  bin: 7.5e0
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1771
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31837
  bin: 2.5e0
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 31475
  bin: 7.5e0
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 3.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 3055
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Ala6dup
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
population: Other
reference allele: A
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: DP

16-30134513-A-AGCCGCC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30134513
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30134519
    reference: chr 16
allele count: 1
allele frequency: 2.600104004160167e-4
allele num: 3846
alternate allele: AGCCGCC
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000102882
  ensembl protein: ENSP00000378625
  ensembl transcript: ENST00000395199
  gene symbol: MAPK3
  hgvsc: ENST00000395199.3:c.12_17dupGGCGGC
  hgvsp: ENSP00000378625.3:p.Ala5_Ala6dup
  variant of: http://identifiers.org/hgnc/6877
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000102882
  ensembl protein: ENSP00000327293
  ensembl transcript: ENST00000322266
  gene symbol: MAPK3
  hgvsc: ENST00000322266.5:c.12_17dupGGCGGC
  hgvsp: ENSP00000327293.5:p.Ala5_Ala6dup
  variant of: http://identifiers.org/hgnc/6877
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000102882
  ensembl protein: ENSP00000378628
  ensembl transcript: ENST00000395202
  gene symbol: MAPK3
  hgvsc: ENST00000395202.1:c.12_17dupGGCGGC
  hgvsp: ENSP00000378628.1:p.Ala5_Ala6dup
  variant of: http://identifiers.org/hgnc/6877
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000102882
  ensembl protein: ENSP00000433746
  ensembl transcript: ENST00000466521
  gene symbol: MAPK3
  hgvsc: ENST00000466521.1:c.12_17dupGGCGGC
  hgvsp: ENSP00000433746.1:p.Ala5_Ala6dup
  variant of: http://identifiers.org/hgnc/6877
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000102882
  ensembl protein: ENSP00000432479
  ensembl transcript: ENST00000490298
  gene symbol: MAPK3
  hgvsc: ENST00000490298.1:c.12_17dupGGCGGC
  hgvsp: ENSP00000432479.1:p.Ala5_Ala6dup
  variant of: http://identifiers.org/hgnc/6877
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000102882
  ensembl protein: ENSP00000384895
  ensembl transcript: ENST00000403394
  gene symbol: MAPK3
  hgvsc: ENST00000403394.1:c.12_17dupGGCGGC
  hgvsp: ENSP00000384895.1:p.Ala5_Ala6dup
  variant of: http://identifiers.org/hgnc/6877
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102882
  ensembl protein: ENSP00000433639
  ensembl transcript: ENST00000481230
  gene symbol: MAPK3
  hgvsc: ENST00000481230.1:c.-173+278_-173+283dupGGCGGC
  variant of: http://identifiers.org/hgnc/6877
annotation: Annotation
  canonical: true
  consequence: inframe_insertion
  ensembl gene: ENSG00000102882
  ensembl protein: ENSP00000263025
  ensembl transcript: ENST00000263025
  gene symbol: MAPK3
  hgvsc: ENST00000263025.4:c.12_17dupGGCGGC
  hgvsp: ENSP00000263025.4:p.Ala5_Ala6dup
  variant of: http://identifiers.org/hgnc/6877
canonical: true
consequence: inframe insertion
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31837
  bin: 2.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1771
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8398
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3055
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1145
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Ala5_Ala6dup
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Other
population: African
population: European (Finnish)
population: Latino
reference allele: A
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: QD

16-30134515-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30134515
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30134515
    reference: chr 16
allele count: 0
allele frequency: 0.0e0
allele num: 2382
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102882
  ensembl protein: ENSP00000378628
  ensembl transcript: ENST00000395202
  gene symbol: MAPK3
  hgvsc: ENST00000395202.1:c.16G>A
  hgvsp: ENSP00000378628.1:p.Ala6Thr
  variant of: http://identifiers.org/hgnc/6877
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000102882
  ensembl protein: ENSP00000433746
  ensembl transcript: ENST00000466521
  gene symbol: MAPK3
  hgvsc: ENST00000466521.1:c.16G>A
  hgvsp: ENSP00000433746.1:p.Ala6Thr
  variant of: http://identifiers.org/hgnc/6877
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000102882
  ensembl protein: ENSP00000263025
  ensembl transcript: ENST00000263025
  gene symbol: MAPK3
  hgvsc: ENST00000263025.4:c.16G>A
  hgvsp: ENSP00000263025.4:p.Ala6Thr
  variant of: http://identifiers.org/hgnc/6877
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000102882
  ensembl protein: ENSP00000432479
  ensembl transcript: ENST00000490298
  gene symbol: MAPK3
  hgvsc: ENST00000490298.1:c.16G>A
  hgvsp: ENSP00000432479.1:p.Ala6Thr
  variant of: http://identifiers.org/hgnc/6877
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102882
  ensembl protein: ENSP00000327293
  ensembl transcript: ENST00000322266
  gene symbol: MAPK3
  hgvsc: ENST00000322266.5:c.16G>A
  hgvsp: ENSP00000327293.5:p.Ala6Thr
  variant of: http://identifiers.org/hgnc/6877
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102882
  ensembl protein: ENSP00000378625
  ensembl transcript: ENST00000395199
  gene symbol: MAPK3
  hgvsc: ENST00000395199.3:c.16G>A
  hgvsp: ENSP00000378625.3:p.Ala6Thr
  variant of: http://identifiers.org/hgnc/6877
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102882
  ensembl protein: ENSP00000384895
  ensembl transcript: ENST00000403394
  gene symbol: MAPK3
  hgvsc: ENST00000403394.1:c.16G>A
  hgvsp: ENSP00000384895.1:p.Ala6Thr
  variant of: http://identifiers.org/hgnc/6877
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102882
  ensembl protein: ENSP00000433639
  ensembl transcript: ENST00000481230
  gene symbol: MAPK3
  hgvsc: ENST00000481230.1:c.-173+282G>A
  variant of: http://identifiers.org/hgnc/6877
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1113
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7236
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31439
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1145
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3529
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 211
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 107
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Ala6Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: African
population: Latino
population: East Asian
population: South Asian
reference allele: C
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: FS

16-30134517-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30134517
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30134517
    reference: chr 16
allele count: 2
allele frequency: 8.857395925597874e-4
allele num: 2258
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102882
  ensembl protein: ENSP00000327293
  ensembl transcript: ENST00000322266
  gene symbol: MAPK3
  hgvsc: ENST00000322266.5:c.14C>T
  hgvsp: ENSP00000327293.5:p.Ala5Val
  variant of: http://identifiers.org/hgnc/6877
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102882
  ensembl protein: ENSP00000378628
  ensembl transcript: ENST00000395202
  gene symbol: MAPK3
  hgvsc: ENST00000395202.1:c.14C>T
  hgvsp: ENSP00000378628.1:p.Ala5Val
  variant of: http://identifiers.org/hgnc/6877
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102882
  ensembl protein: ENSP00000433639
  ensembl transcript: ENST00000481230
  gene symbol: MAPK3
  hgvsc: ENST00000481230.1:c.-173+280C>T
  variant of: http://identifiers.org/hgnc/6877
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000102882
  ensembl protein: ENSP00000432479
  ensembl transcript: ENST00000490298
  gene symbol: MAPK3
  hgvsc: ENST00000490298.1:c.14C>T
  hgvsp: ENSP00000432479.1:p.Ala5Val
  variant of: http://identifiers.org/hgnc/6877
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102882
  ensembl protein: ENSP00000384895
  ensembl transcript: ENST00000403394
  gene symbol: MAPK3
  hgvsc: ENST00000403394.1:c.14C>T
  hgvsp: ENSP00000384895.1:p.Ala5Val
  variant of: http://identifiers.org/hgnc/6877
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000102882
  ensembl protein: ENSP00000433746
  ensembl transcript: ENST00000466521
  gene symbol: MAPK3
  hgvsc: ENST00000466521.1:c.14C>T
  hgvsp: ENSP00000433746.1:p.Ala5Val
  variant of: http://identifiers.org/hgnc/6877
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000102882
  ensembl protein: ENSP00000263025
  ensembl transcript: ENST00000263025
  gene symbol: MAPK3
  hgvsc: ENST00000263025.4:c.14C>T
  hgvsp: ENSP00000263025.4:p.Ala5Val
  variant of: http://identifiers.org/hgnc/6877
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102882
  ensembl protein: ENSP00000378625
  ensembl transcript: ENST00000395199
  gene symbol: MAPK3
  hgvsc: ENST00000395199.3:c.14C>T
  hgvsp: ENSP00000378625.3:p.Ala5Val
  variant of: http://identifiers.org/hgnc/6877
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7078
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1022
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31735
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30398
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Ala5Val
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: South Asian
population: African
population: Other
population: European (Non-Finnish)
population: Latino
reference allele: G
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP

16-30134791-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30134791
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30134791
    reference: chr 16
allele count: 5
allele frequency: 4.68427955780401e-4
allele num: 10674
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102882
  ensembl protein: ENSP00000433639
  ensembl transcript: ENST00000481230
  gene symbol: MAPK3
  hgvsc: ENST00000481230.1:c.-173+6G>A
  variant of: http://identifiers.org/hgnc/6877
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2433
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1020
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1477
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1832
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 770
  bin: 9.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 1955
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 407
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 514
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 377
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 406
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2055
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 276
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 762
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 192
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.75e1
  variant carriers: 0
hgvs: c.-173+6G>A
num of homozygotes: 0
population: African
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 190
  num of homozygotes: 0
population: European (Non-Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 2666
  num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: Other
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff

16-30134826-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30134826
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30134826
    reference: chr 16
allele count: 1
allele frequency: 9.321401938851603e-5
allele num: 10728
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000102882
  ensembl protein: ENSP00000433639
  ensembl transcript: ENST00000481230
  gene symbol: MAPK3
  hgvsc: ENST00000481230.1:c.-202C>T
  variant of: http://identifiers.org/hgnc/6877
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1032
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4448
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1839
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 1
genotype depth: GenotypeDepth
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  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1507
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 2.25e1
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 7.5e0
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genotype quality: GenotypeQuality
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  bin: 6.75e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 9.25e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 191
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  variant carriers: 0
num of homozygotes: 0
population: Other
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 118
  num of homozygotes: 0
population: European (Finnish)
  type: Population
  allele count: 0
  allele frequency: NaN
  allele num: 0
  num of homozygotes: 0
population: European (Non-Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 2694
  num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: Latino
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP

16-30134841-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30134841
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30134841
    reference: chr 16
allele count: 10
allele frequency: 9.31619154089808e-4
allele num: 10734
alternate allele: T
canonical: true
consequence: upstream gene
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1517
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 3.75e1
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genotype depth: GenotypeDepth
  all individuals: 253
  bin: 4.25e1
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genotype depth: GenotypeDepth
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  bin: 7.75e1
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genotype depth: GenotypeDepth
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  bin: 3.25e1
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genotype depth: GenotypeDepth
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  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 2
genotype depth: GenotypeDepth
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  bin: 5.25e1
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genotype depth: GenotypeDepth
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  bin: 2.25e1
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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  bin: 3.25e1
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 1.25e1
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genotype quality: GenotypeQuality
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  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 1.75e1
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genotype quality: GenotypeQuality
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  bin: 7.5e0
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genotype quality: GenotypeQuality
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  bin: 7.25e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 8.75e1
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genotype quality: GenotypeQuality
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  bin: 9.75e1
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 516
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 1
population: European (Non-Finnish)
  type: Population
  allele count: 5
  allele frequency: 1.851851851851852e-3
  allele num: 2700
  num of homozygotes: 0
population: South Asian
  type: Population
  allele count: 4
  allele frequency: 5.333333333333334e-4
  allele num: 7500
  num of homozygotes: 1
population: African
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 192
  num of homozygotes: 0
population: European (Finnish)
  type: Population
  allele count: 0
  allele frequency: NaN
  allele num: 0
  num of homozygotes: 0
population: Other
population: Latino
population: East Asian
reference allele: C
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP

16-30134845-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30134845
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30134845
    reference: chr 16
allele count: 2
allele frequency: 1.862891207153502e-4
allele num: 10736
alternate allele: T
canonical: true
consequence: upstream gene
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1520
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6242
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
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  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1789
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 254
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.5e0
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genotype depth: GenotypeDepth
  all individuals: 5
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genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.25e1
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genotype depth: GenotypeDepth
  all individuals: 1031
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
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genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
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genotype depth: GenotypeDepth
  all individuals: 2
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 190
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genotype quality: GenotypeQuality
  all individuals: 25
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genotype quality: GenotypeQuality
  all individuals: 918
  bin: 2.5e0
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genotype quality: GenotypeQuality
  all individuals: 5310
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 1.25e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 518
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genotype quality: GenotypeQuality
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  bin: 1.75e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
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genotype quality: GenotypeQuality
  all individuals: 407
  bin: 8.25e1
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genotype quality: GenotypeQuality
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  bin: 4.25e1
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genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.25e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 771
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 277
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 92
  num of homozygotes: 0
population: European (Non-Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 2704
  num of homozygotes: 0
population: South Asian
  type: Population
  allele count: 2
  allele frequency: 2.667377967457989e-4
  allele num: 7498
  num of homozygotes: 0
population: African
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 192
  num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Other
reference allele: C
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: DP

16-30194312-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30194312
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30194312
    reference: chr 16
allele count: 1
allele frequency: 9.342301943198804e-5
allele num: 10704
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456266
  ensembl transcript: ENST00000563778
  gene symbol: CORO1A
  hgvsc: ENST00000563778.1:c.-24G>T
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456756
  ensembl transcript: ENST00000561815
  gene symbol: CORO1A
  hgvsc: ENST00000561815.1:c.-36G>T
  variant of: http://identifiers.org/hgnc/2252
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1473
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4176
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2727
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 188
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  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 719
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 143
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genotype quality: GenotypeQuality
  all individuals: 3693
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 181
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 3.75e1
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genotype quality: GenotypeQuality
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  bin: 5.75e1
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genotype quality: GenotypeQuality
  all individuals: 3120
  bin: 7.5e0
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 85
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  variant carriers: 0
num of homozygotes: 0
population: Other
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 118
  num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
reference allele: G
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: MQ

16-30194314-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30194314
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30194314
    reference: chr 16
allele count: 3
allele frequency: 2.803214352457484e-4
allele num: 10702
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456266
  ensembl transcript: ENST00000563778
  gene symbol: CORO1A
  hgvsc: ENST00000563778.1:c.-22C>G
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456756
  ensembl transcript: ENST00000561815
  gene symbol: CORO1A
  hgvsc: ENST00000561815.1:c.-34C>G
  variant of: http://identifiers.org/hgnc/2252
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2733
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 172
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 17
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 182
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
num of homozygotes: 0
population: Other
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 118
  num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/16-30194322-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30194322
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30194322
    reference: chr 16
allele count: 1
allele frequency: 9.342301943198804e-5
allele num: 10704
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456756
  ensembl transcript: ENST00000561815
  gene symbol: CORO1A
  hgvsc: ENST00000561815.1:c.-26C>A
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456266
  ensembl transcript: ENST00000563778
  gene symbol: CORO1A
  hgvsc: ENST00000563778.1:c.-14C>A
  variant of: http://identifiers.org/hgnc/2252
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 7.5e0
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genotype depth: GenotypeDepth
  all individuals: 12
  bin: 5.75e1
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 2759
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 194
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num of homozygotes: 0
population: Latino
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 92
  num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum

16-30194328-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30194328
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30194328
    reference: chr 16
allele count: 567
allele frequency: 5.289179104477612e-2
allele num: 10720
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456266
  ensembl transcript: ENST00000563778
  gene symbol: CORO1A
  hgvsc: ENST00000563778.1:c.-8G>C
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456756
  ensembl transcript: ENST00000561815
  gene symbol: CORO1A
  hgvsc: ENST00000561815.1:c.-20G>C
  variant of: http://identifiers.org/hgnc/2252
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.25e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 3460
  bin: 2.5e0
  variant carriers: 50
genotype depth: GenotypeDepth
  all individuals: 1419
  bin: 2.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 4.25e1
  variant carriers: 78
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 7.5e0
  variant carriers: 41
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 2710
  bin: 2.75e1
  variant carriers: 48
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.75e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 3.25e1
  variant carriers: 65
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 5.25e1
  variant carriers: 54
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 4.75e1
  variant carriers: 63
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 3.75e1
  variant carriers: 64
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 5.75e1
  variant carriers: 43
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 6.25e1
  variant carriers: 28
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 2735
  bin: 7.5e0
  variant carriers: 27
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 1.75e1
  variant carriers: 10
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 533
  bin: 9.75e1
  variant carriers: 525
genotype quality: GenotypeQuality
  all individuals: 734
  bin: 2.5e0
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 1.25e1
  variant carriers: 13
genotype quality: GenotypeQuality
  all individuals: 141
  bin: 7.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 2.75e1
  variant carriers: 12
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 9.25e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 8.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 8.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 169
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3689
  bin: 6.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 3.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 109
  bin: 2.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 684
  bin: 6.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 5.25e1
  variant carriers: 1
num of homozygotes: 32
population: South Asian
  type: Population
  allele count: 226
  allele frequency: 3.017356475300401e-2
  allele num: 7490
  num of homozygotes: 9
population: European (Non-Finnish)
population: Latino
population: Other
population: African
population: East Asian
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ

16-30194358-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30194358
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30194358
    reference: chr 16
allele count: 1
allele frequency: 9.359790340696369e-5
allele num: 10684
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456266
  ensembl transcript: ENST00000563778
  gene symbol: CORO1A
  hgvsc: ENST00000563778.1:c.-2+24A>G
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456756
  ensembl transcript: ENST00000561815
  gene symbol: CORO1A
  hgvsc: ENST00000561815.1:c.11A>G
  hgvsp: ENSP00000456756.1:p.Tyr4Cys
  variant of: http://identifiers.org/hgnc/2252
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 716
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3380
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1496
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3000
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 8.75e1
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genotype quality: GenotypeQuality
  all individuals: 4071
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 278
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3103
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
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genotype quality: GenotypeQuality
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 9
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 769
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 141
  bin: 7.75e1
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genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 5.75e1
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genotype quality: GenotypeQuality
  all individuals: 9
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
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genotype quality: GenotypeQuality
  all individuals: 157
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 186
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Tyr4Cys
num of homozygotes: 0
population: South Asian
  type: Population
  allele count: 1
  allele frequency: 1.337255950788981e-4
  allele num: 7478
  num of homozygotes: 0
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
reference allele: A
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD

16-30194378-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30194378
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30194378
    reference: chr 16
allele count: 3
allele frequency: 2.837684449489217e-4
allele num: 10572
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456266
  ensembl transcript: ENST00000563778
  gene symbol: CORO1A
  hgvsc: ENST00000563778.1:c.-2+44G>A
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456756
  ensembl transcript: ENST00000561815
  gene symbol: CORO1A
  hgvsc: ENST00000561815.1:c.31G>A
  hgvsp: ENSP00000456756.1:p.Val11Met
  variant of: http://identifiers.org/hgnc/2252
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1432
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2957
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3138
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 698
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2869
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 218
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 136
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 275
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  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 18
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genotype quality: GenotypeQuality
  all individuals: 19
  bin: 1.25e1
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genotype quality: GenotypeQuality
  all individuals: 3971
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genotype quality: GenotypeQuality
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 175
  bin: 7.25e1
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genotype quality: GenotypeQuality
  all individuals: 737
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 6
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genotype quality: GenotypeQuality
  all individuals: 9
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genotype quality: GenotypeQuality
  all individuals: 13
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
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  variant carriers: 0
hgvs: p.Val11Met
num of homozygotes: 0
population: European (Finnish)
  type: Population
  allele count: 0
  allele frequency: NaN
  allele num: 0
  num of homozygotes: 0
population: East Asian
population: Other
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD

16-30194398-AG-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30194398
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30194397
    reference: chr 16
allele count: 1
allele frequency: 9.735202492211838e-5
allele num: 10272
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456756
  ensembl transcript: ENST00000561815
  gene symbol: CORO1A
  hgvsc: ENST00000561815.1:c.52delG
  hgvsp: ENSP00000456756.1:p.Asp18IlefsTer14
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456266
  ensembl transcript: ENST00000563778
  gene symbol: CORO1A
  hgvsc: ENST00000563778.1:c.-2+65delG
  variant of: http://identifiers.org/hgnc/2252
canonical: false
consequence: frameshift
filter: VQSRTrancheINDEL96.00to97.00
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2750
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1373
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  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
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genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2840
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genotype depth: GenotypeDepth
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  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 8.75e1
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genotype depth: GenotypeDepth
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  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 637
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 5.75e1
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genotype quality: GenotypeQuality
  all individuals: 143
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 4.75e1
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genotype quality: GenotypeQuality
  all individuals: 11
  bin: 4.25e1
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genotype quality: GenotypeQuality
  all individuals: 264
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genotype quality: GenotypeQuality
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  bin: 1.25e1
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genotype quality: GenotypeQuality
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  bin: 3.75e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 1.75e1
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genotype quality: GenotypeQuality
  all individuals: 41
  bin: 8.25e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 3729
  bin: 6.25e1
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genotype quality: GenotypeQuality
  all individuals: 4
  bin: 9.75e1
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genotype quality: GenotypeQuality
  all individuals: 110
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genotype quality: GenotypeQuality
  all individuals: 48
  bin: 2.75e1
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genotype quality: GenotypeQuality
  all individuals: 444
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genotype quality: GenotypeQuality
  all individuals: 653
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genotype quality: GenotypeQuality
  all individuals: 10
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
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  variant carriers: 0
hgvs: p.Asp18IlefsTer14
num of homozygotes: 0
population: Latino
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 88
  num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: South Asian
population: Other
population: European (Finnish)
population: East Asian
reference allele: AG
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum

http://identifiers.org/exac.variant/16-30194402-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30194402
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30194402
    reference: chr 16
allele count: 2
allele frequency: 1.958480219349785e-4
allele num: 10212
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456756
  ensembl transcript: ENST00000561815
  gene symbol: CORO1A
  hgvsc: ENST00000561815.1:c.55C>A
  hgvsp: ENSP00000456756.1:p.Pro19Thr
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456266
  ensembl transcript: ENST00000563778
  gene symbol: CORO1A
  hgvsc: ENST00000563778.1:c.-2+68C>A
  variant of: http://identifiers.org/hgnc/2252
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2719
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2821
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 9.25e1
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genotype depth: GenotypeDepth
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  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 5.75e1
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1353
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 240
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3697
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2581
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 646
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 137
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 501
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 103
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Pro19Thr
num of homozygotes: 0
population: European (Finnish)
  type: Population
  allele count: 0
  allele frequency: NaN
  allele num: 0
  num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD

http://identifiers.org/exac.variant/16-30194447-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30194447
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30194447
    reference: chr 16
allele count: 40
allele frequency: 5.817335660267597e-3
allele num: 6876
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456266
  ensembl transcript: ENST00000563778
  gene symbol: CORO1A
  hgvsc: ENST00000563778.1:c.-2+113A>C
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456756
  ensembl transcript: ENST00000561815
  gene symbol: CORO1A
  hgvsc: ENST00000561815.1:c.100A>C
  hgvsp: ENST00000561815.1:c.100A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2252
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 2.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 1822
  bin: 2.5e0
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1887
  bin: 1.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 1.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1756
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 617
  bin: 2.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 3.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 139
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 201
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 105
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 9.75e1
  variant carriers: 36
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1647
  bin: 7.5e0
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 3125
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 919
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 312
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 253
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Arg34Arg
num of homozygotes: 2
population: African
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 126
  num of homozygotes: 0
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: A
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum

16-30194447-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30194447
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30194447
    reference: chr 16
allele count: 3
allele frequency: 4.363001745200698e-4
allele num: 6876
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456756
  ensembl transcript: ENST00000561815
  gene symbol: CORO1A
  hgvsc: ENST00000561815.1:c.100A>T
  hgvsp: ENSP00000456756.1:p.Arg34Ter
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456266
  ensembl transcript: ENST00000563778
  gene symbol: CORO1A
  hgvsc: ENST00000563778.1:c.-2+113A>T
  variant of: http://identifiers.org/hgnc/2252
canonical: false
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1822
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 617
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1756
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1887
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 139
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 919
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1647
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3125
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 201
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 312
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 253
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 105
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Arg34Ter
num of homozygotes: 0
population: European (Non-Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 1686
  num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: Other
population: South Asian
reference allele: A
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: QD

16-30196487-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30196487
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30196487
    reference: chr 16
allele count: 2
allele frequency: 1.697937006537057e-5
allele num: 117790
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000219150
  ensembl transcript: ENST00000219150
  gene symbol: CORO1A
  hgvsc: ENST00000219150.5:c.-1-43G>A
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000457332
  ensembl transcript: ENST00000570244
  gene symbol: CORO1A
  hgvsc: ENST00000570244.1:c.-1-43G>A
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000457509
  ensembl transcript: ENST00000569970
  gene symbol: CORO1A
  hgvsc: ENST00000569970.1:c.-1-43G>A
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456266
  ensembl transcript: ENST00000563778
  gene symbol: CORO1A
  hgvsc: ENST00000563778.1:c.-1-43G>A
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000568763
  gene symbol: CORO1A
  hgvsc: ENST00000568763.1:n.122-43G>A
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000569469
  gene symbol: CORO1A
  hgvsc: ENST00000569469.1:n.110-43G>A
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000455552
  ensembl transcript: ENST00000570045
  gene symbol: CORO1A
  hgvsc: ENST00000570045.1:c.-1-43G>A
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000561849
  gene symbol: CORO1A
  hgvsc: ENST00000561849.1:n.127-43G>A
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000568982
  gene symbol: CORO1A
  hgvsc: ENST00000568982.1:n.118-43G>A
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456457
  ensembl transcript: ENST00000565497
  gene symbol: CORO1A
  hgvsc: ENST00000565497.1:c.-1-43G>A
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000566619
  gene symbol: CORO1A
  hgvsc: ENST00000566619.1:n.118-43G>A
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000454752
  ensembl transcript: ENST00000569203
  gene symbol: CORO1A
  hgvsc: ENST00000569203.1:c.-1-43G>A
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456756
  ensembl transcript: ENST00000561815
  gene symbol: CORO1A
  hgvsc: ENST00000561815.1:c.108-43G>A
  variant of: http://identifiers.org/hgnc/2252
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19328
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1553
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1233
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6034
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7497
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5960
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17861
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum

16-30196490-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30196490
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30196490
    reference: chr 16
allele count: 1
allele frequency: 8.48824378236143e-6
allele num: 117810
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000568763
  gene symbol: CORO1A
  hgvsc: ENST00000568763.1:n.122-40G>C
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000457509
  ensembl transcript: ENST00000569970
  gene symbol: CORO1A
  hgvsc: ENST00000569970.1:c.-1-40G>C
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000455552
  ensembl transcript: ENST00000570045
  gene symbol: CORO1A
  hgvsc: ENST00000570045.1:c.-1-40G>C
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000568982
  gene symbol: CORO1A
  hgvsc: ENST00000568982.1:n.118-40G>C
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456457
  ensembl transcript: ENST00000565497
  gene symbol: CORO1A
  hgvsc: ENST00000565497.1:c.-1-40G>C
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000219150
  ensembl transcript: ENST00000219150
  gene symbol: CORO1A
  hgvsc: ENST00000219150.5:c.-1-40G>C
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456756
  ensembl transcript: ENST00000561815
  gene symbol: CORO1A
  hgvsc: ENST00000561815.1:c.108-40G>C
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000457332
  ensembl transcript: ENST00000570244
  gene symbol: CORO1A
  hgvsc: ENST00000570244.1:c.-1-40G>C
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000561849
  gene symbol: CORO1A
  hgvsc: ENST00000561849.1:n.127-40G>C
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000569469
  gene symbol: CORO1A
  hgvsc: ENST00000569469.1:n.110-40G>C
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000454752
  ensembl transcript: ENST00000569203
  gene symbol: CORO1A
  hgvsc: ENST00000569203.1:c.-1-40G>C
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000566619
  gene symbol: CORO1A
  hgvsc: ENST00000566619.1:n.118-40G>C
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456266
  ensembl transcript: ENST00000563778
  gene symbol: CORO1A
  hgvsc: ENST00000563778.1:c.-1-40G>C
  variant of: http://identifiers.org/hgnc/2252
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1238
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6028
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1538
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18135
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5756
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
population: European (Finnish)
reference allele: G
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum

16-30196495-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30196495
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30196495
    reference: chr 16
allele count: 1
allele frequency: 8.472996559963397e-6
allele num: 118022
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000457332
  ensembl transcript: ENST00000570244
  gene symbol: CORO1A
  hgvsc: ENST00000570244.1:c.-1-35G>A
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456266
  ensembl transcript: ENST00000563778
  gene symbol: CORO1A
  hgvsc: ENST00000563778.1:c.-1-35G>A
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000561849
  gene symbol: CORO1A
  hgvsc: ENST00000561849.1:n.127-35G>A
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000219150
  ensembl transcript: ENST00000219150
  gene symbol: CORO1A
  hgvsc: ENST00000219150.5:c.-1-35G>A
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000455552
  ensembl transcript: ENST00000570045
  gene symbol: CORO1A
  hgvsc: ENST00000570045.1:c.-1-35G>A
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000454752
  ensembl transcript: ENST00000569203
  gene symbol: CORO1A
  hgvsc: ENST00000569203.1:c.-1-35G>A
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000566619
  gene symbol: CORO1A
  hgvsc: ENST00000566619.1:n.118-35G>A
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456756
  ensembl transcript: ENST00000561815
  gene symbol: CORO1A
  hgvsc: ENST00000561815.1:c.108-35G>A
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000457509
  ensembl transcript: ENST00000569970
  gene symbol: CORO1A
  hgvsc: ENST00000569970.1:c.-1-35G>A
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000569469
  gene symbol: CORO1A
  hgvsc: ENST00000569469.1:n.110-35G>A
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456457
  ensembl transcript: ENST00000565497
  gene symbol: CORO1A
  hgvsc: ENST00000565497.1:c.-1-35G>A
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000568982
  gene symbol: CORO1A
  hgvsc: ENST00000568982.1:n.118-35G>A
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000568763
  gene symbol: CORO1A
  hgvsc: ENST00000568763.1:n.122-35G>A
  variant of: http://identifiers.org/hgnc/2252
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1241
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6213
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18797
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1493
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2936
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24171
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4658
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: QD

16-30196498-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30196498
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30196498
    reference: chr 16
allele count: 1
allele frequency: 8.464247020585048e-6
allele num: 118144
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456756
  ensembl transcript: ENST00000561815
  gene symbol: CORO1A
  hgvsc: ENST00000561815.1:c.108-32G>A
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000457332
  ensembl transcript: ENST00000570244
  gene symbol: CORO1A
  hgvsc: ENST00000570244.1:c.-1-32G>A
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000561849
  gene symbol: CORO1A
  hgvsc: ENST00000561849.1:n.127-32G>A
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000568982
  gene symbol: CORO1A
  hgvsc: ENST00000568982.1:n.118-32G>A
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456266
  ensembl transcript: ENST00000563778
  gene symbol: CORO1A
  hgvsc: ENST00000563778.1:c.-1-32G>A
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456457
  ensembl transcript: ENST00000565497
  gene symbol: CORO1A
  hgvsc: ENST00000565497.1:c.-1-32G>A
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000455552
  ensembl transcript: ENST00000570045
  gene symbol: CORO1A
  hgvsc: ENST00000570045.1:c.-1-32G>A
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000219150
  ensembl transcript: ENST00000219150
  gene symbol: CORO1A
  hgvsc: ENST00000219150.5:c.-1-32G>A
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000568763
  gene symbol: CORO1A
  hgvsc: ENST00000568763.1:n.122-32G>A
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000569469
  gene symbol: CORO1A
  hgvsc: ENST00000569469.1:n.110-32G>A
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000454752
  ensembl transcript: ENST00000569203
  gene symbol: CORO1A
  hgvsc: ENST00000569203.1:c.-1-32G>A
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000457509
  ensembl transcript: ENST00000569970
  gene symbol: CORO1A
  hgvsc: ENST00000569970.1:c.-1-32G>A
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000566619
  gene symbol: CORO1A
  hgvsc: ENST00000566619.1:n.118-32G>A
  variant of: http://identifiers.org/hgnc/2252
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1963
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19252
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1448
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1244
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 496
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25472
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
reference allele: G
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: QD

16-30196512-T-TA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30196512
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30196513
    reference: chr 16
allele count: 3
allele frequency: 2.513152162986295e-5
allele num: 119372
alternate allele: TA
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000569469
  gene symbol: CORO1A
  hgvsc: ENST00000569469.1:n.110-17dupA
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000457332
  ensembl transcript: ENST00000570244
  gene symbol: CORO1A
  hgvsc: ENST00000570244.1:c.-1-17dupA
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000561849
  gene symbol: CORO1A
  hgvsc: ENST00000561849.1:n.127-17dupA
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000457509
  ensembl transcript: ENST00000569970
  gene symbol: CORO1A
  hgvsc: ENST00000569970.1:c.-1-17dupA
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000219150
  ensembl transcript: ENST00000219150
  gene symbol: CORO1A
  hgvsc: ENST00000219150.5:c.-1-17dupA
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456756
  ensembl transcript: ENST00000561815
  gene symbol: CORO1A
  hgvsc: ENST00000561815.1:c.108-17dupA
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000566619
  gene symbol: CORO1A
  hgvsc: ENST00000566619.1:n.118-17dupA
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000455552
  ensembl transcript: ENST00000570045
  gene symbol: CORO1A
  hgvsc: ENST00000570045.1:c.-1-17dupA
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456266
  ensembl transcript: ENST00000563778
  gene symbol: CORO1A
  hgvsc: ENST00000563778.1:c.-1-17dupA
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456457
  ensembl transcript: ENST00000565497
  gene symbol: CORO1A
  hgvsc: ENST00000565497.1:c.-1-17dupA
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000568982
  gene symbol: CORO1A
  hgvsc: ENST00000568982.1:n.118-17dupA
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000454752
  ensembl transcript: ENST00000569203
  gene symbol: CORO1A
  hgvsc: ENST00000569203.1:c.-1-17dupA
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000568763
  gene symbol: CORO1A
  hgvsc: ENST00000568763.1:n.122-17dupA
  variant of: http://identifiers.org/hgnc/2252
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 935
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1330
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6527
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28475
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20574
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1246
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: Latino
reference allele: T
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ

16-30196539-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30196539
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30196539
    reference: chr 16
allele count: 1
allele frequency: 8.291873963515755e-6
allele num: 120600
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000454752
  ensembl transcript: ENST00000569203
  gene symbol: CORO1A
  hgvsc: ENST00000569203.1:c.9G>A
  hgvsp: ENST00000569203.1:c.9G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456457
  ensembl transcript: ENST00000565497
  gene symbol: CORO1A
  hgvsc: ENST00000565497.1:c.9G>A
  hgvsp: ENST00000565497.1:c.9G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000457509
  ensembl transcript: ENST00000569970
  gene symbol: CORO1A
  hgvsc: ENST00000569970.1:c.9G>A
  hgvsp: ENST00000569970.1:c.9G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000566619
  gene symbol: CORO1A
  hgvsc: ENST00000566619.1:n.127G>A
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456266
  ensembl transcript: ENST00000563778
  gene symbol: CORO1A
  hgvsc: ENST00000563778.1:c.9G>A
  hgvsp: ENST00000563778.1:c.9G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000568763
  gene symbol: CORO1A
  hgvsc: ENST00000568763.1:n.131G>A
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456756
  ensembl transcript: ENST00000561815
  gene symbol: CORO1A
  hgvsc: ENST00000561815.1:c.117G>A
  hgvsp: ENST00000561815.1:c.117G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000219150
  ensembl transcript: ENST00000219150
  gene symbol: CORO1A
  hgvsc: ENST00000219150.5:c.9G>A
  hgvsp: ENST00000219150.5:c.9G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000561849
  gene symbol: CORO1A
  hgvsc: ENST00000561849.1:n.136G>A
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000455552
  ensembl transcript: ENST00000570045
  gene symbol: CORO1A
  hgvsc: ENST00000570045.1:c.9G>A
  hgvsp: ENST00000570045.1:c.9G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000457332
  ensembl transcript: ENST00000570244
  gene symbol: CORO1A
  hgvsc: ENST00000570244.1:c.9G>A
  hgvsp: ENST00000570244.1:c.9G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000569469
  gene symbol: CORO1A
  hgvsc: ENST00000569469.1:n.119G>A
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000568982
  gene symbol: CORO1A
  hgvsc: ENST00000568982.1:n.127G>A
  variant of: http://identifiers.org/hgnc/2252
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1255
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21803
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6785
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28914
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg3Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
population: Other
population: East Asian
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum

16-30196540-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30196540
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30196540
    reference: chr 16
allele count: 1
allele frequency: 8.28953694646617e-6
allele num: 120634
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000569469
  gene symbol: CORO1A
  hgvsc: ENST00000569469.1:n.120C>G
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000455552
  ensembl transcript: ENST00000570045
  gene symbol: CORO1A
  hgvsc: ENST00000570045.1:c.10C>G
  hgvsp: ENSP00000455552.1:p.Gln4Glu
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000457332
  ensembl transcript: ENST00000570244
  gene symbol: CORO1A
  hgvsc: ENST00000570244.1:c.10C>G
  hgvsp: ENSP00000457332.1:p.Gln4Glu
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000568982
  gene symbol: CORO1A
  hgvsc: ENST00000568982.1:n.128C>G
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000568763
  gene symbol: CORO1A
  hgvsc: ENST00000568763.1:n.132C>G
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456756
  ensembl transcript: ENST00000561815
  gene symbol: CORO1A
  hgvsc: ENST00000561815.1:c.118C>G
  hgvsp: ENSP00000456756.1:p.Gln40Glu
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456457
  ensembl transcript: ENST00000565497
  gene symbol: CORO1A
  hgvsc: ENST00000565497.1:c.10C>G
  hgvsp: ENSP00000456457.1:p.Gln4Glu
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000454752
  ensembl transcript: ENST00000569203
  gene symbol: CORO1A
  hgvsc: ENST00000569203.1:c.10C>G
  hgvsp: ENSP00000454752.1:p.Gln4Glu
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456266
  ensembl transcript: ENST00000563778
  gene symbol: CORO1A
  hgvsc: ENST00000563778.1:c.10C>G
  hgvsp: ENSP00000456266.1:p.Gln4Glu
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000219150
  ensembl transcript: ENST00000219150
  gene symbol: CORO1A
  hgvsc: ENST00000219150.5:c.10C>G
  hgvsp: ENSP00000219150.5:p.Gln4Glu
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000457509
  ensembl transcript: ENST00000569970
  gene symbol: CORO1A
  hgvsc: ENST00000569970.1:c.10C>G
  hgvsp: ENSP00000457509.1:p.Gln4Glu
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000566619
  gene symbol: CORO1A
  hgvsc: ENST00000566619.1:n.128C>G
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000561849
  gene symbol: CORO1A
  hgvsc: ENST00000561849.1:n.137C>G
  variant of: http://identifiers.org/hgnc/2252
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6792
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21819
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1255
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28924
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln4Glu
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: DP

16-30196559-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30196559
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30196559
    reference: chr 16
allele count: 1
allele frequency: 8.273214640280627e-6
allele num: 120872
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456756
  ensembl transcript: ENST00000561815
  gene symbol: CORO1A
  hgvsc: ENST00000561815.1:c.137A>G
  hgvsp: ENSP00000456756.1:p.Lys46Arg
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456457
  ensembl transcript: ENST00000565497
  gene symbol: CORO1A
  hgvsc: ENST00000565497.1:c.29A>G
  hgvsp: ENSP00000456457.1:p.Lys10Arg
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000454752
  ensembl transcript: ENST00000569203
  gene symbol: CORO1A
  hgvsc: ENST00000569203.1:c.29A>G
  hgvsp: ENSP00000454752.1:p.Lys10Arg
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000455552
  ensembl transcript: ENST00000570045
  gene symbol: CORO1A
  hgvsc: ENST00000570045.1:c.29A>G
  hgvsp: ENSP00000455552.1:p.Lys10Arg
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000566619
  gene symbol: CORO1A
  hgvsc: ENST00000566619.1:n.147A>G
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000457332
  ensembl transcript: ENST00000570244
  gene symbol: CORO1A
  hgvsc: ENST00000570244.1:c.29A>G
  hgvsp: ENSP00000457332.1:p.Lys10Arg
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000569469
  gene symbol: CORO1A
  hgvsc: ENST00000569469.1:n.139A>G
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000561849
  gene symbol: CORO1A
  hgvsc: ENST00000561849.1:n.156A>G
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000568982
  gene symbol: CORO1A
  hgvsc: ENST00000568982.1:n.147A>G
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000568763
  gene symbol: CORO1A
  hgvsc: ENST00000568763.1:n.151A>G
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000457509
  ensembl transcript: ENST00000569970
  gene symbol: CORO1A
  hgvsc: ENST00000569970.1:c.29A>G
  hgvsp: ENSP00000457509.1:p.Lys10Arg
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000219150
  ensembl transcript: ENST00000219150
  gene symbol: CORO1A
  hgvsc: ENST00000219150.5:c.29A>G
  hgvsp: ENSP00000219150.5:p.Lys10Arg
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456266
  ensembl transcript: ENST00000563778
  gene symbol: CORO1A
  hgvsc: ENST00000563778.1:c.29A>G
  hgvsp: ENSP00000456266.1:p.Lys10Arg
  variant of: http://identifiers.org/hgnc/2252
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6858
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28874
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22090
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1264
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys10Arg
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: A
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: DP

16-30196566-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30196566
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30196566
    reference: chr 16
allele count: 1
allele frequency: 8.271161767381846e-6
allele num: 120902
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000457509
  ensembl transcript: ENST00000569970
  gene symbol: CORO1A
  hgvsc: ENST00000569970.1:c.36C>G
  hgvsp: ENST00000569970.1:c.36C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000454752
  ensembl transcript: ENST00000569203
  gene symbol: CORO1A
  hgvsc: ENST00000569203.1:c.36C>G
  hgvsp: ENST00000569203.1:c.36C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000455552
  ensembl transcript: ENST00000570045
  gene symbol: CORO1A
  hgvsc: ENST00000570045.1:c.36C>G
  hgvsp: ENST00000570045.1:c.36C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000568982
  gene symbol: CORO1A
  hgvsc: ENST00000568982.1:n.154C>G
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000219150
  ensembl transcript: ENST00000219150
  gene symbol: CORO1A
  hgvsc: ENST00000219150.5:c.36C>G
  hgvsp: ENST00000219150.5:c.36C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000561849
  gene symbol: CORO1A
  hgvsc: ENST00000561849.1:n.163C>G
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456756
  ensembl transcript: ENST00000561815
  gene symbol: CORO1A
  hgvsc: ENST00000561815.1:c.144C>G
  hgvsp: ENST00000561815.1:c.144C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000568763
  gene symbol: CORO1A
  hgvsc: ENST00000568763.1:n.158C>G
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456457
  ensembl transcript: ENST00000565497
  gene symbol: CORO1A
  hgvsc: ENST00000565497.1:c.36C>G
  hgvsp: ENST00000565497.1:c.36C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456266
  ensembl transcript: ENST00000563778
  gene symbol: CORO1A
  hgvsc: ENST00000563778.1:c.36C>G
  hgvsp: ENST00000563778.1:c.36C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000457332
  ensembl transcript: ENST00000570244
  gene symbol: CORO1A
  hgvsc: ENST00000570244.1:c.36C>G
  hgvsp: ENST00000570244.1:c.36C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000569469
  gene symbol: CORO1A
  hgvsc: ENST00000569469.1:n.146C>G
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000566619
  gene symbol: CORO1A
  hgvsc: ENST00000566619.1:n.154C>G
  variant of: http://identifiers.org/hgnc/2252
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28834
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22161
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 495
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6864
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg12Arg
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: C
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

16-30196569-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30196569
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30196569
    reference: chr 16
allele count: 1
allele frequency: 8.27034090345204e-6
allele num: 120914
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000568763
  gene symbol: CORO1A
  hgvsc: ENST00000568763.1:n.161C>T
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000455552
  ensembl transcript: ENST00000570045
  gene symbol: CORO1A
  hgvsc: ENST00000570045.1:c.39C>T
  hgvsp: ENST00000570045.1:c.39C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000219150
  ensembl transcript: ENST00000219150
  gene symbol: CORO1A
  hgvsc: ENST00000219150.5:c.39C>T
  hgvsp: ENST00000219150.5:c.39C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000457332
  ensembl transcript: ENST00000570244
  gene symbol: CORO1A
  hgvsc: ENST00000570244.1:c.39C>T
  hgvsp: ENST00000570244.1:c.39C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000454752
  ensembl transcript: ENST00000569203
  gene symbol: CORO1A
  hgvsc: ENST00000569203.1:c.39C>T
  hgvsp: ENST00000569203.1:c.39C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456457
  ensembl transcript: ENST00000565497
  gene symbol: CORO1A
  hgvsc: ENST00000565497.1:c.39C>T
  hgvsp: ENST00000565497.1:c.39C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000561849
  gene symbol: CORO1A
  hgvsc: ENST00000561849.1:n.166C>T
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000566619
  gene symbol: CORO1A
  hgvsc: ENST00000566619.1:n.157C>T
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456266
  ensembl transcript: ENST00000563778
  gene symbol: CORO1A
  hgvsc: ENST00000563778.1:c.39C>T
  hgvsp: ENST00000563778.1:c.39C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000568982
  gene symbol: CORO1A
  hgvsc: ENST00000568982.1:n.157C>T
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456756
  ensembl transcript: ENST00000561815
  gene symbol: CORO1A
  hgvsc: ENST00000561815.1:c.147C>T
  hgvsp: ENST00000561815.1:c.147C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000569469
  gene symbol: CORO1A
  hgvsc: ENST00000569469.1:n.149C>T
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000457509
  ensembl transcript: ENST00000569970
  gene symbol: CORO1A
  hgvsc: ENST00000569970.1:c.39C>T
  hgvsp: ENST00000569970.1:c.39C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2252
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22193
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28809
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6870
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1271
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His13His
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: ClippingRankSum

16-30196572-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30196572
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30196572
    reference: chr 16
allele count: 1
allele frequency: 8.268289456277286e-6
allele num: 120944
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456266
  ensembl transcript: ENST00000563778
  gene symbol: CORO1A
  hgvsc: ENST00000563778.1:c.42G>A
  hgvsp: ENST00000563778.1:c.42G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000455552
  ensembl transcript: ENST00000570045
  gene symbol: CORO1A
  hgvsc: ENST00000570045.1:c.42G>A
  hgvsp: ENST00000570045.1:c.42G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000454752
  ensembl transcript: ENST00000569203
  gene symbol: CORO1A
  hgvsc: ENST00000569203.1:c.42G>A
  hgvsp: ENST00000569203.1:c.42G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000457332
  ensembl transcript: ENST00000570244
  gene symbol: CORO1A
  hgvsc: ENST00000570244.1:c.42G>A
  hgvsp: ENST00000570244.1:c.42G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000457509
  ensembl transcript: ENST00000569970
  gene symbol: CORO1A
  hgvsc: ENST00000569970.1:c.42G>A
  hgvsp: ENST00000569970.1:c.42G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000568982
  gene symbol: CORO1A
  hgvsc: ENST00000568982.1:n.160G>A
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000566619
  gene symbol: CORO1A
  hgvsc: ENST00000566619.1:n.160G>A
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456756
  ensembl transcript: ENST00000561815
  gene symbol: CORO1A
  hgvsc: ENST00000561815.1:c.150G>A
  hgvsp: ENST00000561815.1:c.150G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000219150
  ensembl transcript: ENST00000219150
  gene symbol: CORO1A
  hgvsc: ENST00000219150.5:c.42G>A
  hgvsp: ENST00000219150.5:c.42G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000568763
  gene symbol: CORO1A
  hgvsc: ENST00000568763.1:n.164G>A
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456457
  ensembl transcript: ENST00000565497
  gene symbol: CORO1A
  hgvsc: ENST00000565497.1:c.42G>A
  hgvsp: ENST00000565497.1:c.42G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000569469
  gene symbol: CORO1A
  hgvsc: ENST00000569469.1:n.152G>A
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000561849
  gene symbol: CORO1A
  hgvsc: ENST00000561849.1:n.169G>A
  variant of: http://identifiers.org/hgnc/2252
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6870
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22196
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28818
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Val14Val
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP

16-30196578-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30196578
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30196578
    reference: chr 16
allele count: 1
allele frequency: 8.267742575567167e-6
allele num: 120952
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000568982
  gene symbol: CORO1A
  hgvsc: ENST00000568982.1:n.166A>G
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456756
  ensembl transcript: ENST00000561815
  gene symbol: CORO1A
  hgvsc: ENST00000561815.1:c.156A>G
  hgvsp: ENST00000561815.1:c.156A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000569469
  gene symbol: CORO1A
  hgvsc: ENST00000569469.1:n.158A>G
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000566619
  gene symbol: CORO1A
  hgvsc: ENST00000566619.1:n.166A>G
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000454752
  ensembl transcript: ENST00000569203
  gene symbol: CORO1A
  hgvsc: ENST00000569203.1:c.48A>G
  hgvsp: ENST00000569203.1:c.48A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456457
  ensembl transcript: ENST00000565497
  gene symbol: CORO1A
  hgvsc: ENST00000565497.1:c.48A>G
  hgvsp: ENST00000565497.1:c.48A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000457332
  ensembl transcript: ENST00000570244
  gene symbol: CORO1A
  hgvsc: ENST00000570244.1:c.48A>G
  hgvsp: ENST00000570244.1:c.48A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000457509
  ensembl transcript: ENST00000569970
  gene symbol: CORO1A
  hgvsc: ENST00000569970.1:c.48A>G
  hgvsp: ENST00000569970.1:c.48A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000455552
  ensembl transcript: ENST00000570045
  gene symbol: CORO1A
  hgvsc: ENST00000570045.1:c.48A>G
  hgvsp: ENST00000570045.1:c.48A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000568763
  gene symbol: CORO1A
  hgvsc: ENST00000568763.1:n.170A>G
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000561849
  gene symbol: CORO1A
  hgvsc: ENST00000561849.1:n.175A>G
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000219150
  ensembl transcript: ENST00000219150
  gene symbol: CORO1A
  hgvsc: ENST00000219150.5:c.48A>G
  hgvsp: ENST00000219150.5:c.48A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456266
  ensembl transcript: ENST00000563778
  gene symbol: CORO1A
  hgvsc: ENST00000563778.1:c.48A>G
  hgvsp: ENST00000563778.1:c.48A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2252
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1275
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22213
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6877
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28802
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly16Gly
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: A
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: InbreedingCoeff

16-30196580-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30196580
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30196580
    reference: chr 16
allele count: 1
allele frequency: 8.267742575567167e-6
allele num: 120952
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000561849
  gene symbol: CORO1A
  hgvsc: ENST00000561849.1:n.177A>T
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456756
  ensembl transcript: ENST00000561815
  gene symbol: CORO1A
  hgvsc: ENST00000561815.1:c.158A>T
  hgvsp: ENSP00000456756.1:p.Gln53Leu
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000455552
  ensembl transcript: ENST00000570045
  gene symbol: CORO1A
  hgvsc: ENST00000570045.1:c.50A>T
  hgvsp: ENSP00000455552.1:p.Gln17Leu
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456457
  ensembl transcript: ENST00000565497
  gene symbol: CORO1A
  hgvsc: ENST00000565497.1:c.50A>T
  hgvsp: ENSP00000456457.1:p.Gln17Leu
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000457509
  ensembl transcript: ENST00000569970
  gene symbol: CORO1A
  hgvsc: ENST00000569970.1:c.50A>T
  hgvsp: ENSP00000457509.1:p.Gln17Leu
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000568763
  gene symbol: CORO1A
  hgvsc: ENST00000568763.1:n.172A>T
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000219150
  ensembl transcript: ENST00000219150
  gene symbol: CORO1A
  hgvsc: ENST00000219150.5:c.50A>T
  hgvsp: ENSP00000219150.5:p.Gln17Leu
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000566619
  gene symbol: CORO1A
  hgvsc: ENST00000566619.1:n.168A>T
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000454752
  ensembl transcript: ENST00000569203
  gene symbol: CORO1A
  hgvsc: ENST00000569203.1:c.50A>T
  hgvsp: ENSP00000454752.1:p.Gln17Leu
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000569469
  gene symbol: CORO1A
  hgvsc: ENST00000569469.1:n.160A>T
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000457332
  ensembl transcript: ENST00000570244
  gene symbol: CORO1A
  hgvsc: ENST00000570244.1:c.50A>T
  hgvsp: ENSP00000457332.1:p.Gln17Leu
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456266
  ensembl transcript: ENST00000563778
  gene symbol: CORO1A
  hgvsc: ENST00000563778.1:c.50A>T
  hgvsp: ENSP00000456266.1:p.Gln17Leu
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000568982
  gene symbol: CORO1A
  hgvsc: ENST00000568982.1:n.168A>T
  variant of: http://identifiers.org/hgnc/2252
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6880
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22221
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28795
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln17Leu
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
population: European (Finnish)
population: African
reference allele: A
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: MQ

http://identifiers.org/exac.variant/16-30196593-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30196593
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30196593
    reference: chr 16
allele count: 5
allele frequency: 4.133187845121185e-5
allele num: 120972
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000455552
  ensembl transcript: ENST00000570045
  gene symbol: CORO1A
  hgvsc: ENST00000570045.1:c.63C>A
  hgvsp: ENST00000570045.1:c.63C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000568763
  gene symbol: CORO1A
  hgvsc: ENST00000568763.1:n.185C>A
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000561849
  gene symbol: CORO1A
  hgvsc: ENST00000561849.1:n.190C>A
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000568982
  gene symbol: CORO1A
  hgvsc: ENST00000568982.1:n.181C>A
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456266
  ensembl transcript: ENST00000563778
  gene symbol: CORO1A
  hgvsc: ENST00000563778.1:c.63C>A
  hgvsp: ENST00000563778.1:c.63C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456756
  ensembl transcript: ENST00000561815
  gene symbol: CORO1A
  hgvsc: ENST00000561815.1:c.171C>A
  hgvsp: ENST00000561815.1:c.171C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000566619
  gene symbol: CORO1A
  hgvsc: ENST00000566619.1:n.181C>A
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000457332
  ensembl transcript: ENST00000570244
  gene symbol: CORO1A
  hgvsc: ENST00000570244.1:c.63C>A
  hgvsp: ENST00000570244.1:c.63C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000457509
  ensembl transcript: ENST00000569970
  gene symbol: CORO1A
  hgvsc: ENST00000569970.1:c.63C>A
  hgvsp: ENST00000569970.1:c.63C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456457
  ensembl transcript: ENST00000565497
  gene symbol: CORO1A
  hgvsc: ENST00000565497.1:c.63C>A
  hgvsp: ENST00000565497.1:c.63C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000569469
  gene symbol: CORO1A
  hgvsc: ENST00000569469.1:n.173C>A
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000219150
  ensembl transcript: ENST00000219150
  gene symbol: CORO1A
  hgvsc: ENST00000219150.5:c.63C>A
  hgvsp: ENST00000219150.5:c.63C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000454752
  ensembl transcript: ENST00000569203
  gene symbol: CORO1A
  hgvsc: ENST00000569203.1:c.63C>A
  hgvsp: ENST00000569203.1:c.63C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2252
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28743
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6906
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1275
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Ala21Ala
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: FS

16-30196594-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30196594
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30196594
    reference: chr 16
allele count: 1
allele frequency: 8.266375690242371e-6
allele num: 120972
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000568763
  gene symbol: CORO1A
  hgvsc: ENST00000568763.1:n.186G>A
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000568982
  gene symbol: CORO1A
  hgvsc: ENST00000568982.1:n.182G>A
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456457
  ensembl transcript: ENST00000565497
  gene symbol: CORO1A
  hgvsc: ENST00000565497.1:c.64G>A
  hgvsp: ENSP00000456457.1:p.Asp22Asn
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000457509
  ensembl transcript: ENST00000569970
  gene symbol: CORO1A
  hgvsc: ENST00000569970.1:c.64G>A
  hgvsp: ENSP00000457509.1:p.Asp22Asn
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000561849
  gene symbol: CORO1A
  hgvsc: ENST00000561849.1:n.191G>A
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456756
  ensembl transcript: ENST00000561815
  gene symbol: CORO1A
  hgvsc: ENST00000561815.1:c.172G>A
  hgvsp: ENSP00000456756.1:p.Asp58Asn
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000454752
  ensembl transcript: ENST00000569203
  gene symbol: CORO1A
  hgvsc: ENST00000569203.1:c.64G>A
  hgvsp: ENSP00000454752.1:p.Asp22Asn
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456266
  ensembl transcript: ENST00000563778
  gene symbol: CORO1A
  hgvsc: ENST00000563778.1:c.64G>A
  hgvsp: ENSP00000456266.1:p.Asp22Asn
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000569469
  gene symbol: CORO1A
  hgvsc: ENST00000569469.1:n.174G>A
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000455552
  ensembl transcript: ENST00000570045
  gene symbol: CORO1A
  hgvsc: ENST00000570045.1:c.64G>A
  hgvsp: ENSP00000455552.1:p.Asp22Asn
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000566619
  gene symbol: CORO1A
  hgvsc: ENST00000566619.1:n.182G>A
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000457332
  ensembl transcript: ENST00000570244
  gene symbol: CORO1A
  hgvsc: ENST00000570244.1:c.64G>A
  hgvsp: ENSP00000457332.1:p.Asp22Asn
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000219150
  ensembl transcript: ENST00000219150
  gene symbol: CORO1A
  hgvsc: ENST00000219150.5:c.64G>A
  hgvsp: ENSP00000219150.5:p.Asp22Asn
  variant of: http://identifiers.org/hgnc/2252
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28733
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 495
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1278
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp22Asn
num of homozygotes: 0
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ

16-30196599-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30196599
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30196599
    reference: chr 16
allele count: 1
allele frequency: 8.265555775970376e-6
allele num: 120984
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000569469
  gene symbol: CORO1A
  hgvsc: ENST00000569469.1:n.179G>C
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456266
  ensembl transcript: ENST00000563778
  gene symbol: CORO1A
  hgvsc: ENST00000563778.1:c.69G>C
  hgvsp: ENSP00000456266.1:p.Gln23His
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000457332
  ensembl transcript: ENST00000570244
  gene symbol: CORO1A
  hgvsc: ENST00000570244.1:c.69G>C
  hgvsp: ENSP00000457332.1:p.Gln23His
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000219150
  ensembl transcript: ENST00000219150
  gene symbol: CORO1A
  hgvsc: ENST00000219150.5:c.69G>C
  hgvsp: ENSP00000219150.5:p.Gln23His
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456756
  ensembl transcript: ENST00000561815
  gene symbol: CORO1A
  hgvsc: ENST00000561815.1:c.177G>C
  hgvsp: ENSP00000456756.1:p.Gln59His
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000561849
  gene symbol: CORO1A
  hgvsc: ENST00000561849.1:n.196G>C
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000455552
  ensembl transcript: ENST00000570045
  gene symbol: CORO1A
  hgvsc: ENST00000570045.1:c.69G>C
  hgvsp: ENSP00000455552.1:p.Gln23His
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000566619
  gene symbol: CORO1A
  hgvsc: ENST00000566619.1:n.187G>C
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456457
  ensembl transcript: ENST00000565497
  gene symbol: CORO1A
  hgvsc: ENST00000565497.1:c.69G>C
  hgvsp: ENSP00000456457.1:p.Gln23His
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000454752
  ensembl transcript: ENST00000569203
  gene symbol: CORO1A
  hgvsc: ENST00000569203.1:c.69G>C
  hgvsp: ENSP00000454752.1:p.Gln23His
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000457509
  ensembl transcript: ENST00000569970
  gene symbol: CORO1A
  hgvsc: ENST00000569970.1:c.69G>C
  hgvsp: ENSP00000457509.1:p.Gln23His
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000568763
  gene symbol: CORO1A
  hgvsc: ENST00000568763.1:n.191G>C
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000568982
  gene symbol: CORO1A
  hgvsc: ENST00000568982.1:n.187G>C
  variant of: http://identifiers.org/hgnc/2252
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1277
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28711
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22308
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6904
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln23His
num of homozygotes: 0
population: European (Finnish)
population: Other
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP

16-30196617-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30196617
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30196617
    reference: chr 16
allele count: 5
allele frequency: 4.133666231253823e-5
allele num: 120958
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000568982
  gene symbol: CORO1A
  hgvsc: ENST00000568982.1:n.205C>T
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000455552
  ensembl transcript: ENST00000570045
  gene symbol: CORO1A
  hgvsc: ENST00000570045.1:c.87C>T
  hgvsp: ENST00000570045.1:c.87C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000457332
  ensembl transcript: ENST00000570244
  gene symbol: CORO1A
  hgvsc: ENST00000570244.1:c.87C>T
  hgvsp: ENST00000570244.1:c.87C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000457509
  ensembl transcript: ENST00000569970
  gene symbol: CORO1A
  hgvsc: ENST00000569970.1:c.87C>T
  hgvsp: ENST00000569970.1:c.87C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000568763
  gene symbol: CORO1A
  hgvsc: ENST00000568763.1:n.209C>T
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456457
  ensembl transcript: ENST00000565497
  gene symbol: CORO1A
  hgvsc: ENST00000565497.1:c.87C>T
  hgvsp: ENST00000565497.1:c.87C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000561849
  gene symbol: CORO1A
  hgvsc: ENST00000561849.1:n.214C>T
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000454752
  ensembl transcript: ENST00000569203
  gene symbol: CORO1A
  hgvsc: ENST00000569203.1:c.87C>T
  hgvsp: ENST00000569203.1:c.87C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456756
  ensembl transcript: ENST00000561815
  gene symbol: CORO1A
  hgvsc: ENST00000561815.1:c.195C>T
  hgvsp: ENST00000561815.1:c.195C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000566619
  gene symbol: CORO1A
  hgvsc: ENST00000566619.1:n.205C>T
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456266
  ensembl transcript: ENST00000563778
  gene symbol: CORO1A
  hgvsc: ENST00000563778.1:c.87C>T
  hgvsp: ENST00000563778.1:c.87C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000219150
  ensembl transcript: ENST00000219150
  gene symbol: CORO1A
  hgvsc: ENST00000219150.5:c.87C>T
  hgvsp: ENST00000219150.5:c.87C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000569469
  gene symbol: CORO1A
  hgvsc: ENST00000569469.1:n.197C>T
  variant of: http://identifiers.org/hgnc/2252
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 28656
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6916
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1275
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg29Arg
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum

16-30196618-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30196618
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30196618
    reference: chr 16
allele count: 2
allele frequency: 1.653466492501529e-5
allele num: 120958
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456457
  ensembl transcript: ENST00000565497
  gene symbol: CORO1A
  hgvsc: ENST00000565497.1:c.88G>A
  hgvsp: ENSP00000456457.1:p.Val30Ile
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000566619
  gene symbol: CORO1A
  hgvsc: ENST00000566619.1:n.206G>A
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000568763
  gene symbol: CORO1A
  hgvsc: ENST00000568763.1:n.210G>A
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000561849
  gene symbol: CORO1A
  hgvsc: ENST00000561849.1:n.215G>A
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000219150
  ensembl transcript: ENST00000219150
  gene symbol: CORO1A
  hgvsc: ENST00000219150.5:c.88G>A
  hgvsp: ENSP00000219150.5:p.Val30Ile
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000457332
  ensembl transcript: ENST00000570244
  gene symbol: CORO1A
  hgvsc: ENST00000570244.1:c.88G>A
  hgvsp: ENSP00000457332.1:p.Val30Ile
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000455552
  ensembl transcript: ENST00000570045
  gene symbol: CORO1A
  hgvsc: ENST00000570045.1:c.88G>A
  hgvsp: ENSP00000455552.1:p.Val30Ile
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000457509
  ensembl transcript: ENST00000569970
  gene symbol: CORO1A
  hgvsc: ENST00000569970.1:c.88G>A
  hgvsp: ENSP00000457509.1:p.Val30Ile
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000568982
  gene symbol: CORO1A
  hgvsc: ENST00000568982.1:n.206G>A
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456266
  ensembl transcript: ENST00000563778
  gene symbol: CORO1A
  hgvsc: ENST00000563778.1:c.88G>A
  hgvsp: ENSP00000456266.1:p.Val30Ile
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000454752
  ensembl transcript: ENST00000569203
  gene symbol: CORO1A
  hgvsc: ENST00000569203.1:c.88G>A
  hgvsp: ENSP00000454752.1:p.Val30Ile
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000569469
  gene symbol: CORO1A
  hgvsc: ENST00000569469.1:n.198G>A
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456756
  ensembl transcript: ENST00000561815
  gene symbol: CORO1A
  hgvsc: ENST00000561815.1:c.196G>A
  hgvsp: ENSP00000456756.1:p.Val66Ile
  variant of: http://identifiers.org/hgnc/2252
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22358
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1279
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28641
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6921
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 497
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val30Ile
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/16-30196625-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30196625
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30196625
    reference: chr 16
allele count: 1
allele frequency: 8.268836409340477e-6
allele num: 120936
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000455552
  ensembl transcript: ENST00000570045
  gene symbol: CORO1A
  hgvsc: ENST00000570045.1:c.95A>C
  hgvsp: ENSP00000455552.1:p.Gln32Pro
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000454752
  ensembl transcript: ENST00000569203
  gene symbol: CORO1A
  hgvsc: ENST00000569203.1:c.95A>C
  hgvsp: ENSP00000454752.1:p.Gln32Pro
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456756
  ensembl transcript: ENST00000561815
  gene symbol: CORO1A
  hgvsc: ENST00000561815.1:c.203A>C
  hgvsp: ENSP00000456756.1:p.Gln68Pro
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000457332
  ensembl transcript: ENST00000570244
  gene symbol: CORO1A
  hgvsc: ENST00000570244.1:c.95A>C
  hgvsp: ENSP00000457332.1:p.Gln32Pro
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000219150
  ensembl transcript: ENST00000219150
  gene symbol: CORO1A
  hgvsc: ENST00000219150.5:c.95A>C
  hgvsp: ENSP00000219150.5:p.Gln32Pro
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456457
  ensembl transcript: ENST00000565497
  gene symbol: CORO1A
  hgvsc: ENST00000565497.1:c.95A>C
  hgvsp: ENSP00000456457.1:p.Gln32Pro
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000561849
  gene symbol: CORO1A
  hgvsc: ENST00000561849.1:n.222A>C
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000457509
  ensembl transcript: ENST00000569970
  gene symbol: CORO1A
  hgvsc: ENST00000569970.1:c.95A>C
  hgvsp: ENSP00000457509.1:p.Gln32Pro
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456266
  ensembl transcript: ENST00000563778
  gene symbol: CORO1A
  hgvsc: ENST00000563778.1:c.95A>C
  hgvsp: ENSP00000456266.1:p.Gln32Pro
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000569469
  gene symbol: CORO1A
  hgvsc: ENST00000569469.1:n.205A>C
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000568982
  gene symbol: CORO1A
  hgvsc: ENST00000568982.1:n.213A>C
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000566619
  gene symbol: CORO1A
  hgvsc: ENST00000566619.1:n.213A>C
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000568763
  gene symbol: CORO1A
  hgvsc: ENST00000568763.1:n.217A>C
  variant of: http://identifiers.org/hgnc/2252
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28593
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22366
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1279
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 495
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln32Pro
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: A
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum

16-30196647-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30196647
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30196647
    reference: chr 16
allele count: 3
allele frequency: 2.506140043105609e-5
allele num: 119706
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000569469
  gene symbol: CORO1A
  hgvsc: ENST00000569469.1:n.227C>T
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456266
  ensembl transcript: ENST00000563778
  gene symbol: CORO1A
  hgvsc: ENST00000563778.1:c.117C>T
  hgvsp: ENST00000563778.1:c.117C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456457
  ensembl transcript: ENST00000565497
  gene symbol: CORO1A
  hgvsc: ENST00000565497.1:c.117C>T
  hgvsp: ENST00000565497.1:c.117C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000454752
  ensembl transcript: ENST00000569203
  gene symbol: CORO1A
  hgvsc: ENST00000569203.1:c.117C>T
  hgvsp: ENST00000569203.1:c.117C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000455552
  ensembl transcript: ENST00000570045
  gene symbol: CORO1A
  hgvsc: ENST00000570045.1:c.117C>T
  hgvsp: ENST00000570045.1:c.117C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456756
  ensembl transcript: ENST00000561815
  gene symbol: CORO1A
  hgvsc: ENST00000561815.1:c.225C>T
  hgvsp: ENST00000561815.1:c.225C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000566619
  gene symbol: CORO1A
  hgvsc: ENST00000566619.1:n.235C>T
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000561849
  gene symbol: CORO1A
  hgvsc: ENST00000561849.1:n.244C>T
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000457332
  ensembl transcript: ENST00000570244
  gene symbol: CORO1A
  hgvsc: ENST00000570244.1:c.117C>T
  hgvsp: ENST00000570244.1:c.117C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000219150
  ensembl transcript: ENST00000219150
  gene symbol: CORO1A
  hgvsc: ENST00000219150.5:c.117C>T
  hgvsp: ENST00000219150.5:c.117C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000457509
  ensembl transcript: ENST00000569970
  gene symbol: CORO1A
  hgvsc: ENST00000569970.1:c.117C>T
  hgvsp: ENST00000569970.1:c.117C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000568982
  gene symbol: CORO1A
  hgvsc: ENST00000568982.1:n.235C>T
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000568763
  gene symbol: CORO1A
  hgvsc: ENST00000568763.1:n.239C>T
  variant of: http://identifiers.org/hgnc/2252
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.95to100.00
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1258
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28146
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22152
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Phe39Phe
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum

16-30196655-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30196655
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30196655
    reference: chr 16
allele count: 1
allele frequency: 8.281573498964803e-6
allele num: 120750
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000568763
  gene symbol: CORO1A
  hgvsc: ENST00000568763.1:n.247T>C
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456756
  ensembl transcript: ENST00000561815
  gene symbol: CORO1A
  hgvsc: ENST00000561815.1:c.233T>C
  hgvsp: ENSP00000456756.1:p.Val78Ala
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456266
  ensembl transcript: ENST00000563778
  gene symbol: CORO1A
  hgvsc: ENST00000563778.1:c.125T>C
  hgvsp: ENSP00000456266.1:p.Val42Ala
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000561849
  gene symbol: CORO1A
  hgvsc: ENST00000561849.1:n.252T>C
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000455552
  ensembl transcript: ENST00000570045
  gene symbol: CORO1A
  hgvsc: ENST00000570045.1:c.125T>C
  hgvsp: ENSP00000455552.1:p.Val42Ala
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000569469
  gene symbol: CORO1A
  hgvsc: ENST00000569469.1:n.235T>C
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000457509
  ensembl transcript: ENST00000569970
  gene symbol: CORO1A
  hgvsc: ENST00000569970.1:c.125T>C
  hgvsp: ENSP00000457509.1:p.Val42Ala
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000566619
  gene symbol: CORO1A
  hgvsc: ENST00000566619.1:n.243T>C
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456457
  ensembl transcript: ENST00000565497
  gene symbol: CORO1A
  hgvsc: ENST00000565497.1:c.125T>C
  hgvsp: ENSP00000456457.1:p.Val42Ala
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000457332
  ensembl transcript: ENST00000570244
  gene symbol: CORO1A
  hgvsc: ENST00000570244.1:c.125T>C
  hgvsp: ENSP00000457332.1:p.Val42Ala
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000454752
  ensembl transcript: ENST00000569203
  gene symbol: CORO1A
  hgvsc: ENST00000569203.1:c.125T>C
  hgvsp: ENSP00000454752.1:p.Val42Ala
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000219150
  ensembl transcript: ENST00000219150
  gene symbol: CORO1A
  hgvsc: ENST00000219150.5:c.125T>C
  hgvsp: ENSP00000219150.5:p.Val42Ala
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000568982
  gene symbol: CORO1A
  hgvsc: ENST00000568982.1:n.243T>C
  variant of: http://identifiers.org/hgnc/2252
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 22513
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6949
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28300
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val42Ala
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
population: Other
population: Latino
reference allele: T
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum

16-30196686-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30196686
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30196686
    reference: chr 16
allele count: 4
allele frequency: 3.328728592114242e-5
allele num: 120166
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000454752
  ensembl transcript: ENST00000569203
  gene symbol: CORO1A
  hgvsc: ENST00000569203.1:c.156G>C
  hgvsp: ENSP00000454752.1:p.Glu52Asp
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000219150
  ensembl transcript: ENST00000219150
  gene symbol: CORO1A
  hgvsc: ENST00000219150.5:c.156G>C
  hgvsp: ENSP00000219150.5:p.Glu52Asp
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000457509
  ensembl transcript: ENST00000569970
  gene symbol: CORO1A
  hgvsc: ENST00000569970.1:c.156G>C
  hgvsp: ENSP00000457509.1:p.Glu52Asp
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000455552
  ensembl transcript: ENST00000570045
  gene symbol: CORO1A
  hgvsc: ENST00000570045.1:c.156G>C
  hgvsp: ENSP00000455552.1:p.Glu52Asp
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000568763
  gene symbol: CORO1A
  hgvsc: ENST00000568763.1:n.278G>C
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000561849
  gene symbol: CORO1A
  hgvsc: ENST00000561849.1:n.283G>C
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000566619
  gene symbol: CORO1A
  hgvsc: ENST00000566619.1:n.274G>C
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000457332
  ensembl transcript: ENST00000570244
  gene symbol: CORO1A
  hgvsc: ENST00000570244.1:c.156G>C
  hgvsp: ENSP00000457332.1:p.Glu52Asp
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456756
  ensembl transcript: ENST00000561815
  gene symbol: CORO1A
  hgvsc: ENST00000561815.1:c.264G>C
  hgvsp: ENSP00000456756.1:p.Glu88Asp
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456266
  ensembl transcript: ENST00000563778
  gene symbol: CORO1A
  hgvsc: ENST00000563778.1:c.156G>C
  hgvsp: ENSP00000456266.1:p.Glu52Asp
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456457
  ensembl transcript: ENST00000565497
  gene symbol: CORO1A
  hgvsc: ENST00000565497.1:c.156G>C
  hgvsp: ENSP00000456457.1:p.Glu52Asp
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000569469
  gene symbol: CORO1A
  hgvsc: ENST00000569469.1:n.266G>C
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000568982
  gene symbol: CORO1A
  hgvsc: ENST00000568982.1:n.274G>C
  variant of: http://identifiers.org/hgnc/2252
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27703
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22391
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 647
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6923
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu52Asp
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: G
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD

16-30196690-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30196690
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30196690
    reference: chr 16
allele count: 1
allele frequency: 8.328058896032513e-6
allele num: 120076
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000568763
  gene symbol: CORO1A
  hgvsc: ENST00000568763.1:n.282A>T
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456457
  ensembl transcript: ENST00000565497
  gene symbol: CORO1A
  hgvsc: ENST00000565497.1:c.160A>T
  hgvsp: ENSP00000456457.1:p.Ser54Cys
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000219150
  ensembl transcript: ENST00000219150
  gene symbol: CORO1A
  hgvsc: ENST00000219150.5:c.160A>T
  hgvsp: ENSP00000219150.5:p.Ser54Cys
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456266
  ensembl transcript: ENST00000563778
  gene symbol: CORO1A
  hgvsc: ENST00000563778.1:c.160A>T
  hgvsp: ENSP00000456266.1:p.Ser54Cys
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456756
  ensembl transcript: ENST00000561815
  gene symbol: CORO1A
  hgvsc: ENST00000561815.1:c.268A>T
  hgvsp: ENSP00000456756.1:p.Ser90Cys
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000455552
  ensembl transcript: ENST00000570045
  gene symbol: CORO1A
  hgvsc: ENST00000570045.1:c.160A>T
  hgvsp: ENSP00000455552.1:p.Ser54Cys
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000457332
  ensembl transcript: ENST00000570244
  gene symbol: CORO1A
  hgvsc: ENST00000570244.1:c.160A>T
  hgvsp: ENSP00000457332.1:p.Ser54Cys
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000566619
  gene symbol: CORO1A
  hgvsc: ENST00000566619.1:n.278A>T
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000568982
  gene symbol: CORO1A
  hgvsc: ENST00000568982.1:n.278A>T
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000454752
  ensembl transcript: ENST00000569203
  gene symbol: CORO1A
  hgvsc: ENST00000569203.1:c.160A>T
  hgvsp: ENSP00000454752.1:p.Ser54Cys
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000569469
  gene symbol: CORO1A
  hgvsc: ENST00000569469.1:n.270A>T
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000457509
  ensembl transcript: ENST00000569970
  gene symbol: CORO1A
  hgvsc: ENST00000569970.1:c.160A>T
  hgvsp: ENSP00000457509.1:p.Ser54Cys
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000561849
  gene symbol: CORO1A
  hgvsc: ENST00000561849.1:n.287A>T
  variant of: http://identifiers.org/hgnc/2252
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 548
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22372
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 689
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6907
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27660
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser54Cys
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum

16-30196692-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30196692
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30196692
    reference: chr 16
allele count: 1
allele frequency: 8.334861391255063e-6
allele num: 119978
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000561849
  gene symbol: CORO1A
  hgvsc: ENST00000561849.1:n.289C>T
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000457509
  ensembl transcript: ENST00000569970
  gene symbol: CORO1A
  hgvsc: ENST00000569970.1:c.162C>T
  hgvsp: ENST00000569970.1:c.162C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000457332
  ensembl transcript: ENST00000570244
  gene symbol: CORO1A
  hgvsc: ENST00000570244.1:c.162C>T
  hgvsp: ENST00000570244.1:c.162C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456266
  ensembl transcript: ENST00000563778
  gene symbol: CORO1A
  hgvsc: ENST00000563778.1:c.162C>T
  hgvsp: ENST00000563778.1:c.162C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000566619
  gene symbol: CORO1A
  hgvsc: ENST00000566619.1:n.280C>T
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000569469
  gene symbol: CORO1A
  hgvsc: ENST00000569469.1:n.272C>T
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000219150
  ensembl transcript: ENST00000219150
  gene symbol: CORO1A
  hgvsc: ENST00000219150.5:c.162C>T
  hgvsp: ENST00000219150.5:c.162C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456756
  ensembl transcript: ENST00000561815
  gene symbol: CORO1A
  hgvsc: ENST00000561815.1:c.270C>T
  hgvsp: ENST00000561815.1:c.270C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456457
  ensembl transcript: ENST00000565497
  gene symbol: CORO1A
  hgvsc: ENST00000565497.1:c.162C>T
  hgvsp: ENST00000565497.1:c.162C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000455552
  ensembl transcript: ENST00000570045
  gene symbol: CORO1A
  hgvsc: ENST00000570045.1:c.162C>T
  hgvsp: ENST00000570045.1:c.162C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000568982
  gene symbol: CORO1A
  hgvsc: ENST00000568982.1:n.280C>T
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000454752
  ensembl transcript: ENST00000569203
  gene symbol: CORO1A
  hgvsc: ENST00000569203.1:c.162C>T
  hgvsp: ENST00000569203.1:c.162C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000568763
  gene symbol: CORO1A
  hgvsc: ENST00000568763.1:n.284C>T
  variant of: http://identifiers.org/hgnc/2252
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27581
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6910
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22336
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 731
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser54Ser
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: East Asian
population: South Asian
population: Latino
reference allele: C
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum

16-30196698-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30196698
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30196698
    reference: chr 16
allele count: 2
allele frequency: 1.670090351888037e-5
allele num: 119754
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000455552
  ensembl transcript: ENST00000570045
  gene symbol: CORO1A
  hgvsc: ENST00000570045.1:c.168A>G
  hgvsp: ENST00000570045.1:c.168A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000568982
  gene symbol: CORO1A
  hgvsc: ENST00000568982.1:n.286A>G
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000561849
  gene symbol: CORO1A
  hgvsc: ENST00000561849.1:n.295A>G
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456457
  ensembl transcript: ENST00000565497
  gene symbol: CORO1A
  hgvsc: ENST00000565497.1:c.168A>G
  hgvsp: ENST00000565497.1:c.168A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000457509
  ensembl transcript: ENST00000569970
  gene symbol: CORO1A
  hgvsc: ENST00000569970.1:c.168A>G
  hgvsp: ENST00000569970.1:c.168A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000219150
  ensembl transcript: ENST00000219150
  gene symbol: CORO1A
  hgvsc: ENST00000219150.5:c.168A>G
  hgvsp: ENST00000219150.5:c.168A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456266
  ensembl transcript: ENST00000563778
  gene symbol: CORO1A
  hgvsc: ENST00000563778.1:c.168A>G
  hgvsp: ENST00000563778.1:c.168A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000454752
  ensembl transcript: ENST00000569203
  gene symbol: CORO1A
  hgvsc: ENST00000569203.1:c.168A>G
  hgvsp: ENST00000569203.1:c.168A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000569469
  gene symbol: CORO1A
  hgvsc: ENST00000569469.1:n.278A>G
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456756
  ensembl transcript: ENST00000561815
  gene symbol: CORO1A
  hgvsc: ENST00000561815.1:c.276A>G
  hgvsp: ENST00000561815.1:c.276A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000566619
  gene symbol: CORO1A
  hgvsc: ENST00000566619.1:n.286A>G
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000457332
  ensembl transcript: ENST00000570244
  gene symbol: CORO1A
  hgvsc: ENST00000570244.1:c.168A>G
  hgvsp: ENST00000570244.1:c.168A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000568763
  gene symbol: CORO1A
  hgvsc: ENST00000568763.1:n.290A>G
  variant of: http://identifiers.org/hgnc/2252
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1221
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27359
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 889
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 685
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly56Gly
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: DP

16-30196701-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30196701
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30196701
    reference: chr 16
allele count: 1
allele frequency: 8.362742310458446e-6
allele num: 119578
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000566619
  gene symbol: CORO1A
  hgvsc: ENST00000566619.1:n.289G>A
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456756
  ensembl transcript: ENST00000561815
  gene symbol: CORO1A
  hgvsc: ENST00000561815.1:c.279G>A
  hgvsp: ENST00000561815.1:c.279G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000457509
  ensembl transcript: ENST00000569970
  gene symbol: CORO1A
  hgvsc: ENST00000569970.1:c.171G>A
  hgvsp: ENST00000569970.1:c.171G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000219150
  ensembl transcript: ENST00000219150
  gene symbol: CORO1A
  hgvsc: ENST00000219150.5:c.171G>A
  hgvsp: ENST00000219150.5:c.171G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000561849
  gene symbol: CORO1A
  hgvsc: ENST00000561849.1:n.298G>A
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000568982
  gene symbol: CORO1A
  hgvsc: ENST00000568982.1:n.289G>A
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000457332
  ensembl transcript: ENST00000570244
  gene symbol: CORO1A
  hgvsc: ENST00000570244.1:c.171G>A
  hgvsp: ENST00000570244.1:c.171G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000455552
  ensembl transcript: ENST00000570045
  gene symbol: CORO1A
  hgvsc: ENST00000570045.1:c.171G>A
  hgvsp: ENST00000570045.1:c.171G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000454752
  ensembl transcript: ENST00000569203
  gene symbol: CORO1A
  hgvsc: ENST00000569203.1:c.171G>A
  hgvsp: ENST00000569203.1:c.171G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456457
  ensembl transcript: ENST00000565497
  gene symbol: CORO1A
  hgvsc: ENST00000565497.1:c.171G>A
  hgvsp: ENST00000565497.1:c.171G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000569469
  gene symbol: CORO1A
  hgvsc: ENST00000569469.1:n.281G>A
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000568763
  gene symbol: CORO1A
  hgvsc: ENST00000568763.1:n.293G>A
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456266
  ensembl transcript: ENST00000563778
  gene symbol: CORO1A
  hgvsc: ENST00000563778.1:c.171G>A
  hgvsp: ENST00000563778.1:c.171G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2252
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 779
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22249
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27112
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1062
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6870
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly57Gly
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: DP

16-30196701-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30196701
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30196701
    reference: chr 16
allele count: 1
allele frequency: 8.362742310458446e-6
allele num: 119578
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456457
  ensembl transcript: ENST00000565497
  gene symbol: CORO1A
  hgvsc: ENST00000565497.1:c.171G>T
  hgvsp: ENST00000565497.1:c.171G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000568763
  gene symbol: CORO1A
  hgvsc: ENST00000568763.1:n.293G>T
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000454752
  ensembl transcript: ENST00000569203
  gene symbol: CORO1A
  hgvsc: ENST00000569203.1:c.171G>T
  hgvsp: ENST00000569203.1:c.171G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000457332
  ensembl transcript: ENST00000570244
  gene symbol: CORO1A
  hgvsc: ENST00000570244.1:c.171G>T
  hgvsp: ENST00000570244.1:c.171G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000569469
  gene symbol: CORO1A
  hgvsc: ENST00000569469.1:n.281G>T
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000566619
  gene symbol: CORO1A
  hgvsc: ENST00000566619.1:n.289G>T
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000457509
  ensembl transcript: ENST00000569970
  gene symbol: CORO1A
  hgvsc: ENST00000569970.1:c.171G>T
  hgvsp: ENST00000569970.1:c.171G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000219150
  ensembl transcript: ENST00000219150
  gene symbol: CORO1A
  hgvsc: ENST00000219150.5:c.171G>T
  hgvsp: ENST00000219150.5:c.171G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456756
  ensembl transcript: ENST00000561815
  gene symbol: CORO1A
  hgvsc: ENST00000561815.1:c.279G>T
  hgvsp: ENST00000561815.1:c.279G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000568982
  gene symbol: CORO1A
  hgvsc: ENST00000568982.1:n.289G>T
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000455552
  ensembl transcript: ENST00000570045
  gene symbol: CORO1A
  hgvsc: ENST00000570045.1:c.171G>T
  hgvsp: ENST00000570045.1:c.171G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456266
  ensembl transcript: ENST00000563778
  gene symbol: CORO1A
  hgvsc: ENST00000563778.1:c.171G>T
  hgvsp: ENST00000563778.1:c.171G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000561849
  gene symbol: CORO1A
  hgvsc: ENST00000561849.1:n.298G>T
  variant of: http://identifiers.org/hgnc/2252
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 779
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6870
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22249
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27112
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly57Gly
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD

16-30196702-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30196702
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30196702
    reference: chr 16
allele count: 1
allele frequency: 8.363581620193032e-6
allele num: 119566
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000454752
  ensembl transcript: ENST00000569203
  gene symbol: CORO1A
  hgvsc: ENST00000569203.1:c.172G>T
  hgvsp: ENSP00000454752.1:p.Ala58Ser
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456756
  ensembl transcript: ENST00000561815
  gene symbol: CORO1A
  hgvsc: ENST00000561815.1:c.280G>T
  hgvsp: ENSP00000456756.1:p.Ala94Ser
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000569469
  gene symbol: CORO1A
  hgvsc: ENST00000569469.1:n.282G>T
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000561849
  gene symbol: CORO1A
  hgvsc: ENST00000561849.1:n.299G>T
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456457
  ensembl transcript: ENST00000565497
  gene symbol: CORO1A
  hgvsc: ENST00000565497.1:c.172G>T
  hgvsp: ENSP00000456457.1:p.Ala58Ser
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000568763
  gene symbol: CORO1A
  hgvsc: ENST00000568763.1:n.294G>T
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000566619
  gene symbol: CORO1A
  hgvsc: ENST00000566619.1:n.290G>T
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000568982
  gene symbol: CORO1A
  hgvsc: ENST00000568982.1:n.290G>T
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000455552
  ensembl transcript: ENST00000570045
  gene symbol: CORO1A
  hgvsc: ENST00000570045.1:c.172G>T
  hgvsp: ENSP00000455552.1:p.Ala58Ser
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456266
  ensembl transcript: ENST00000563778
  gene symbol: CORO1A
  hgvsc: ENST00000563778.1:c.172G>T
  hgvsp: ENSP00000456266.1:p.Ala58Ser
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000219150
  ensembl transcript: ENST00000219150
  gene symbol: CORO1A
  hgvsc: ENST00000219150.5:c.172G>T
  hgvsp: ENSP00000219150.5:p.Ala58Ser
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000457509
  ensembl transcript: ENST00000569970
  gene symbol: CORO1A
  hgvsc: ENST00000569970.1:c.172G>T
  hgvsp: ENSP00000457509.1:p.Ala58Ser
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000457332
  ensembl transcript: ENST00000570244
  gene symbol: CORO1A
  hgvsc: ENST00000570244.1:c.172G>T
  hgvsp: ENSP00000457332.1:p.Ala58Ser
  variant of: http://identifiers.org/hgnc/2252
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6870
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22279
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27079
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1070
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 780
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1219
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala58Ser
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: South Asian
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: VQSLOD

16-30196712-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30196712
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30196712
    reference: chr 16
allele count: 1
allele frequency: 8.431703204047217e-6
allele num: 118600
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000569469
  gene symbol: CORO1A
  hgvsc: ENST00000569469.1:n.292T>C
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456756
  ensembl transcript: ENST00000561815
  gene symbol: CORO1A
  hgvsc: ENST00000561815.1:c.290T>C
  hgvsp: ENSP00000456756.1:p.Val97Ala
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456457
  ensembl transcript: ENST00000565497
  gene symbol: CORO1A
  hgvsc: ENST00000565497.1:c.182T>C
  hgvsp: ENSP00000456457.1:p.Val61Ala
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000454752
  ensembl transcript: ENST00000569203
  gene symbol: CORO1A
  hgvsc: ENST00000569203.1:c.182T>C
  hgvsp: ENSP00000454752.1:p.Val61Ala
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000568982
  gene symbol: CORO1A
  hgvsc: ENST00000568982.1:n.300T>C
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000219150
  ensembl transcript: ENST00000219150
  gene symbol: CORO1A
  hgvsc: ENST00000219150.5:c.182T>C
  hgvsp: ENSP00000219150.5:p.Val61Ala
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000457332
  ensembl transcript: ENST00000570244
  gene symbol: CORO1A
  hgvsc: ENST00000570244.1:c.182T>C
  hgvsp: ENSP00000457332.1:p.Val61Ala
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000457509
  ensembl transcript: ENST00000569970
  gene symbol: CORO1A
  hgvsc: ENST00000569970.1:c.182T>C
  hgvsp: ENSP00000457509.1:p.Val61Ala
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000566619
  gene symbol: CORO1A
  hgvsc: ENST00000566619.1:n.300T>C
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456266
  ensembl transcript: ENST00000563778
  gene symbol: CORO1A
  hgvsc: ENST00000563778.1:c.182T>C
  hgvsp: ENSP00000456266.1:p.Val61Ala
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000455552
  ensembl transcript: ENST00000570045
  gene symbol: CORO1A
  hgvsc: ENST00000570045.1:c.182T>C
  hgvsp: ENSP00000455552.1:p.Val61Ala
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000568763
  gene symbol: CORO1A
  hgvsc: ENST00000568763.1:n.304T>C
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000561849
  gene symbol: CORO1A
  hgvsc: ENST00000561849.1:n.309T>C
  variant of: http://identifiers.org/hgnc/2252
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1841
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6782
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26133
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val61Ala
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: T
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD

16-30196713-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30196713
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30196713
    reference: chr 16
allele count: 1
allele frequency: 8.442095665828085e-6
allele num: 118454
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000568763
  gene symbol: CORO1A
  hgvsc: ENST00000568763.1:n.305G>A
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000455552
  ensembl transcript: ENST00000570045
  gene symbol: CORO1A
  hgvsc: ENST00000570045.1:c.183G>A
  hgvsp: ENST00000570045.1:c.183G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000457332
  ensembl transcript: ENST00000570244
  gene symbol: CORO1A
  hgvsc: ENST00000570244.1:c.183G>A
  hgvsp: ENST00000570244.1:c.183G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000457509
  ensembl transcript: ENST00000569970
  gene symbol: CORO1A
  hgvsc: ENST00000569970.1:c.183G>A
  hgvsp: ENST00000569970.1:c.183G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000561849
  gene symbol: CORO1A
  hgvsc: ENST00000561849.1:n.310G>A
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456457
  ensembl transcript: ENST00000565497
  gene symbol: CORO1A
  hgvsc: ENST00000565497.1:c.183G>A
  hgvsp: ENST00000565497.1:c.183G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000566619
  gene symbol: CORO1A
  hgvsc: ENST00000566619.1:n.301G>A
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456756
  ensembl transcript: ENST00000561815
  gene symbol: CORO1A
  hgvsc: ENST00000561815.1:c.291G>A
  hgvsp: ENST00000561815.1:c.291G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000219150
  ensembl transcript: ENST00000219150
  gene symbol: CORO1A
  hgvsc: ENST00000219150.5:c.183G>A
  hgvsp: ENST00000219150.5:c.183G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456266
  ensembl transcript: ENST00000563778
  gene symbol: CORO1A
  hgvsc: ENST00000563778.1:c.183G>A
  hgvsp: ENST00000563778.1:c.183G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000454752
  ensembl transcript: ENST00000569203
  gene symbol: CORO1A
  hgvsc: ENST00000569203.1:c.183G>A
  hgvsp: ENST00000569203.1:c.183G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000568982
  gene symbol: CORO1A
  hgvsc: ENST00000568982.1:n.301G>A
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000569469
  gene symbol: CORO1A
  hgvsc: ENST00000569469.1:n.293G>A
  variant of: http://identifiers.org/hgnc/2252
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1939
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21831
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6796
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1289
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25936
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1220
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val61Val
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
population: East Asian
reference allele: G
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: QD

16-30196714-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30196714
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30196714
    reference: chr 16
allele count: 2
allele frequency: 1.688618709895306e-5
allele num: 118440
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000566619
  gene symbol: CORO1A
  hgvsc: ENST00000566619.1:n.302C>T
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000568763
  gene symbol: CORO1A
  hgvsc: ENST00000568763.1:n.306C>T
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000457332
  ensembl transcript: ENST00000570244
  gene symbol: CORO1A
  hgvsc: ENST00000570244.1:c.184C>T
  hgvsp: ENST00000570244.1:c.184C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456756
  ensembl transcript: ENST00000561815
  gene symbol: CORO1A
  hgvsc: ENST00000561815.1:c.292C>T
  hgvsp: ENST00000561815.1:c.292C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456457
  ensembl transcript: ENST00000565497
  gene symbol: CORO1A
  hgvsc: ENST00000565497.1:c.184C>T
  hgvsp: ENST00000565497.1:c.184C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000561849
  gene symbol: CORO1A
  hgvsc: ENST00000561849.1:n.311C>T
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456266
  ensembl transcript: ENST00000563778
  gene symbol: CORO1A
  hgvsc: ENST00000563778.1:c.184C>T
  hgvsp: ENST00000563778.1:c.184C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000455552
  ensembl transcript: ENST00000570045
  gene symbol: CORO1A
  hgvsc: ENST00000570045.1:c.184C>T
  hgvsp: ENST00000570045.1:c.184C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000569469
  gene symbol: CORO1A
  hgvsc: ENST00000569469.1:n.294C>T
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000568982
  gene symbol: CORO1A
  hgvsc: ENST00000568982.1:n.302C>T
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000457509
  ensembl transcript: ENST00000569970
  gene symbol: CORO1A
  hgvsc: ENST00000569970.1:c.184C>T
  hgvsp: ENST00000569970.1:c.184C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000219150
  ensembl transcript: ENST00000219150
  gene symbol: CORO1A
  hgvsc: ENST00000219150.5:c.184C>T
  hgvsp: ENST00000219150.5:c.184C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000454752
  ensembl transcript: ENST00000569203
  gene symbol: CORO1A
  hgvsc: ENST00000569203.1:c.184C>T
  hgvsp: ENST00000569203.1:c.184C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2252
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1947
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21835
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1220
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25927
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1292
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6797
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu62Leu
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
population: Other
population: East Asian
reference allele: C
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ

16-30196731-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30196731
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30196731
    reference: chr 16
allele count: 2
allele frequency: 1.757098678661794e-5
allele num: 113824
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000454752
  ensembl transcript: ENST00000569203
  gene symbol: CORO1A
  hgvsc: ENST00000569203.1:c.198+3G>T
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456457
  ensembl transcript: ENST00000565497
  gene symbol: CORO1A
  hgvsc: ENST00000565497.1:c.198+3G>T
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000568982
  gene symbol: CORO1A
  hgvsc: ENST00000568982.1:n.316+3G>T
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000457332
  ensembl transcript: ENST00000570244
  gene symbol: CORO1A
  hgvsc: ENST00000570244.1:c.198+3G>T
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000455552
  ensembl transcript: ENST00000570045
  gene symbol: CORO1A
  hgvsc: ENST00000570045.1:c.198+3G>T
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000566619
  gene symbol: CORO1A
  hgvsc: ENST00000566619.1:n.316+3G>T
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000569469
  gene symbol: CORO1A
  hgvsc: ENST00000569469.1:n.308+3G>T
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000568763
  gene symbol: CORO1A
  hgvsc: ENST00000568763.1:n.323G>T
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456756
  ensembl transcript: ENST00000561815
  gene symbol: CORO1A
  hgvsc: ENST00000561815.1:c.306+3G>T
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456266
  ensembl transcript: ENST00000563778
  gene symbol: CORO1A
  hgvsc: ENST00000563778.1:c.198+3G>T
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000457509
  ensembl transcript: ENST00000569970
  gene symbol: CORO1A
  hgvsc: ENST00000569970.1:c.198+3G>T
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000561849
  gene symbol: CORO1A
  hgvsc: ENST00000561849.1:n.328G>T
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000219150
  ensembl transcript: ENST00000219150
  gene symbol: CORO1A
  hgvsc: ENST00000219150.5:c.198+3G>T
  variant of: http://identifiers.org/hgnc/2252
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19578
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6291
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2022
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3331
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20213
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6784
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.198+3G>T
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Latino
reference allele: G
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD

16-30196736-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30196736
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30196736
    reference: chr 16
allele count: 1
allele frequency: 9.027226113959703e-6
allele num: 110776
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000569469
  gene symbol: CORO1A
  hgvsc: ENST00000569469.1:n.308+8C>T
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000566619
  gene symbol: CORO1A
  hgvsc: ENST00000566619.1:n.316+8C>T
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000457509
  ensembl transcript: ENST00000569970
  gene symbol: CORO1A
  hgvsc: ENST00000569970.1:c.198+8C>T
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000457332
  ensembl transcript: ENST00000570244
  gene symbol: CORO1A
  hgvsc: ENST00000570244.1:c.198+8C>T
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456457
  ensembl transcript: ENST00000565497
  gene symbol: CORO1A
  hgvsc: ENST00000565497.1:c.198+8C>T
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000568763
  gene symbol: CORO1A
  hgvsc: ENST00000568763.1:n.328C>T
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000568982
  gene symbol: CORO1A
  hgvsc: ENST00000568982.1:n.316+8C>T
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000454752
  ensembl transcript: ENST00000569203
  gene symbol: CORO1A
  hgvsc: ENST00000569203.1:c.198+8C>T
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456756
  ensembl transcript: ENST00000561815
  gene symbol: CORO1A
  hgvsc: ENST00000561815.1:c.306+8C>T
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000219150
  ensembl transcript: ENST00000219150
  gene symbol: CORO1A
  hgvsc: ENST00000219150.5:c.198+8C>T
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000455552
  ensembl transcript: ENST00000570045
  gene symbol: CORO1A
  hgvsc: ENST00000570045.1:c.198+8C>T
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456266
  ensembl transcript: ENST00000563778
  gene symbol: CORO1A
  hgvsc: ENST00000563778.1:c.198+8C>T
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000561849
  gene symbol: CORO1A
  hgvsc: ENST00000561849.1:n.333C>T
  variant of: http://identifiers.org/hgnc/2252
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17345
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3619
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4538
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15826
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1020
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11321
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.198+8C>T
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: DP

16-30196745-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30196745
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30196745
    reference: chr 16
allele count: 11
allele frequency: 1.00961891475145e-4
allele num: 108952
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456457
  ensembl transcript: ENST00000565497
  gene symbol: CORO1A
  hgvsc: ENST00000565497.1:c.198+17C>T
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000561849
  gene symbol: CORO1A
  hgvsc: ENST00000561849.1:n.342C>T
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456266
  ensembl transcript: ENST00000563778
  gene symbol: CORO1A
  hgvsc: ENST00000563778.1:c.198+17C>T
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000457332
  ensembl transcript: ENST00000570244
  gene symbol: CORO1A
  hgvsc: ENST00000570244.1:c.198+17C>T
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000568763
  gene symbol: CORO1A
  hgvsc: ENST00000568763.1:n.337C>T
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000219150
  ensembl transcript: ENST00000219150
  gene symbol: CORO1A
  hgvsc: ENST00000219150.5:c.198+17C>T
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456756
  ensembl transcript: ENST00000561815
  gene symbol: CORO1A
  hgvsc: ENST00000561815.1:c.306+17C>T
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000454752
  ensembl transcript: ENST00000569203
  gene symbol: CORO1A
  hgvsc: ENST00000569203.1:c.198+17C>T
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000568982
  gene symbol: CORO1A
  hgvsc: ENST00000568982.1:n.316+17C>T
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000457509
  ensembl transcript: ENST00000569970
  gene symbol: CORO1A
  hgvsc: ENST00000569970.1:c.198+17C>T
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000455552
  ensembl transcript: ENST00000570045
  gene symbol: CORO1A
  hgvsc: ENST00000570045.1:c.198+17C>T
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000566619
  gene symbol: CORO1A
  hgvsc: ENST00000566619.1:n.316+17C>T
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000569469
  gene symbol: CORO1A
  hgvsc: ENST00000569469.1:n.308+17C>T
  variant of: http://identifiers.org/hgnc/2252
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 833
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 685
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4464
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5254
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4790
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15643
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14320
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13798
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum

16-30196746-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30196746
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30196746
    reference: chr 16
allele count: 1
allele frequency: 9.199970560094207e-6
allele num: 108696
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000569469
  gene symbol: CORO1A
  hgvsc: ENST00000569469.1:n.308+18T>C
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000561849
  gene symbol: CORO1A
  hgvsc: ENST00000561849.1:n.343T>C
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000566619
  gene symbol: CORO1A
  hgvsc: ENST00000566619.1:n.316+18T>C
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000454752
  ensembl transcript: ENST00000569203
  gene symbol: CORO1A
  hgvsc: ENST00000569203.1:c.198+18T>C
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000455552
  ensembl transcript: ENST00000570045
  gene symbol: CORO1A
  hgvsc: ENST00000570045.1:c.198+18T>C
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000568763
  gene symbol: CORO1A
  hgvsc: ENST00000568763.1:n.338T>C
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456457
  ensembl transcript: ENST00000565497
  gene symbol: CORO1A
  hgvsc: ENST00000565497.1:c.198+18T>C
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000457509
  ensembl transcript: ENST00000569970
  gene symbol: CORO1A
  hgvsc: ENST00000569970.1:c.198+18T>C
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000457332
  ensembl transcript: ENST00000570244
  gene symbol: CORO1A
  hgvsc: ENST00000570244.1:c.198+18T>C
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000568982
  gene symbol: CORO1A
  hgvsc: ENST00000568982.1:n.316+18T>C
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456266
  ensembl transcript: ENST00000563778
  gene symbol: CORO1A
  hgvsc: ENST00000563778.1:c.198+18T>C
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000219150
  ensembl transcript: ENST00000219150
  gene symbol: CORO1A
  hgvsc: ENST00000219150.5:c.198+18T>C
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456756
  ensembl transcript: ENST00000561815
  gene symbol: CORO1A
  hgvsc: ENST00000561815.1:c.306+18T>C
  variant of: http://identifiers.org/hgnc/2252
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4781
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15639
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14362
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4470
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13727
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5294
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 687
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
population: African
population: Latino
reference allele: T
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: BaseQRankSum

16-30196747-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30196747
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30196747
    reference: chr 16
allele count: 2
allele frequency: 1.854083619171225e-5
allele num: 107870
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000566619
  gene symbol: CORO1A
  hgvsc: ENST00000566619.1:n.316+19G>T
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000568982
  gene symbol: CORO1A
  hgvsc: ENST00000568982.1:n.316+19G>T
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000561849
  gene symbol: CORO1A
  hgvsc: ENST00000561849.1:n.344G>T
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000568763
  gene symbol: CORO1A
  hgvsc: ENST00000568763.1:n.339G>T
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000457332
  ensembl transcript: ENST00000570244
  gene symbol: CORO1A
  hgvsc: ENST00000570244.1:c.198+19G>T
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456756
  ensembl transcript: ENST00000561815
  gene symbol: CORO1A
  hgvsc: ENST00000561815.1:c.306+19G>T
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000569469
  gene symbol: CORO1A
  hgvsc: ENST00000569469.1:n.308+19G>T
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000457509
  ensembl transcript: ENST00000569970
  gene symbol: CORO1A
  hgvsc: ENST00000569970.1:c.198+19G>T
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456266
  ensembl transcript: ENST00000563778
  gene symbol: CORO1A
  hgvsc: ENST00000563778.1:c.198+19G>T
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000454752
  ensembl transcript: ENST00000569203
  gene symbol: CORO1A
  hgvsc: ENST00000569203.1:c.198+19G>T
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456457
  ensembl transcript: ENST00000565497
  gene symbol: CORO1A
  hgvsc: ENST00000565497.1:c.198+19G>T
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000455552
  ensembl transcript: ENST00000570045
  gene symbol: CORO1A
  hgvsc: ENST00000570045.1:c.198+19G>T
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000219150
  ensembl transcript: ENST00000219150
  gene symbol: CORO1A
  hgvsc: ENST00000219150.5:c.198+19G>T
  variant of: http://identifiers.org/hgnc/2252
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12644
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 813
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4213
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5689
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15600
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14550
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5484
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 806
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ

16-30196748-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30196748
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30196748
    reference: chr 16
allele count: 4
allele frequency: 3.712228079293192e-5
allele num: 107752
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456756
  ensembl transcript: ENST00000561815
  gene symbol: CORO1A
  hgvsc: ENST00000561815.1:c.306+20G>A
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000568763
  gene symbol: CORO1A
  hgvsc: ENST00000568763.1:n.340G>A
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000457509
  ensembl transcript: ENST00000569970
  gene symbol: CORO1A
  hgvsc: ENST00000569970.1:c.198+20G>A
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456266
  ensembl transcript: ENST00000563778
  gene symbol: CORO1A
  hgvsc: ENST00000563778.1:c.198+20G>A
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000569469
  gene symbol: CORO1A
  hgvsc: ENST00000569469.1:n.308+20G>A
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000219150
  ensembl transcript: ENST00000219150
  gene symbol: CORO1A
  hgvsc: ENST00000219150.5:c.198+20G>A
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000568982
  gene symbol: CORO1A
  hgvsc: ENST00000568982.1:n.316+20G>A
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000561849
  gene symbol: CORO1A
  hgvsc: ENST00000561849.1:n.345G>A
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000566619
  gene symbol: CORO1A
  hgvsc: ENST00000566619.1:n.316+20G>A
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456457
  ensembl transcript: ENST00000565497
  gene symbol: CORO1A
  hgvsc: ENST00000565497.1:c.198+20G>A
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000455552
  ensembl transcript: ENST00000570045
  gene symbol: CORO1A
  hgvsc: ENST00000570045.1:c.198+20G>A
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000454752
  ensembl transcript: ENST00000569203
  gene symbol: CORO1A
  hgvsc: ENST00000569203.1:c.198+20G>A
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000457332
  ensembl transcript: ENST00000570244
  gene symbol: CORO1A
  hgvsc: ENST00000570244.1:c.198+20G>A
  variant of: http://identifiers.org/hgnc/2252
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 811
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5526
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14542
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4180
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5660
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 797
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12653
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15639
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff

16-30196757-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30196757
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30196757
    reference: chr 16
allele count: 1
allele frequency: 9.485146260955344e-6
allele num: 105428
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000219150
  ensembl transcript: ENST00000219150
  gene symbol: CORO1A
  hgvsc: ENST00000219150.5:c.198+29G>T
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456457
  ensembl transcript: ENST00000565497
  gene symbol: CORO1A
  hgvsc: ENST00000565497.1:c.198+29G>T
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000457509
  ensembl transcript: ENST00000569970
  gene symbol: CORO1A
  hgvsc: ENST00000569970.1:c.198+29G>T
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456266
  ensembl transcript: ENST00000563778
  gene symbol: CORO1A
  hgvsc: ENST00000563778.1:c.198+29G>T
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000561849
  gene symbol: CORO1A
  hgvsc: ENST00000561849.1:n.354G>T
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456756
  ensembl transcript: ENST00000561815
  gene symbol: CORO1A
  hgvsc: ENST00000561815.1:c.306+29G>T
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000568763
  gene symbol: CORO1A
  hgvsc: ENST00000568763.1:n.349G>T
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000569469
  gene symbol: CORO1A
  hgvsc: ENST00000569469.1:n.308+29G>T
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000566619
  gene symbol: CORO1A
  hgvsc: ENST00000566619.1:n.316+29G>T
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000454752
  ensembl transcript: ENST00000569203
  gene symbol: CORO1A
  hgvsc: ENST00000569203.1:c.198+29G>T
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000457332
  ensembl transcript: ENST00000570244
  gene symbol: CORO1A
  hgvsc: ENST00000570244.1:c.198+29G>T
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000455552
  ensembl transcript: ENST00000570045
  gene symbol: CORO1A
  hgvsc: ENST00000570045.1:c.198+29G>T
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000568982
  gene symbol: CORO1A
  hgvsc: ENST00000568982.1:n.316+29G>T
  variant of: http://identifiers.org/hgnc/2252
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10320
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18984
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6349
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1221
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9674
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2976
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9585
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: African
population: Latino
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: FS

16-30196759-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30196759
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30196759
    reference: chr 16
allele count: 1
allele frequency: 9.554566127152167e-6
allele num: 104662
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456266
  ensembl transcript: ENST00000563778
  gene symbol: CORO1A
  hgvsc: ENST00000563778.1:c.198+31T>A
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000568763
  gene symbol: CORO1A
  hgvsc: ENST00000568763.1:n.351T>A
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000561849
  gene symbol: CORO1A
  hgvsc: ENST00000561849.1:n.356T>A
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456756
  ensembl transcript: ENST00000561815
  gene symbol: CORO1A
  hgvsc: ENST00000561815.1:c.306+31T>A
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000454752
  ensembl transcript: ENST00000569203
  gene symbol: CORO1A
  hgvsc: ENST00000569203.1:c.198+31T>A
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000568982
  gene symbol: CORO1A
  hgvsc: ENST00000568982.1:n.316+31T>A
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000569469
  gene symbol: CORO1A
  hgvsc: ENST00000569469.1:n.308+31T>A
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456457
  ensembl transcript: ENST00000565497
  gene symbol: CORO1A
  hgvsc: ENST00000565497.1:c.198+31T>A
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000566619
  gene symbol: CORO1A
  hgvsc: ENST00000566619.1:n.316+31T>A
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000455552
  ensembl transcript: ENST00000570045
  gene symbol: CORO1A
  hgvsc: ENST00000570045.1:c.198+31T>A
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000457509
  ensembl transcript: ENST00000569970
  gene symbol: CORO1A
  hgvsc: ENST00000569970.1:c.198+31T>A
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000457332
  ensembl transcript: ENST00000570244
  gene symbol: CORO1A
  hgvsc: ENST00000570244.1:c.198+31T>A
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000219150
  ensembl transcript: ENST00000219150
  gene symbol: CORO1A
  hgvsc: ENST00000219150.5:c.198+31T>A
  variant of: http://identifiers.org/hgnc/2252
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19403
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1340
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6584
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8995
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8531
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2713
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11560
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
reference allele: T
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum

16-30196760-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30196760
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30196760
    reference: chr 16
allele count: 1
allele frequency: 9.591774094536525e-6
allele num: 104256
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000569469
  gene symbol: CORO1A
  hgvsc: ENST00000569469.1:n.308+32C>G
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456756
  ensembl transcript: ENST00000561815
  gene symbol: CORO1A
  hgvsc: ENST00000561815.1:c.306+32C>G
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000455552
  ensembl transcript: ENST00000570045
  gene symbol: CORO1A
  hgvsc: ENST00000570045.1:c.198+32C>G
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000219150
  ensembl transcript: ENST00000219150
  gene symbol: CORO1A
  hgvsc: ENST00000219150.5:c.198+32C>G
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000566619
  gene symbol: CORO1A
  hgvsc: ENST00000566619.1:n.316+32C>G
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000454752
  ensembl transcript: ENST00000569203
  gene symbol: CORO1A
  hgvsc: ENST00000569203.1:c.198+32C>G
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456457
  ensembl transcript: ENST00000565497
  gene symbol: CORO1A
  hgvsc: ENST00000565497.1:c.198+32C>G
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456266
  ensembl transcript: ENST00000563778
  gene symbol: CORO1A
  hgvsc: ENST00000563778.1:c.198+32C>G
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000568763
  gene symbol: CORO1A
  hgvsc: ENST00000568763.1:n.352C>G
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000561849
  gene symbol: CORO1A
  hgvsc: ENST00000561849.1:n.357C>G
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000568982
  gene symbol: CORO1A
  hgvsc: ENST00000568982.1:n.316+32C>G
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000457509
  ensembl transcript: ENST00000569970
  gene symbol: CORO1A
  hgvsc: ENST00000569970.1:c.198+32C>G
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000457332
  ensembl transcript: ENST00000570244
  gene symbol: CORO1A
  hgvsc: ENST00000570244.1:c.198+32C>G
  variant of: http://identifiers.org/hgnc/2252
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12234
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2650
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8580
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1379
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6680
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19423
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: C
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: FS
site quality: ReadPosRankSum

16-30196767-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30196767
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30196767
    reference: chr 16
allele count: 7
allele frequency: 6.906077348066299e-5
allele num: 101360
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000561849
  gene symbol: CORO1A
  hgvsc: ENST00000561849.1:n.364C>T
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000457509
  ensembl transcript: ENST00000569970
  gene symbol: CORO1A
  hgvsc: ENST00000569970.1:c.198+39C>T
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000568763
  gene symbol: CORO1A
  hgvsc: ENST00000568763.1:n.359C>T
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000455552
  ensembl transcript: ENST00000570045
  gene symbol: CORO1A
  hgvsc: ENST00000570045.1:c.198+39C>T
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000457332
  ensembl transcript: ENST00000570244
  gene symbol: CORO1A
  hgvsc: ENST00000570244.1:c.198+39C>T
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000569469
  gene symbol: CORO1A
  hgvsc: ENST00000569469.1:n.308+39C>T
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000568982
  gene symbol: CORO1A
  hgvsc: ENST00000568982.1:n.316+39C>T
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456266
  ensembl transcript: ENST00000563778
  gene symbol: CORO1A
  hgvsc: ENST00000563778.1:c.198+39C>T
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456457
  ensembl transcript: ENST00000565497
  gene symbol: CORO1A
  hgvsc: ENST00000565497.1:c.198+39C>T
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000454752
  ensembl transcript: ENST00000569203
  gene symbol: CORO1A
  hgvsc: ENST00000569203.1:c.198+39C>T
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456756
  ensembl transcript: ENST00000561815
  gene symbol: CORO1A
  hgvsc: ENST00000561815.1:c.306+39C>T
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000566619
  gene symbol: CORO1A
  hgvsc: ENST00000566619.1:n.316+39C>T
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000219150
  ensembl transcript: ENST00000219150
  gene symbol: CORO1A
  hgvsc: ENST00000219150.5:c.198+39C>T
  variant of: http://identifiers.org/hgnc/2252
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15811
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6910
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 19193
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1563
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2027
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6095
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7603
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 596
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: South Asian
population: African
population: Latino
population: East Asian
reference allele: C
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum

16-30196768-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30196768
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30196768
    reference: chr 16
allele count: 8
allele frequency: 7.932258512304916e-5
allele num: 100854
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000457509
  ensembl transcript: ENST00000569970
  gene symbol: CORO1A
  hgvsc: ENST00000569970.1:c.198+40G>A
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000457332
  ensembl transcript: ENST00000570244
  gene symbol: CORO1A
  hgvsc: ENST00000570244.1:c.198+40G>A
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000568763
  gene symbol: CORO1A
  hgvsc: ENST00000568763.1:n.360G>A
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000454752
  ensembl transcript: ENST00000569203
  gene symbol: CORO1A
  hgvsc: ENST00000569203.1:c.198+40G>A
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456756
  ensembl transcript: ENST00000561815
  gene symbol: CORO1A
  hgvsc: ENST00000561815.1:c.306+40G>A
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000219150
  ensembl transcript: ENST00000219150
  gene symbol: CORO1A
  hgvsc: ENST00000219150.5:c.198+40G>A
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000455552
  ensembl transcript: ENST00000570045
  gene symbol: CORO1A
  hgvsc: ENST00000570045.1:c.198+40G>A
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000568982
  gene symbol: CORO1A
  hgvsc: ENST00000568982.1:n.316+40G>A
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456457
  ensembl transcript: ENST00000565497
  gene symbol: CORO1A
  hgvsc: ENST00000565497.1:c.198+40G>A
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000569469
  gene symbol: CORO1A
  hgvsc: ENST00000569469.1:n.308+40G>A
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000561849
  gene symbol: CORO1A
  hgvsc: ENST00000561849.1:n.365G>A
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456266
  ensembl transcript: ENST00000563778
  gene symbol: CORO1A
  hgvsc: ENST00000563778.1:c.198+40G>A
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000566619
  gene symbol: CORO1A
  hgvsc: ENST00000566619.1:n.316+40G>A
  variant of: http://identifiers.org/hgnc/2252
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5817
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6889
  bin: 2.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 7812
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1927
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19168
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1573
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: South Asian
population: Latino
reference allele: G
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP

16-30196777-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30196777
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30196777
    reference: chr 16
allele count: 1
allele frequency: 1.025830409716666e-5
allele num: 97482
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000569469
  gene symbol: CORO1A
  hgvsc: ENST00000569469.1:n.308+49G>A
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000455552
  ensembl transcript: ENST00000570045
  gene symbol: CORO1A
  hgvsc: ENST00000570045.1:c.198+49G>A
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456266
  ensembl transcript: ENST00000563778
  gene symbol: CORO1A
  hgvsc: ENST00000563778.1:c.198+49G>A
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000566619
  gene symbol: CORO1A
  hgvsc: ENST00000566619.1:n.316+49G>A
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000561849
  gene symbol: CORO1A
  hgvsc: ENST00000561849.1:n.374G>A
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000454752
  ensembl transcript: ENST00000569203
  gene symbol: CORO1A
  hgvsc: ENST00000569203.1:c.198+49G>A
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000568763
  gene symbol: CORO1A
  hgvsc: ENST00000568763.1:n.369G>A
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456756
  ensembl transcript: ENST00000561815
  gene symbol: CORO1A
  hgvsc: ENST00000561815.1:c.306+49G>A
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000457332
  ensembl transcript: ENST00000570244
  gene symbol: CORO1A
  hgvsc: ENST00000570244.1:c.198+49G>A
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000219150
  ensembl transcript: ENST00000219150
  gene symbol: CORO1A
  hgvsc: ENST00000219150.5:c.198+49G>A
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000457509
  ensembl transcript: ENST00000569970
  gene symbol: CORO1A
  hgvsc: ENST00000569970.1:c.198+49G>A
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000568982
  gene symbol: CORO1A
  hgvsc: ENST00000568982.1:n.316+49G>A
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456457
  ensembl transcript: ENST00000565497
  gene symbol: CORO1A
  hgvsc: ENST00000565497.1:c.198+49G>A
  variant of: http://identifiers.org/hgnc/2252
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15816
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9291
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18248
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1507
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3870
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1612
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8857
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: Other
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum

16-30196780-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30196780
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30196780
    reference: chr 16
allele count: 0
allele frequency: 0.0e0
allele num: 96346
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456457
  ensembl transcript: ENST00000565497
  gene symbol: CORO1A
  hgvsc: ENST00000565497.1:c.198+52C>G
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000568982
  gene symbol: CORO1A
  hgvsc: ENST00000568982.1:n.316+52C>G
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000454752
  ensembl transcript: ENST00000569203
  gene symbol: CORO1A
  hgvsc: ENST00000569203.1:c.198+52C>G
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000568763
  gene symbol: CORO1A
  hgvsc: ENST00000568763.1:n.372C>G
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456756
  ensembl transcript: ENST00000561815
  gene symbol: CORO1A
  hgvsc: ENST00000561815.1:c.306+52C>G
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000569469
  gene symbol: CORO1A
  hgvsc: ENST00000569469.1:n.308+52C>G
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456266
  ensembl transcript: ENST00000563778
  gene symbol: CORO1A
  hgvsc: ENST00000563778.1:c.198+52C>G
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000561849
  gene symbol: CORO1A
  hgvsc: ENST00000561849.1:n.377C>G
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000566619
  gene symbol: CORO1A
  hgvsc: ENST00000566619.1:n.316+52C>G
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000457332
  ensembl transcript: ENST00000570244
  gene symbol: CORO1A
  hgvsc: ENST00000570244.1:c.198+52C>G
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000219150
  ensembl transcript: ENST00000219150
  gene symbol: CORO1A
  hgvsc: ENST00000219150.5:c.198+52C>G
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000455552
  ensembl transcript: ENST00000570045
  gene symbol: CORO1A
  hgvsc: ENST00000570045.1:c.198+52C>G
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000457509
  ensembl transcript: ENST00000569970
  gene symbol: CORO1A
  hgvsc: ENST00000569970.1:c.198+52C>G
  variant of: http://identifiers.org/hgnc/2252
canonical: false
consequence: non coding transcript exon
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9320
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1466
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15745
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3916
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1604
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18258
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8889
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: DP

16-30197871-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30197871
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30197871
    reference: chr 16
allele count: 1
allele frequency: 8.298617450332775e-6
allele num: 120502
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000457332
  ensembl transcript: ENST00000570244
  gene symbol: CORO1A
  hgvsc: ENST00000570244.1:c.199-266T>C
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000568982
  gene symbol: CORO1A
  hgvsc: ENST00000568982.1:n.317-48T>C
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000567034
  gene symbol: CORO1A
  hgvsc: ENST00000567034.1:n.619T>C
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456266
  ensembl transcript: ENST00000563778
  gene symbol: CORO1A
  hgvsc: ENST00000563778.1:c.199-48T>C
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000568763
  gene symbol: CORO1A
  hgvsc: ENST00000568763.1:n.1463T>C
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000454752
  ensembl transcript: ENST00000569203
  gene symbol: CORO1A
  hgvsc: ENST00000569203.1:c.199-48T>C
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456756
  ensembl transcript: ENST00000561815
  gene symbol: CORO1A
  hgvsc: ENST00000561815.1:c.307-48T>C
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000455552
  ensembl transcript: ENST00000570045
  gene symbol: CORO1A
  hgvsc: ENST00000570045.1:c.199-48T>C
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000219150
  ensembl transcript: ENST00000219150
  gene symbol: CORO1A
  hgvsc: ENST00000219150.5:c.199-48T>C
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000457509
  ensembl transcript: ENST00000569970
  gene symbol: CORO1A
  hgvsc: ENST00000569970.1:c.199-48T>C
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456457
  ensembl transcript: ENST00000565497
  gene symbol: CORO1A
  hgvsc: ENST00000565497.1:c.199-48T>C
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000569469
  gene symbol: CORO1A
  hgvsc: ENST00000569469.1:n.309-48T>C
  variant of: http://identifiers.org/hgnc/2252
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 536
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26853
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11965
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 857
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3338
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9671
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 668
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1464
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 640
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: T
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: BaseQRankSum

http://identifiers.org/exac.variant/16-30197885-CA-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30197885
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30197884
    reference: chr 16
allele count: 1
allele frequency: 8.300546175938376e-6
allele num: 120474
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000219150
  ensembl transcript: ENST00000219150
  gene symbol: CORO1A
  hgvsc: ENST00000219150.5:c.199-30delA
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000568982
  gene symbol: CORO1A
  hgvsc: ENST00000568982.1:n.317-30delA
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456266
  ensembl transcript: ENST00000563778
  gene symbol: CORO1A
  hgvsc: ENST00000563778.1:c.199-30delA
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000457332
  ensembl transcript: ENST00000570244
  gene symbol: CORO1A
  hgvsc: ENST00000570244.1:c.199-248delA
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000568763
  gene symbol: CORO1A
  hgvsc: ENST00000568763.1:n.1481delA
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000569469
  gene symbol: CORO1A
  hgvsc: ENST00000569469.1:n.309-30delA
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000454752
  ensembl transcript: ENST00000569203
  gene symbol: CORO1A
  hgvsc: ENST00000569203.1:c.199-30delA
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000567034
  gene symbol: CORO1A
  hgvsc: ENST00000567034.1:n.637delA
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000455552
  ensembl transcript: ENST00000570045
  gene symbol: CORO1A
  hgvsc: ENST00000570045.1:c.199-30delA
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456756
  ensembl transcript: ENST00000561815
  gene symbol: CORO1A
  hgvsc: ENST00000561815.1:c.307-30delA
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000457509
  ensembl transcript: ENST00000569970
  gene symbol: CORO1A
  hgvsc: ENST00000569970.1:c.199-30delA
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456457
  ensembl transcript: ENST00000565497
  gene symbol: CORO1A
  hgvsc: ENST00000565497.1:c.199-30delA
  variant of: http://identifiers.org/hgnc/2252
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1452
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9984
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3314
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26932
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 641
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11926
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 852
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 536
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: South Asian
population: African
population: Latino
reference allele: CA
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP

16-30197903-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30197903
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30197903
    reference: chr 16
allele count: 4
allele frequency: 3.32021847037535e-5
allele num: 120474
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000219150
  ensembl transcript: ENST00000219150
  gene symbol: CORO1A
  hgvsc: ENST00000219150.5:c.199-16C>G
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000455552
  ensembl transcript: ENST00000570045
  gene symbol: CORO1A
  hgvsc: ENST00000570045.1:c.199-16C>G
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000457332
  ensembl transcript: ENST00000570244
  gene symbol: CORO1A
  hgvsc: ENST00000570244.1:c.199-234C>G
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456457
  ensembl transcript: ENST00000565497
  gene symbol: CORO1A
  hgvsc: ENST00000565497.1:c.199-16C>G
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000567034
  gene symbol: CORO1A
  hgvsc: ENST00000567034.1:n.651C>G
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456756
  ensembl transcript: ENST00000561815
  gene symbol: CORO1A
  hgvsc: ENST00000561815.1:c.307-16C>G
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000569469
  gene symbol: CORO1A
  hgvsc: ENST00000569469.1:n.309-16C>G
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000568763
  gene symbol: CORO1A
  hgvsc: ENST00000568763.1:n.1495C>G
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456266
  ensembl transcript: ENST00000563778
  gene symbol: CORO1A
  hgvsc: ENST00000563778.1:c.199-16C>G
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000568982
  gene symbol: CORO1A
  hgvsc: ENST00000568982.1:n.317-16C>G
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000457509
  ensembl transcript: ENST00000569970
  gene symbol: CORO1A
  hgvsc: ENST00000569970.1:c.199-16C>G
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000454752
  ensembl transcript: ENST00000569203
  gene symbol: CORO1A
  hgvsc: ENST00000569203.1:c.199-16C>G
  variant of: http://identifiers.org/hgnc/2252
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 693
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3290
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 848
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27026
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 536
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11860
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10166
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 640
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1437
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum

16-30197906-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30197906
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30197906
    reference: chr 16
allele count: 9
allele frequency: 7.46999551800269e-5
allele num: 120482
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456457
  ensembl transcript: ENST00000565497
  gene symbol: CORO1A
  hgvsc: ENST00000565497.1:c.199-13G>A
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000569469
  gene symbol: CORO1A
  hgvsc: ENST00000569469.1:n.309-13G>A
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000457332
  ensembl transcript: ENST00000570244
  gene symbol: CORO1A
  hgvsc: ENST00000570244.1:c.199-231G>A
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000567034
  gene symbol: CORO1A
  hgvsc: ENST00000567034.1:n.654G>A
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456266
  ensembl transcript: ENST00000563778
  gene symbol: CORO1A
  hgvsc: ENST00000563778.1:c.199-13G>A
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000568982
  gene symbol: CORO1A
  hgvsc: ENST00000568982.1:n.317-13G>A
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000568763
  gene symbol: CORO1A
  hgvsc: ENST00000568763.1:n.1498G>A
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000219150
  ensembl transcript: ENST00000219150
  gene symbol: CORO1A
  hgvsc: ENST00000219150.5:c.199-13G>A
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000454752
  ensembl transcript: ENST00000569203
  gene symbol: CORO1A
  hgvsc: ENST00000569203.1:c.199-13G>A
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456756
  ensembl transcript: ENST00000561815
  gene symbol: CORO1A
  hgvsc: ENST00000561815.1:c.307-13G>A
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000457509
  ensembl transcript: ENST00000569970
  gene symbol: CORO1A
  hgvsc: ENST00000569970.1:c.199-13G>A
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000455552
  ensembl transcript: ENST00000570045
  gene symbol: CORO1A
  hgvsc: ENST00000570045.1:c.199-13G>A
  variant of: http://identifiers.org/hgnc/2252
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 536
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11856
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27029
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10214
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 696
  bin: 9.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 640
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 844
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3286
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1432
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Other
population: African
population: Latino
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS

16-30197909-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30197909
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30197909
    reference: chr 16
allele count: 1
allele frequency: 8.301097405076952e-6
allele num: 120466
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000567034
  gene symbol: CORO1A
  hgvsc: ENST00000567034.1:n.657G>A
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456457
  ensembl transcript: ENST00000565497
  gene symbol: CORO1A
  hgvsc: ENST00000565497.1:c.199-10G>A
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000454752
  ensembl transcript: ENST00000569203
  gene symbol: CORO1A
  hgvsc: ENST00000569203.1:c.199-10G>A
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456266
  ensembl transcript: ENST00000563778
  gene symbol: CORO1A
  hgvsc: ENST00000563778.1:c.199-10G>A
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000568982
  gene symbol: CORO1A
  hgvsc: ENST00000568982.1:n.317-10G>A
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000457332
  ensembl transcript: ENST00000570244
  gene symbol: CORO1A
  hgvsc: ENST00000570244.1:c.199-228G>A
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000568763
  gene symbol: CORO1A
  hgvsc: ENST00000568763.1:n.1501G>A
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000219150
  ensembl transcript: ENST00000219150
  gene symbol: CORO1A
  hgvsc: ENST00000219150.5:c.199-10G>A
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456756
  ensembl transcript: ENST00000561815
  gene symbol: CORO1A
  hgvsc: ENST00000561815.1:c.307-10G>A
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000457509
  ensembl transcript: ENST00000569970
  gene symbol: CORO1A
  hgvsc: ENST00000569970.1:c.199-10G>A
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000569469
  gene symbol: CORO1A
  hgvsc: ENST00000569469.1:n.309-10G>A
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000455552
  ensembl transcript: ENST00000570045
  gene symbol: CORO1A
  hgvsc: ENST00000570045.1:c.199-10G>A
  variant of: http://identifiers.org/hgnc/2252
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 692
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 639
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11845
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10237
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27024
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 844
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3281
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1431
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 536
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: Other
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum

16-30197913-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30197913
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30197913
    reference: chr 16
allele count: 3
allele frequency: 2.490742739484914e-5
allele num: 120446
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000569469
  gene symbol: CORO1A
  hgvsc: ENST00000569469.1:n.309-6C>T
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456457
  ensembl transcript: ENST00000565497
  gene symbol: CORO1A
  hgvsc: ENST00000565497.1:c.199-6C>T
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000457509
  ensembl transcript: ENST00000569970
  gene symbol: CORO1A
  hgvsc: ENST00000569970.1:c.199-6C>T
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456266
  ensembl transcript: ENST00000563778
  gene symbol: CORO1A
  hgvsc: ENST00000563778.1:c.199-6C>T
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000568982
  gene symbol: CORO1A
  hgvsc: ENST00000568982.1:n.317-6C>T
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000455552
  ensembl transcript: ENST00000570045
  gene symbol: CORO1A
  hgvsc: ENST00000570045.1:c.199-6C>T
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000219150
  ensembl transcript: ENST00000219150
  gene symbol: CORO1A
  hgvsc: ENST00000219150.5:c.199-6C>T
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000454752
  ensembl transcript: ENST00000569203
  gene symbol: CORO1A
  hgvsc: ENST00000569203.1:c.199-6C>T
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000568763
  gene symbol: CORO1A
  hgvsc: ENST00000568763.1:n.1505C>T
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000457332
  ensembl transcript: ENST00000570244
  gene symbol: CORO1A
  hgvsc: ENST00000570244.1:c.199-224C>T
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102879
  ensembl protein: ENSP00000456756
  ensembl transcript: ENST00000561815
  gene symbol: CORO1A
  hgvsc: ENST00000561815.1:c.307-6C>T
  variant of: http://identifiers.org/hgnc/2252
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102879
  ensembl transcript: ENST00000567034
  gene symbol: CORO1A
  hgvsc: ENST00000567034.1:n.661C>T
  variant of: http://identifiers.org/hgnc/2252
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3275
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10234
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 536
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 844
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 7.5e0
  variant carriers: 0
hgvs: c.199-6C>T
num of homozygotes: 0
reference allele: C

GenotypeQuality
all individuals: 8
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7597
bin: 2.25e1
variant carriers: 1

GenotypeQuality
all individuals: 3
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 312
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1803
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2852
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 8.25e1
variant carriers: 2

GenotypeQuality
all individuals: 9
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 287
bin: 6.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 686
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 622
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.98019801980198e-3
allele num: 1010
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 428
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 54
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 150
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3968
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.06e-1

QD
type: SiteQuality
SIO_000300: 1.019e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 3.788e0

DP
type: SiteQuality
SIO_000300: 2.14772e5

MQRankSum
type: SiteQuality
SIO_000300: 3.22e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.01e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.94e0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.27e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.63e-1

GenotypeQuality
all individuals: 62
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 971
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5208
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1145
bin: 1.25e1
variant carriers: 1

GenotypeQuality
all individuals: 10
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 183
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 8.25e1
variant carriers: 2

GenotypeQuality
all individuals: 2
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 240
bin: 6.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 72
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2076
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.582278481012658e-3
allele num: 632
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 432
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 380
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 32
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.678e0

MQRankSum
type: SiteQuality
SIO_000300: -5.5e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.27e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.76e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.73e-1

QD
type: SiteQuality
SIO_000300: 1.587e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.759999999999999e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.43e-1

MQ
type: SiteQuality
SIO_000300: 5.742e1

DP
type: SiteQuality
SIO_000300: 1.72398e5

GenotypeQuality
all individuals: 22
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31475
bin: 7.5e0
variant carriers: 1

GenotypeQuality
all individuals: 10
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5208
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 183
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 971
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 96
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 240
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 62
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 5
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 2
bin: 8.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 632
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2076
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 380
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 32
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 2.314814814814815e-3
allele num: 432
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 72
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.759999999999999e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.76e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.73e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.27e-1

FS
type: SiteQuality
SIO_000300: 1.678e0

MQRankSum
type: SiteQuality
SIO_000300: -5.5e-1

MQ
type: SiteQuality
SIO_000300: 5.742e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.43e-1

DP
type: SiteQuality
SIO_000300: 1.72398e5

QD
type: SiteQuality
SIO_000300: 1.587e1

GenotypeQuality
all individuals: 30319
bin: 7.5e0
variant carriers: 1

GenotypeQuality
all individuals: 3344
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1371
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 12
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1200
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 52
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 18
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 330
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 146
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 194
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 442
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.53123e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.51e-2

QD
type: SiteQuality
SIO_000300: 1.095e1

MQ
type: SiteQuality
SIO_000300: 4.596e1

VQSLOD
type: SiteQuality
SIO_000300: 7.24e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
all individuals: 1030
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 100
bin: 2.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3573
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1137
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 211
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 6
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3616
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
all individuals: 12
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variant carriers: 1

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 50
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 182
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 412
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African
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allele count: 0
allele frequency: 0.0e0
allele num: 322
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Other
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allele count: 0
allele frequency: 0.0e0
allele num: 16
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European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 8.741258741258741e-4
allele num: 1144
num of homozygotes: 0

Latino
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allele frequency: 7.575757575757576e-3
allele num: 132
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 4.78e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 2.96e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.96e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.092e0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -9.703000000000001e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.96e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.74e-2

DP
type: SiteQuality
SIO_000300: 1.51235e5

South Asian
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allele frequency: 6.688068485821295e-4
allele num: 7476
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East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 132
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Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 92
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 118
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European (Finnish)
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.384e0

FS
type: SiteQuality
SIO_000300: 1.035e0

QD
type: SiteQuality
SIO_000300: 1.038e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -4.53e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.07e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.47e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.07e-1

DP
type: SiteQuality
SIO_000300: 1.5993e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.64e-2

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 132
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African
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allele count: 0
allele frequency: 0.0e0
allele num: 190
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South Asian
type: Population
allele count: 1
allele frequency: 1.332977872567315e-4
allele num: 7502
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Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 92
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ClippingRankSum
type: SiteQuality
SIO_000300: -1.112e0

FS
type: SiteQuality
SIO_000300: 8.579000000000001e0

MQRankSum
type: SiteQuality
SIO_000300: 2.22e-1

MQ
type: SiteQuality
SIO_000300: 5.972e1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.19e-1

QD
type: SiteQuality
SIO_000300: 1.064e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.23e-2

VQSLOD
type: SiteQuality
SIO_000300: -1.017e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.6e-2

DP
type: SiteQuality
SIO_000300: 1.64908e5

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 118
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Latino
type: Population
allele count: 1
allele frequency: 1.08695652173913e-2
allele num: 92
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 132
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QD
type: SiteQuality
SIO_000300: 1.002e1

MQ
type: SiteQuality
SIO_000300: 5.973e1

MQRankSum
type: SiteQuality
SIO_000300: 2.45e-1

VQSLOD
type: SiteQuality
SIO_000300: -5.923e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.1e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.161e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.3e-1

FS
type: SiteQuality
SIO_000300: 5.31e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.08e-2

DP
type: SiteQuality
SIO_000300: 1.6763e5

European (Finnish)
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 132
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 118
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MQRankSum
type: SiteQuality
SIO_000300: 4.46e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 9.460000000000001e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.38e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -5.49e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.825e0

FS
type: SiteQuality
SIO_000300: 6.79e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.31e0

DP
type: SiteQuality
SIO_000300: 1.68807e5

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7488
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4
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East Asian
type: Population
allele count: 1
allele frequency: 7.462686567164179e-3
allele num: 134
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European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2674
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African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 194
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 92
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ReadPosRankSum
type: SiteQuality
SIO_000300: 1.99e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.42e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 3.0e-2

QD
type: SiteQuality
SIO_000300: 9.19e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.909e0

VQSLOD
type: SiteQuality
SIO_000300: -1.602e0

DP
type: SiteQuality
SIO_000300: 1.52617e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.67e-2

MQ
type: SiteQuality
SIO_000300: 5.924e1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 192
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South Asian
type: Population
allele count: 3
allele frequency: 4.006410256410256e-4
allele num: 7488
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 134
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 92
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European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2674
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.86e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.4e-2

FS
type: SiteQuality
SIO_000300: 7.536e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.77e-1

QD
type: SiteQuality
SIO_000300: 1.147e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -9.7e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.77e-1

DP
type: SiteQuality
SIO_000300: 1.52204e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.54e-2

South Asian
type: Population
allele count: 1
allele frequency: 1.335470085470086e-4
allele num: 7488
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2678
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African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 192
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 134
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 118
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.249e0

DP
type: SiteQuality
SIO_000300: 1.52796e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.58e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.679e0

FS
type: SiteQuality
SIO_000300: 7.702e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.32e-2

QD
type: SiteQuality
SIO_000300: 1.164e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.1e-2

MQRankSum
type: SiteQuality
SIO_000300: -1.056e0

European (Non-Finnish)
type: Population
allele count: 315
allele frequency: 1.171003717472119e-1
allele num: 2690
num of homozygotes: 23

Latino
type: Population
allele count: 7
allele frequency: 7.608695652173914e-2
allele num: 92
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Other
type: Population
allele count: 9
allele frequency: 7.627118644067797e-2
allele num: 118
num of homozygotes: 0

African
type: Population
allele count: 10
allele frequency: 5.208333333333334e-2
allele num: 192
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 134
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 3.34e-1

DP
type: SiteQuality
SIO_000300: 1.59437e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.47e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.67e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.89e-2

QD
type: SiteQuality
SIO_000300: 1.323e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.77e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.29e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 118
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 190
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2668
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 92
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 134
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.48497e5

BaseQRankSum
type: SiteQuality
SIO_000300: 3.23e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.3e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.1e-1

VQSLOD
type: SiteQuality
SIO_000300: -6.881e-1

FS
type: SiteQuality
SIO_000300: 4.055e0

MQRankSum
type: SiteQuality
SIO_000300: 1.5e-1

MQ
type: SiteQuality
SIO_000300: 5.953e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.85e-2

QD
type: SiteQuality
SIO_000300: 1.262e1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 132
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 116
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 90
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South Asian
type: Population
allele count: 3
allele frequency: 4.044216770018873e-4
allele num: 7418
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 188
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2628
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.963e1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.72e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.534e0

DP
type: SiteQuality
SIO_000300: 1.45927e5

FS
type: SiteQuality
SIO_000300: 7.157e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.71e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.487e0

MQRankSum
type: SiteQuality
SIO_000300: 1.75e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.65e-1

QD
type: SiteQuality
SIO_000300: 1.063e1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 188
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2564
num of homozygotes: 0

South Asian
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allele count: 1
allele frequency: 1.391594767603674e-4
allele num: 7186
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 114
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 132
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.39463e5

VQSLOD
type: SiteQuality
SIO_000300: 9.0e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.53e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -7.09e-1

FS
type: SiteQuality
SIO_000300: 2.831e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 3.36e-1

QD
type: SiteQuality
SIO_000300: 7.75e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.83e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.34e-1

Latino
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allele count: 0
allele frequency: 0.0e0
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African
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allele count: 0
allele frequency: 0.0e0
allele num: 186
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South Asian
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allele count: 2
allele frequency: 2.796420581655481e-4
allele num: 7152
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
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Other
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allele count: 0
allele frequency: 0.0e0
allele num: 114
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 2540
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.66e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.15e-1

DP
type: SiteQuality
SIO_000300: 1.38422e5

FS
type: SiteQuality
SIO_000300: 4.754e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.366e0

QD
type: SiteQuality
SIO_000300: 1.078e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.9e-1

MQ
type: SiteQuality
SIO_000300: 5.942e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.55e-2

VQSLOD
type: SiteQuality
SIO_000300: -6.736e-1

East Asian
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allele count: 10
allele frequency: 1.020408163265306e-1
allele num: 98
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Other
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allele count: 1
allele frequency: 1.31578947368421e-2
allele num: 76
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 1.779359430604982e-3
allele num: 1686
num of homozygotes: 0

Latino
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allele count: 4
allele frequency: 6.896551724137931e-2
allele num: 58
num of homozygotes: 1

South Asian
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allele count: 22
allele frequency: 4.552980132450331e-3
allele num: 4832
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.468e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.46e1

MQRankSum
type: SiteQuality
SIO_000300: 8.400000000000001e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.7e-2

VQSLOD
type: SiteQuality
SIO_000300: 5.94e0

DP
type: SiteQuality
SIO_000300: 7.6713e4

ClippingRankSum
type: SiteQuality
SIO_000300: -2.44e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.24e-1

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 58
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 126
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 98
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 76
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 6.208609271523179e-4
allele num: 4832
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 7.6713e4

MQRankSum
type: SiteQuality
SIO_000300: 8.400000000000001e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.24e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.7e-2

VQSLOD
type: SiteQuality
SIO_000300: 5.94e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.44e-1

QD
type: SiteQuality
SIO_000300: 1.46e1

GenotypeDepth
all individuals: 2
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variant carriers: 0

GenotypeDepth
all individuals: 8
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variant carriers: 0

GenotypeDepth
all individuals: 25
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variant carriers: 0

GenotypeQuality
all individuals: 136
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variant carriers: 0

GenotypeQuality
all individuals: 235
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variant carriers: 0

GenotypeQuality
all individuals: 1472
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 32791
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GenotypeQuality
all individuals: 1383
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variant carriers: 0

GenotypeQuality
all individuals: 2543
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 281
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variant carriers: 0

GenotypeQuality
all individuals: 6243
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variant carriers: 0

GenotypeQuality
all individuals: 118
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variant carriers: 0

GenotypeQuality
all individuals: 1525
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1923
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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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Other
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European (Non-Finnish)
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African
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East Asian
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Latino
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FS
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VQSLOD
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MQ
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ReadPosRankSum
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QD
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InbreedingCoeff
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BaseQRankSum
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DP
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MQRankSum
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ClippingRankSum
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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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Latino
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European (Non-Finnish)
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Other
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South Asian
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European (Finnish)
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QD
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MQRankSum
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VQSLOD
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FS
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DP
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ClippingRankSum
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InbreedingCoeff
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MQ
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BaseQRankSum
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ReadPosRankSum
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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 frequency: 0.0e0
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European (Finnish)
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South Asian
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African
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East Asian
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Other
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European (Non-Finnish)
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InbreedingCoeff
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VQSLOD
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MQ
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BaseQRankSum
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MQRankSum
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ClippingRankSum
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FS
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ReadPosRankSum
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DP
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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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African
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European (Non-Finnish)
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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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InbreedingCoeff
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MQRankSum
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ClippingRankSum
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BaseQRankSum
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FS
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ReadPosRankSum
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VQSLOD
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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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East Asian
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South Asian
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African
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European (Non-Finnish)
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Other
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European (Finnish)
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Latino
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VQSLOD
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QD
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InbreedingCoeff
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ReadPosRankSum
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DP
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ClippingRankSum
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FS
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MQRankSum
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BaseQRankSum
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MQ
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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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Latino
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European (Finnish)
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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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MQ
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FS
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InbreedingCoeff
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QD
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DP
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VQSLOD
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ReadPosRankSum
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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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African
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South Asian
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QD
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MQRankSum
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BaseQRankSum
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VQSLOD
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MQ
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FS
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DP
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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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num of homozygotes: 0

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

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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Latino
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South Asian
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European (Non-Finnish)
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Other
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MQRankSum
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InbreedingCoeff
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FS
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QD
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VQSLOD
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BaseQRankSum
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ReadPosRankSum
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MQ
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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European (Non-Finnish)
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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 num: 11552
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East Asian
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South Asian
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European (Finnish)
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BaseQRankSum
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QD
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InbreedingCoeff
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VQSLOD
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FS
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ReadPosRankSum
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MQ
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MQRankSum
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ClippingRankSum
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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allele num: 6584
num of homozygotes: 0

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

European (Non-Finnish)
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East 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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ClippingRankSum
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BaseQRankSum
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InbreedingCoeff
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ReadPosRankSum
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MQRankSum
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FS
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QD
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DP
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VQSLOD
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MQ
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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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African
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East Asian
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European (Finnish)
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Other
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European (Non-Finnish)
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South Asian
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MQRankSum
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DP
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BaseQRankSum
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InbreedingCoeff
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VQSLOD
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ClippingRankSum
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QD
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ReadPosRankSum
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MQ
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SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 4.08e-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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 5.25e1
variant carriers: 0

Other
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allele frequency: 0.0e0
allele num: 902
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
allele num: 8644
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66418
num of homozygotes: 0

European (Finnish)
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allele frequency: 1.519295047098146e-4
allele num: 6582
num of homozygotes: 0

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 frequency: 0.0e0
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South Asian
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BaseQRankSum
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FS
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DP
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MQRankSum
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VQSLOD
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ReadPosRankSum
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ClippingRankSum
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InbreedingCoeff
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QD
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MQ
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SIO_000300: 5.883e1

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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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 6584
num of homozygotes: 0

Other
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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

African
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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 (Non-Finnish)
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num of homozygotes: 0

East Asian
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InbreedingCoeff
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BaseQRankSum
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ClippingRankSum
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MQ
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FS
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QD
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MQRankSum
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VQSLOD
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ReadPosRankSum
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DP
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 count: 0
allele frequency: 0.0e0
allele num: 10366
num of homozygotes: 0

European (Finnish)
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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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num of homozygotes: 0

European (Non-Finnish)
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allele num: 66394
num of homozygotes: 0

Latino
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East Asian
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South Asian
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ClippingRankSum
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FS
type: SiteQuality
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MQRankSum
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DP
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InbreedingCoeff
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MQ
type: SiteQuality
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VQSLOD
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ReadPosRankSum
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QD
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BaseQRankSum
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 count: 0
allele frequency: 0.0e0
allele num: 10366
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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European (Finnish)
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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
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allele num: 66398
num of homozygotes: 0

Latino
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num of homozygotes: 0

South Asian
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VQSLOD
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InbreedingCoeff
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QD
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ClippingRankSum
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DP
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MQ
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MQRankSum
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FS
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SIO_000300: 2.499e0

BaseQRankSum
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ReadPosRankSum
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

European (Finnish)
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East Asian
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Latino
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European (Non-Finnish)
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Other
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South Asian
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BaseQRankSum
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ReadPosRankSum
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QD
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MQ
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InbreedingCoeff
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MQRankSum
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FS
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VQSLOD
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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African
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East Asian
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Other
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European (Finnish)
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European (Non-Finnish)
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MQ
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InbreedingCoeff
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DP
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ClippingRankSum
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VQSLOD
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QD
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FS
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ReadPosRankSum
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 (Non-Finnish)
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East Asian
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European (Finnish)
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Other
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MQRankSum
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InbreedingCoeff
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DP
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VQSLOD
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MQ
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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East Asian
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DP
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MQRankSum
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VQSLOD
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MQ
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BaseQRankSum
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InbreedingCoeff
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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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Latino
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South Asian
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East Asian
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European (Non-Finnish)
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European (Finnish)
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ClippingRankSum
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VQSLOD
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DP
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FS
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QD
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InbreedingCoeff
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ReadPosRankSum
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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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African
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European (Non-Finnish)
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European (Finnish)
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Other
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East Asian
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South Asian
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Latino
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ClippingRankSum
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QD
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MQ
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FS
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MQRankSum
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BaseQRankSum
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DP
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VQSLOD
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ReadPosRankSum
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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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South Asian
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African
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Latino
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East Asian
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European (Non-Finnish)
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European (Finnish)
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InbreedingCoeff
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MQ
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FS
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MQRankSum
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QD
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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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GenotypeQuality
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African
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East Asian
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European (Non-Finnish)
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MQ
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FS
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DP
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East Asian
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African
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European (Non-Finnish)
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MQ
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DP
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FS
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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Latino
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South Asian
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East Asian
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Other
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European (Non-Finnish)
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DP
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BaseQRankSum
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MQRankSum
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ReadPosRankSum
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ClippingRankSum
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InbreedingCoeff
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FS
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MQ
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VQSLOD
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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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African
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East Asian
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South Asian
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European (Non-Finnish)
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European (Finnish)
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Other
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ReadPosRankSum
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DP
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MQRankSum
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InbreedingCoeff
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FS
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MQ
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ClippingRankSum
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VQSLOD
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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European (Non-Finnish)
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Other
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South Asian
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East Asian
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ReadPosRankSum
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FS
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MQRankSum
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VQSLOD
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ClippingRankSum
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InbreedingCoeff
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BaseQRankSum
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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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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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allele frequency: 0.0e0
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European (Non-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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DP
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ReadPosRankSum
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FS
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QD
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VQSLOD
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BaseQRankSum
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MQRankSum
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ClippingRankSum
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InbreedingCoeff
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MQ
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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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East Asian
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European (Non-Finnish)
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South Asian
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European (Finnish)
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Latino
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InbreedingCoeff
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ClippingRankSum
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BaseQRankSum
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MQRankSum
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DP
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FS
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MQ
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ReadPosRankSum
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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East Asian
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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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BaseQRankSum
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InbreedingCoeff
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MQ
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ClippingRankSum
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ReadPosRankSum
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QD
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MQRankSum
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FS
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VQSLOD
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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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South Asian
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allele num: 15594
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East Asian
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European (Finnish)
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Latino
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European (Non-Finnish)
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African
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ReadPosRankSum
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DP
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MQRankSum
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ClippingRankSum
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MQ
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FS
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VQSLOD
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InbreedingCoeff
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SIO_000300: -2.6e-3

QD
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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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GenotypeQuality
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bin: 5.25e1
variant carriers: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 15580
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5298
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.669449081803005e-5
allele num: 59900
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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num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9138
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10074
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -7.819e-1

FS
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ClippingRankSum
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DP
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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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SIO_000300: 2.12e-1

GenotypeDepth
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variant carriers: 0

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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bin: 5.25e1
variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9094
num of homozygotes: 0

South Asian
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allele count: 2
allele frequency: 1.28783000643915e-4
allele num: 15530
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 9964
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

East 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 count: 0
allele frequency: 0.0e0
allele num: 59410
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

DP
type: SiteQuality
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QD
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InbreedingCoeff
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ClippingRankSum
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VQSLOD
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BaseQRankSum
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ReadPosRankSum
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SIO_000300: 8.699999999999999e-2

MQRankSum
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SIO_000300: -1.09e-1

FS
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SIO_000300: 0.0e0

MQ
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SIO_000300: 6.0e1

GenotypeDepth
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GenotypeDepth
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variant carriers: 1

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 count: 3
allele frequency: 3.302509907529723e-4
allele num: 9084
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 59346
num of homozygotes: 0

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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num of homozygotes: 0

East Asian
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allele count: 1
allele frequency: 1.277465508431272e-4
allele num: 7828
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5256
num of homozygotes: 0

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

BaseQRankSum
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SIO_000300: -8.61e-1

DP
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ClippingRankSum
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MQ
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VQSLOD
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MQRankSum
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ReadPosRankSum
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FS
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SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.1e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-3

GenotypeDepth
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variant carriers: 0

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

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

African
type: Population
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

South Asian
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allele count: 1
allele frequency: 6.510416666666667e-5
allele num: 15360
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

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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DP
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ClippingRankSum
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VQSLOD
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ReadPosRankSum
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BaseQRankSum
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InbreedingCoeff
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MQ
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QD
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MQRankSum
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FS
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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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num of homozygotes: 0

African
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num of homozygotes: 0

East Asian
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allele frequency: 1.325556733828208e-4
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South Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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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 frequency: 0.0e0
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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

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

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

East Asian
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allele frequency: 1.334044823906083e-4
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South Asian
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Latino
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 0.0e0
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European (Finnish)
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Other
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QD
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BaseQRankSum
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ClippingRankSum
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MQRankSum
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VQSLOD
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InbreedingCoeff
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MQ
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DP
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FS
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ReadPosRankSum
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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 (Non-Finnish)
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allele count: 3
allele frequency: 5.377886132224294e-5
allele num: 55784
num of homozygotes: 0

European (Finnish)
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allele frequency: 2.084201750729471e-4
allele num: 4798
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Other
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South Asian
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African
type: Population
allele count: 0
allele frequency: 0.0e0
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Latino
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allele frequency: 1.086012163336229e-4
allele num: 9208
num of homozygotes: 0

East Asian
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allele count: 2
allele frequency: 2.751031636863824e-4
allele num: 7270
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.9e-1

MQ
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SIO_000300: 6.0e1

QD
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VQSLOD
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InbreedingCoeff
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SIO_000300: -6.7e-3

MQRankSum
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SIO_000300: -3.8e-1

FS
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SIO_000300: 9.779999999999999e0

DP
type: SiteQuality
SIO_000300: 1.000405e6

ReadPosRankSum
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SIO_000300: -1.74e-1

GenotypeDepth
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variant carriers: 0

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: 1
allele frequency: 1.171234481143125e-4
allele num: 8538
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

European (Finnish)
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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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num of homozygotes: 0

European (Non-Finnish)
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allele count: 4
allele frequency: 7.205908845253108e-5
allele num: 55510
num of homozygotes: 0

South Asian
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allele count: 3
allele frequency: 2.003740315255143e-4
allele num: 14972
num of homozygotes: 0

Latino
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MQRankSum
type: SiteQuality
SIO_000300: 3.1e-2

ClippingRankSum
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InbreedingCoeff
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FS
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MQ
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QD
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ReadPosRankSum
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VQSLOD
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BaseQRankSum
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SIO_000300: -2.83e-1

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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 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 (Finnish)
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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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num of homozygotes: 0

European (Non-Finnish)
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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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num of homozygotes: 0

South Asian
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num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.09e-1

FS
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SIO_000300: 0.0e0

QD
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MQ
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ReadPosRankSum
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VQSLOD
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InbreedingCoeff
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SIO_000300: -7.8e-3

DP
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SIO_000300: 9.65301e5

BaseQRankSum
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SIO_000300: -1.927e0

ClippingRankSum
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SIO_000300: 1.45e0

GenotypeDepth
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variant carriers: 0

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: 6782
num of homozygotes: 0

African
type: Population
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 (Finnish)
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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 frequency: 0.0e0
allele num: 684
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 53022
num of homozygotes: 0

South Asian
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QD
type: SiteQuality
SIO_000300: 1.693e1

BaseQRankSum
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SIO_000300: 1.98e-1

ClippingRankSum
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SIO_000300: 7.27e-1

VQSLOD
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SIO_000300: 7.57e-1

MQRankSum
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SIO_000300: 7.27e-1

ReadPosRankSum
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SIO_000300: 9.22e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
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SIO_000300: -8.1e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 9.64803e5

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 count: 0
allele frequency: 0.0e0
allele num: 10328
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
allele num: 6536
num of homozygotes: 0

Latino
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allele frequency: 8.665511265164645e-5
allele num: 11540
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 66074
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South Asian
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Other
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ReadPosRankSum
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SIO_000300: 3.75e-1

FS
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MQRankSum
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InbreedingCoeff
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ClippingRankSum
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DP
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VQSLOD
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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: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 frequency: 0.0e0
allele num: 8618
num of homozygotes: 0

European (Finnish)
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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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South Asian
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African
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allele num: 10328
num of homozygotes: 0

Latino
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FS
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MQ
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BaseQRankSum
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MQRankSum
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ReadPosRankSum
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QD
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VQSLOD
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InbreedingCoeff
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ClippingRankSum
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DP
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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

South Asian
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African
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allele frequency: 3.873716831299632e-4
allele num: 10326
num of homozygotes: 0

Latino
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European (Finnish)
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European (Non-Finnish)
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East Asian
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Other
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InbreedingCoeff
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DP
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MQ
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MQRankSum
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BaseQRankSum
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ClippingRankSum
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FS
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QD
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VQSLOD
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ReadPosRankSum
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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: 6500
num of homozygotes: 0

Other
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African
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allele count: 0
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Latino
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South Asian
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East Asian
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European (Non-Finnish)
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allele frequency: 0.0e0
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QD
type: SiteQuality
SIO_000300: 1.094e1

MQRankSum
type: SiteQuality
SIO_000300: -4.69e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.94e-1

MQ
type: SiteQuality
SIO_000300: 5.952e1

DP
type: SiteQuality
SIO_000300: 1.937345e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -5.141e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.5e-2

VQSLOD
type: SiteQuality
SIO_000300: 7.47e-1

FS
type: SiteQuality
SIO_000300: 3.657e0

GenotypeDepth
all individuals: 493
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 102
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 132
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 129
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6796
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 83
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 859
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32546
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 588
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 812
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3601
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9517
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1908
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3391
bin: 7.75e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 8.668515950069348e-5
allele num: 11536
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8620
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6492
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10322
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66096
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16506
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.25e-1

FS
type: SiteQuality
SIO_000300: 1.714e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

DP
type: SiteQuality
SIO_000300: 1.93653e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.38e-1

MQRankSum
type: SiteQuality
SIO_000300: -5.35e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.207e0

QD
type: SiteQuality
SIO_000300: 2.336e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.065e0