12-102036210-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102036210
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 102036210
    reference: chr 12
allele count: 1
allele frequency: 8.351986102295126e-6
allele num: 119732
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000442847
  ensembl transcript: ENST00000541119
  gene symbol: MYBPC1
  hgvsc: ENST00000541119.1:c.568C>G
  hgvsp: ENSP00000442847.1:p.Gln190Glu
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000354849
  ensembl transcript: ENST00000361466
  gene symbol: MYBPC1
  hgvsc: ENST00000361466.2:c.679C>G
  hgvsp: ENSP00000354849.2:p.Gln227Glu
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000388989
  ensembl transcript: ENST00000441232
  gene symbol: MYBPC1
  hgvsc: ENST00000441232.1:c.604C>G
  hgvsp: ENSP00000388989.1:p.Gln202Glu
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000400908
  ensembl transcript: ENST00000452455
  gene symbol: MYBPC1
  hgvsc: ENST00000452455.2:c.604C>G
  hgvsp: ENSP00000400908.2:p.Gln202Glu
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447362
  ensembl transcript: ENST00000547509
  gene symbol: MYBPC1
  hgvsc: ENST00000547509.1:c.562C>G
  hgvsp: ENSP00000447362.1:p.Gln188Glu
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000448175
  ensembl transcript: ENST00000547405
  gene symbol: MYBPC1
  hgvsc: ENST00000547405.1:c.526C>G
  hgvsp: ENSP00000448175.1:p.Gln176Glu
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447404
  ensembl transcript: ENST00000550514
  gene symbol: MYBPC1
  hgvsc: ENST00000550514.1:c.307C>G
  hgvsp: ENSP00000447404.1:p.Gln103Glu
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000449702
  ensembl transcript: ENST00000550270
  gene symbol: MYBPC1
  hgvsc: ENST00000550270.1:c.604C>G
  hgvsp: ENSP00000449702.1:p.Gln202Glu
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447660
  ensembl transcript: ENST00000549145
  gene symbol: MYBPC1
  hgvsc: ENST00000549145.1:c.643C>G
  hgvsp: ENSP00000447660.1:p.Gln215Glu
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000446128
  ensembl transcript: ENST00000536007
  gene symbol: MYBPC1
  hgvsc: ENST00000536007.1:c.547C>G
  hgvsp: ENSP00000446128.1:p.Gln183Glu
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000376665
  ensembl transcript: ENST00000392934
  gene symbol: MYBPC1
  hgvsc: ENST00000392934.3:c.565C>G
  hgvsp: ENSP00000376665.3:p.Gln189Glu
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl transcript: ENST00000550501
  gene symbol: MYBPC1
  hgvsc: ENST00000550501.1:n.574+27488C>G
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000354845
  ensembl transcript: ENST00000361685
  gene symbol: MYBPC1
  hgvsc: ENST00000361685.2:c.679C>G
  hgvsp: ENSP00000354845.2:p.Gln227Glu
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196091
  ensembl transcript: ENST00000552198
  gene symbol: MYBPC1
  hgvsc: ENST00000552198.1:n.566C>G
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000353822
  ensembl transcript: ENST00000360610
  gene symbol: MYBPC1
  hgvsc: ENST00000360610.2:c.604C>G
  hgvsp: ENSP00000353822.2:p.Gln202Glu
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447116
  ensembl transcript: ENST00000551300
  gene symbol: MYBPC1
  hgvsc: ENST00000551300.1:c.307C>G
  hgvsp: ENSP00000447116.1:p.Gln103Glu
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000440034
  ensembl transcript: ENST00000545503
  gene symbol: MYBPC1
  hgvsc: ENST00000545503.2:c.604C>G
  hgvsp: ENSP00000440034.2:p.Gln202Glu
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447900
  ensembl transcript: ENST00000553190
  gene symbol: MYBPC1
  hgvsc: ENST00000553190.1:c.604C>G
  hgvsp: ENSP00000447900.1:p.Gln202Glu
  variant of: http://identifiers.org/hgnc/7549
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1671
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln202Glu
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: Latino
population: East Asian
reference allele: C
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP

12-102036239-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102036239
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 102036239
    reference: chr 12
allele count: 2
allele frequency: 1.671849399806065e-5
allele num: 119628
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000448175
  ensembl transcript: ENST00000547405
  gene symbol: MYBPC1
  hgvsc: ENST00000547405.1:c.555G>T
  hgvsp: ENSP00000448175.1:p.Trp185Cys
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447900
  ensembl transcript: ENST00000553190
  gene symbol: MYBPC1
  hgvsc: ENST00000553190.1:c.633G>T
  hgvsp: ENSP00000447900.1:p.Trp211Cys
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447362
  ensembl transcript: ENST00000547509
  gene symbol: MYBPC1
  hgvsc: ENST00000547509.1:c.591G>T
  hgvsp: ENSP00000447362.1:p.Trp197Cys
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000376665
  ensembl transcript: ENST00000392934
  gene symbol: MYBPC1
  hgvsc: ENST00000392934.3:c.594G>T
  hgvsp: ENSP00000376665.3:p.Trp198Cys
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000442847
  ensembl transcript: ENST00000541119
  gene symbol: MYBPC1
  hgvsc: ENST00000541119.1:c.597G>T
  hgvsp: ENSP00000442847.1:p.Trp199Cys
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000354845
  ensembl transcript: ENST00000361685
  gene symbol: MYBPC1
  hgvsc: ENST00000361685.2:c.708G>T
  hgvsp: ENSP00000354845.2:p.Trp236Cys
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000446128
  ensembl transcript: ENST00000536007
  gene symbol: MYBPC1
  hgvsc: ENST00000536007.1:c.576G>T
  hgvsp: ENSP00000446128.1:p.Trp192Cys
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000400908
  ensembl transcript: ENST00000452455
  gene symbol: MYBPC1
  hgvsc: ENST00000452455.2:c.633G>T
  hgvsp: ENSP00000400908.2:p.Trp211Cys
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447116
  ensembl transcript: ENST00000551300
  gene symbol: MYBPC1
  hgvsc: ENST00000551300.1:c.336G>T
  hgvsp: ENSP00000447116.1:p.Trp112Cys
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000440034
  ensembl transcript: ENST00000545503
  gene symbol: MYBPC1
  hgvsc: ENST00000545503.2:c.633G>T
  hgvsp: ENSP00000440034.2:p.Trp211Cys
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000353822
  ensembl transcript: ENST00000360610
  gene symbol: MYBPC1
  hgvsc: ENST00000360610.2:c.633G>T
  hgvsp: ENSP00000353822.2:p.Trp211Cys
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000449702
  ensembl transcript: ENST00000550270
  gene symbol: MYBPC1
  hgvsc: ENST00000550270.1:c.633G>T
  hgvsp: ENSP00000449702.1:p.Trp211Cys
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000354849
  ensembl transcript: ENST00000361466
  gene symbol: MYBPC1
  hgvsc: ENST00000361466.2:c.708G>T
  hgvsp: ENSP00000354849.2:p.Trp236Cys
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl transcript: ENST00000550501
  gene symbol: MYBPC1
  hgvsc: ENST00000550501.1:n.574+27517G>T
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000388989
  ensembl transcript: ENST00000441232
  gene symbol: MYBPC1
  hgvsc: ENST00000441232.1:c.633G>T
  hgvsp: ENSP00000388989.1:p.Trp211Cys
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447660
  ensembl transcript: ENST00000549145
  gene symbol: MYBPC1
  hgvsc: ENST00000549145.1:c.672G>T
  hgvsp: ENSP00000447660.1:p.Trp224Cys
  variant of: http://identifiers.org/hgnc/7549
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 931
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1671
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 834
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2559
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Trp211Cys
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: Other
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum

12-102036240-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102036240
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 102036240
    reference: chr 12
allele count: 1
allele frequency: 8.359666282122017e-6
allele num: 119622
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000449702
  ensembl transcript: ENST00000550270
  gene symbol: MYBPC1
  hgvsc: ENST00000550270.1:c.634G>A
  hgvsp: ENSP00000449702.1:p.Glu212Lys
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447116
  ensembl transcript: ENST00000551300
  gene symbol: MYBPC1
  hgvsc: ENST00000551300.1:c.337G>A
  hgvsp: ENSP00000447116.1:p.Glu113Lys
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000388989
  ensembl transcript: ENST00000441232
  gene symbol: MYBPC1
  hgvsc: ENST00000441232.1:c.634G>A
  hgvsp: ENSP00000388989.1:p.Glu212Lys
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000354849
  ensembl transcript: ENST00000361466
  gene symbol: MYBPC1
  hgvsc: ENST00000361466.2:c.709G>A
  hgvsp: ENSP00000354849.2:p.Glu237Lys
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl transcript: ENST00000550501
  gene symbol: MYBPC1
  hgvsc: ENST00000550501.1:n.574+27518G>A
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000448175
  ensembl transcript: ENST00000547405
  gene symbol: MYBPC1
  hgvsc: ENST00000547405.1:c.556G>A
  hgvsp: ENSP00000448175.1:p.Glu186Lys
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000353822
  ensembl transcript: ENST00000360610
  gene symbol: MYBPC1
  hgvsc: ENST00000360610.2:c.634G>A
  hgvsp: ENSP00000353822.2:p.Glu212Lys
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447362
  ensembl transcript: ENST00000547509
  gene symbol: MYBPC1
  hgvsc: ENST00000547509.1:c.592G>A
  hgvsp: ENSP00000447362.1:p.Glu198Lys
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000446128
  ensembl transcript: ENST00000536007
  gene symbol: MYBPC1
  hgvsc: ENST00000536007.1:c.577G>A
  hgvsp: ENSP00000446128.1:p.Glu193Lys
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000376665
  ensembl transcript: ENST00000392934
  gene symbol: MYBPC1
  hgvsc: ENST00000392934.3:c.595G>A
  hgvsp: ENSP00000376665.3:p.Glu199Lys
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000440034
  ensembl transcript: ENST00000545503
  gene symbol: MYBPC1
  hgvsc: ENST00000545503.2:c.634G>A
  hgvsp: ENSP00000440034.2:p.Glu212Lys
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000442847
  ensembl transcript: ENST00000541119
  gene symbol: MYBPC1
  hgvsc: ENST00000541119.1:c.598G>A
  hgvsp: ENSP00000442847.1:p.Glu200Lys
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000354845
  ensembl transcript: ENST00000361685
  gene symbol: MYBPC1
  hgvsc: ENST00000361685.2:c.709G>A
  hgvsp: ENSP00000354845.2:p.Glu237Lys
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447900
  ensembl transcript: ENST00000553190
  gene symbol: MYBPC1
  hgvsc: ENST00000553190.1:c.634G>A
  hgvsp: ENSP00000447900.1:p.Glu212Lys
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447660
  ensembl transcript: ENST00000549145
  gene symbol: MYBPC1
  hgvsc: ENST00000549145.1:c.673G>A
  hgvsp: ENSP00000447660.1:p.Glu225Lys
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000400908
  ensembl transcript: ENST00000452455
  gene symbol: MYBPC1
  hgvsc: ENST00000452455.2:c.634G>A
  hgvsp: ENSP00000400908.2:p.Glu212Lys
  variant of: http://identifiers.org/hgnc/7549
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 948
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3157
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 845
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu212Lys
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
population: East Asian
reference allele: G
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum

12-102036242-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102036242
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 102036242
    reference: chr 12
allele count: 2
allele frequency: 1.67238063383226e-5
allele num: 119590
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000442847
  ensembl transcript: ENST00000541119
  gene symbol: MYBPC1
  hgvsc: ENST00000541119.1:c.600G>A
  hgvsp: ENST00000541119.1:c.600G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447660
  ensembl transcript: ENST00000549145
  gene symbol: MYBPC1
  hgvsc: ENST00000549145.1:c.675G>A
  hgvsp: ENST00000549145.1:c.675G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000354849
  ensembl transcript: ENST00000361466
  gene symbol: MYBPC1
  hgvsc: ENST00000361466.2:c.711G>A
  hgvsp: ENST00000361466.2:c.711G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447362
  ensembl transcript: ENST00000547509
  gene symbol: MYBPC1
  hgvsc: ENST00000547509.1:c.594G>A
  hgvsp: ENST00000547509.1:c.594G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000449702
  ensembl transcript: ENST00000550270
  gene symbol: MYBPC1
  hgvsc: ENST00000550270.1:c.636G>A
  hgvsp: ENST00000550270.1:c.636G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447116
  ensembl transcript: ENST00000551300
  gene symbol: MYBPC1
  hgvsc: ENST00000551300.1:c.339G>A
  hgvsp: ENST00000551300.1:c.339G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000376665
  ensembl transcript: ENST00000392934
  gene symbol: MYBPC1
  hgvsc: ENST00000392934.3:c.597G>A
  hgvsp: ENST00000392934.3:c.597G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447900
  ensembl transcript: ENST00000553190
  gene symbol: MYBPC1
  hgvsc: ENST00000553190.1:c.636G>A
  hgvsp: ENST00000553190.1:c.636G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000440034
  ensembl transcript: ENST00000545503
  gene symbol: MYBPC1
  hgvsc: ENST00000545503.2:c.636G>A
  hgvsp: ENST00000545503.2:c.636G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000448175
  ensembl transcript: ENST00000547405
  gene symbol: MYBPC1
  hgvsc: ENST00000547405.1:c.558G>A
  hgvsp: ENST00000547405.1:c.558G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl transcript: ENST00000550501
  gene symbol: MYBPC1
  hgvsc: ENST00000550501.1:n.574+27520G>A
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000353822
  ensembl transcript: ENST00000360610
  gene symbol: MYBPC1
  hgvsc: ENST00000360610.2:c.636G>A
  hgvsp: ENST00000360610.2:c.636G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000388989
  ensembl transcript: ENST00000441232
  gene symbol: MYBPC1
  hgvsc: ENST00000441232.1:c.636G>A
  hgvsp: ENST00000441232.1:c.636G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000354845
  ensembl transcript: ENST00000361685
  gene symbol: MYBPC1
  hgvsc: ENST00000361685.2:c.711G>A
  hgvsp: ENST00000361685.2:c.711G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000400908
  ensembl transcript: ENST00000452455
  gene symbol: MYBPC1
  hgvsc: ENST00000452455.2:c.636G>A
  hgvsp: ENST00000452455.2:c.636G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000446128
  ensembl transcript: ENST00000536007
  gene symbol: MYBPC1
  hgvsc: ENST00000536007.1:c.579G>A
  hgvsp: ENST00000536007.1:c.579G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17552
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1274
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 941
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 859
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6410
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu212Glu
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: G
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD

12-102036245-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102036245
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 102036245
    reference: chr 12
allele count: 1
allele frequency: 8.369041242635244e-6
allele num: 119488
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447660
  ensembl transcript: ENST00000549145
  gene symbol: MYBPC1
  hgvsc: ENST00000549145.1:c.678G>A
  hgvsp: ENST00000549145.1:c.678G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000448175
  ensembl transcript: ENST00000547405
  gene symbol: MYBPC1
  hgvsc: ENST00000547405.1:c.561G>A
  hgvsp: ENST00000547405.1:c.561G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl transcript: ENST00000550501
  gene symbol: MYBPC1
  hgvsc: ENST00000550501.1:n.574+27523G>A
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000388989
  ensembl transcript: ENST00000441232
  gene symbol: MYBPC1
  hgvsc: ENST00000441232.1:c.639G>A
  hgvsp: ENST00000441232.1:c.639G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000449702
  ensembl transcript: ENST00000550270
  gene symbol: MYBPC1
  hgvsc: ENST00000550270.1:c.639G>A
  hgvsp: ENST00000550270.1:c.639G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000440034
  ensembl transcript: ENST00000545503
  gene symbol: MYBPC1
  hgvsc: ENST00000545503.2:c.639G>A
  hgvsp: ENST00000545503.2:c.639G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000442847
  ensembl transcript: ENST00000541119
  gene symbol: MYBPC1
  hgvsc: ENST00000541119.1:c.603G>A
  hgvsp: ENST00000541119.1:c.603G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000400908
  ensembl transcript: ENST00000452455
  gene symbol: MYBPC1
  hgvsc: ENST00000452455.2:c.639G>A
  hgvsp: ENST00000452455.2:c.639G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447900
  ensembl transcript: ENST00000553190
  gene symbol: MYBPC1
  hgvsc: ENST00000553190.1:c.639G>A
  hgvsp: ENST00000553190.1:c.639G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000354845
  ensembl transcript: ENST00000361685
  gene symbol: MYBPC1
  hgvsc: ENST00000361685.2:c.714G>A
  hgvsp: ENST00000361685.2:c.714G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447116
  ensembl transcript: ENST00000551300
  gene symbol: MYBPC1
  hgvsc: ENST00000551300.1:c.342G>A
  hgvsp: ENST00000551300.1:c.342G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000354849
  ensembl transcript: ENST00000361466
  gene symbol: MYBPC1
  hgvsc: ENST00000361466.2:c.714G>A
  hgvsp: ENST00000361466.2:c.714G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000446128
  ensembl transcript: ENST00000536007
  gene symbol: MYBPC1
  hgvsc: ENST00000536007.1:c.582G>A
  hgvsp: ENST00000536007.1:c.582G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447362
  ensembl transcript: ENST00000547509
  gene symbol: MYBPC1
  hgvsc: ENST00000547509.1:c.597G>A
  hgvsp: ENST00000547509.1:c.597G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000376665
  ensembl transcript: ENST00000392934
  gene symbol: MYBPC1
  hgvsc: ENST00000392934.3:c.600G>A
  hgvsp: ENST00000392934.3:c.600G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000353822
  ensembl transcript: ENST00000360610
  gene symbol: MYBPC1
  hgvsc: ENST00000360610.2:c.639G>A
  hgvsp: ENST00000360610.2:c.639G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1671
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1141
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 613
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu213Leu
num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
reference allele: G
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: QD

12-102036254-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102036254
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 102036254
    reference: chr 12
allele count: 1
allele frequency: 8.377735330585436e-6
allele num: 119364
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000388989
  ensembl transcript: ENST00000441232
  gene symbol: MYBPC1
  hgvsc: ENST00000441232.1:c.648C>G
  hgvsp: ENSP00000388989.1:p.Asn216Lys
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447900
  ensembl transcript: ENST00000553190
  gene symbol: MYBPC1
  hgvsc: ENST00000553190.1:c.648C>G
  hgvsp: ENSP00000447900.1:p.Asn216Lys
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447116
  ensembl transcript: ENST00000551300
  gene symbol: MYBPC1
  hgvsc: ENST00000551300.1:c.351C>G
  hgvsp: ENSP00000447116.1:p.Asn117Lys
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447660
  ensembl transcript: ENST00000549145
  gene symbol: MYBPC1
  hgvsc: ENST00000549145.1:c.687C>G
  hgvsp: ENSP00000447660.1:p.Asn229Lys
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000354849
  ensembl transcript: ENST00000361466
  gene symbol: MYBPC1
  hgvsc: ENST00000361466.2:c.723C>G
  hgvsp: ENSP00000354849.2:p.Asn241Lys
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000440034
  ensembl transcript: ENST00000545503
  gene symbol: MYBPC1
  hgvsc: ENST00000545503.2:c.648C>G
  hgvsp: ENSP00000440034.2:p.Asn216Lys
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000354845
  ensembl transcript: ENST00000361685
  gene symbol: MYBPC1
  hgvsc: ENST00000361685.2:c.723C>G
  hgvsp: ENSP00000354845.2:p.Asn241Lys
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000448175
  ensembl transcript: ENST00000547405
  gene symbol: MYBPC1
  hgvsc: ENST00000547405.1:c.570C>G
  hgvsp: ENSP00000448175.1:p.Asn190Lys
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000446128
  ensembl transcript: ENST00000536007
  gene symbol: MYBPC1
  hgvsc: ENST00000536007.1:c.591C>G
  hgvsp: ENSP00000446128.1:p.Asn197Lys
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000449702
  ensembl transcript: ENST00000550270
  gene symbol: MYBPC1
  hgvsc: ENST00000550270.1:c.648C>G
  hgvsp: ENSP00000449702.1:p.Asn216Lys
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000442847
  ensembl transcript: ENST00000541119
  gene symbol: MYBPC1
  hgvsc: ENST00000541119.1:c.612C>G
  hgvsp: ENSP00000442847.1:p.Asn204Lys
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000400908
  ensembl transcript: ENST00000452455
  gene symbol: MYBPC1
  hgvsc: ENST00000452455.2:c.648C>G
  hgvsp: ENSP00000400908.2:p.Asn216Lys
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000353822
  ensembl transcript: ENST00000360610
  gene symbol: MYBPC1
  hgvsc: ENST00000360610.2:c.648C>G
  hgvsp: ENSP00000353822.2:p.Asn216Lys
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl transcript: ENST00000550501
  gene symbol: MYBPC1
  hgvsc: ENST00000550501.1:n.574+27532C>G
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447362
  ensembl transcript: ENST00000547509
  gene symbol: MYBPC1
  hgvsc: ENST00000547509.1:c.606C>G
  hgvsp: ENSP00000447362.1:p.Asn202Lys
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000376665
  ensembl transcript: ENST00000392934
  gene symbol: MYBPC1
  hgvsc: ENST00000392934.3:c.609C>G
  hgvsp: ENSP00000376665.3:p.Asn203Lys
  variant of: http://identifiers.org/hgnc/7549
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 942
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1672
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6404
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn216Lys
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Latino
population: East Asian
reference allele: C
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP

12-102036267-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102036267
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 102036267
    reference: chr 12
allele count: 1
allele frequency: 8.41864224137931e-6
allele num: 118784
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000388989
  ensembl transcript: ENST00000441232
  gene symbol: MYBPC1
  hgvsc: ENST00000441232.1:c.661G>C
  hgvsp: ENSP00000388989.1:p.Glu221Gln
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000449702
  ensembl transcript: ENST00000550270
  gene symbol: MYBPC1
  hgvsc: ENST00000550270.1:c.661G>C
  hgvsp: ENSP00000449702.1:p.Glu221Gln
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000446128
  ensembl transcript: ENST00000536007
  gene symbol: MYBPC1
  hgvsc: ENST00000536007.1:c.604G>C
  hgvsp: ENSP00000446128.1:p.Glu202Gln
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl transcript: ENST00000550501
  gene symbol: MYBPC1
  hgvsc: ENST00000550501.1:n.574+27545G>C
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447116
  ensembl transcript: ENST00000551300
  gene symbol: MYBPC1
  hgvsc: ENST00000551300.1:c.364G>C
  hgvsp: ENSP00000447116.1:p.Glu122Gln
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000442847
  ensembl transcript: ENST00000541119
  gene symbol: MYBPC1
  hgvsc: ENST00000541119.1:c.625G>C
  hgvsp: ENSP00000442847.1:p.Glu209Gln
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000354845
  ensembl transcript: ENST00000361685
  gene symbol: MYBPC1
  hgvsc: ENST00000361685.2:c.736G>C
  hgvsp: ENSP00000354845.2:p.Glu246Gln
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447660
  ensembl transcript: ENST00000549145
  gene symbol: MYBPC1
  hgvsc: ENST00000549145.1:c.700G>C
  hgvsp: ENSP00000447660.1:p.Glu234Gln
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000354849
  ensembl transcript: ENST00000361466
  gene symbol: MYBPC1
  hgvsc: ENST00000361466.2:c.736G>C
  hgvsp: ENSP00000354849.2:p.Glu246Gln
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000400908
  ensembl transcript: ENST00000452455
  gene symbol: MYBPC1
  hgvsc: ENST00000452455.2:c.661G>C
  hgvsp: ENSP00000400908.2:p.Glu221Gln
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000376665
  ensembl transcript: ENST00000392934
  gene symbol: MYBPC1
  hgvsc: ENST00000392934.3:c.622G>C
  hgvsp: ENSP00000376665.3:p.Glu208Gln
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000440034
  ensembl transcript: ENST00000545503
  gene symbol: MYBPC1
  hgvsc: ENST00000545503.2:c.661G>C
  hgvsp: ENSP00000440034.2:p.Glu221Gln
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000353822
  ensembl transcript: ENST00000360610
  gene symbol: MYBPC1
  hgvsc: ENST00000360610.2:c.661G>C
  hgvsp: ENSP00000353822.2:p.Glu221Gln
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447900
  ensembl transcript: ENST00000553190
  gene symbol: MYBPC1
  hgvsc: ENST00000553190.1:c.661G>C
  hgvsp: ENSP00000447900.1:p.Glu221Gln
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000448175
  ensembl transcript: ENST00000547405
  gene symbol: MYBPC1
  hgvsc: ENST00000547405.1:c.583G>C
  hgvsp: ENSP00000448175.1:p.Glu195Gln
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447362
  ensembl transcript: ENST00000547509
  gene symbol: MYBPC1
  hgvsc: ENST00000547509.1:c.619G>C
  hgvsp: ENSP00000447362.1:p.Glu207Gln
  variant of: http://identifiers.org/hgnc/7549
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2105
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17191
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16520
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 941
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 613
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6362
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu221Gln
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: QD

12-102036273-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102036273
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 102036273
    reference: chr 12
allele count: 3
allele frequency: 2.534554425332027e-5
allele num: 118364
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000449702
  ensembl transcript: ENST00000550270
  gene symbol: MYBPC1
  hgvsc: ENST00000550270.1:c.667G>C
  hgvsp: ENSP00000449702.1:p.Glu223Gln
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000440034
  ensembl transcript: ENST00000545503
  gene symbol: MYBPC1
  hgvsc: ENST00000545503.2:c.667G>C
  hgvsp: ENSP00000440034.2:p.Glu223Gln
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447660
  ensembl transcript: ENST00000549145
  gene symbol: MYBPC1
  hgvsc: ENST00000549145.1:c.706G>C
  hgvsp: ENSP00000447660.1:p.Glu236Gln
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447362
  ensembl transcript: ENST00000547509
  gene symbol: MYBPC1
  hgvsc: ENST00000547509.1:c.625G>C
  hgvsp: ENSP00000447362.1:p.Glu209Gln
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000446128
  ensembl transcript: ENST00000536007
  gene symbol: MYBPC1
  hgvsc: ENST00000536007.1:c.610G>C
  hgvsp: ENSP00000446128.1:p.Glu204Gln
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447116
  ensembl transcript: ENST00000551300
  gene symbol: MYBPC1
  hgvsc: ENST00000551300.1:c.370G>C
  hgvsp: ENSP00000447116.1:p.Glu124Gln
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000442847
  ensembl transcript: ENST00000541119
  gene symbol: MYBPC1
  hgvsc: ENST00000541119.1:c.631G>C
  hgvsp: ENSP00000442847.1:p.Glu211Gln
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000448175
  ensembl transcript: ENST00000547405
  gene symbol: MYBPC1
  hgvsc: ENST00000547405.1:c.589G>C
  hgvsp: ENSP00000448175.1:p.Glu197Gln
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000376665
  ensembl transcript: ENST00000392934
  gene symbol: MYBPC1
  hgvsc: ENST00000392934.3:c.628G>C
  hgvsp: ENSP00000376665.3:p.Glu210Gln
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000354849
  ensembl transcript: ENST00000361466
  gene symbol: MYBPC1
  hgvsc: ENST00000361466.2:c.742G>C
  hgvsp: ENSP00000354849.2:p.Glu248Gln
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl transcript: ENST00000550501
  gene symbol: MYBPC1
  hgvsc: ENST00000550501.1:n.574+27551G>C
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000400908
  ensembl transcript: ENST00000452455
  gene symbol: MYBPC1
  hgvsc: ENST00000452455.2:c.667G>C
  hgvsp: ENSP00000400908.2:p.Glu223Gln
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000353822
  ensembl transcript: ENST00000360610
  gene symbol: MYBPC1
  hgvsc: ENST00000360610.2:c.667G>C
  hgvsp: ENSP00000353822.2:p.Glu223Gln
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447900
  ensembl transcript: ENST00000553190
  gene symbol: MYBPC1
  hgvsc: ENST00000553190.1:c.667G>C
  hgvsp: ENSP00000447900.1:p.Glu223Gln
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000354845
  ensembl transcript: ENST00000361685
  gene symbol: MYBPC1
  hgvsc: ENST00000361685.2:c.742G>C
  hgvsp: ENSP00000354845.2:p.Glu248Gln
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000388989
  ensembl transcript: ENST00000441232
  gene symbol: MYBPC1
  hgvsc: ENST00000441232.1:c.667G>C
  hgvsp: ENSP00000388989.1:p.Glu223Gln
  variant of: http://identifiers.org/hgnc/7549
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2558
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 942
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3153
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16692
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1670
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu223Gln
num of homozygotes: 0
population: East Asian
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
reference allele: G
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD

http://identifiers.org/exac.variant/12-102036281-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102036281
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 102036281
    reference: chr 12
allele count: 19
allele frequency: 1.612437836278154e-4
allele num: 117834
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447900
  ensembl transcript: ENST00000553190
  gene symbol: MYBPC1
  hgvsc: ENST00000553190.1:c.675C>A
  hgvsp: ENST00000553190.1:c.675C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000388989
  ensembl transcript: ENST00000441232
  gene symbol: MYBPC1
  hgvsc: ENST00000441232.1:c.675C>A
  hgvsp: ENST00000441232.1:c.675C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000449702
  ensembl transcript: ENST00000550270
  gene symbol: MYBPC1
  hgvsc: ENST00000550270.1:c.675C>A
  hgvsp: ENST00000550270.1:c.675C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447116
  ensembl transcript: ENST00000551300
  gene symbol: MYBPC1
  hgvsc: ENST00000551300.1:c.378C>A
  hgvsp: ENST00000551300.1:c.378C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000448175
  ensembl transcript: ENST00000547405
  gene symbol: MYBPC1
  hgvsc: ENST00000547405.1:c.597C>A
  hgvsp: ENST00000547405.1:c.597C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000442847
  ensembl transcript: ENST00000541119
  gene symbol: MYBPC1
  hgvsc: ENST00000541119.1:c.639C>A
  hgvsp: ENST00000541119.1:c.639C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000446128
  ensembl transcript: ENST00000536007
  gene symbol: MYBPC1
  hgvsc: ENST00000536007.1:c.618C>A
  hgvsp: ENST00000536007.1:c.618C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000376665
  ensembl transcript: ENST00000392934
  gene symbol: MYBPC1
  hgvsc: ENST00000392934.3:c.636C>A
  hgvsp: ENST00000392934.3:c.636C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000354845
  ensembl transcript: ENST00000361685
  gene symbol: MYBPC1
  hgvsc: ENST00000361685.2:c.750C>A
  hgvsp: ENST00000361685.2:c.750C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl transcript: ENST00000550501
  gene symbol: MYBPC1
  hgvsc: ENST00000550501.1:n.574+27559C>A
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000400908
  ensembl transcript: ENST00000452455
  gene symbol: MYBPC1
  hgvsc: ENST00000452455.2:c.675C>A
  hgvsp: ENST00000452455.2:c.675C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000354849
  ensembl transcript: ENST00000361466
  gene symbol: MYBPC1
  hgvsc: ENST00000361466.2:c.750C>A
  hgvsp: ENST00000361466.2:c.750C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447660
  ensembl transcript: ENST00000549145
  gene symbol: MYBPC1
  hgvsc: ENST00000549145.1:c.714C>A
  hgvsp: ENST00000549145.1:c.714C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000440034
  ensembl transcript: ENST00000545503
  gene symbol: MYBPC1
  hgvsc: ENST00000545503.2:c.675C>A
  hgvsp: ENST00000545503.2:c.675C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000353822
  ensembl transcript: ENST00000360610
  gene symbol: MYBPC1
  hgvsc: ENST00000360610.2:c.675C>A
  hgvsp: ENST00000360610.2:c.675C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447362
  ensembl transcript: ENST00000547509
  gene symbol: MYBPC1
  hgvsc: ENST00000547509.1:c.633C>A
  hgvsp: ENST00000547509.1:c.633C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6222
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3119
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1673
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1670
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2928
  bin: 1.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Ile225Ile
num of homozygotes: 1
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD

12-102036287-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102036287
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 102036287
    reference: chr 12
allele count: 4
allele frequency: 3.405704555129843e-5
allele num: 117450
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000442847
  ensembl transcript: ENST00000541119
  gene symbol: MYBPC1
  hgvsc: ENST00000541119.1:c.645C>T
  hgvsp: ENST00000541119.1:c.645C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl transcript: ENST00000550501
  gene symbol: MYBPC1
  hgvsc: ENST00000550501.1:n.574+27565C>T
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447900
  ensembl transcript: ENST00000553190
  gene symbol: MYBPC1
  hgvsc: ENST00000553190.1:c.681C>T
  hgvsp: ENST00000553190.1:c.681C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000446128
  ensembl transcript: ENST00000536007
  gene symbol: MYBPC1
  hgvsc: ENST00000536007.1:c.624C>T
  hgvsp: ENST00000536007.1:c.624C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000449702
  ensembl transcript: ENST00000550270
  gene symbol: MYBPC1
  hgvsc: ENST00000550270.1:c.681C>T
  hgvsp: ENST00000550270.1:c.681C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000354845
  ensembl transcript: ENST00000361685
  gene symbol: MYBPC1
  hgvsc: ENST00000361685.2:c.756C>T
  hgvsp: ENST00000361685.2:c.756C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000400908
  ensembl transcript: ENST00000452455
  gene symbol: MYBPC1
  hgvsc: ENST00000452455.2:c.681C>T
  hgvsp: ENST00000452455.2:c.681C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000376665
  ensembl transcript: ENST00000392934
  gene symbol: MYBPC1
  hgvsc: ENST00000392934.3:c.642C>T
  hgvsp: ENST00000392934.3:c.642C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000388989
  ensembl transcript: ENST00000441232
  gene symbol: MYBPC1
  hgvsc: ENST00000441232.1:c.681C>T
  hgvsp: ENST00000441232.1:c.681C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447116
  ensembl transcript: ENST00000551300
  gene symbol: MYBPC1
  hgvsc: ENST00000551300.1:c.384C>T
  hgvsp: ENST00000551300.1:c.384C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000448175
  ensembl transcript: ENST00000547405
  gene symbol: MYBPC1
  hgvsc: ENST00000547405.1:c.603C>T
  hgvsp: ENST00000547405.1:c.603C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000440034
  ensembl transcript: ENST00000545503
  gene symbol: MYBPC1
  hgvsc: ENST00000545503.2:c.681C>T
  hgvsp: ENST00000545503.2:c.681C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000353822
  ensembl transcript: ENST00000360610
  gene symbol: MYBPC1
  hgvsc: ENST00000360610.2:c.681C>T
  hgvsp: ENST00000360610.2:c.681C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000354849
  ensembl transcript: ENST00000361466
  gene symbol: MYBPC1
  hgvsc: ENST00000361466.2:c.756C>T
  hgvsp: ENST00000361466.2:c.756C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447660
  ensembl transcript: ENST00000549145
  gene symbol: MYBPC1
  hgvsc: ENST00000549145.1:c.720C>T
  hgvsp: ENST00000549145.1:c.720C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447362
  ensembl transcript: ENST00000547509
  gene symbol: MYBPC1
  hgvsc: ENST00000547509.1:c.639C>T
  hgvsp: ENST00000547509.1:c.639C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3142
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1668
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1757
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6139
  bin: 3.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
hgvs: p.Phe227Phe
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD

12-102036291-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102036291
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 102036291
    reference: chr 12
allele count: 1
allele frequency: 8.536356341659126e-6
allele num: 117146
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl transcript: ENST00000550501
  gene symbol: MYBPC1
  hgvsc: ENST00000550501.1:n.574+27569T>A
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447362
  ensembl transcript: ENST00000547509
  gene symbol: MYBPC1
  hgvsc: ENST00000547509.1:c.643T>A
  hgvsp: ENSP00000447362.1:p.Tyr215Asn
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000448175
  ensembl transcript: ENST00000547405
  gene symbol: MYBPC1
  hgvsc: ENST00000547405.1:c.607T>A
  hgvsp: ENSP00000448175.1:p.Tyr203Asn
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447660
  ensembl transcript: ENST00000549145
  gene symbol: MYBPC1
  hgvsc: ENST00000549145.1:c.724T>A
  hgvsp: ENSP00000447660.1:p.Tyr242Asn
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000446128
  ensembl transcript: ENST00000536007
  gene symbol: MYBPC1
  hgvsc: ENST00000536007.1:c.628T>A
  hgvsp: ENSP00000446128.1:p.Tyr210Asn
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000376665
  ensembl transcript: ENST00000392934
  gene symbol: MYBPC1
  hgvsc: ENST00000392934.3:c.646T>A
  hgvsp: ENSP00000376665.3:p.Tyr216Asn
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000442847
  ensembl transcript: ENST00000541119
  gene symbol: MYBPC1
  hgvsc: ENST00000541119.1:c.649T>A
  hgvsp: ENSP00000442847.1:p.Tyr217Asn
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000354845
  ensembl transcript: ENST00000361685
  gene symbol: MYBPC1
  hgvsc: ENST00000361685.2:c.760T>A
  hgvsp: ENSP00000354845.2:p.Tyr254Asn
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000353822
  ensembl transcript: ENST00000360610
  gene symbol: MYBPC1
  hgvsc: ENST00000360610.2:c.685T>A
  hgvsp: ENSP00000353822.2:p.Tyr229Asn
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000354849
  ensembl transcript: ENST00000361466
  gene symbol: MYBPC1
  hgvsc: ENST00000361466.2:c.760T>A
  hgvsp: ENSP00000354849.2:p.Tyr254Asn
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000440034
  ensembl transcript: ENST00000545503
  gene symbol: MYBPC1
  hgvsc: ENST00000545503.2:c.685T>A
  hgvsp: ENSP00000440034.2:p.Tyr229Asn
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000449702
  ensembl transcript: ENST00000550270
  gene symbol: MYBPC1
  hgvsc: ENST00000550270.1:c.685T>A
  hgvsp: ENSP00000449702.1:p.Tyr229Asn
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447116
  ensembl transcript: ENST00000551300
  gene symbol: MYBPC1
  hgvsc: ENST00000551300.1:c.388T>A
  hgvsp: ENSP00000447116.1:p.Tyr130Asn
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447900
  ensembl transcript: ENST00000553190
  gene symbol: MYBPC1
  hgvsc: ENST00000553190.1:c.685T>A
  hgvsp: ENSP00000447900.1:p.Tyr229Asn
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000400908
  ensembl transcript: ENST00000452455
  gene symbol: MYBPC1
  hgvsc: ENST00000452455.2:c.685T>A
  hgvsp: ENSP00000400908.2:p.Tyr229Asn
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000388989
  ensembl transcript: ENST00000441232
  gene symbol: MYBPC1
  hgvsc: ENST00000441232.1:c.685T>A
  hgvsp: ENSP00000388989.1:p.Tyr229Asn
  variant of: http://identifiers.org/hgnc/7549
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14155
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15207
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3133
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1757
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1273
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3466
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Tyr229Asn
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: DP

12-102036302-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102036302
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 102036302
    reference: chr 12
allele count: 1
allele frequency: 8.660108078148815e-6
allele num: 115472
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447362
  ensembl transcript: ENST00000547509
  gene symbol: MYBPC1
  hgvsc: ENST00000547509.1:c.654C>T
  hgvsp: ENST00000547509.1:c.654C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000388989
  ensembl transcript: ENST00000441232
  gene symbol: MYBPC1
  hgvsc: ENST00000441232.1:c.696C>T
  hgvsp: ENST00000441232.1:c.696C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000376665
  ensembl transcript: ENST00000392934
  gene symbol: MYBPC1
  hgvsc: ENST00000392934.3:c.657C>T
  hgvsp: ENST00000392934.3:c.657C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447900
  ensembl transcript: ENST00000553190
  gene symbol: MYBPC1
  hgvsc: ENST00000553190.1:c.696C>T
  hgvsp: ENST00000553190.1:c.696C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000442847
  ensembl transcript: ENST00000541119
  gene symbol: MYBPC1
  hgvsc: ENST00000541119.1:c.660C>T
  hgvsp: ENST00000541119.1:c.660C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000400908
  ensembl transcript: ENST00000452455
  gene symbol: MYBPC1
  hgvsc: ENST00000452455.2:c.696C>T
  hgvsp: ENST00000452455.2:c.696C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000354845
  ensembl transcript: ENST00000361685
  gene symbol: MYBPC1
  hgvsc: ENST00000361685.2:c.771C>T
  hgvsp: ENST00000361685.2:c.771C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000446128
  ensembl transcript: ENST00000536007
  gene symbol: MYBPC1
  hgvsc: ENST00000536007.1:c.639C>T
  hgvsp: ENST00000536007.1:c.639C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000449702
  ensembl transcript: ENST00000550270
  gene symbol: MYBPC1
  hgvsc: ENST00000550270.1:c.696C>T
  hgvsp: ENST00000550270.1:c.696C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000448175
  ensembl transcript: ENST00000547405
  gene symbol: MYBPC1
  hgvsc: ENST00000547405.1:c.618C>T
  hgvsp: ENST00000547405.1:c.618C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000354849
  ensembl transcript: ENST00000361466
  gene symbol: MYBPC1
  hgvsc: ENST00000361466.2:c.771C>T
  hgvsp: ENST00000361466.2:c.771C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000353822
  ensembl transcript: ENST00000360610
  gene symbol: MYBPC1
  hgvsc: ENST00000360610.2:c.696C>T
  hgvsp: ENST00000360610.2:c.696C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447116
  ensembl transcript: ENST00000551300
  gene symbol: MYBPC1
  hgvsc: ENST00000551300.1:c.399C>T
  hgvsp: ENST00000551300.1:c.399C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl transcript: ENST00000550501
  gene symbol: MYBPC1
  hgvsc: ENST00000550501.1:n.574+27580C>T
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000440034
  ensembl transcript: ENST00000545503
  gene symbol: MYBPC1
  hgvsc: ENST00000545503.2:c.696C>T
  hgvsp: ENST00000545503.2:c.696C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447660
  ensembl transcript: ENST00000549145
  gene symbol: MYBPC1
  hgvsc: ENST00000549145.1:c.735C>T
  hgvsp: ENST00000549145.1:c.735C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 612
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13408
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2056
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr232Thr
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum

12-102036305-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102036305
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 102036305
    reference: chr 12
allele count: 34473
allele frequency: 3.002560707939936e-1
allele num: 114812
alternate allele: T
annotation: Annotation
  canonical: true
  clinical significance: benign
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000400908
  ensembl transcript: ENST00000452455
  gene symbol: MYBPC1
  hgvsc: ENST00000452455.2:c.699C>T
  hgvsp: ENST00000452455.2:c.699C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000448175
  ensembl transcript: ENST00000547405
  gene symbol: MYBPC1
  hgvsc: ENST00000547405.1:c.621C>T
  hgvsp: ENST00000547405.1:c.621C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000354845
  ensembl transcript: ENST00000361685
  gene symbol: MYBPC1
  hgvsc: ENST00000361685.2:c.774C>T
  hgvsp: ENST00000361685.2:c.774C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000446128
  ensembl transcript: ENST00000536007
  gene symbol: MYBPC1
  hgvsc: ENST00000536007.1:c.642C>T
  hgvsp: ENST00000536007.1:c.642C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000376665
  ensembl transcript: ENST00000392934
  gene symbol: MYBPC1
  hgvsc: ENST00000392934.3:c.660C>T
  hgvsp: ENST00000392934.3:c.660C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000388989
  ensembl transcript: ENST00000441232
  gene symbol: MYBPC1
  hgvsc: ENST00000441232.1:c.699C>T
  hgvsp: ENST00000441232.1:c.699C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000442847
  ensembl transcript: ENST00000541119
  gene symbol: MYBPC1
  hgvsc: ENST00000541119.1:c.663C>T
  hgvsp: ENST00000541119.1:c.663C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447660
  ensembl transcript: ENST00000549145
  gene symbol: MYBPC1
  hgvsc: ENST00000549145.1:c.738C>T
  hgvsp: ENST00000549145.1:c.738C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000449702
  ensembl transcript: ENST00000550270
  gene symbol: MYBPC1
  hgvsc: ENST00000550270.1:c.699C>T
  hgvsp: ENST00000550270.1:c.699C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000354849
  ensembl transcript: ENST00000361466
  gene symbol: MYBPC1
  hgvsc: ENST00000361466.2:c.774C>T
  hgvsp: ENST00000361466.2:c.774C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000353822
  ensembl transcript: ENST00000360610
  gene symbol: MYBPC1
  hgvsc: ENST00000360610.2:c.699C>T
  hgvsp: ENST00000360610.2:c.699C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl transcript: ENST00000550501
  gene symbol: MYBPC1
  hgvsc: ENST00000550501.1:n.574+27583C>T
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000440034
  ensembl transcript: ENST00000545503
  gene symbol: MYBPC1
  hgvsc: ENST00000545503.2:c.699C>T
  hgvsp: ENST00000545503.2:c.699C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447116
  ensembl transcript: ENST00000551300
  gene symbol: MYBPC1
  hgvsc: ENST00000551300.1:c.402C>T
  hgvsp: ENST00000551300.1:c.402C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447900
  ensembl transcript: ENST00000553190
  gene symbol: MYBPC1
  hgvsc: ENST00000553190.1:c.699C>T
  hgvsp: ENST00000553190.1:c.699C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447362
  ensembl transcript: ENST00000547509
  gene symbol: MYBPC1
  hgvsc: ENST00000547509.1:c.657C>T
  hgvsp: ENST00000547509.1:c.657C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1791
  bin: 5.25e1
  variant carriers: 1308
genotype depth: GenotypeDepth
  all individuals: 2666
  bin: 7.5e0
  variant carriers: 235
genotype quality: GenotypeQuality
hgvs: p.Asp233Asp
num of homozygotes: 5074
population: European (Non-Finnish)
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: Other
population: East Asian
reference allele: C
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD

http://identifiers.org/exac.variant/12-102036311-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102036311
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 102036311
    reference: chr 12
allele count: 1
allele frequency: 9.195233191113726e-6
allele num: 108752
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000448175
  ensembl transcript: ENST00000547405
  gene symbol: MYBPC1
  hgvsc: ENST00000547405.1:c.627C>A
  hgvsp: ENST00000547405.1:c.627C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447900
  ensembl transcript: ENST00000553190
  gene symbol: MYBPC1
  hgvsc: ENST00000553190.1:c.705C>A
  hgvsp: ENST00000553190.1:c.705C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000442847
  ensembl transcript: ENST00000541119
  gene symbol: MYBPC1
  hgvsc: ENST00000541119.1:c.669C>A
  hgvsp: ENST00000541119.1:c.669C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000354845
  ensembl transcript: ENST00000361685
  gene symbol: MYBPC1
  hgvsc: ENST00000361685.2:c.780C>A
  hgvsp: ENST00000361685.2:c.780C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000400908
  ensembl transcript: ENST00000452455
  gene symbol: MYBPC1
  hgvsc: ENST00000452455.2:c.705C>A
  hgvsp: ENST00000452455.2:c.705C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447116
  ensembl transcript: ENST00000551300
  gene symbol: MYBPC1
  hgvsc: ENST00000551300.1:c.408C>A
  hgvsp: ENST00000551300.1:c.408C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000449702
  ensembl transcript: ENST00000550270
  gene symbol: MYBPC1
  hgvsc: ENST00000550270.1:c.705C>A
  hgvsp: ENST00000550270.1:c.705C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000376665
  ensembl transcript: ENST00000392934
  gene symbol: MYBPC1
  hgvsc: ENST00000392934.3:c.666C>A
  hgvsp: ENST00000392934.3:c.666C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000440034
  ensembl transcript: ENST00000545503
  gene symbol: MYBPC1
  hgvsc: ENST00000545503.2:c.705C>A
  hgvsp: ENST00000545503.2:c.705C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000354849
  ensembl transcript: ENST00000361466
  gene symbol: MYBPC1
  hgvsc: ENST00000361466.2:c.780C>A
  hgvsp: ENST00000361466.2:c.780C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000446128
  ensembl transcript: ENST00000536007
  gene symbol: MYBPC1
  hgvsc: ENST00000536007.1:c.648C>A
  hgvsp: ENST00000536007.1:c.648C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000388989
  ensembl transcript: ENST00000441232
  gene symbol: MYBPC1
  hgvsc: ENST00000441232.1:c.705C>A
  hgvsp: ENST00000441232.1:c.705C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000353822
  ensembl transcript: ENST00000360610
  gene symbol: MYBPC1
  hgvsc: ENST00000360610.2:c.705C>A
  hgvsp: ENST00000360610.2:c.705C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447660
  ensembl transcript: ENST00000549145
  gene symbol: MYBPC1
  hgvsc: ENST00000549145.1:c.744C>A
  hgvsp: ENST00000549145.1:c.744C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl transcript: ENST00000550501
  gene symbol: MYBPC1
  hgvsc: ENST00000550501.1:n.574+27589C>A
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447362
  ensembl transcript: ENST00000547509
  gene symbol: MYBPC1
  hgvsc: ENST00000547509.1:c.663C>A
  hgvsp: ENST00000547509.1:c.663C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5945
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 787
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1577
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13731
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1192
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg235Arg
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD

12-102036333-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102036333
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 102036333
    reference: chr 12
allele count: 1
allele frequency: 9.963930571331778e-6
allele num: 100362
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000376665
  ensembl transcript: ENST00000392934
  gene symbol: MYBPC1
  hgvsc: ENST00000392934.3:c.688C>G
  hgvsp: ENSP00000376665.3:p.Arg230Gly
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000400908
  ensembl transcript: ENST00000452455
  gene symbol: MYBPC1
  hgvsc: ENST00000452455.2:c.727C>G
  hgvsp: ENSP00000400908.2:p.Arg243Gly
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000449702
  ensembl transcript: ENST00000550270
  gene symbol: MYBPC1
  hgvsc: ENST00000550270.1:c.727C>G
  hgvsp: ENSP00000449702.1:p.Arg243Gly
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000354845
  ensembl transcript: ENST00000361685
  gene symbol: MYBPC1
  hgvsc: ENST00000361685.2:c.802C>G
  hgvsp: ENSP00000354845.2:p.Arg268Gly
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl transcript: ENST00000550501
  gene symbol: MYBPC1
  hgvsc: ENST00000550501.1:n.574+27611C>G
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000446128
  ensembl transcript: ENST00000536007
  gene symbol: MYBPC1
  hgvsc: ENST00000536007.1:c.670C>G
  hgvsp: ENSP00000446128.1:p.Arg224Gly
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000353822
  ensembl transcript: ENST00000360610
  gene symbol: MYBPC1
  hgvsc: ENST00000360610.2:c.727C>G
  hgvsp: ENSP00000353822.2:p.Arg243Gly
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000442847
  ensembl transcript: ENST00000541119
  gene symbol: MYBPC1
  hgvsc: ENST00000541119.1:c.691C>G
  hgvsp: ENSP00000442847.1:p.Arg231Gly
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000448175
  ensembl transcript: ENST00000547405
  gene symbol: MYBPC1
  hgvsc: ENST00000547405.1:c.649C>G
  hgvsp: ENSP00000448175.1:p.Arg217Gly
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447362
  ensembl transcript: ENST00000547509
  gene symbol: MYBPC1
  hgvsc: ENST00000547509.1:c.685C>G
  hgvsp: ENSP00000447362.1:p.Arg229Gly
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447116
  ensembl transcript: ENST00000551300
  gene symbol: MYBPC1
  hgvsc: ENST00000551300.1:c.430C>G
  hgvsp: ENSP00000447116.1:p.Arg144Gly
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447660
  ensembl transcript: ENST00000549145
  gene symbol: MYBPC1
  hgvsc: ENST00000549145.1:c.766C>G
  hgvsp: ENSP00000447660.1:p.Arg256Gly
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000388989
  ensembl transcript: ENST00000441232
  gene symbol: MYBPC1
  hgvsc: ENST00000441232.1:c.727C>G
  hgvsp: ENSP00000388989.1:p.Arg243Gly
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447900
  ensembl transcript: ENST00000553190
  gene symbol: MYBPC1
  hgvsc: ENST00000553190.1:c.727C>G
  hgvsp: ENSP00000447900.1:p.Arg243Gly
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000440034
  ensembl transcript: ENST00000545503
  gene symbol: MYBPC1
  hgvsc: ENST00000545503.2:c.727C>G
  hgvsp: ENSP00000440034.2:p.Arg243Gly
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000354849
  ensembl transcript: ENST00000361466
  gene symbol: MYBPC1
  hgvsc: ENST00000361466.2:c.802C>G
  hgvsp: ENSP00000354849.2:p.Arg268Gly
  variant of: http://identifiers.org/hgnc/7549
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15355
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1147
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9925
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1414
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg243Gly
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
reference allele: C
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP

12-102036344-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102036344
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 102036344
    reference: chr 12
allele count: 1
allele frequency: 1.050199537912203e-5
allele num: 95220
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000354849
  ensembl transcript: ENST00000361466
  gene symbol: MYBPC1
  hgvsc: ENST00000361466.2:c.813A>G
  hgvsp: ENST00000361466.2:c.813A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447660
  ensembl transcript: ENST00000549145
  gene symbol: MYBPC1
  hgvsc: ENST00000549145.1:c.777A>G
  hgvsp: ENST00000549145.1:c.777A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000442847
  ensembl transcript: ENST00000541119
  gene symbol: MYBPC1
  hgvsc: ENST00000541119.1:c.702A>G
  hgvsp: ENST00000541119.1:c.702A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447362
  ensembl transcript: ENST00000547509
  gene symbol: MYBPC1
  hgvsc: ENST00000547509.1:c.696A>G
  hgvsp: ENST00000547509.1:c.696A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000388989
  ensembl transcript: ENST00000441232
  gene symbol: MYBPC1
  hgvsc: ENST00000441232.1:c.738A>G
  hgvsp: ENST00000441232.1:c.738A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl transcript: ENST00000550501
  gene symbol: MYBPC1
  hgvsc: ENST00000550501.1:n.574+27622A>G
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000376665
  ensembl transcript: ENST00000392934
  gene symbol: MYBPC1
  hgvsc: ENST00000392934.3:c.699A>G
  hgvsp: ENST00000392934.3:c.699A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447900
  ensembl transcript: ENST00000553190
  gene symbol: MYBPC1
  hgvsc: ENST00000553190.1:c.738A>G
  hgvsp: ENST00000553190.1:c.738A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000353822
  ensembl transcript: ENST00000360610
  gene symbol: MYBPC1
  hgvsc: ENST00000360610.2:c.738A>G
  hgvsp: ENST00000360610.2:c.738A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000354845
  ensembl transcript: ENST00000361685
  gene symbol: MYBPC1
  hgvsc: ENST00000361685.2:c.813A>G
  hgvsp: ENST00000361685.2:c.813A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000446128
  ensembl transcript: ENST00000536007
  gene symbol: MYBPC1
  hgvsc: ENST00000536007.1:c.681A>G
  hgvsp: ENST00000536007.1:c.681A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000440034
  ensembl transcript: ENST00000545503
  gene symbol: MYBPC1
  hgvsc: ENST00000545503.2:c.738A>G
  hgvsp: ENST00000545503.2:c.738A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000448175
  ensembl transcript: ENST00000547405
  gene symbol: MYBPC1
  hgvsc: ENST00000547405.1:c.660A>G
  hgvsp: ENST00000547405.1:c.660A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000449702
  ensembl transcript: ENST00000550270
  gene symbol: MYBPC1
  hgvsc: ENST00000550270.1:c.738A>G
  hgvsp: ENST00000550270.1:c.738A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447116
  ensembl transcript: ENST00000551300
  gene symbol: MYBPC1
  hgvsc: ENST00000551300.1:c.441A>G
  hgvsp: ENST00000551300.1:c.441A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000400908
  ensembl transcript: ENST00000452455
  gene symbol: MYBPC1
  hgvsc: ENST00000452455.2:c.738A>G
  hgvsp: ENST00000452455.2:c.738A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12300
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12863
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1131
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 665
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1328
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg246Arg
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: African
population: European (Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: DP

12-102036348-GAGA-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102036348
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 102036345
    reference: chr 12
allele count: 2
allele frequency: 2.14712071112638e-5
allele num: 93148
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000449702
  ensembl transcript: ENST00000550270
  gene symbol: MYBPC1
  hgvsc: ENST00000550270.1:c.749_751delAGA
  hgvsp: ENSP00000449702.1:p.Lys250del
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000448175
  ensembl transcript: ENST00000547405
  gene symbol: MYBPC1
  hgvsc: ENST00000547405.1:c.671_673delAGA
  hgvsp: ENSP00000448175.1:p.Lys224del
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000442847
  ensembl transcript: ENST00000541119
  gene symbol: MYBPC1
  hgvsc: ENST00000541119.1:c.713_715delAGA
  hgvsp: ENSP00000442847.1:p.Lys238del
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447900
  ensembl transcript: ENST00000553190
  gene symbol: MYBPC1
  hgvsc: ENST00000553190.1:c.749_751delAGA
  hgvsp: ENSP00000447900.1:p.Lys250del
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000446128
  ensembl transcript: ENST00000536007
  gene symbol: MYBPC1
  hgvsc: ENST00000536007.1:c.692_694delAGA
  hgvsp: ENSP00000446128.1:p.Lys231del
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000388989
  ensembl transcript: ENST00000441232
  gene symbol: MYBPC1
  hgvsc: ENST00000441232.1:c.749_751delAGA
  hgvsp: ENSP00000388989.1:p.Lys250del
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447116
  ensembl transcript: ENST00000551300
  gene symbol: MYBPC1
  hgvsc: ENST00000551300.1:c.452_454delAGA
  hgvsp: ENSP00000447116.1:p.Lys151del
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl transcript: ENST00000550501
  gene symbol: MYBPC1
  hgvsc: ENST00000550501.1:n.574+27633_574+27635delAGA
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000354849
  ensembl transcript: ENST00000361466
  gene symbol: MYBPC1
  hgvsc: ENST00000361466.2:c.824_826delAGA
  hgvsp: ENSP00000354849.2:p.Lys275del
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000440034
  ensembl transcript: ENST00000545503
  gene symbol: MYBPC1
  hgvsc: ENST00000545503.2:c.749_751delAGA
  hgvsp: ENSP00000440034.2:p.Lys250del
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000354845
  ensembl transcript: ENST00000361685
  gene symbol: MYBPC1
  hgvsc: ENST00000361685.2:c.824_826delAGA
  hgvsp: ENSP00000354845.2:p.Lys275del
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000353822
  ensembl transcript: ENST00000360610
  gene symbol: MYBPC1
  hgvsc: ENST00000360610.2:c.749_751delAGA
  hgvsp: ENSP00000353822.2:p.Lys250del
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000376665
  ensembl transcript: ENST00000392934
  gene symbol: MYBPC1
  hgvsc: ENST00000392934.3:c.710_712delAGA
  hgvsp: ENSP00000376665.3:p.Lys237del
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447362
  ensembl transcript: ENST00000547509
  gene symbol: MYBPC1
  hgvsc: ENST00000547509.1:c.707_709delAGA
  hgvsp: ENSP00000447362.1:p.Lys236del
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: true
  consequence: inframe_deletion
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000400908
  ensembl transcript: ENST00000452455
  gene symbol: MYBPC1
  hgvsc: ENST00000452455.2:c.749_751delAGA
  hgvsp: ENSP00000400908.2:p.Lys250del
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447660
  ensembl transcript: ENST00000549145
  gene symbol: MYBPC1
  hgvsc: ENST00000549145.1:c.788_790delAGA
  hgvsp: ENSP00000447660.1:p.Lys263del
  variant of: http://identifiers.org/hgnc/7549
canonical: true
consequence: inframe deletion
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9249
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1314
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys250del
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
population: European (Finnish)
reference allele: GAGA
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD

12-102036359-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102036359
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 102036359
    reference: chr 12
allele count: 1
allele frequency: 1.162736616901539e-5
allele num: 86004
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447900
  ensembl transcript: ENST00000553190
  gene symbol: MYBPC1
  hgvsc: ENST00000553190.1:c.753C>T
  hgvsp: ENST00000553190.1:c.753C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000376665
  ensembl transcript: ENST00000392934
  gene symbol: MYBPC1
  hgvsc: ENST00000392934.3:c.714C>T
  hgvsp: ENST00000392934.3:c.714C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000354845
  ensembl transcript: ENST00000361685
  gene symbol: MYBPC1
  hgvsc: ENST00000361685.2:c.828C>T
  hgvsp: ENST00000361685.2:c.828C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000354849
  ensembl transcript: ENST00000361466
  gene symbol: MYBPC1
  hgvsc: ENST00000361466.2:c.828C>T
  hgvsp: ENST00000361466.2:c.828C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000448175
  ensembl transcript: ENST00000547405
  gene symbol: MYBPC1
  hgvsc: ENST00000547405.1:c.675C>T
  hgvsp: ENST00000547405.1:c.675C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000446128
  ensembl transcript: ENST00000536007
  gene symbol: MYBPC1
  hgvsc: ENST00000536007.1:c.696C>T
  hgvsp: ENST00000536007.1:c.696C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000449702
  ensembl transcript: ENST00000550270
  gene symbol: MYBPC1
  hgvsc: ENST00000550270.1:c.753C>T
  hgvsp: ENST00000550270.1:c.753C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447660
  ensembl transcript: ENST00000549145
  gene symbol: MYBPC1
  hgvsc: ENST00000549145.1:c.792C>T
  hgvsp: ENST00000549145.1:c.792C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000442847
  ensembl transcript: ENST00000541119
  gene symbol: MYBPC1
  hgvsc: ENST00000541119.1:c.717C>T
  hgvsp: ENST00000541119.1:c.717C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000353822
  ensembl transcript: ENST00000360610
  gene symbol: MYBPC1
  hgvsc: ENST00000360610.2:c.753C>T
  hgvsp: ENST00000360610.2:c.753C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447116
  ensembl transcript: ENST00000551300
  gene symbol: MYBPC1
  hgvsc: ENST00000551300.1:c.456C>T
  hgvsp: ENST00000551300.1:c.456C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447362
  ensembl transcript: ENST00000547509
  gene symbol: MYBPC1
  hgvsc: ENST00000547509.1:c.711C>T
  hgvsp: ENST00000547509.1:c.711C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000388989
  ensembl transcript: ENST00000441232
  gene symbol: MYBPC1
  hgvsc: ENST00000441232.1:c.753C>T
  hgvsp: ENST00000441232.1:c.753C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl transcript: ENST00000550501
  gene symbol: MYBPC1
  hgvsc: ENST00000550501.1:n.574+27637C>T
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000400908
  ensembl transcript: ENST00000452455
  gene symbol: MYBPC1
  hgvsc: ENST00000452455.2:c.753C>T
  hgvsp: ENST00000452455.2:c.753C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000440034
  ensembl transcript: ENST00000545503
  gene symbol: MYBPC1
  hgvsc: ENST00000545503.2:c.753C>T
  hgvsp: ENST00000545503.2:c.753C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17014
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1077
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1154
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser251Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: African
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: QD

12-102036360-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102036360
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 102036360
    reference: chr 12
allele count: 1
allele frequency: 1.163575434595425e-5
allele num: 85942
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000376665
  ensembl transcript: ENST00000392934
  gene symbol: MYBPC1
  hgvsc: ENST00000392934.3:c.715G>A
  hgvsp: ENSP00000376665.3:p.Ala239Thr
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000354849
  ensembl transcript: ENST00000361466
  gene symbol: MYBPC1
  hgvsc: ENST00000361466.2:c.829G>A
  hgvsp: ENSP00000354849.2:p.Ala277Thr
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447900
  ensembl transcript: ENST00000553190
  gene symbol: MYBPC1
  hgvsc: ENST00000553190.1:c.754G>A
  hgvsp: ENSP00000447900.1:p.Ala252Thr
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000353822
  ensembl transcript: ENST00000360610
  gene symbol: MYBPC1
  hgvsc: ENST00000360610.2:c.754G>A
  hgvsp: ENSP00000353822.2:p.Ala252Thr
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447362
  ensembl transcript: ENST00000547509
  gene symbol: MYBPC1
  hgvsc: ENST00000547509.1:c.712G>A
  hgvsp: ENSP00000447362.1:p.Ala238Thr
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447660
  ensembl transcript: ENST00000549145
  gene symbol: MYBPC1
  hgvsc: ENST00000549145.1:c.793G>A
  hgvsp: ENSP00000447660.1:p.Ala265Thr
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000400908
  ensembl transcript: ENST00000452455
  gene symbol: MYBPC1
  hgvsc: ENST00000452455.2:c.754G>A
  hgvsp: ENSP00000400908.2:p.Ala252Thr
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000446128
  ensembl transcript: ENST00000536007
  gene symbol: MYBPC1
  hgvsc: ENST00000536007.1:c.697G>A
  hgvsp: ENSP00000446128.1:p.Ala233Thr
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000448175
  ensembl transcript: ENST00000547405
  gene symbol: MYBPC1
  hgvsc: ENST00000547405.1:c.676G>A
  hgvsp: ENSP00000448175.1:p.Ala226Thr
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000449702
  ensembl transcript: ENST00000550270
  gene symbol: MYBPC1
  hgvsc: ENST00000550270.1:c.754G>A
  hgvsp: ENSP00000449702.1:p.Ala252Thr
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000442847
  ensembl transcript: ENST00000541119
  gene symbol: MYBPC1
  hgvsc: ENST00000541119.1:c.718G>A
  hgvsp: ENSP00000442847.1:p.Ala240Thr
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447116
  ensembl transcript: ENST00000551300
  gene symbol: MYBPC1
  hgvsc: ENST00000551300.1:c.457G>A
  hgvsp: ENSP00000447116.1:p.Ala153Thr
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000388989
  ensembl transcript: ENST00000441232
  gene symbol: MYBPC1
  hgvsc: ENST00000441232.1:c.754G>A
  hgvsp: ENSP00000388989.1:p.Ala252Thr
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000440034
  ensembl transcript: ENST00000545503
  gene symbol: MYBPC1
  hgvsc: ENST00000545503.2:c.754G>A
  hgvsp: ENSP00000440034.2:p.Ala252Thr
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl transcript: ENST00000550501
  gene symbol: MYBPC1
  hgvsc: ENST00000550501.1:n.574+27638G>A
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000354845
  ensembl transcript: ENST00000361685
  gene symbol: MYBPC1
  hgvsc: ENST00000361685.2:c.829G>A
  hgvsp: ENSP00000354845.2:p.Ala277Thr
  variant of: http://identifiers.org/hgnc/7549
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 917
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2342
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7442
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15561
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala252Thr
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: East Asian
reference allele: G
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS

12-102036375-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102036375
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 102036375
    reference: chr 12
allele count: 2
allele frequency: 2.551476028882709e-5
allele num: 78386
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447900
  ensembl transcript: ENST00000553190
  gene symbol: MYBPC1
  hgvsc: ENST00000553190.1:c.757+12C>T
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447116
  ensembl transcript: ENST00000551300
  gene symbol: MYBPC1
  hgvsc: ENST00000551300.1:c.460+12C>T
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000449702
  ensembl transcript: ENST00000550270
  gene symbol: MYBPC1
  hgvsc: ENST00000550270.1:c.757+12C>T
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000354845
  ensembl transcript: ENST00000361685
  gene symbol: MYBPC1
  hgvsc: ENST00000361685.2:c.832+12C>T
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000353822
  ensembl transcript: ENST00000360610
  gene symbol: MYBPC1
  hgvsc: ENST00000360610.2:c.757+12C>T
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000448175
  ensembl transcript: ENST00000547405
  gene symbol: MYBPC1
  hgvsc: ENST00000547405.1:c.679+12C>T
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000376665
  ensembl transcript: ENST00000392934
  gene symbol: MYBPC1
  hgvsc: ENST00000392934.3:c.718+12C>T
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000354849
  ensembl transcript: ENST00000361466
  gene symbol: MYBPC1
  hgvsc: ENST00000361466.2:c.832+12C>T
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000442847
  ensembl transcript: ENST00000541119
  gene symbol: MYBPC1
  hgvsc: ENST00000541119.1:c.721+12C>T
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl transcript: ENST00000550501
  gene symbol: MYBPC1
  hgvsc: ENST00000550501.1:n.574+27653C>T
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000388989
  ensembl transcript: ENST00000441232
  gene symbol: MYBPC1
  hgvsc: ENST00000441232.1:c.757+12C>T
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447362
  ensembl transcript: ENST00000547509
  gene symbol: MYBPC1
  hgvsc: ENST00000547509.1:c.715+12C>T
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000440034
  ensembl transcript: ENST00000545503
  gene symbol: MYBPC1
  hgvsc: ENST00000545503.2:c.757+12C>T
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000446128
  ensembl transcript: ENST00000536007
  gene symbol: MYBPC1
  hgvsc: ENST00000536007.1:c.700+12C>T
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447660
  ensembl transcript: ENST00000549145
  gene symbol: MYBPC1
  hgvsc: ENST00000549145.1:c.796+12C>T
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000400908
  ensembl transcript: ENST00000452455
  gene symbol: MYBPC1
  hgvsc: ENST00000452455.2:c.757+12C>T
  variant of: http://identifiers.org/hgnc/7549
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5502
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1624
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 849
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 920
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3084
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5644
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19393
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ

12-102036377-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102036377
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 102036377
    reference: chr 12
allele count: 1
allele frequency: 1.282182787978254e-5
allele num: 77992
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447900
  ensembl transcript: ENST00000553190
  gene symbol: MYBPC1
  hgvsc: ENST00000553190.1:c.757+14G>T
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000400908
  ensembl transcript: ENST00000452455
  gene symbol: MYBPC1
  hgvsc: ENST00000452455.2:c.757+14G>T
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000354849
  ensembl transcript: ENST00000361466
  gene symbol: MYBPC1
  hgvsc: ENST00000361466.2:c.832+14G>T
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000446128
  ensembl transcript: ENST00000536007
  gene symbol: MYBPC1
  hgvsc: ENST00000536007.1:c.700+14G>T
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000448175
  ensembl transcript: ENST00000547405
  gene symbol: MYBPC1
  hgvsc: ENST00000547405.1:c.679+14G>T
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447660
  ensembl transcript: ENST00000549145
  gene symbol: MYBPC1
  hgvsc: ENST00000549145.1:c.796+14G>T
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000354845
  ensembl transcript: ENST00000361685
  gene symbol: MYBPC1
  hgvsc: ENST00000361685.2:c.832+14G>T
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000442847
  ensembl transcript: ENST00000541119
  gene symbol: MYBPC1
  hgvsc: ENST00000541119.1:c.721+14G>T
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000440034
  ensembl transcript: ENST00000545503
  gene symbol: MYBPC1
  hgvsc: ENST00000545503.2:c.757+14G>T
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447116
  ensembl transcript: ENST00000551300
  gene symbol: MYBPC1
  hgvsc: ENST00000551300.1:c.460+14G>T
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl transcript: ENST00000550501
  gene symbol: MYBPC1
  hgvsc: ENST00000550501.1:n.574+27655G>T
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000449702
  ensembl transcript: ENST00000550270
  gene symbol: MYBPC1
  hgvsc: ENST00000550270.1:c.757+14G>T
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000353822
  ensembl transcript: ENST00000360610
  gene symbol: MYBPC1
  hgvsc: ENST00000360610.2:c.757+14G>T
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000376665
  ensembl transcript: ENST00000392934
  gene symbol: MYBPC1
  hgvsc: ENST00000392934.3:c.718+14G>T
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447362
  ensembl transcript: ENST00000547509
  gene symbol: MYBPC1
  hgvsc: ENST00000547509.1:c.715+14G>T
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000388989
  ensembl transcript: ENST00000441232
  gene symbol: MYBPC1
  hgvsc: ENST00000441232.1:c.757+14G>T
  variant of: http://identifiers.org/hgnc/7549
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 849
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 760
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5212
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17810
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19743
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5333
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1532
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 919
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
population: Latino
population: East Asian
reference allele: G
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum

12-102036378-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102036378
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 102036378
    reference: chr 12
allele count: 2
allele frequency: 2.585582790360947e-5
allele num: 77352
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000440034
  ensembl transcript: ENST00000545503
  gene symbol: MYBPC1
  hgvsc: ENST00000545503.2:c.757+15G>C
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000354849
  ensembl transcript: ENST00000361466
  gene symbol: MYBPC1
  hgvsc: ENST00000361466.2:c.832+15G>C
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000442847
  ensembl transcript: ENST00000541119
  gene symbol: MYBPC1
  hgvsc: ENST00000541119.1:c.721+15G>C
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000354845
  ensembl transcript: ENST00000361685
  gene symbol: MYBPC1
  hgvsc: ENST00000361685.2:c.832+15G>C
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000400908
  ensembl transcript: ENST00000452455
  gene symbol: MYBPC1
  hgvsc: ENST00000452455.2:c.757+15G>C
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447900
  ensembl transcript: ENST00000553190
  gene symbol: MYBPC1
  hgvsc: ENST00000553190.1:c.757+15G>C
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000448175
  ensembl transcript: ENST00000547405
  gene symbol: MYBPC1
  hgvsc: ENST00000547405.1:c.679+15G>C
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl transcript: ENST00000550501
  gene symbol: MYBPC1
  hgvsc: ENST00000550501.1:n.574+27656G>C
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000376665
  ensembl transcript: ENST00000392934
  gene symbol: MYBPC1
  hgvsc: ENST00000392934.3:c.718+15G>C
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447660
  ensembl transcript: ENST00000549145
  gene symbol: MYBPC1
  hgvsc: ENST00000549145.1:c.796+15G>C
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000388989
  ensembl transcript: ENST00000441232
  gene symbol: MYBPC1
  hgvsc: ENST00000441232.1:c.757+15G>C
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000449702
  ensembl transcript: ENST00000550270
  gene symbol: MYBPC1
  hgvsc: ENST00000550270.1:c.757+15G>C
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447116
  ensembl transcript: ENST00000551300
  gene symbol: MYBPC1
  hgvsc: ENST00000551300.1:c.460+15G>C
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000353822
  ensembl transcript: ENST00000360610
  gene symbol: MYBPC1
  hgvsc: ENST00000360610.2:c.757+15G>C
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000446128
  ensembl transcript: ENST00000536007
  gene symbol: MYBPC1
  hgvsc: ENST00000536007.1:c.700+15G>C
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447362
  ensembl transcript: ENST00000547509
  gene symbol: MYBPC1
  hgvsc: ENST00000547509.1:c.715+15G>C
  variant of: http://identifiers.org/hgnc/7549
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3078
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20252
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17884
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 849
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 863
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 918
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3730
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1479
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: QD

12-102036379-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102036379
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 102036379
    reference: chr 12
allele count: 114
allele frequency: 1.474926253687316e-3
allele num: 77292
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000376665
  ensembl transcript: ENST00000392934
  gene symbol: MYBPC1
  hgvsc: ENST00000392934.3:c.718+16G>A
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000354845
  ensembl transcript: ENST00000361685
  gene symbol: MYBPC1
  hgvsc: ENST00000361685.2:c.832+16G>A
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447362
  ensembl transcript: ENST00000547509
  gene symbol: MYBPC1
  hgvsc: ENST00000547509.1:c.715+16G>A
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000449702
  ensembl transcript: ENST00000550270
  gene symbol: MYBPC1
  hgvsc: ENST00000550270.1:c.757+16G>A
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000442847
  ensembl transcript: ENST00000541119
  gene symbol: MYBPC1
  hgvsc: ENST00000541119.1:c.721+16G>A
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000440034
  ensembl transcript: ENST00000545503
  gene symbol: MYBPC1
  hgvsc: ENST00000545503.2:c.757+16G>A
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl transcript: ENST00000550501
  gene symbol: MYBPC1
  hgvsc: ENST00000550501.1:n.574+27657G>A
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000354849
  ensembl transcript: ENST00000361466
  gene symbol: MYBPC1
  hgvsc: ENST00000361466.2:c.832+16G>A
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000388989
  ensembl transcript: ENST00000441232
  gene symbol: MYBPC1
  hgvsc: ENST00000441232.1:c.757+16G>A
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447900
  ensembl transcript: ENST00000553190
  gene symbol: MYBPC1
  hgvsc: ENST00000553190.1:c.757+16G>A
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447660
  ensembl transcript: ENST00000549145
  gene symbol: MYBPC1
  hgvsc: ENST00000549145.1:c.796+16G>A
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000400908
  ensembl transcript: ENST00000452455
  gene symbol: MYBPC1
  hgvsc: ENST00000452455.2:c.757+16G>A
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447116
  ensembl transcript: ENST00000551300
  gene symbol: MYBPC1
  hgvsc: ENST00000551300.1:c.460+16G>A
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000448175
  ensembl transcript: ENST00000547405
  gene symbol: MYBPC1
  hgvsc: ENST00000547405.1:c.679+16G>A
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000446128
  ensembl transcript: ENST00000536007
  gene symbol: MYBPC1
  hgvsc: ENST00000536007.1:c.700+16G>A
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000353822
  ensembl transcript: ENST00000360610
  gene symbol: MYBPC1
  hgvsc: ENST00000360610.2:c.757+16G>A
  variant of: http://identifiers.org/hgnc/7549
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4736
  bin: 2.25e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 17947
  bin: 7.5e0
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 20256
  bin: 1.25e1
  variant carriers: 35
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 861
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4840
  bin: 2.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 3011
  bin: 1.75e1
  variant carriers: 35
genotype quality: GenotypeQuality
num of homozygotes: 2
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: East Asian
population: Latino
population: African
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff

12-102036379-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102036379
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 102036379
    reference: chr 12
allele count: 1
allele frequency: 1.293794959374838e-5
allele num: 77292
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447660
  ensembl transcript: ENST00000549145
  gene symbol: MYBPC1
  hgvsc: ENST00000549145.1:c.796+16G>T
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447900
  ensembl transcript: ENST00000553190
  gene symbol: MYBPC1
  hgvsc: ENST00000553190.1:c.757+16G>T
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000448175
  ensembl transcript: ENST00000547405
  gene symbol: MYBPC1
  hgvsc: ENST00000547405.1:c.679+16G>T
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000376665
  ensembl transcript: ENST00000392934
  gene symbol: MYBPC1
  hgvsc: ENST00000392934.3:c.718+16G>T
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447116
  ensembl transcript: ENST00000551300
  gene symbol: MYBPC1
  hgvsc: ENST00000551300.1:c.460+16G>T
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000353822
  ensembl transcript: ENST00000360610
  gene symbol: MYBPC1
  hgvsc: ENST00000360610.2:c.757+16G>T
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000400908
  ensembl transcript: ENST00000452455
  gene symbol: MYBPC1
  hgvsc: ENST00000452455.2:c.757+16G>T
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000446128
  ensembl transcript: ENST00000536007
  gene symbol: MYBPC1
  hgvsc: ENST00000536007.1:c.700+16G>T
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000388989
  ensembl transcript: ENST00000441232
  gene symbol: MYBPC1
  hgvsc: ENST00000441232.1:c.757+16G>T
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000354845
  ensembl transcript: ENST00000361685
  gene symbol: MYBPC1
  hgvsc: ENST00000361685.2:c.832+16G>T
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000449702
  ensembl transcript: ENST00000550270
  gene symbol: MYBPC1
  hgvsc: ENST00000550270.1:c.757+16G>T
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000354849
  ensembl transcript: ENST00000361466
  gene symbol: MYBPC1
  hgvsc: ENST00000361466.2:c.832+16G>T
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000442847
  ensembl transcript: ENST00000541119
  gene symbol: MYBPC1
  hgvsc: ENST00000541119.1:c.721+16G>T
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447362
  ensembl transcript: ENST00000547509
  gene symbol: MYBPC1
  hgvsc: ENST00000547509.1:c.715+16G>T
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000440034
  ensembl transcript: ENST00000545503
  gene symbol: MYBPC1
  hgvsc: ENST00000545503.2:c.757+16G>T
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl transcript: ENST00000550501
  gene symbol: MYBPC1
  hgvsc: ENST00000550501.1:n.574+27657G>T
  variant of: http://identifiers.org/hgnc/7549
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3740
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17947
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3011
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20256
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 918
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4840
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum

12-102036380-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102036380
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 102036380
    reference: chr 12
allele count: 2
allele frequency: 2.631578947368421e-5
allele num: 76000
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000354845
  ensembl transcript: ENST00000361685
  gene symbol: MYBPC1
  hgvsc: ENST00000361685.2:c.832+17G>A
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000448175
  ensembl transcript: ENST00000547405
  gene symbol: MYBPC1
  hgvsc: ENST00000547405.1:c.679+17G>A
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447660
  ensembl transcript: ENST00000549145
  gene symbol: MYBPC1
  hgvsc: ENST00000549145.1:c.796+17G>A
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000442847
  ensembl transcript: ENST00000541119
  gene symbol: MYBPC1
  hgvsc: ENST00000541119.1:c.721+17G>A
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000449702
  ensembl transcript: ENST00000550270
  gene symbol: MYBPC1
  hgvsc: ENST00000550270.1:c.757+17G>A
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000446128
  ensembl transcript: ENST00000536007
  gene symbol: MYBPC1
  hgvsc: ENST00000536007.1:c.700+17G>A
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447116
  ensembl transcript: ENST00000551300
  gene symbol: MYBPC1
  hgvsc: ENST00000551300.1:c.460+17G>A
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000440034
  ensembl transcript: ENST00000545503
  gene symbol: MYBPC1
  hgvsc: ENST00000545503.2:c.757+17G>A
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447362
  ensembl transcript: ENST00000547509
  gene symbol: MYBPC1
  hgvsc: ENST00000547509.1:c.715+17G>A
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000353822
  ensembl transcript: ENST00000360610
  gene symbol: MYBPC1
  hgvsc: ENST00000360610.2:c.757+17G>A
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000400908
  ensembl transcript: ENST00000452455
  gene symbol: MYBPC1
  hgvsc: ENST00000452455.2:c.757+17G>A
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000388989
  ensembl transcript: ENST00000441232
  gene symbol: MYBPC1
  hgvsc: ENST00000441232.1:c.757+17G>A
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447900
  ensembl transcript: ENST00000553190
  gene symbol: MYBPC1
  hgvsc: ENST00000553190.1:c.757+17G>A
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000354849
  ensembl transcript: ENST00000361466
  gene symbol: MYBPC1
  hgvsc: ENST00000361466.2:c.832+17G>A
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000376665
  ensembl transcript: ENST00000392934
  gene symbol: MYBPC1
  hgvsc: ENST00000392934.3:c.718+17G>A
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl transcript: ENST00000550501
  gene symbol: MYBPC1
  hgvsc: ENST00000550501.1:n.574+27658G>A
  variant of: http://identifiers.org/hgnc/7549
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20774
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4037
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 852
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17959
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 761
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1415
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4218
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
reference allele: G
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD

12-102036382-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102036382
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 102036382
    reference: chr 12
allele count: 1
allele frequency: 1.330176381388172e-5
allele num: 75178
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000376665
  ensembl transcript: ENST00000392934
  gene symbol: MYBPC1
  hgvsc: ENST00000392934.3:c.718+19G>A
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000442847
  ensembl transcript: ENST00000541119
  gene symbol: MYBPC1
  hgvsc: ENST00000541119.1:c.721+19G>A
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000448175
  ensembl transcript: ENST00000547405
  gene symbol: MYBPC1
  hgvsc: ENST00000547405.1:c.679+19G>A
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447660
  ensembl transcript: ENST00000549145
  gene symbol: MYBPC1
  hgvsc: ENST00000549145.1:c.796+19G>A
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000400908
  ensembl transcript: ENST00000452455
  gene symbol: MYBPC1
  hgvsc: ENST00000452455.2:c.757+19G>A
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl transcript: ENST00000550501
  gene symbol: MYBPC1
  hgvsc: ENST00000550501.1:n.574+27660G>A
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000354845
  ensembl transcript: ENST00000361685
  gene symbol: MYBPC1
  hgvsc: ENST00000361685.2:c.832+19G>A
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000446128
  ensembl transcript: ENST00000536007
  gene symbol: MYBPC1
  hgvsc: ENST00000536007.1:c.700+19G>A
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000388989
  ensembl transcript: ENST00000441232
  gene symbol: MYBPC1
  hgvsc: ENST00000441232.1:c.757+19G>A
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000440034
  ensembl transcript: ENST00000545503
  gene symbol: MYBPC1
  hgvsc: ENST00000545503.2:c.757+19G>A
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000449702
  ensembl transcript: ENST00000550270
  gene symbol: MYBPC1
  hgvsc: ENST00000550270.1:c.757+19G>A
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000354849
  ensembl transcript: ENST00000361466
  gene symbol: MYBPC1
  hgvsc: ENST00000361466.2:c.832+19G>A
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447116
  ensembl transcript: ENST00000551300
  gene symbol: MYBPC1
  hgvsc: ENST00000551300.1:c.460+19G>A
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000353822
  ensembl transcript: ENST00000360610
  gene symbol: MYBPC1
  hgvsc: ENST00000360610.2:c.757+19G>A
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447900
  ensembl transcript: ENST00000553190
  gene symbol: MYBPC1
  hgvsc: ENST00000553190.1:c.757+19G>A
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447362
  ensembl transcript: ENST00000547509
  gene symbol: MYBPC1
  hgvsc: ENST00000547509.1:c.715+19G>A
  variant of: http://identifiers.org/hgnc/7549
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4401
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3204
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 761
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18105
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4169
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20880
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 852
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1358
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum

12-102036383-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102036383
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 102036383
    reference: chr 12
allele count: 58
allele frequency: 7.718924673941975e-4
allele num: 75140
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000388989
  ensembl transcript: ENST00000441232
  gene symbol: MYBPC1
  hgvsc: ENST00000441232.1:c.757+20A>G
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000440034
  ensembl transcript: ENST00000545503
  gene symbol: MYBPC1
  hgvsc: ENST00000545503.2:c.757+20A>G
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000449702
  ensembl transcript: ENST00000550270
  gene symbol: MYBPC1
  hgvsc: ENST00000550270.1:c.757+20A>G
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000446128
  ensembl transcript: ENST00000536007
  gene symbol: MYBPC1
  hgvsc: ENST00000536007.1:c.700+20A>G
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000442847
  ensembl transcript: ENST00000541119
  gene symbol: MYBPC1
  hgvsc: ENST00000541119.1:c.721+20A>G
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447900
  ensembl transcript: ENST00000553190
  gene symbol: MYBPC1
  hgvsc: ENST00000553190.1:c.757+20A>G
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000400908
  ensembl transcript: ENST00000452455
  gene symbol: MYBPC1
  hgvsc: ENST00000452455.2:c.757+20A>G
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000376665
  ensembl transcript: ENST00000392934
  gene symbol: MYBPC1
  hgvsc: ENST00000392934.3:c.718+20A>G
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000354845
  ensembl transcript: ENST00000361685
  gene symbol: MYBPC1
  hgvsc: ENST00000361685.2:c.832+20A>G
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000448175
  ensembl transcript: ENST00000547405
  gene symbol: MYBPC1
  hgvsc: ENST00000547405.1:c.679+20A>G
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447660
  ensembl transcript: ENST00000549145
  gene symbol: MYBPC1
  hgvsc: ENST00000549145.1:c.796+20A>G
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447362
  ensembl transcript: ENST00000547509
  gene symbol: MYBPC1
  hgvsc: ENST00000547509.1:c.715+20A>G
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000353822
  ensembl transcript: ENST00000360610
  gene symbol: MYBPC1
  hgvsc: ENST00000360610.2:c.757+20A>G
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000354849
  ensembl transcript: ENST00000361466
  gene symbol: MYBPC1
  hgvsc: ENST00000361466.2:c.832+20A>G
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl transcript: ENST00000550501
  gene symbol: MYBPC1
  hgvsc: ENST00000550501.1:n.574+27661A>G
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447116
  ensembl transcript: ENST00000551300
  gene symbol: MYBPC1
  hgvsc: ENST00000551300.1:c.460+20A>G
  variant of: http://identifiers.org/hgnc/7549
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 849
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 761
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1330
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Other
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
reference allele: A
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: QD

12-102036384-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102036384
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 102036384
    reference: chr 12
allele count: 2
allele frequency: 2.719608376393799e-5
allele num: 73540
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000388989
  ensembl transcript: ENST00000441232
  gene symbol: MYBPC1
  hgvsc: ENST00000441232.1:c.757+21G>A
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000354845
  ensembl transcript: ENST00000361685
  gene symbol: MYBPC1
  hgvsc: ENST00000361685.2:c.832+21G>A
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447362
  ensembl transcript: ENST00000547509
  gene symbol: MYBPC1
  hgvsc: ENST00000547509.1:c.715+21G>A
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000400908
  ensembl transcript: ENST00000452455
  gene symbol: MYBPC1
  hgvsc: ENST00000452455.2:c.757+21G>A
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000446128
  ensembl transcript: ENST00000536007
  gene symbol: MYBPC1
  hgvsc: ENST00000536007.1:c.700+21G>A
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000442847
  ensembl transcript: ENST00000541119
  gene symbol: MYBPC1
  hgvsc: ENST00000541119.1:c.721+21G>A
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447116
  ensembl transcript: ENST00000551300
  gene symbol: MYBPC1
  hgvsc: ENST00000551300.1:c.460+21G>A
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000354849
  ensembl transcript: ENST00000361466
  gene symbol: MYBPC1
  hgvsc: ENST00000361466.2:c.832+21G>A
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000353822
  ensembl transcript: ENST00000360610
  gene symbol: MYBPC1
  hgvsc: ENST00000360610.2:c.757+21G>A
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000440034
  ensembl transcript: ENST00000545503
  gene symbol: MYBPC1
  hgvsc: ENST00000545503.2:c.757+21G>A
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl transcript: ENST00000550501
  gene symbol: MYBPC1
  hgvsc: ENST00000550501.1:n.574+27662G>A
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000448175
  ensembl transcript: ENST00000547405
  gene symbol: MYBPC1
  hgvsc: ENST00000547405.1:c.679+21G>A
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447660
  ensembl transcript: ENST00000549145
  gene symbol: MYBPC1
  hgvsc: ENST00000549145.1:c.796+21G>A
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000449702
  ensembl transcript: ENST00000550270
  gene symbol: MYBPC1
  hgvsc: ENST00000550270.1:c.757+21G>A
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000376665
  ensembl transcript: ENST00000392934
  gene symbol: MYBPC1
  hgvsc: ENST00000392934.3:c.718+21G>A
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447900
  ensembl transcript: ENST00000553190
  gene symbol: MYBPC1
  hgvsc: ENST00000553190.1:c.757+21G>A
  variant of: http://identifiers.org/hgnc/7549
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3054
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18139
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3560
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 761
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 853
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21245
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3530
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP

12-102036388-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102036388
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 102036388
    reference: chr 12
allele count: 1
allele frequency: 1.407697288775022e-5
allele num: 71038
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000442847
  ensembl transcript: ENST00000541119
  gene symbol: MYBPC1
  hgvsc: ENST00000541119.1:c.721+25G>A
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000449702
  ensembl transcript: ENST00000550270
  gene symbol: MYBPC1
  hgvsc: ENST00000550270.1:c.757+25G>A
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447116
  ensembl transcript: ENST00000551300
  gene symbol: MYBPC1
  hgvsc: ENST00000551300.1:c.460+25G>A
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000400908
  ensembl transcript: ENST00000452455
  gene symbol: MYBPC1
  hgvsc: ENST00000452455.2:c.757+25G>A
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000354845
  ensembl transcript: ENST00000361685
  gene symbol: MYBPC1
  hgvsc: ENST00000361685.2:c.832+25G>A
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000354849
  ensembl transcript: ENST00000361466
  gene symbol: MYBPC1
  hgvsc: ENST00000361466.2:c.832+25G>A
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000448175
  ensembl transcript: ENST00000547405
  gene symbol: MYBPC1
  hgvsc: ENST00000547405.1:c.679+25G>A
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000376665
  ensembl transcript: ENST00000392934
  gene symbol: MYBPC1
  hgvsc: ENST00000392934.3:c.718+25G>A
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447900
  ensembl transcript: ENST00000553190
  gene symbol: MYBPC1
  hgvsc: ENST00000553190.1:c.757+25G>A
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000353822
  ensembl transcript: ENST00000360610
  gene symbol: MYBPC1
  hgvsc: ENST00000360610.2:c.757+25G>A
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000446128
  ensembl transcript: ENST00000536007
  gene symbol: MYBPC1
  hgvsc: ENST00000536007.1:c.700+25G>A
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl transcript: ENST00000550501
  gene symbol: MYBPC1
  hgvsc: ENST00000550501.1:n.574+27666G>A
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000388989
  ensembl transcript: ENST00000441232
  gene symbol: MYBPC1
  hgvsc: ENST00000441232.1:c.757+25G>A
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447660
  ensembl transcript: ENST00000549145
  gene symbol: MYBPC1
  hgvsc: ENST00000549145.1:c.796+25G>A
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447362
  ensembl transcript: ENST00000547509
  gene symbol: MYBPC1
  hgvsc: ENST00000547509.1:c.715+25G>A
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000440034
  ensembl transcript: ENST00000545503
  gene symbol: MYBPC1
  hgvsc: ENST00000545503.2:c.757+25G>A
  variant of: http://identifiers.org/hgnc/7549
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2889
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 838
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18337
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2332
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6081
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3887
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ

12-102036393-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102036393
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 102036393
    reference: chr 12
allele count: 1
allele frequency: 1.47592762050949e-5
allele num: 67754
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000354845
  ensembl transcript: ENST00000361685
  gene symbol: MYBPC1
  hgvsc: ENST00000361685.2:c.832+30C>T
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447116
  ensembl transcript: ENST00000551300
  gene symbol: MYBPC1
  hgvsc: ENST00000551300.1:c.460+30C>T
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000388989
  ensembl transcript: ENST00000441232
  gene symbol: MYBPC1
  hgvsc: ENST00000441232.1:c.757+30C>T
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447362
  ensembl transcript: ENST00000547509
  gene symbol: MYBPC1
  hgvsc: ENST00000547509.1:c.715+30C>T
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000448175
  ensembl transcript: ENST00000547405
  gene symbol: MYBPC1
  hgvsc: ENST00000547405.1:c.679+30C>T
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000354849
  ensembl transcript: ENST00000361466
  gene symbol: MYBPC1
  hgvsc: ENST00000361466.2:c.832+30C>T
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447900
  ensembl transcript: ENST00000553190
  gene symbol: MYBPC1
  hgvsc: ENST00000553190.1:c.757+30C>T
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000442847
  ensembl transcript: ENST00000541119
  gene symbol: MYBPC1
  hgvsc: ENST00000541119.1:c.721+30C>T
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000353822
  ensembl transcript: ENST00000360610
  gene symbol: MYBPC1
  hgvsc: ENST00000360610.2:c.757+30C>T
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000449702
  ensembl transcript: ENST00000550270
  gene symbol: MYBPC1
  hgvsc: ENST00000550270.1:c.757+30C>T
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000376665
  ensembl transcript: ENST00000392934
  gene symbol: MYBPC1
  hgvsc: ENST00000392934.3:c.718+30C>T
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl transcript: ENST00000550501
  gene symbol: MYBPC1
  hgvsc: ENST00000550501.1:n.574+27671C>T
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000446128
  ensembl transcript: ENST00000536007
  gene symbol: MYBPC1
  hgvsc: ENST00000536007.1:c.700+30C>T
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447660
  ensembl transcript: ENST00000549145
  gene symbol: MYBPC1
  hgvsc: ENST00000549145.1:c.796+30C>T
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000400908
  ensembl transcript: ENST00000452455
  gene symbol: MYBPC1
  hgvsc: ENST00000452455.2:c.757+30C>T
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000440034
  ensembl transcript: ENST00000545503
  gene symbol: MYBPC1
  hgvsc: ENST00000545503.2:c.757+30C>T
  variant of: http://identifiers.org/hgnc/7549
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2231
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4109
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 850
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20628
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7011
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 999
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 761
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
reference allele: C
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: MQRankSum

12-102036394-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102036394
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 102036394
    reference: chr 12
allele count: 1
allele frequency: 1.515794579518584e-5
allele num: 65972
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000353822
  ensembl transcript: ENST00000360610
  gene symbol: MYBPC1
  hgvsc: ENST00000360610.2:c.757+31G>T
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000442847
  ensembl transcript: ENST00000541119
  gene symbol: MYBPC1
  hgvsc: ENST00000541119.1:c.721+31G>T
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000400908
  ensembl transcript: ENST00000452455
  gene symbol: MYBPC1
  hgvsc: ENST00000452455.2:c.757+31G>T
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000354849
  ensembl transcript: ENST00000361466
  gene symbol: MYBPC1
  hgvsc: ENST00000361466.2:c.832+31G>T
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000446128
  ensembl transcript: ENST00000536007
  gene symbol: MYBPC1
  hgvsc: ENST00000536007.1:c.700+31G>T
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl transcript: ENST00000550501
  gene symbol: MYBPC1
  hgvsc: ENST00000550501.1:n.574+27672G>T
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000388989
  ensembl transcript: ENST00000441232
  gene symbol: MYBPC1
  hgvsc: ENST00000441232.1:c.757+31G>T
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000354845
  ensembl transcript: ENST00000361685
  gene symbol: MYBPC1
  hgvsc: ENST00000361685.2:c.832+31G>T
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447660
  ensembl transcript: ENST00000549145
  gene symbol: MYBPC1
  hgvsc: ENST00000549145.1:c.796+31G>T
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000449702
  ensembl transcript: ENST00000550270
  gene symbol: MYBPC1
  hgvsc: ENST00000550270.1:c.757+31G>T
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447116
  ensembl transcript: ENST00000551300
  gene symbol: MYBPC1
  hgvsc: ENST00000551300.1:c.460+31G>T
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447900
  ensembl transcript: ENST00000553190
  gene symbol: MYBPC1
  hgvsc: ENST00000553190.1:c.757+31G>T
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000448175
  ensembl transcript: ENST00000547405
  gene symbol: MYBPC1
  hgvsc: ENST00000547405.1:c.679+31G>T
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000376665
  ensembl transcript: ENST00000392934
  gene symbol: MYBPC1
  hgvsc: ENST00000392934.3:c.718+31G>T
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000440034
  ensembl transcript: ENST00000545503
  gene symbol: MYBPC1
  hgvsc: ENST00000545503.2:c.757+31G>T
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447362
  ensembl transcript: ENST00000547509
  gene symbol: MYBPC1
  hgvsc: ENST00000547509.1:c.715+31G>T
  variant of: http://identifiers.org/hgnc/7549
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2015
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 911
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7383
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4315
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19357
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 827
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
reference allele: G
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: ReadPosRankSum

12-102036401-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102036401
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 102036401
    reference: chr 12
allele count: 1
allele frequency: 1.632759690428763e-5
allele num: 61246
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000353822
  ensembl transcript: ENST00000360610
  gene symbol: MYBPC1
  hgvsc: ENST00000360610.2:c.757+38G>T
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000354845
  ensembl transcript: ENST00000361685
  gene symbol: MYBPC1
  hgvsc: ENST00000361685.2:c.832+38G>T
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000442847
  ensembl transcript: ENST00000541119
  gene symbol: MYBPC1
  hgvsc: ENST00000541119.1:c.721+38G>T
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000388989
  ensembl transcript: ENST00000441232
  gene symbol: MYBPC1
  hgvsc: ENST00000441232.1:c.757+38G>T
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447362
  ensembl transcript: ENST00000547509
  gene symbol: MYBPC1
  hgvsc: ENST00000547509.1:c.715+38G>T
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000440034
  ensembl transcript: ENST00000545503
  gene symbol: MYBPC1
  hgvsc: ENST00000545503.2:c.757+38G>T
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000376665
  ensembl transcript: ENST00000392934
  gene symbol: MYBPC1
  hgvsc: ENST00000392934.3:c.718+38G>T
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000448175
  ensembl transcript: ENST00000547405
  gene symbol: MYBPC1
  hgvsc: ENST00000547405.1:c.679+38G>T
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000446128
  ensembl transcript: ENST00000536007
  gene symbol: MYBPC1
  hgvsc: ENST00000536007.1:c.700+38G>T
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000449702
  ensembl transcript: ENST00000550270
  gene symbol: MYBPC1
  hgvsc: ENST00000550270.1:c.757+38G>T
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447116
  ensembl transcript: ENST00000551300
  gene symbol: MYBPC1
  hgvsc: ENST00000551300.1:c.460+38G>T
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000400908
  ensembl transcript: ENST00000452455
  gene symbol: MYBPC1
  hgvsc: ENST00000452455.2:c.757+38G>T
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl transcript: ENST00000550501
  gene symbol: MYBPC1
  hgvsc: ENST00000550501.1:n.574+27679G>T
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000354849
  ensembl transcript: ENST00000361466
  gene symbol: MYBPC1
  hgvsc: ENST00000361466.2:c.832+38G>T
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447660
  ensembl transcript: ENST00000549145
  gene symbol: MYBPC1
  hgvsc: ENST00000549145.1:c.796+38G>T
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447900
  ensembl transcript: ENST00000553190
  gene symbol: MYBPC1
  hgvsc: ENST00000553190.1:c.757+38G>T
  variant of: http://identifiers.org/hgnc/7549
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4852
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 761
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20878
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8302
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1364
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: Other
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum

12-102036411-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102036411
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 102036411
    reference: chr 12
allele count: 0
allele frequency: 0.0e0
allele num: 52768
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000440034
  ensembl transcript: ENST00000545503
  gene symbol: MYBPC1
  hgvsc: ENST00000545503.2:c.757+48T>G
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000354845
  ensembl transcript: ENST00000361685
  gene symbol: MYBPC1
  hgvsc: ENST00000361685.2:c.832+48T>G
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447362
  ensembl transcript: ENST00000547509
  gene symbol: MYBPC1
  hgvsc: ENST00000547509.1:c.715+48T>G
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000376665
  ensembl transcript: ENST00000392934
  gene symbol: MYBPC1
  hgvsc: ENST00000392934.3:c.718+48T>G
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000446128
  ensembl transcript: ENST00000536007
  gene symbol: MYBPC1
  hgvsc: ENST00000536007.1:c.700+48T>G
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000353822
  ensembl transcript: ENST00000360610
  gene symbol: MYBPC1
  hgvsc: ENST00000360610.2:c.757+48T>G
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447116
  ensembl transcript: ENST00000551300
  gene symbol: MYBPC1
  hgvsc: ENST00000551300.1:c.460+48T>G
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000448175
  ensembl transcript: ENST00000547405
  gene symbol: MYBPC1
  hgvsc: ENST00000547405.1:c.679+48T>G
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447900
  ensembl transcript: ENST00000553190
  gene symbol: MYBPC1
  hgvsc: ENST00000553190.1:c.757+48T>G
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000354849
  ensembl transcript: ENST00000361466
  gene symbol: MYBPC1
  hgvsc: ENST00000361466.2:c.832+48T>G
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000442847
  ensembl transcript: ENST00000541119
  gene symbol: MYBPC1
  hgvsc: ENST00000541119.1:c.721+48T>G
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000449702
  ensembl transcript: ENST00000550270
  gene symbol: MYBPC1
  hgvsc: ENST00000550270.1:c.757+48T>G
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000388989
  ensembl transcript: ENST00000441232
  gene symbol: MYBPC1
  hgvsc: ENST00000441232.1:c.757+48T>G
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447660
  ensembl transcript: ENST00000549145
  gene symbol: MYBPC1
  hgvsc: ENST00000549145.1:c.796+48T>G
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl transcript: ENST00000550501
  gene symbol: MYBPC1
  hgvsc: ENST00000550501.1:n.574+27689T>G
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000400908
  ensembl transcript: ENST00000452455
  gene symbol: MYBPC1
  hgvsc: ENST00000452455.2:c.757+48T>G
  variant of: http://identifiers.org/hgnc/7549
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 8638
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 761
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 847
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 900
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4778
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 696
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 792
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
reference allele: T
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: InbreedingCoeff

12-102036412-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102036412
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 102036412
    reference: chr 12
allele count: 6
allele frequency: 1.139557851553597e-4
allele num: 52652
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000376665
  ensembl transcript: ENST00000392934
  gene symbol: MYBPC1
  hgvsc: ENST00000392934.3:c.718+49C>T
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl transcript: ENST00000550501
  gene symbol: MYBPC1
  hgvsc: ENST00000550501.1:n.574+27690C>T
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000440034
  ensembl transcript: ENST00000545503
  gene symbol: MYBPC1
  hgvsc: ENST00000545503.2:c.757+49C>T
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447116
  ensembl transcript: ENST00000551300
  gene symbol: MYBPC1
  hgvsc: ENST00000551300.1:c.460+49C>T
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447900
  ensembl transcript: ENST00000553190
  gene symbol: MYBPC1
  hgvsc: ENST00000553190.1:c.757+49C>T
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000353822
  ensembl transcript: ENST00000360610
  gene symbol: MYBPC1
  hgvsc: ENST00000360610.2:c.757+49C>T
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000388989
  ensembl transcript: ENST00000441232
  gene symbol: MYBPC1
  hgvsc: ENST00000441232.1:c.757+49C>T
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000448175
  ensembl transcript: ENST00000547405
  gene symbol: MYBPC1
  hgvsc: ENST00000547405.1:c.679+49C>T
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447660
  ensembl transcript: ENST00000549145
  gene symbol: MYBPC1
  hgvsc: ENST00000549145.1:c.796+49C>T
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000400908
  ensembl transcript: ENST00000452455
  gene symbol: MYBPC1
  hgvsc: ENST00000452455.2:c.757+49C>T
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000442847
  ensembl transcript: ENST00000541119
  gene symbol: MYBPC1
  hgvsc: ENST00000541119.1:c.721+49C>T
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000449702
  ensembl transcript: ENST00000550270
  gene symbol: MYBPC1
  hgvsc: ENST00000550270.1:c.757+49C>T
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447362
  ensembl transcript: ENST00000547509
  gene symbol: MYBPC1
  hgvsc: ENST00000547509.1:c.715+49C>T
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000354849
  ensembl transcript: ENST00000361466
  gene symbol: MYBPC1
  hgvsc: ENST00000361466.2:c.832+49C>T
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000354845
  ensembl transcript: ENST00000361685
  gene symbol: MYBPC1
  hgvsc: ENST00000361685.2:c.832+49C>T
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000446128
  ensembl transcript: ENST00000536007
  gene symbol: MYBPC1
  hgvsc: ENST00000536007.1:c.700+49C>T
  variant of: http://identifiers.org/hgnc/7549
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8637
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 696
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24374
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 792
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14882
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 847
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 777
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Other
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: DP

http://identifiers.org/exac.variant/12-102036415-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102036415
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 102036415
    reference: chr 12
allele count: 2
allele frequency: 3.880631766851643e-5
allele num: 51538
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000446128
  ensembl transcript: ENST00000536007
  gene symbol: MYBPC1
  hgvsc: ENST00000536007.1:c.700+52A>C
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000353822
  ensembl transcript: ENST00000360610
  gene symbol: MYBPC1
  hgvsc: ENST00000360610.2:c.757+52A>C
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000354849
  ensembl transcript: ENST00000361466
  gene symbol: MYBPC1
  hgvsc: ENST00000361466.2:c.832+52A>C
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000442847
  ensembl transcript: ENST00000541119
  gene symbol: MYBPC1
  hgvsc: ENST00000541119.1:c.721+52A>C
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447116
  ensembl transcript: ENST00000551300
  gene symbol: MYBPC1
  hgvsc: ENST00000551300.1:c.460+52A>C
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000448175
  ensembl transcript: ENST00000547405
  gene symbol: MYBPC1
  hgvsc: ENST00000547405.1:c.679+52A>C
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000449702
  ensembl transcript: ENST00000550270
  gene symbol: MYBPC1
  hgvsc: ENST00000550270.1:c.757+52A>C
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000440034
  ensembl transcript: ENST00000545503
  gene symbol: MYBPC1
  hgvsc: ENST00000545503.2:c.757+52A>C
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447362
  ensembl transcript: ENST00000547509
  gene symbol: MYBPC1
  hgvsc: ENST00000547509.1:c.715+52A>C
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000354845
  ensembl transcript: ENST00000361685
  gene symbol: MYBPC1
  hgvsc: ENST00000361685.2:c.832+52A>C
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000388989
  ensembl transcript: ENST00000441232
  gene symbol: MYBPC1
  hgvsc: ENST00000441232.1:c.757+52A>C
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000400908
  ensembl transcript: ENST00000452455
  gene symbol: MYBPC1
  hgvsc: ENST00000452455.2:c.757+52A>C
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl transcript: ENST00000550501
  gene symbol: MYBPC1
  hgvsc: ENST00000550501.1:n.574+27693A>C
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447660
  ensembl transcript: ENST00000549145
  gene symbol: MYBPC1
  hgvsc: ENST00000549145.1:c.796+52A>C
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447900
  ensembl transcript: ENST00000553190
  gene symbol: MYBPC1
  hgvsc: ENST00000553190.1:c.757+52A>C
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000376665
  ensembl transcript: ENST00000392934
  gene symbol: MYBPC1
  hgvsc: ENST00000392934.3:c.718+52A>C
  variant of: http://identifiers.org/hgnc/7549
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8678
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 761
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 899
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 779
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14716
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 531
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
reference allele: A
site quality: DP
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD

12-102038391-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102038391
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 102038391
    reference: chr 12
allele count: 2
allele frequency: 1.730792529899441e-5
allele num: 115554
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000388989
  ensembl transcript: ENST00000441232
  gene symbol: MYBPC1
  hgvsc: ENST00000441232.1:c.758-51T>A
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000400908
  ensembl transcript: ENST00000452455
  gene symbol: MYBPC1
  hgvsc: ENST00000452455.2:c.758-51T>A
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447660
  ensembl transcript: ENST00000549145
  gene symbol: MYBPC1
  hgvsc: ENST00000549145.1:c.797-51T>A
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000442847
  ensembl transcript: ENST00000541119
  gene symbol: MYBPC1
  hgvsc: ENST00000541119.1:c.722-51T>A
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000354849
  ensembl transcript: ENST00000361466
  gene symbol: MYBPC1
  hgvsc: ENST00000361466.2:c.833-51T>A
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000448175
  ensembl transcript: ENST00000547405
  gene symbol: MYBPC1
  hgvsc: ENST00000547405.1:c.680-51T>A
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447116
  ensembl transcript: ENST00000551300
  gene symbol: MYBPC1
  hgvsc: ENST00000551300.1:c.461-51T>A
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000353822
  ensembl transcript: ENST00000360610
  gene symbol: MYBPC1
  hgvsc: ENST00000360610.2:c.758-51T>A
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000354845
  ensembl transcript: ENST00000361685
  gene symbol: MYBPC1
  hgvsc: ENST00000361685.2:c.833-51T>A
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447900
  ensembl transcript: ENST00000553190
  gene symbol: MYBPC1
  hgvsc: ENST00000553190.1:c.758-51T>A
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447362
  ensembl transcript: ENST00000547509
  gene symbol: MYBPC1
  hgvsc: ENST00000547509.1:c.716-51T>A
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000449702
  ensembl transcript: ENST00000550270
  gene symbol: MYBPC1
  hgvsc: ENST00000550270.1:c.758-51T>A
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000446128
  ensembl transcript: ENST00000536007
  gene symbol: MYBPC1
  hgvsc: ENST00000536007.1:c.701-51T>A
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000376665
  ensembl transcript: ENST00000392934
  gene symbol: MYBPC1
  hgvsc: ENST00000392934.3:c.719-51T>A
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl transcript: ENST00000550501
  gene symbol: MYBPC1
  hgvsc: ENST00000550501.1:n.574+29669T>A
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000440034
  ensembl transcript: ENST00000545503
  gene symbol: MYBPC1
  hgvsc: ENST00000545503.2:c.758-51T>A
  variant of: http://identifiers.org/hgnc/7549
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10115
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 688
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8435
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14404
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2610
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 916
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 980
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2306
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
population: Latino
reference allele: T
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum

12-102038391-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102038391
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 102038391
    reference: chr 12
allele count: 2
allele frequency: 1.730792529899441e-5
allele num: 115554
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000449702
  ensembl transcript: ENST00000550270
  gene symbol: MYBPC1
  hgvsc: ENST00000550270.1:c.758-51T>C
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000353822
  ensembl transcript: ENST00000360610
  gene symbol: MYBPC1
  hgvsc: ENST00000360610.2:c.758-51T>C
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000442847
  ensembl transcript: ENST00000541119
  gene symbol: MYBPC1
  hgvsc: ENST00000541119.1:c.722-51T>C
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000376665
  ensembl transcript: ENST00000392934
  gene symbol: MYBPC1
  hgvsc: ENST00000392934.3:c.719-51T>C
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000354849
  ensembl transcript: ENST00000361466
  gene symbol: MYBPC1
  hgvsc: ENST00000361466.2:c.833-51T>C
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447362
  ensembl transcript: ENST00000547509
  gene symbol: MYBPC1
  hgvsc: ENST00000547509.1:c.716-51T>C
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447660
  ensembl transcript: ENST00000549145
  gene symbol: MYBPC1
  hgvsc: ENST00000549145.1:c.797-51T>C
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447116
  ensembl transcript: ENST00000551300
  gene symbol: MYBPC1
  hgvsc: ENST00000551300.1:c.461-51T>C
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000354845
  ensembl transcript: ENST00000361685
  gene symbol: MYBPC1
  hgvsc: ENST00000361685.2:c.833-51T>C
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl transcript: ENST00000550501
  gene symbol: MYBPC1
  hgvsc: ENST00000550501.1:n.574+29669T>C
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000400908
  ensembl transcript: ENST00000452455
  gene symbol: MYBPC1
  hgvsc: ENST00000452455.2:c.758-51T>C
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000448175
  ensembl transcript: ENST00000547405
  gene symbol: MYBPC1
  hgvsc: ENST00000547405.1:c.680-51T>C
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447900
  ensembl transcript: ENST00000553190
  gene symbol: MYBPC1
  hgvsc: ENST00000553190.1:c.758-51T>C
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000440034
  ensembl transcript: ENST00000545503
  gene symbol: MYBPC1
  hgvsc: ENST00000545503.2:c.758-51T>C
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000388989
  ensembl transcript: ENST00000441232
  gene symbol: MYBPC1
  hgvsc: ENST00000441232.1:c.758-51T>C
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000446128
  ensembl transcript: ENST00000536007
  gene symbol: MYBPC1
  hgvsc: ENST00000536007.1:c.701-51T>C
  variant of: http://identifiers.org/hgnc/7549
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10115
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2610
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 914
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13240
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2306
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1135
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14404
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: DP
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

12-102038397-ATG-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102038397
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 102038395
    reference: chr 12
allele count: 1
allele frequency: 8.643640009680878e-6
allele num: 115692
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000448175
  ensembl transcript: ENST00000547405
  gene symbol: MYBPC1
  hgvsc: ENST00000547405.1:c.680-43_680-42delGT
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447362
  ensembl transcript: ENST00000547509
  gene symbol: MYBPC1
  hgvsc: ENST00000547509.1:c.716-43_716-42delGT
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000354845
  ensembl transcript: ENST00000361685
  gene symbol: MYBPC1
  hgvsc: ENST00000361685.2:c.833-43_833-42delGT
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447116
  ensembl transcript: ENST00000551300
  gene symbol: MYBPC1
  hgvsc: ENST00000551300.1:c.461-43_461-42delGT
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000446128
  ensembl transcript: ENST00000536007
  gene symbol: MYBPC1
  hgvsc: ENST00000536007.1:c.701-43_701-42delGT
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl transcript: ENST00000550501
  gene symbol: MYBPC1
  hgvsc: ENST00000550501.1:n.574+29677_574+29678delGT
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000354849
  ensembl transcript: ENST00000361466
  gene symbol: MYBPC1
  hgvsc: ENST00000361466.2:c.833-43_833-42delGT
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000388989
  ensembl transcript: ENST00000441232
  gene symbol: MYBPC1
  hgvsc: ENST00000441232.1:c.758-43_758-42delGT
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000376665
  ensembl transcript: ENST00000392934
  gene symbol: MYBPC1
  hgvsc: ENST00000392934.3:c.719-43_719-42delGT
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000440034
  ensembl transcript: ENST00000545503
  gene symbol: MYBPC1
  hgvsc: ENST00000545503.2:c.758-43_758-42delGT
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000442847
  ensembl transcript: ENST00000541119
  gene symbol: MYBPC1
  hgvsc: ENST00000541119.1:c.722-43_722-42delGT
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000449702
  ensembl transcript: ENST00000550270
  gene symbol: MYBPC1
  hgvsc: ENST00000550270.1:c.758-43_758-42delGT
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447900
  ensembl transcript: ENST00000553190
  gene symbol: MYBPC1
  hgvsc: ENST00000553190.1:c.758-43_758-42delGT
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000353822
  ensembl transcript: ENST00000360610
  gene symbol: MYBPC1
  hgvsc: ENST00000360610.2:c.758-43_758-42delGT
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447660
  ensembl transcript: ENST00000549145
  gene symbol: MYBPC1
  hgvsc: ENST00000549145.1:c.797-43_797-42delGT
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000400908
  ensembl transcript: ENST00000452455
  gene symbol: MYBPC1
  hgvsc: ENST00000452455.2:c.758-43_758-42delGT
  variant of: http://identifiers.org/hgnc/7549
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 965
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 916
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2312
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 979
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 688
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8676
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 915
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10045
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
population: European (Finnish)
reference allele: ATG
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum

12-102038399-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102038399
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 102038399
    reference: chr 12
allele count: 2
allele frequency: 1.730223544881999e-5
allele num: 115592
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000353822
  ensembl transcript: ENST00000360610
  gene symbol: MYBPC1
  hgvsc: ENST00000360610.2:c.758-43G>A
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000442847
  ensembl transcript: ENST00000541119
  gene symbol: MYBPC1
  hgvsc: ENST00000541119.1:c.722-43G>A
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447116
  ensembl transcript: ENST00000551300
  gene symbol: MYBPC1
  hgvsc: ENST00000551300.1:c.461-43G>A
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000354845
  ensembl transcript: ENST00000361685
  gene symbol: MYBPC1
  hgvsc: ENST00000361685.2:c.833-43G>A
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447362
  ensembl transcript: ENST00000547509
  gene symbol: MYBPC1
  hgvsc: ENST00000547509.1:c.716-43G>A
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447660
  ensembl transcript: ENST00000549145
  gene symbol: MYBPC1
  hgvsc: ENST00000549145.1:c.797-43G>A
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000354849
  ensembl transcript: ENST00000361466
  gene symbol: MYBPC1
  hgvsc: ENST00000361466.2:c.833-43G>A
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000400908
  ensembl transcript: ENST00000452455
  gene symbol: MYBPC1
  hgvsc: ENST00000452455.2:c.758-43G>A
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000449702
  ensembl transcript: ENST00000550270
  gene symbol: MYBPC1
  hgvsc: ENST00000550270.1:c.758-43G>A
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447900
  ensembl transcript: ENST00000553190
  gene symbol: MYBPC1
  hgvsc: ENST00000553190.1:c.758-43G>A
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000448175
  ensembl transcript: ENST00000547405
  gene symbol: MYBPC1
  hgvsc: ENST00000547405.1:c.680-43G>A
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000388989
  ensembl transcript: ENST00000441232
  gene symbol: MYBPC1
  hgvsc: ENST00000441232.1:c.758-43G>A
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000440034
  ensembl transcript: ENST00000545503
  gene symbol: MYBPC1
  hgvsc: ENST00000545503.2:c.758-43G>A
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl transcript: ENST00000550501
  gene symbol: MYBPC1
  hgvsc: ENST00000550501.1:n.574+29677G>A
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000376665
  ensembl transcript: ENST00000392934
  gene symbol: MYBPC1
  hgvsc: ENST00000392934.3:c.719-43G>A
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000446128
  ensembl transcript: ENST00000536007
  gene symbol: MYBPC1
  hgvsc: ENST00000536007.1:c.701-43G>A
  variant of: http://identifiers.org/hgnc/7549
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2581
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1135
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 796
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 688
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9876
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2334
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 985
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9898
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 978
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: Other
population: South Asian
reference allele: G
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD

12-102038418-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102038418
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 102038418
    reference: chr 12
allele count: 1
allele frequency: 8.541898009737763e-6
allele num: 117070
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl transcript: ENST00000550501
  gene symbol: MYBPC1
  hgvsc: ENST00000550501.1:n.574+29696C>G
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000400908
  ensembl transcript: ENST00000452455
  gene symbol: MYBPC1
  hgvsc: ENST00000452455.2:c.758-24C>G
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000449702
  ensembl transcript: ENST00000550270
  gene symbol: MYBPC1
  hgvsc: ENST00000550270.1:c.758-24C>G
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000388989
  ensembl transcript: ENST00000441232
  gene symbol: MYBPC1
  hgvsc: ENST00000441232.1:c.758-24C>G
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000354849
  ensembl transcript: ENST00000361466
  gene symbol: MYBPC1
  hgvsc: ENST00000361466.2:c.833-24C>G
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000448175
  ensembl transcript: ENST00000547405
  gene symbol: MYBPC1
  hgvsc: ENST00000547405.1:c.680-24C>G
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000354845
  ensembl transcript: ENST00000361685
  gene symbol: MYBPC1
  hgvsc: ENST00000361685.2:c.833-24C>G
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447116
  ensembl transcript: ENST00000551300
  gene symbol: MYBPC1
  hgvsc: ENST00000551300.1:c.461-24C>G
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447900
  ensembl transcript: ENST00000553190
  gene symbol: MYBPC1
  hgvsc: ENST00000553190.1:c.758-24C>G
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000376665
  ensembl transcript: ENST00000392934
  gene symbol: MYBPC1
  hgvsc: ENST00000392934.3:c.719-24C>G
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447660
  ensembl transcript: ENST00000549145
  gene symbol: MYBPC1
  hgvsc: ENST00000549145.1:c.797-24C>G
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000446128
  ensembl transcript: ENST00000536007
  gene symbol: MYBPC1
  hgvsc: ENST00000536007.1:c.701-24C>G
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000440034
  ensembl transcript: ENST00000545503
  gene symbol: MYBPC1
  hgvsc: ENST00000545503.2:c.758-24C>G
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000442847
  ensembl transcript: ENST00000541119
  gene symbol: MYBPC1
  hgvsc: ENST00000541119.1:c.722-24C>G
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000353822
  ensembl transcript: ENST00000360610
  gene symbol: MYBPC1
  hgvsc: ENST00000360610.2:c.758-24C>G
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447362
  ensembl transcript: ENST00000547509
  gene symbol: MYBPC1
  hgvsc: ENST00000547509.1:c.716-24C>G
  variant of: http://identifiers.org/hgnc/7549
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 914
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 970
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 796
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1139
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 979
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 725
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2083
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 915
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: African
population: East Asian
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: QD

12-102038418-CT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102038418
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 102038417
    reference: chr 12
allele count: 1
allele frequency: 8.541898009737763e-6
allele num: 117070
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000449702
  ensembl transcript: ENST00000550270
  gene symbol: MYBPC1
  hgvsc: ENST00000550270.1:c.758-20delT
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447362
  ensembl transcript: ENST00000547509
  gene symbol: MYBPC1
  hgvsc: ENST00000547509.1:c.716-20delT
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000376665
  ensembl transcript: ENST00000392934
  gene symbol: MYBPC1
  hgvsc: ENST00000392934.3:c.719-20delT
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000446128
  ensembl transcript: ENST00000536007
  gene symbol: MYBPC1
  hgvsc: ENST00000536007.1:c.701-20delT
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000354849
  ensembl transcript: ENST00000361466
  gene symbol: MYBPC1
  hgvsc: ENST00000361466.2:c.833-20delT
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000440034
  ensembl transcript: ENST00000545503
  gene symbol: MYBPC1
  hgvsc: ENST00000545503.2:c.758-20delT
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447116
  ensembl transcript: ENST00000551300
  gene symbol: MYBPC1
  hgvsc: ENST00000551300.1:c.461-20delT
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000400908
  ensembl transcript: ENST00000452455
  gene symbol: MYBPC1
  hgvsc: ENST00000452455.2:c.758-20delT
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000388989
  ensembl transcript: ENST00000441232
  gene symbol: MYBPC1
  hgvsc: ENST00000441232.1:c.758-20delT
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000448175
  ensembl transcript: ENST00000547405
  gene symbol: MYBPC1
  hgvsc: ENST00000547405.1:c.680-20delT
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000353822
  ensembl transcript: ENST00000360610
  gene symbol: MYBPC1
  hgvsc: ENST00000360610.2:c.758-20delT
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000442847
  ensembl transcript: ENST00000541119
  gene symbol: MYBPC1
  hgvsc: ENST00000541119.1:c.722-20delT
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000354845
  ensembl transcript: ENST00000361685
  gene symbol: MYBPC1
  hgvsc: ENST00000361685.2:c.833-20delT
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl transcript: ENST00000550501
  gene symbol: MYBPC1
  hgvsc: ENST00000550501.1:n.574+29700delT
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447660
  ensembl transcript: ENST00000549145
  gene symbol: MYBPC1
  hgvsc: ENST00000549145.1:c.797-20delT
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447900
  ensembl transcript: ENST00000553190
  gene symbol: MYBPC1
  hgvsc: ENST00000553190.1:c.758-20delT
  variant of: http://identifiers.org/hgnc/7549
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2083
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4728
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 915
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29393
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 914
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1873
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 970
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 796
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
population: Other
reference allele: CT
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD

12-102038428-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102038428
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 102038428
    reference: chr 12
allele count: 1
allele frequency: 8.426019548365353e-6
allele num: 118680
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447900
  ensembl transcript: ENST00000553190
  gene symbol: MYBPC1
  hgvsc: ENST00000553190.1:c.758-14T>C
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000442847
  ensembl transcript: ENST00000541119
  gene symbol: MYBPC1
  hgvsc: ENST00000541119.1:c.722-14T>C
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000446128
  ensembl transcript: ENST00000536007
  gene symbol: MYBPC1
  hgvsc: ENST00000536007.1:c.701-14T>C
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000400908
  ensembl transcript: ENST00000452455
  gene symbol: MYBPC1
  hgvsc: ENST00000452455.2:c.758-14T>C
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl transcript: ENST00000550501
  gene symbol: MYBPC1
  hgvsc: ENST00000550501.1:n.574+29706T>C
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447660
  ensembl transcript: ENST00000549145
  gene symbol: MYBPC1
  hgvsc: ENST00000549145.1:c.797-14T>C
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000376665
  ensembl transcript: ENST00000392934
  gene symbol: MYBPC1
  hgvsc: ENST00000392934.3:c.719-14T>C
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000388989
  ensembl transcript: ENST00000441232
  gene symbol: MYBPC1
  hgvsc: ENST00000441232.1:c.758-14T>C
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000354845
  ensembl transcript: ENST00000361685
  gene symbol: MYBPC1
  hgvsc: ENST00000361685.2:c.833-14T>C
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000354849
  ensembl transcript: ENST00000361466
  gene symbol: MYBPC1
  hgvsc: ENST00000361466.2:c.833-14T>C
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000449702
  ensembl transcript: ENST00000550270
  gene symbol: MYBPC1
  hgvsc: ENST00000550270.1:c.758-14T>C
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000448175
  ensembl transcript: ENST00000547405
  gene symbol: MYBPC1
  hgvsc: ENST00000547405.1:c.680-14T>C
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000440034
  ensembl transcript: ENST00000545503
  gene symbol: MYBPC1
  hgvsc: ENST00000545503.2:c.758-14T>C
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447362
  ensembl transcript: ENST00000547509
  gene symbol: MYBPC1
  hgvsc: ENST00000547509.1:c.716-14T>C
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447116
  ensembl transcript: ENST00000551300
  gene symbol: MYBPC1
  hgvsc: ENST00000551300.1:c.461-14T>C
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000353822
  ensembl transcript: ENST00000360610
  gene symbol: MYBPC1
  hgvsc: ENST00000360610.2:c.758-14T>C
  variant of: http://identifiers.org/hgnc/7549
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 688
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1141
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 796
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 914
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11588
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 979
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 985
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1348
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 724
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: Other
population: East Asian
population: South Asian
reference allele: T
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum

12-102038430-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102038430
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 102038430
    reference: chr 12
allele count: 2
allele frequency: 1.681972617485787e-5
allele num: 118908
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000354849
  ensembl transcript: ENST00000361466
  gene symbol: MYBPC1
  hgvsc: ENST00000361466.2:c.833-12C>G
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000448175
  ensembl transcript: ENST00000547405
  gene symbol: MYBPC1
  hgvsc: ENST00000547405.1:c.680-12C>G
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000376665
  ensembl transcript: ENST00000392934
  gene symbol: MYBPC1
  hgvsc: ENST00000392934.3:c.719-12C>G
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447362
  ensembl transcript: ENST00000547509
  gene symbol: MYBPC1
  hgvsc: ENST00000547509.1:c.716-12C>G
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000449702
  ensembl transcript: ENST00000550270
  gene symbol: MYBPC1
  hgvsc: ENST00000550270.1:c.758-12C>G
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000354845
  ensembl transcript: ENST00000361685
  gene symbol: MYBPC1
  hgvsc: ENST00000361685.2:c.833-12C>G
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000446128
  ensembl transcript: ENST00000536007
  gene symbol: MYBPC1
  hgvsc: ENST00000536007.1:c.701-12C>G
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447660
  ensembl transcript: ENST00000549145
  gene symbol: MYBPC1
  hgvsc: ENST00000549145.1:c.797-12C>G
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000440034
  ensembl transcript: ENST00000545503
  gene symbol: MYBPC1
  hgvsc: ENST00000545503.2:c.758-12C>G
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000353822
  ensembl transcript: ENST00000360610
  gene symbol: MYBPC1
  hgvsc: ENST00000360610.2:c.758-12C>G
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl transcript: ENST00000550501
  gene symbol: MYBPC1
  hgvsc: ENST00000550501.1:n.574+29708C>G
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447116
  ensembl transcript: ENST00000551300
  gene symbol: MYBPC1
  hgvsc: ENST00000551300.1:c.461-12C>G
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447900
  ensembl transcript: ENST00000553190
  gene symbol: MYBPC1
  hgvsc: ENST00000553190.1:c.758-12C>G
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000442847
  ensembl transcript: ENST00000541119
  gene symbol: MYBPC1
  hgvsc: ENST00000541119.1:c.722-12C>G
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000400908
  ensembl transcript: ENST00000452455
  gene symbol: MYBPC1
  hgvsc: ENST00000452455.2:c.758-12C>G
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000388989
  ensembl transcript: ENST00000441232
  gene symbol: MYBPC1
  hgvsc: ENST00000441232.1:c.758-12C>G
  variant of: http://identifiers.org/hgnc/7549
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2590
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1774
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 688
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 979
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1206
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1143
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33429
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 915
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Other
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum

12-102038436-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102038436
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 102038436
    reference: chr 12
allele count: 1
allele frequency: 8.351707088928977e-6
allele num: 119736
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000376665
  ensembl transcript: ENST00000392934
  gene symbol: MYBPC1
  hgvsc: ENST00000392934.3:c.719-6T>C
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000400908
  ensembl transcript: ENST00000452455
  gene symbol: MYBPC1
  hgvsc: ENST00000452455.2:c.758-6T>C
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447116
  ensembl transcript: ENST00000551300
  gene symbol: MYBPC1
  hgvsc: ENST00000551300.1:c.461-6T>C
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000448175
  ensembl transcript: ENST00000547405
  gene symbol: MYBPC1
  hgvsc: ENST00000547405.1:c.680-6T>C
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000354845
  ensembl transcript: ENST00000361685
  gene symbol: MYBPC1
  hgvsc: ENST00000361685.2:c.833-6T>C
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000442847
  ensembl transcript: ENST00000541119
  gene symbol: MYBPC1
  hgvsc: ENST00000541119.1:c.722-6T>C
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000388989
  ensembl transcript: ENST00000441232
  gene symbol: MYBPC1
  hgvsc: ENST00000441232.1:c.758-6T>C
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000353822
  ensembl transcript: ENST00000360610
  gene symbol: MYBPC1
  hgvsc: ENST00000360610.2:c.758-6T>C
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000446128
  ensembl transcript: ENST00000536007
  gene symbol: MYBPC1
  hgvsc: ENST00000536007.1:c.701-6T>C
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000449702
  ensembl transcript: ENST00000550270
  gene symbol: MYBPC1
  hgvsc: ENST00000550270.1:c.758-6T>C
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000354849
  ensembl transcript: ENST00000361466
  gene symbol: MYBPC1
  hgvsc: ENST00000361466.2:c.833-6T>C
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl transcript: ENST00000550501
  gene symbol: MYBPC1
  hgvsc: ENST00000550501.1:n.574+29714T>C
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447900
  ensembl transcript: ENST00000553190
  gene symbol: MYBPC1
  hgvsc: ENST00000553190.1:c.758-6T>C
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447362
  ensembl transcript: ENST00000547509
  gene symbol: MYBPC1
  hgvsc: ENST00000547509.1:c.716-6T>C
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000440034
  ensembl transcript: ENST00000545503
  gene symbol: MYBPC1
  hgvsc: ENST00000545503.2:c.758-6T>C
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447660
  ensembl transcript: ENST00000549145
  gene symbol: MYBPC1
  hgvsc: ENST00000549145.1:c.797-6T>C
  variant of: http://identifiers.org/hgnc/7549
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12116
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 915
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 914
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1145
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: c.758-6T>C
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
population: South Asian
population: European (Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff

12-102038446-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102038446
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 102038446
    reference: chr 12
allele count: 1
allele frequency: 8.296276631047985e-6
allele num: 120536
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000354849
  ensembl transcript: ENST00000361466
  gene symbol: MYBPC1
  hgvsc: ENST00000361466.2:c.837T>C
  hgvsp: ENST00000361466.2:c.837T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000446128
  ensembl transcript: ENST00000536007
  gene symbol: MYBPC1
  hgvsc: ENST00000536007.1:c.705T>C
  hgvsp: ENST00000536007.1:c.705T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447900
  ensembl transcript: ENST00000553190
  gene symbol: MYBPC1
  hgvsc: ENST00000553190.1:c.762T>C
  hgvsp: ENST00000553190.1:c.762T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000388989
  ensembl transcript: ENST00000441232
  gene symbol: MYBPC1
  hgvsc: ENST00000441232.1:c.762T>C
  hgvsp: ENST00000441232.1:c.762T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000400908
  ensembl transcript: ENST00000452455
  gene symbol: MYBPC1
  hgvsc: ENST00000452455.2:c.762T>C
  hgvsp: ENST00000452455.2:c.762T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447116
  ensembl transcript: ENST00000551300
  gene symbol: MYBPC1
  hgvsc: ENST00000551300.1:c.465T>C
  hgvsp: ENST00000551300.1:c.465T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000354845
  ensembl transcript: ENST00000361685
  gene symbol: MYBPC1
  hgvsc: ENST00000361685.2:c.837T>C
  hgvsp: ENST00000361685.2:c.837T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl transcript: ENST00000550501
  gene symbol: MYBPC1
  hgvsc: ENST00000550501.1:n.574+29724T>C
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000353822
  ensembl transcript: ENST00000360610
  gene symbol: MYBPC1
  hgvsc: ENST00000360610.2:c.762T>C
  hgvsp: ENST00000360610.2:c.762T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000449702
  ensembl transcript: ENST00000550270
  gene symbol: MYBPC1
  hgvsc: ENST00000550270.1:c.762T>C
  hgvsp: ENST00000550270.1:c.762T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000448175
  ensembl transcript: ENST00000547405
  gene symbol: MYBPC1
  hgvsc: ENST00000547405.1:c.684T>C
  hgvsp: ENST00000547405.1:c.684T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000442847
  ensembl transcript: ENST00000541119
  gene symbol: MYBPC1
  hgvsc: ENST00000541119.1:c.726T>C
  hgvsp: ENST00000541119.1:c.726T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447660
  ensembl transcript: ENST00000549145
  gene symbol: MYBPC1
  hgvsc: ENST00000549145.1:c.801T>C
  hgvsp: ENST00000549145.1:c.801T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447362
  ensembl transcript: ENST00000547509
  gene symbol: MYBPC1
  hgvsc: ENST00000547509.1:c.720T>C
  hgvsp: ENST00000547509.1:c.720T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000440034
  ensembl transcript: ENST00000545503
  gene symbol: MYBPC1
  hgvsc: ENST00000545503.2:c.762T>C
  hgvsp: ENST00000545503.2:c.762T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000376665
  ensembl transcript: ENST00000392934
  gene symbol: MYBPC1
  hgvsc: ENST00000392934.3:c.723T>C
  hgvsp: ENST00000392934.3:c.723T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 915
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1143
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12548
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 985
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Phe254Phe
num of homozygotes: 0
population: African
population: Other
population: European (Finnish)
population: East Asian
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: T
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ

12-102038449-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102038449
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 102038449
    reference: chr 12
allele count: 1
allele frequency: 8.286239870071759e-6
allele num: 120682
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000354849
  ensembl transcript: ENST00000361466
  gene symbol: MYBPC1
  hgvsc: ENST00000361466.2:c.840A>G
  hgvsp: ENST00000361466.2:c.840A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000354845
  ensembl transcript: ENST00000361685
  gene symbol: MYBPC1
  hgvsc: ENST00000361685.2:c.840A>G
  hgvsp: ENST00000361685.2:c.840A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000446128
  ensembl transcript: ENST00000536007
  gene symbol: MYBPC1
  hgvsc: ENST00000536007.1:c.708A>G
  hgvsp: ENST00000536007.1:c.708A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000442847
  ensembl transcript: ENST00000541119
  gene symbol: MYBPC1
  hgvsc: ENST00000541119.1:c.729A>G
  hgvsp: ENST00000541119.1:c.729A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000449702
  ensembl transcript: ENST00000550270
  gene symbol: MYBPC1
  hgvsc: ENST00000550270.1:c.765A>G
  hgvsp: ENST00000550270.1:c.765A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447362
  ensembl transcript: ENST00000547509
  gene symbol: MYBPC1
  hgvsc: ENST00000547509.1:c.723A>G
  hgvsp: ENST00000547509.1:c.723A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000388989
  ensembl transcript: ENST00000441232
  gene symbol: MYBPC1
  hgvsc: ENST00000441232.1:c.765A>G
  hgvsp: ENST00000441232.1:c.765A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000353822
  ensembl transcript: ENST00000360610
  gene symbol: MYBPC1
  hgvsc: ENST00000360610.2:c.765A>G
  hgvsp: ENST00000360610.2:c.765A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000440034
  ensembl transcript: ENST00000545503
  gene symbol: MYBPC1
  hgvsc: ENST00000545503.2:c.765A>G
  hgvsp: ENST00000545503.2:c.765A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447116
  ensembl transcript: ENST00000551300
  gene symbol: MYBPC1
  hgvsc: ENST00000551300.1:c.468A>G
  hgvsp: ENST00000551300.1:c.468A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447900
  ensembl transcript: ENST00000553190
  gene symbol: MYBPC1
  hgvsc: ENST00000553190.1:c.765A>G
  hgvsp: ENST00000553190.1:c.765A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000448175
  ensembl transcript: ENST00000547405
  gene symbol: MYBPC1
  hgvsc: ENST00000547405.1:c.687A>G
  hgvsp: ENST00000547405.1:c.687A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447660
  ensembl transcript: ENST00000549145
  gene symbol: MYBPC1
  hgvsc: ENST00000549145.1:c.804A>G
  hgvsp: ENST00000549145.1:c.804A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000376665
  ensembl transcript: ENST00000392934
  gene symbol: MYBPC1
  hgvsc: ENST00000392934.3:c.726A>G
  hgvsp: ENST00000392934.3:c.726A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl transcript: ENST00000550501
  gene symbol: MYBPC1
  hgvsc: ENST00000550501.1:n.574+29727A>G
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000400908
  ensembl transcript: ENST00000452455
  gene symbol: MYBPC1
  hgvsc: ENST00000452455.2:c.765A>G
  hgvsp: ENST00000452455.2:c.765A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 688
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 986
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 796
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala255Ala
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: European (Finnish)
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD

http://identifiers.org/exac.variant/12-102038452-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102038452
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 102038452
    reference: chr 12
allele count: 1
allele frequency: 8.27841981522567e-6
allele num: 120796
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000448175
  ensembl transcript: ENST00000547405
  gene symbol: MYBPC1
  hgvsc: ENST00000547405.1:c.690A>C
  hgvsp: ENSP00000448175.1:p.Lys230Asn
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000388989
  ensembl transcript: ENST00000441232
  gene symbol: MYBPC1
  hgvsc: ENST00000441232.1:c.768A>C
  hgvsp: ENSP00000388989.1:p.Lys256Asn
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447660
  ensembl transcript: ENST00000549145
  gene symbol: MYBPC1
  hgvsc: ENST00000549145.1:c.807A>C
  hgvsp: ENSP00000447660.1:p.Lys269Asn
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000354849
  ensembl transcript: ENST00000361466
  gene symbol: MYBPC1
  hgvsc: ENST00000361466.2:c.843A>C
  hgvsp: ENSP00000354849.2:p.Lys281Asn
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000353822
  ensembl transcript: ENST00000360610
  gene symbol: MYBPC1
  hgvsc: ENST00000360610.2:c.768A>C
  hgvsp: ENSP00000353822.2:p.Lys256Asn
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000400908
  ensembl transcript: ENST00000452455
  gene symbol: MYBPC1
  hgvsc: ENST00000452455.2:c.768A>C
  hgvsp: ENSP00000400908.2:p.Lys256Asn
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000442847
  ensembl transcript: ENST00000541119
  gene symbol: MYBPC1
  hgvsc: ENST00000541119.1:c.732A>C
  hgvsp: ENSP00000442847.1:p.Lys244Asn
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl transcript: ENST00000550501
  gene symbol: MYBPC1
  hgvsc: ENST00000550501.1:n.574+29730A>C
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447116
  ensembl transcript: ENST00000551300
  gene symbol: MYBPC1
  hgvsc: ENST00000551300.1:c.471A>C
  hgvsp: ENSP00000447116.1:p.Lys157Asn
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000449702
  ensembl transcript: ENST00000550270
  gene symbol: MYBPC1
  hgvsc: ENST00000550270.1:c.768A>C
  hgvsp: ENSP00000449702.1:p.Lys256Asn
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000376665
  ensembl transcript: ENST00000392934
  gene symbol: MYBPC1
  hgvsc: ENST00000392934.3:c.729A>C
  hgvsp: ENSP00000376665.3:p.Lys243Asn
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000440034
  ensembl transcript: ENST00000545503
  gene symbol: MYBPC1
  hgvsc: ENST00000545503.2:c.768A>C
  hgvsp: ENSP00000440034.2:p.Lys256Asn
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000354845
  ensembl transcript: ENST00000361685
  gene symbol: MYBPC1
  hgvsc: ENST00000361685.2:c.843A>C
  hgvsp: ENSP00000354845.2:p.Lys281Asn
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000446128
  ensembl transcript: ENST00000536007
  gene symbol: MYBPC1
  hgvsc: ENST00000536007.1:c.711A>C
  hgvsp: ENSP00000446128.1:p.Lys237Asn
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447362
  ensembl transcript: ENST00000547509
  gene symbol: MYBPC1
  hgvsc: ENST00000547509.1:c.726A>C
  hgvsp: ENSP00000447362.1:p.Lys242Asn
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447900
  ensembl transcript: ENST00000553190
  gene symbol: MYBPC1
  hgvsc: ENST00000553190.1:c.768A>C
  hgvsp: ENSP00000447900.1:p.Lys256Asn
  variant of: http://identifiers.org/hgnc/7549
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 985
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 915
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35116
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 796
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys256Asn
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum

12-102038455-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102038455
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 102038455
    reference: chr 12
allele count: 1
allele frequency: 8.272803984182399e-6
allele num: 120878
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000388989
  ensembl transcript: ENST00000441232
  gene symbol: MYBPC1
  hgvsc: ENST00000441232.1:c.771T>C
  hgvsp: ENST00000441232.1:c.771T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000448175
  ensembl transcript: ENST00000547405
  gene symbol: MYBPC1
  hgvsc: ENST00000547405.1:c.693T>C
  hgvsp: ENST00000547405.1:c.693T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000440034
  ensembl transcript: ENST00000545503
  gene symbol: MYBPC1
  hgvsc: ENST00000545503.2:c.771T>C
  hgvsp: ENST00000545503.2:c.771T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447362
  ensembl transcript: ENST00000547509
  gene symbol: MYBPC1
  hgvsc: ENST00000547509.1:c.729T>C
  hgvsp: ENST00000547509.1:c.729T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447660
  ensembl transcript: ENST00000549145
  gene symbol: MYBPC1
  hgvsc: ENST00000549145.1:c.810T>C
  hgvsp: ENST00000549145.1:c.810T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447116
  ensembl transcript: ENST00000551300
  gene symbol: MYBPC1
  hgvsc: ENST00000551300.1:c.474T>C
  hgvsp: ENST00000551300.1:c.474T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000376665
  ensembl transcript: ENST00000392934
  gene symbol: MYBPC1
  hgvsc: ENST00000392934.3:c.732T>C
  hgvsp: ENST00000392934.3:c.732T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000442847
  ensembl transcript: ENST00000541119
  gene symbol: MYBPC1
  hgvsc: ENST00000541119.1:c.735T>C
  hgvsp: ENST00000541119.1:c.735T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000353822
  ensembl transcript: ENST00000360610
  gene symbol: MYBPC1
  hgvsc: ENST00000360610.2:c.771T>C
  hgvsp: ENST00000360610.2:c.771T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447900
  ensembl transcript: ENST00000553190
  gene symbol: MYBPC1
  hgvsc: ENST00000553190.1:c.771T>C
  hgvsp: ENST00000553190.1:c.771T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000400908
  ensembl transcript: ENST00000452455
  gene symbol: MYBPC1
  hgvsc: ENST00000452455.2:c.771T>C
  hgvsp: ENST00000452455.2:c.771T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000354845
  ensembl transcript: ENST00000361685
  gene symbol: MYBPC1
  hgvsc: ENST00000361685.2:c.846T>C
  hgvsp: ENST00000361685.2:c.846T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000354849
  ensembl transcript: ENST00000361466
  gene symbol: MYBPC1
  hgvsc: ENST00000361466.2:c.846T>C
  hgvsp: ENST00000361466.2:c.846T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl transcript: ENST00000550501
  gene symbol: MYBPC1
  hgvsc: ENST00000550501.1:n.574+29733T>C
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000449702
  ensembl transcript: ENST00000550270
  gene symbol: MYBPC1
  hgvsc: ENST00000550270.1:c.771T>C
  hgvsp: ENST00000550270.1:c.771T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000446128
  ensembl transcript: ENST00000536007
  gene symbol: MYBPC1
  hgvsc: ENST00000536007.1:c.714T>C
  hgvsp: ENST00000536007.1:c.714T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 915
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35151
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 971
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 796
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 985
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile257Ile
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
population: African
reference allele: T
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum

12-102038464-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102038464
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 102038464
    reference: chr 12
allele count: 1
allele frequency: 8.259548037531387e-6
allele num: 121072
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447660
  ensembl transcript: ENST00000549145
  gene symbol: MYBPC1
  hgvsc: ENST00000549145.1:c.819T>C
  hgvsp: ENST00000549145.1:c.819T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000353822
  ensembl transcript: ENST00000360610
  gene symbol: MYBPC1
  hgvsc: ENST00000360610.2:c.780T>C
  hgvsp: ENST00000360610.2:c.780T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000442847
  ensembl transcript: ENST00000541119
  gene symbol: MYBPC1
  hgvsc: ENST00000541119.1:c.744T>C
  hgvsp: ENST00000541119.1:c.744T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000388989
  ensembl transcript: ENST00000441232
  gene symbol: MYBPC1
  hgvsc: ENST00000441232.1:c.780T>C
  hgvsp: ENST00000441232.1:c.780T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447116
  ensembl transcript: ENST00000551300
  gene symbol: MYBPC1
  hgvsc: ENST00000551300.1:c.483T>C
  hgvsp: ENST00000551300.1:c.483T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447362
  ensembl transcript: ENST00000547509
  gene symbol: MYBPC1
  hgvsc: ENST00000547509.1:c.738T>C
  hgvsp: ENST00000547509.1:c.738T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000449702
  ensembl transcript: ENST00000550270
  gene symbol: MYBPC1
  hgvsc: ENST00000550270.1:c.780T>C
  hgvsp: ENST00000550270.1:c.780T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000400908
  ensembl transcript: ENST00000452455
  gene symbol: MYBPC1
  hgvsc: ENST00000452455.2:c.780T>C
  hgvsp: ENST00000452455.2:c.780T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447900
  ensembl transcript: ENST00000553190
  gene symbol: MYBPC1
  hgvsc: ENST00000553190.1:c.780T>C
  hgvsp: ENST00000553190.1:c.780T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000448175
  ensembl transcript: ENST00000547405
  gene symbol: MYBPC1
  hgvsc: ENST00000547405.1:c.702T>C
  hgvsp: ENST00000547405.1:c.702T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000440034
  ensembl transcript: ENST00000545503
  gene symbol: MYBPC1
  hgvsc: ENST00000545503.2:c.780T>C
  hgvsp: ENST00000545503.2:c.780T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000446128
  ensembl transcript: ENST00000536007
  gene symbol: MYBPC1
  hgvsc: ENST00000536007.1:c.723T>C
  hgvsp: ENST00000536007.1:c.723T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000354845
  ensembl transcript: ENST00000361685
  gene symbol: MYBPC1
  hgvsc: ENST00000361685.2:c.855T>C
  hgvsp: ENST00000361685.2:c.855T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000376665
  ensembl transcript: ENST00000392934
  gene symbol: MYBPC1
  hgvsc: ENST00000392934.3:c.741T>C
  hgvsp: ENST00000392934.3:c.741T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl transcript: ENST00000550501
  gene symbol: MYBPC1
  hgvsc: ENST00000550501.1:n.574+29742T>C
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000354849
  ensembl transcript: ENST00000361466
  gene symbol: MYBPC1
  hgvsc: ENST00000361466.2:c.855T>C
  hgvsp: ENST00000361466.2:c.855T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 914
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 979
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 977
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro260Pro
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
population: African
population: East Asian
reference allele: T
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: QD

12-102038467-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102038467
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 102038467
    reference: chr 12
allele count: 3
allele frequency: 2.476841531678803e-5
allele num: 121122
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000440034
  ensembl transcript: ENST00000545503
  gene symbol: MYBPC1
  hgvsc: ENST00000545503.2:c.783A>G
  hgvsp: ENST00000545503.2:c.783A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447362
  ensembl transcript: ENST00000547509
  gene symbol: MYBPC1
  hgvsc: ENST00000547509.1:c.741A>G
  hgvsp: ENST00000547509.1:c.741A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000448175
  ensembl transcript: ENST00000547405
  gene symbol: MYBPC1
  hgvsc: ENST00000547405.1:c.705A>G
  hgvsp: ENST00000547405.1:c.705A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000446128
  ensembl transcript: ENST00000536007
  gene symbol: MYBPC1
  hgvsc: ENST00000536007.1:c.726A>G
  hgvsp: ENST00000536007.1:c.726A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000449702
  ensembl transcript: ENST00000550270
  gene symbol: MYBPC1
  hgvsc: ENST00000550270.1:c.783A>G
  hgvsp: ENST00000550270.1:c.783A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000388989
  ensembl transcript: ENST00000441232
  gene symbol: MYBPC1
  hgvsc: ENST00000441232.1:c.783A>G
  hgvsp: ENST00000441232.1:c.783A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000442847
  ensembl transcript: ENST00000541119
  gene symbol: MYBPC1
  hgvsc: ENST00000541119.1:c.747A>G
  hgvsp: ENST00000541119.1:c.747A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447900
  ensembl transcript: ENST00000553190
  gene symbol: MYBPC1
  hgvsc: ENST00000553190.1:c.783A>G
  hgvsp: ENST00000553190.1:c.783A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl transcript: ENST00000550501
  gene symbol: MYBPC1
  hgvsc: ENST00000550501.1:n.574+29745A>G
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000354849
  ensembl transcript: ENST00000361466
  gene symbol: MYBPC1
  hgvsc: ENST00000361466.2:c.858A>G
  hgvsp: ENST00000361466.2:c.858A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000376665
  ensembl transcript: ENST00000392934
  gene symbol: MYBPC1
  hgvsc: ENST00000392934.3:c.744A>G
  hgvsp: ENST00000392934.3:c.744A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000400908
  ensembl transcript: ENST00000452455
  gene symbol: MYBPC1
  hgvsc: ENST00000452455.2:c.783A>G
  hgvsp: ENST00000452455.2:c.783A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447116
  ensembl transcript: ENST00000551300
  gene symbol: MYBPC1
  hgvsc: ENST00000551300.1:c.486A>G
  hgvsp: ENST00000551300.1:c.486A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447660
  ensembl transcript: ENST00000549145
  gene symbol: MYBPC1
  hgvsc: ENST00000549145.1:c.822A>G
  hgvsp: ENST00000549145.1:c.822A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000354845
  ensembl transcript: ENST00000361685
  gene symbol: MYBPC1
  hgvsc: ENST00000361685.2:c.858A>G
  hgvsp: ENST00000361685.2:c.858A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000353822
  ensembl transcript: ENST00000360610
  gene symbol: MYBPC1
  hgvsc: ENST00000360610.2:c.783A>G
  hgvsp: ENST00000360610.2:c.783A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1144
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35129
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 724
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 979
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala261Ala
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: Latino
population: Other
population: East Asian
population: European (Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum

12-102038487-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102038487
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 102038487
    reference: chr 12
allele count: 2
allele frequency: 1.650328415354656e-5
allele num: 121188
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000449702
  ensembl transcript: ENST00000550270
  gene symbol: MYBPC1
  hgvsc: ENST00000550270.1:c.803G>T
  hgvsp: ENSP00000449702.1:p.Gly268Val
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447116
  ensembl transcript: ENST00000551300
  gene symbol: MYBPC1
  hgvsc: ENST00000551300.1:c.506G>T
  hgvsp: ENSP00000447116.1:p.Gly169Val
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000448175
  ensembl transcript: ENST00000547405
  gene symbol: MYBPC1
  hgvsc: ENST00000547405.1:c.725G>T
  hgvsp: ENSP00000448175.1:p.Gly242Val
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000354845
  ensembl transcript: ENST00000361685
  gene symbol: MYBPC1
  hgvsc: ENST00000361685.2:c.878G>T
  hgvsp: ENSP00000354845.2:p.Gly293Val
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000446128
  ensembl transcript: ENST00000536007
  gene symbol: MYBPC1
  hgvsc: ENST00000536007.1:c.746G>T
  hgvsp: ENSP00000446128.1:p.Gly249Val
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000376665
  ensembl transcript: ENST00000392934
  gene symbol: MYBPC1
  hgvsc: ENST00000392934.3:c.764G>T
  hgvsp: ENSP00000376665.3:p.Gly255Val
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000442847
  ensembl transcript: ENST00000541119
  gene symbol: MYBPC1
  hgvsc: ENST00000541119.1:c.767G>T
  hgvsp: ENSP00000442847.1:p.Gly256Val
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000440034
  ensembl transcript: ENST00000545503
  gene symbol: MYBPC1
  hgvsc: ENST00000545503.2:c.803G>T
  hgvsp: ENSP00000440034.2:p.Gly268Val
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000354849
  ensembl transcript: ENST00000361466
  gene symbol: MYBPC1
  hgvsc: ENST00000361466.2:c.878G>T
  hgvsp: ENSP00000354849.2:p.Gly293Val
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447900
  ensembl transcript: ENST00000553190
  gene symbol: MYBPC1
  hgvsc: ENST00000553190.1:c.803G>T
  hgvsp: ENSP00000447900.1:p.Gly268Val
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447660
  ensembl transcript: ENST00000549145
  gene symbol: MYBPC1
  hgvsc: ENST00000549145.1:c.842G>T
  hgvsp: ENSP00000447660.1:p.Gly281Val
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000400908
  ensembl transcript: ENST00000452455
  gene symbol: MYBPC1
  hgvsc: ENST00000452455.2:c.803G>T
  hgvsp: ENSP00000400908.2:p.Gly268Val
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447362
  ensembl transcript: ENST00000547509
  gene symbol: MYBPC1
  hgvsc: ENST00000547509.1:c.761G>T
  hgvsp: ENSP00000447362.1:p.Gly254Val
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000388989
  ensembl transcript: ENST00000441232
  gene symbol: MYBPC1
  hgvsc: ENST00000441232.1:c.803G>T
  hgvsp: ENSP00000388989.1:p.Gly268Val
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl transcript: ENST00000550501
  gene symbol: MYBPC1
  hgvsc: ENST00000550501.1:n.574+29765G>T
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000353822
  ensembl transcript: ENST00000360610
  gene symbol: MYBPC1
  hgvsc: ENST00000360610.2:c.803G>T
  hgvsp: ENSP00000353822.2:p.Gly268Val
  variant of: http://identifiers.org/hgnc/7549
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 915
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 979
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 913
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 688
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly268Val
num of homozygotes: 0
population: East Asian
population: South Asian
population: Other
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: MQRankSum

12-102038490-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102038490
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 102038490
    reference: chr 12
allele count: 1
allele frequency: 8.251642076773278e-6
allele num: 121188
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000440034
  ensembl transcript: ENST00000545503
  gene symbol: MYBPC1
  hgvsc: ENST00000545503.2:c.806G>A
  hgvsp: ENSP00000440034.2:p.Arg269Lys
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000376665
  ensembl transcript: ENST00000392934
  gene symbol: MYBPC1
  hgvsc: ENST00000392934.3:c.767G>A
  hgvsp: ENSP00000376665.3:p.Arg256Lys
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000449702
  ensembl transcript: ENST00000550270
  gene symbol: MYBPC1
  hgvsc: ENST00000550270.1:c.806G>A
  hgvsp: ENSP00000449702.1:p.Arg269Lys
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000388989
  ensembl transcript: ENST00000441232
  gene symbol: MYBPC1
  hgvsc: ENST00000441232.1:c.806G>A
  hgvsp: ENSP00000388989.1:p.Arg269Lys
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000354845
  ensembl transcript: ENST00000361685
  gene symbol: MYBPC1
  hgvsc: ENST00000361685.2:c.881G>A
  hgvsp: ENSP00000354845.2:p.Arg294Lys
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000448175
  ensembl transcript: ENST00000547405
  gene symbol: MYBPC1
  hgvsc: ENST00000547405.1:c.728G>A
  hgvsp: ENSP00000448175.1:p.Arg243Lys
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000354849
  ensembl transcript: ENST00000361466
  gene symbol: MYBPC1
  hgvsc: ENST00000361466.2:c.881G>A
  hgvsp: ENSP00000354849.2:p.Arg294Lys
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000446128
  ensembl transcript: ENST00000536007
  gene symbol: MYBPC1
  hgvsc: ENST00000536007.1:c.749G>A
  hgvsp: ENSP00000446128.1:p.Arg250Lys
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447660
  ensembl transcript: ENST00000549145
  gene symbol: MYBPC1
  hgvsc: ENST00000549145.1:c.845G>A
  hgvsp: ENSP00000447660.1:p.Arg282Lys
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000400908
  ensembl transcript: ENST00000452455
  gene symbol: MYBPC1
  hgvsc: ENST00000452455.2:c.806G>A
  hgvsp: ENSP00000400908.2:p.Arg269Lys
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000353822
  ensembl transcript: ENST00000360610
  gene symbol: MYBPC1
  hgvsc: ENST00000360610.2:c.806G>A
  hgvsp: ENSP00000353822.2:p.Arg269Lys
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447116
  ensembl transcript: ENST00000551300
  gene symbol: MYBPC1
  hgvsc: ENST00000551300.1:c.509G>A
  hgvsp: ENSP00000447116.1:p.Arg170Lys
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000442847
  ensembl transcript: ENST00000541119
  gene symbol: MYBPC1
  hgvsc: ENST00000541119.1:c.770G>A
  hgvsp: ENSP00000442847.1:p.Arg257Lys
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447900
  ensembl transcript: ENST00000553190
  gene symbol: MYBPC1
  hgvsc: ENST00000553190.1:c.806G>A
  hgvsp: ENSP00000447900.1:p.Arg269Lys
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl transcript: ENST00000550501
  gene symbol: MYBPC1
  hgvsc: ENST00000550501.1:n.574+29768G>A
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447362
  ensembl transcript: ENST00000547509
  gene symbol: MYBPC1
  hgvsc: ENST00000547509.1:c.764G>A
  hgvsp: ENSP00000447362.1:p.Arg255Lys
  variant of: http://identifiers.org/hgnc/7549
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 796
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2786
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 724
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 915
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg269Lys
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: African
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum

12-102038492-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102038492
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 102038492
    reference: chr 12
allele count: 5
allele frequency: 4.125957222075521e-5
allele num: 121184
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000388989
  ensembl transcript: ENST00000441232
  gene symbol: MYBPC1
  hgvsc: ENST00000441232.1:c.808G>A
  hgvsp: ENSP00000388989.1:p.Val270Met
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000354849
  ensembl transcript: ENST00000361466
  gene symbol: MYBPC1
  hgvsc: ENST00000361466.2:c.883G>A
  hgvsp: ENSP00000354849.2:p.Val295Met
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000448175
  ensembl transcript: ENST00000547405
  gene symbol: MYBPC1
  hgvsc: ENST00000547405.1:c.730G>A
  hgvsp: ENSP00000448175.1:p.Val244Met
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447900
  ensembl transcript: ENST00000553190
  gene symbol: MYBPC1
  hgvsc: ENST00000553190.1:c.808G>A
  hgvsp: ENSP00000447900.1:p.Val270Met
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000449702
  ensembl transcript: ENST00000550270
  gene symbol: MYBPC1
  hgvsc: ENST00000550270.1:c.808G>A
  hgvsp: ENSP00000449702.1:p.Val270Met
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000354845
  ensembl transcript: ENST00000361685
  gene symbol: MYBPC1
  hgvsc: ENST00000361685.2:c.883G>A
  hgvsp: ENSP00000354845.2:p.Val295Met
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447116
  ensembl transcript: ENST00000551300
  gene symbol: MYBPC1
  hgvsc: ENST00000551300.1:c.511G>A
  hgvsp: ENSP00000447116.1:p.Val171Met
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447362
  ensembl transcript: ENST00000547509
  gene symbol: MYBPC1
  hgvsc: ENST00000547509.1:c.766G>A
  hgvsp: ENSP00000447362.1:p.Val256Met
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000442847
  ensembl transcript: ENST00000541119
  gene symbol: MYBPC1
  hgvsc: ENST00000541119.1:c.772G>A
  hgvsp: ENSP00000442847.1:p.Val258Met
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447660
  ensembl transcript: ENST00000549145
  gene symbol: MYBPC1
  hgvsc: ENST00000549145.1:c.847G>A
  hgvsp: ENSP00000447660.1:p.Val283Met
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000446128
  ensembl transcript: ENST00000536007
  gene symbol: MYBPC1
  hgvsc: ENST00000536007.1:c.751G>A
  hgvsp: ENSP00000446128.1:p.Val251Met
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl transcript: ENST00000550501
  gene symbol: MYBPC1
  hgvsc: ENST00000550501.1:n.574+29770G>A
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000353822
  ensembl transcript: ENST00000360610
  gene symbol: MYBPC1
  hgvsc: ENST00000360610.2:c.808G>A
  hgvsp: ENSP00000353822.2:p.Val270Met
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000400908
  ensembl transcript: ENST00000452455
  gene symbol: MYBPC1
  hgvsc: ENST00000452455.2:c.808G>A
  hgvsp: ENSP00000400908.2:p.Val270Met
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000376665
  ensembl transcript: ENST00000392934
  gene symbol: MYBPC1
  hgvsc: ENST00000392934.3:c.769G>A
  hgvsp: ENSP00000376665.3:p.Val257Met
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000440034
  ensembl transcript: ENST00000545503
  gene symbol: MYBPC1
  hgvsc: ENST00000545503.2:c.808G>A
  hgvsp: ENSP00000440034.2:p.Val270Met
  variant of: http://identifiers.org/hgnc/7549
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 979
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 915
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val270Met
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum

12-102038527-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102038527
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 102038527
    reference: chr 12
allele count: 1
allele frequency: 8.294900295298451e-6
allele num: 120556
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000354845
  ensembl transcript: ENST00000361685
  gene symbol: MYBPC1
  hgvsc: ENST00000361685.2:c.918G>A
  hgvsp: ENST00000361685.2:c.918G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447900
  ensembl transcript: ENST00000553190
  gene symbol: MYBPC1
  hgvsc: ENST00000553190.1:c.843G>A
  hgvsp: ENST00000553190.1:c.843G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447116
  ensembl transcript: ENST00000551300
  gene symbol: MYBPC1
  hgvsc: ENST00000551300.1:c.546G>A
  hgvsp: ENST00000551300.1:c.546G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447362
  ensembl transcript: ENST00000547509
  gene symbol: MYBPC1
  hgvsc: ENST00000547509.1:c.801G>A
  hgvsp: ENST00000547509.1:c.801G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl transcript: ENST00000550501
  gene symbol: MYBPC1
  hgvsc: ENST00000550501.1:n.574+29805G>A
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447660
  ensembl transcript: ENST00000549145
  gene symbol: MYBPC1
  hgvsc: ENST00000549145.1:c.882G>A
  hgvsp: ENST00000549145.1:c.882G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000400908
  ensembl transcript: ENST00000452455
  gene symbol: MYBPC1
  hgvsc: ENST00000452455.2:c.843G>A
  hgvsp: ENST00000452455.2:c.843G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000448175
  ensembl transcript: ENST00000547405
  gene symbol: MYBPC1
  hgvsc: ENST00000547405.1:c.765G>A
  hgvsp: ENST00000547405.1:c.765G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000449702
  ensembl transcript: ENST00000550270
  gene symbol: MYBPC1
  hgvsc: ENST00000550270.1:c.843G>A
  hgvsp: ENST00000550270.1:c.843G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000353822
  ensembl transcript: ENST00000360610
  gene symbol: MYBPC1
  hgvsc: ENST00000360610.2:c.843G>A
  hgvsp: ENST00000360610.2:c.843G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000440034
  ensembl transcript: ENST00000545503
  gene symbol: MYBPC1
  hgvsc: ENST00000545503.2:c.843G>A
  hgvsp: ENST00000545503.2:c.843G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000442847
  ensembl transcript: ENST00000541119
  gene symbol: MYBPC1
  hgvsc: ENST00000541119.1:c.807G>A
  hgvsp: ENST00000541119.1:c.807G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000376665
  ensembl transcript: ENST00000392934
  gene symbol: MYBPC1
  hgvsc: ENST00000392934.3:c.804G>A
  hgvsp: ENST00000392934.3:c.804G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000354849
  ensembl transcript: ENST00000361466
  gene symbol: MYBPC1
  hgvsc: ENST00000361466.2:c.918G>A
  hgvsp: ENST00000361466.2:c.918G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000388989
  ensembl transcript: ENST00000441232
  gene symbol: MYBPC1
  hgvsc: ENST00000441232.1:c.843G>A
  hgvsp: ENST00000441232.1:c.843G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000446128
  ensembl transcript: ENST00000536007
  gene symbol: MYBPC1
  hgvsc: ENST00000536007.1:c.786G>A
  hgvsp: ENST00000536007.1:c.786G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13643
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 688
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2842
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu281Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: South Asian
population: European (Finnish)
population: African
population: Other
population: East Asian
reference allele: G
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP

12-102038530-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102038530
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 102038530
    reference: chr 12
allele count: 2
allele frequency: 1.661847309469206e-5
allele num: 120348
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000442847
  ensembl transcript: ENST00000541119
  gene symbol: MYBPC1
  hgvsc: ENST00000541119.1:c.810G>A
  hgvsp: ENST00000541119.1:c.810G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000448175
  ensembl transcript: ENST00000547405
  gene symbol: MYBPC1
  hgvsc: ENST00000547405.1:c.768G>A
  hgvsp: ENST00000547405.1:c.768G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000400908
  ensembl transcript: ENST00000452455
  gene symbol: MYBPC1
  hgvsc: ENST00000452455.2:c.846G>A
  hgvsp: ENST00000452455.2:c.846G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000354849
  ensembl transcript: ENST00000361466
  gene symbol: MYBPC1
  hgvsc: ENST00000361466.2:c.921G>A
  hgvsp: ENST00000361466.2:c.921G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447362
  ensembl transcript: ENST00000547509
  gene symbol: MYBPC1
  hgvsc: ENST00000547509.1:c.804G>A
  hgvsp: ENST00000547509.1:c.804G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000354845
  ensembl transcript: ENST00000361685
  gene symbol: MYBPC1
  hgvsc: ENST00000361685.2:c.921G>A
  hgvsp: ENST00000361685.2:c.921G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447116
  ensembl transcript: ENST00000551300
  gene symbol: MYBPC1
  hgvsc: ENST00000551300.1:c.549G>A
  hgvsp: ENST00000551300.1:c.549G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000449702
  ensembl transcript: ENST00000550270
  gene symbol: MYBPC1
  hgvsc: ENST00000550270.1:c.846G>A
  hgvsp: ENST00000550270.1:c.846G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000353822
  ensembl transcript: ENST00000360610
  gene symbol: MYBPC1
  hgvsc: ENST00000360610.2:c.846G>A
  hgvsp: ENST00000360610.2:c.846G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000440034
  ensembl transcript: ENST00000545503
  gene symbol: MYBPC1
  hgvsc: ENST00000545503.2:c.846G>A
  hgvsp: ENST00000545503.2:c.846G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000388989
  ensembl transcript: ENST00000441232
  gene symbol: MYBPC1
  hgvsc: ENST00000441232.1:c.846G>A
  hgvsp: ENST00000441232.1:c.846G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl transcript: ENST00000550501
  gene symbol: MYBPC1
  hgvsc: ENST00000550501.1:n.574+29808G>A
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447660
  ensembl transcript: ENST00000549145
  gene symbol: MYBPC1
  hgvsc: ENST00000549145.1:c.885G>A
  hgvsp: ENST00000549145.1:c.885G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000446128
  ensembl transcript: ENST00000536007
  gene symbol: MYBPC1
  hgvsc: ENST00000536007.1:c.789G>A
  hgvsp: ENST00000536007.1:c.789G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000376665
  ensembl transcript: ENST00000392934
  gene symbol: MYBPC1
  hgvsc: ENST00000392934.3:c.807G>A
  hgvsp: ENST00000392934.3:c.807G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447900
  ensembl transcript: ENST00000553190
  gene symbol: MYBPC1
  hgvsc: ENST00000553190.1:c.846G>A
  hgvsp: ENST00000553190.1:c.846G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 915
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 980
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 796
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 913
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32907
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Glu282Glu
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
population: East Asian
population: African
population: European (Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: MQ

12-102038540-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102038540
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 102038540
    reference: chr 12
allele count: 1
allele frequency: 8.344598541364175e-6
allele num: 119838
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000354845
  ensembl transcript: ENST00000361685
  gene symbol: MYBPC1
  hgvsc: ENST00000361685.2:c.931T>C
  hgvsp: ENSP00000354845.2:p.Tyr311His
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000400908
  ensembl transcript: ENST00000452455
  gene symbol: MYBPC1
  hgvsc: ENST00000452455.2:c.856T>C
  hgvsp: ENSP00000400908.2:p.Tyr286His
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447900
  ensembl transcript: ENST00000553190
  gene symbol: MYBPC1
  hgvsc: ENST00000553190.1:c.856T>C
  hgvsp: ENSP00000447900.1:p.Tyr286His
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000442847
  ensembl transcript: ENST00000541119
  gene symbol: MYBPC1
  hgvsc: ENST00000541119.1:c.820T>C
  hgvsp: ENSP00000442847.1:p.Tyr274His
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000440034
  ensembl transcript: ENST00000545503
  gene symbol: MYBPC1
  hgvsc: ENST00000545503.2:c.856T>C
  hgvsp: ENSP00000440034.2:p.Tyr286His
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000353822
  ensembl transcript: ENST00000360610
  gene symbol: MYBPC1
  hgvsc: ENST00000360610.2:c.856T>C
  hgvsp: ENSP00000353822.2:p.Tyr286His
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000388989
  ensembl transcript: ENST00000441232
  gene symbol: MYBPC1
  hgvsc: ENST00000441232.1:c.856T>C
  hgvsp: ENSP00000388989.1:p.Tyr286His
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000376665
  ensembl transcript: ENST00000392934
  gene symbol: MYBPC1
  hgvsc: ENST00000392934.3:c.817T>C
  hgvsp: ENSP00000376665.3:p.Tyr273His
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000446128
  ensembl transcript: ENST00000536007
  gene symbol: MYBPC1
  hgvsc: ENST00000536007.1:c.799T>C
  hgvsp: ENSP00000446128.1:p.Tyr267His
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447660
  ensembl transcript: ENST00000549145
  gene symbol: MYBPC1
  hgvsc: ENST00000549145.1:c.895T>C
  hgvsp: ENSP00000447660.1:p.Tyr299His
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000354849
  ensembl transcript: ENST00000361466
  gene symbol: MYBPC1
  hgvsc: ENST00000361466.2:c.931T>C
  hgvsp: ENSP00000354849.2:p.Tyr311His
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447362
  ensembl transcript: ENST00000547509
  gene symbol: MYBPC1
  hgvsc: ENST00000547509.1:c.814T>C
  hgvsp: ENSP00000447362.1:p.Tyr272His
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000448175
  ensembl transcript: ENST00000547405
  gene symbol: MYBPC1
  hgvsc: ENST00000547405.1:c.778T>C
  hgvsp: ENSP00000448175.1:p.Tyr260His
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000449702
  ensembl transcript: ENST00000550270
  gene symbol: MYBPC1
  hgvsc: ENST00000550270.1:c.856T>C
  hgvsp: ENSP00000449702.1:p.Tyr286His
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl transcript: ENST00000550501
  gene symbol: MYBPC1
  hgvsc: ENST00000550501.1:n.574+29818T>C
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447116
  ensembl transcript: ENST00000551300
  gene symbol: MYBPC1
  hgvsc: ENST00000551300.1:c.559T>C
  hgvsp: ENSP00000447116.1:p.Tyr187His
  variant of: http://identifiers.org/hgnc/7549
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1331
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 688
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 988
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 749
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Tyr286His
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
population: African
reference allele: T
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD

12-102038542-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102038542
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 102038542
    reference: chr 12
allele count: 1
allele frequency: 8.357709987463435e-6
allele num: 119650
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447660
  ensembl transcript: ENST00000549145
  gene symbol: MYBPC1
  hgvsc: ENST00000549145.1:c.897T>C
  hgvsp: ENST00000549145.1:c.897T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000388989
  ensembl transcript: ENST00000441232
  gene symbol: MYBPC1
  hgvsc: ENST00000441232.1:c.858T>C
  hgvsp: ENST00000441232.1:c.858T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000448175
  ensembl transcript: ENST00000547405
  gene symbol: MYBPC1
  hgvsc: ENST00000547405.1:c.780T>C
  hgvsp: ENST00000547405.1:c.780T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000354845
  ensembl transcript: ENST00000361685
  gene symbol: MYBPC1
  hgvsc: ENST00000361685.2:c.933T>C
  hgvsp: ENST00000361685.2:c.933T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000440034
  ensembl transcript: ENST00000545503
  gene symbol: MYBPC1
  hgvsc: ENST00000545503.2:c.858T>C
  hgvsp: ENST00000545503.2:c.858T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000449702
  ensembl transcript: ENST00000550270
  gene symbol: MYBPC1
  hgvsc: ENST00000550270.1:c.858T>C
  hgvsp: ENST00000550270.1:c.858T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000446128
  ensembl transcript: ENST00000536007
  gene symbol: MYBPC1
  hgvsc: ENST00000536007.1:c.801T>C
  hgvsp: ENST00000536007.1:c.801T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447116
  ensembl transcript: ENST00000551300
  gene symbol: MYBPC1
  hgvsc: ENST00000551300.1:c.561T>C
  hgvsp: ENST00000551300.1:c.561T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447900
  ensembl transcript: ENST00000553190
  gene symbol: MYBPC1
  hgvsc: ENST00000553190.1:c.858T>C
  hgvsp: ENST00000553190.1:c.858T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000400908
  ensembl transcript: ENST00000452455
  gene symbol: MYBPC1
  hgvsc: ENST00000452455.2:c.858T>C
  hgvsp: ENST00000452455.2:c.858T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000442847
  ensembl transcript: ENST00000541119
  gene symbol: MYBPC1
  hgvsc: ENST00000541119.1:c.822T>C
  hgvsp: ENST00000541119.1:c.822T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000354849
  ensembl transcript: ENST00000361466
  gene symbol: MYBPC1
  hgvsc: ENST00000361466.2:c.933T>C
  hgvsp: ENST00000361466.2:c.933T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000353822
  ensembl transcript: ENST00000360610
  gene symbol: MYBPC1
  hgvsc: ENST00000360610.2:c.858T>C
  hgvsp: ENST00000360610.2:c.858T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000376665
  ensembl transcript: ENST00000392934
  gene symbol: MYBPC1
  hgvsc: ENST00000392934.3:c.819T>C
  hgvsp: ENST00000392934.3:c.819T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447362
  ensembl transcript: ENST00000547509
  gene symbol: MYBPC1
  hgvsc: ENST00000547509.1:c.816T>C
  hgvsp: ENST00000547509.1:c.816T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl transcript: ENST00000550501
  gene symbol: MYBPC1
  hgvsc: ENST00000550501.1:n.574+29820T>C
  variant of: http://identifiers.org/hgnc/7549
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1170
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 820
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 846
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1481
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 978
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Tyr286Tyr
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
reference allele: T
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: DP

12-102038583-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102038583
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 102038583
    reference: chr 12
allele count: 1
allele frequency: 8.775778850372971e-6
allele num: 113950
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl transcript: ENST00000550501
  gene symbol: MYBPC1
  hgvsc: ENST00000550501.1:n.574+29861G>C
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000376665
  ensembl transcript: ENST00000392934
  gene symbol: MYBPC1
  hgvsc: ENST00000392934.3:c.851+9G>C
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000353822
  ensembl transcript: ENST00000360610
  gene symbol: MYBPC1
  hgvsc: ENST00000360610.2:c.890+9G>C
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000448175
  ensembl transcript: ENST00000547405
  gene symbol: MYBPC1
  hgvsc: ENST00000547405.1:c.812+9G>C
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000354849
  ensembl transcript: ENST00000361466
  gene symbol: MYBPC1
  hgvsc: ENST00000361466.2:c.965+9G>C
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000442847
  ensembl transcript: ENST00000541119
  gene symbol: MYBPC1
  hgvsc: ENST00000541119.1:c.854+9G>C
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447900
  ensembl transcript: ENST00000553190
  gene symbol: MYBPC1
  hgvsc: ENST00000553190.1:c.890+9G>C
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000400908
  ensembl transcript: ENST00000452455
  gene symbol: MYBPC1
  hgvsc: ENST00000452455.2:c.890+9G>C
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447116
  ensembl transcript: ENST00000551300
  gene symbol: MYBPC1
  hgvsc: ENST00000551300.1:c.593+9G>C
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000388989
  ensembl transcript: ENST00000441232
  gene symbol: MYBPC1
  hgvsc: ENST00000441232.1:c.890+9G>C
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000449702
  ensembl transcript: ENST00000550270
  gene symbol: MYBPC1
  hgvsc: ENST00000550270.1:c.890+9G>C
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447660
  ensembl transcript: ENST00000549145
  gene symbol: MYBPC1
  hgvsc: ENST00000549145.1:c.929+9G>C
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447362
  ensembl transcript: ENST00000547509
  gene symbol: MYBPC1
  hgvsc: ENST00000547509.1:c.848+9G>C
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000354845
  ensembl transcript: ENST00000361685
  gene symbol: MYBPC1
  hgvsc: ENST00000361685.2:c.965+9G>C
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000440034
  ensembl transcript: ENST00000545503
  gene symbol: MYBPC1
  hgvsc: ENST00000545503.2:c.890+9G>C
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000446128
  ensembl transcript: ENST00000536007
  gene symbol: MYBPC1
  hgvsc: ENST00000536007.1:c.833+9G>C
  variant of: http://identifiers.org/hgnc/7549
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 915
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 725
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 978
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11199
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2340
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2427
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3505
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 688
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23497
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: Other
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD

12-102038597-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102038597
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 102038597
    reference: chr 12
allele count: 1
allele frequency: 8.97037980588098e-6
allele num: 111478
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447116
  ensembl transcript: ENST00000551300
  gene symbol: MYBPC1
  hgvsc: ENST00000551300.1:c.593+23A>T
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000442847
  ensembl transcript: ENST00000541119
  gene symbol: MYBPC1
  hgvsc: ENST00000541119.1:c.854+23A>T
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447362
  ensembl transcript: ENST00000547509
  gene symbol: MYBPC1
  hgvsc: ENST00000547509.1:c.848+23A>T
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000449702
  ensembl transcript: ENST00000550270
  gene symbol: MYBPC1
  hgvsc: ENST00000550270.1:c.890+23A>T
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000400908
  ensembl transcript: ENST00000452455
  gene symbol: MYBPC1
  hgvsc: ENST00000452455.2:c.890+23A>T
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000376665
  ensembl transcript: ENST00000392934
  gene symbol: MYBPC1
  hgvsc: ENST00000392934.3:c.851+23A>T
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000354845
  ensembl transcript: ENST00000361685
  gene symbol: MYBPC1
  hgvsc: ENST00000361685.2:c.965+23A>T
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000440034
  ensembl transcript: ENST00000545503
  gene symbol: MYBPC1
  hgvsc: ENST00000545503.2:c.890+23A>T
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000448175
  ensembl transcript: ENST00000547405
  gene symbol: MYBPC1
  hgvsc: ENST00000547405.1:c.812+23A>T
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447660
  ensembl transcript: ENST00000549145
  gene symbol: MYBPC1
  hgvsc: ENST00000549145.1:c.929+23A>T
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl transcript: ENST00000550501
  gene symbol: MYBPC1
  hgvsc: ENST00000550501.1:n.574+29875A>T
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000353822
  ensembl transcript: ENST00000360610
  gene symbol: MYBPC1
  hgvsc: ENST00000360610.2:c.890+23A>T
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000388989
  ensembl transcript: ENST00000441232
  gene symbol: MYBPC1
  hgvsc: ENST00000441232.1:c.890+23A>T
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447900
  ensembl transcript: ENST00000553190
  gene symbol: MYBPC1
  hgvsc: ENST00000553190.1:c.890+23A>T
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000354849
  ensembl transcript: ENST00000361466
  gene symbol: MYBPC1
  hgvsc: ENST00000361466.2:c.965+23A>T
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000446128
  ensembl transcript: ENST00000536007
  gene symbol: MYBPC1
  hgvsc: ENST00000536007.1:c.833+23A>T
  variant of: http://identifiers.org/hgnc/7549
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1104
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4488
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2239
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14584
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 969
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 913
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 977
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15951
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Other
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
reference allele: A
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: FS

12-102038600-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102038600
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 102038600
    reference: chr 12
allele count: 2
allele frequency: 1.803296425866484e-5
allele num: 110908
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000448175
  ensembl transcript: ENST00000547405
  gene symbol: MYBPC1
  hgvsc: ENST00000547405.1:c.812+26G>A
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000354845
  ensembl transcript: ENST00000361685
  gene symbol: MYBPC1
  hgvsc: ENST00000361685.2:c.965+26G>A
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447362
  ensembl transcript: ENST00000547509
  gene symbol: MYBPC1
  hgvsc: ENST00000547509.1:c.848+26G>A
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447116
  ensembl transcript: ENST00000551300
  gene symbol: MYBPC1
  hgvsc: ENST00000551300.1:c.593+26G>A
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000388989
  ensembl transcript: ENST00000441232
  gene symbol: MYBPC1
  hgvsc: ENST00000441232.1:c.890+26G>A
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000442847
  ensembl transcript: ENST00000541119
  gene symbol: MYBPC1
  hgvsc: ENST00000541119.1:c.854+26G>A
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000449702
  ensembl transcript: ENST00000550270
  gene symbol: MYBPC1
  hgvsc: ENST00000550270.1:c.890+26G>A
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000400908
  ensembl transcript: ENST00000452455
  gene symbol: MYBPC1
  hgvsc: ENST00000452455.2:c.890+26G>A
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447660
  ensembl transcript: ENST00000549145
  gene symbol: MYBPC1
  hgvsc: ENST00000549145.1:c.929+26G>A
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000354849
  ensembl transcript: ENST00000361466
  gene symbol: MYBPC1
  hgvsc: ENST00000361466.2:c.965+26G>A
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000446128
  ensembl transcript: ENST00000536007
  gene symbol: MYBPC1
  hgvsc: ENST00000536007.1:c.833+26G>A
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl transcript: ENST00000550501
  gene symbol: MYBPC1
  hgvsc: ENST00000550501.1:n.574+29878G>A
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000440034
  ensembl transcript: ENST00000545503
  gene symbol: MYBPC1
  hgvsc: ENST00000545503.2:c.890+26G>A
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000376665
  ensembl transcript: ENST00000392934
  gene symbol: MYBPC1
  hgvsc: ENST00000392934.3:c.851+26G>A
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447900
  ensembl transcript: ENST00000553190
  gene symbol: MYBPC1
  hgvsc: ENST00000553190.1:c.890+26G>A
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000353822
  ensembl transcript: ENST00000360610
  gene symbol: MYBPC1
  hgvsc: ENST00000360610.2:c.890+26G>A
  variant of: http://identifiers.org/hgnc/7549
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 977
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 725
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13881
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 915
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6126
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 970
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1105
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: African
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: MQ
site quality: InbreedingCoeff

12-102038601-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102038601
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 102038601
    reference: chr 12
allele count: 1
allele frequency: 9.012906482082342e-6
allele num: 110952
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000448175
  ensembl transcript: ENST00000547405
  gene symbol: MYBPC1
  hgvsc: ENST00000547405.1:c.812+27A>G
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000353822
  ensembl transcript: ENST00000360610
  gene symbol: MYBPC1
  hgvsc: ENST00000360610.2:c.890+27A>G
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000354845
  ensembl transcript: ENST00000361685
  gene symbol: MYBPC1
  hgvsc: ENST00000361685.2:c.965+27A>G
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447116
  ensembl transcript: ENST00000551300
  gene symbol: MYBPC1
  hgvsc: ENST00000551300.1:c.593+27A>G
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447362
  ensembl transcript: ENST00000547509
  gene symbol: MYBPC1
  hgvsc: ENST00000547509.1:c.848+27A>G
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000376665
  ensembl transcript: ENST00000392934
  gene symbol: MYBPC1
  hgvsc: ENST00000392934.3:c.851+27A>G
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000442847
  ensembl transcript: ENST00000541119
  gene symbol: MYBPC1
  hgvsc: ENST00000541119.1:c.854+27A>G
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000354849
  ensembl transcript: ENST00000361466
  gene symbol: MYBPC1
  hgvsc: ENST00000361466.2:c.965+27A>G
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000446128
  ensembl transcript: ENST00000536007
  gene symbol: MYBPC1
  hgvsc: ENST00000536007.1:c.833+27A>G
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl transcript: ENST00000550501
  gene symbol: MYBPC1
  hgvsc: ENST00000550501.1:n.574+29879A>G
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000400908
  ensembl transcript: ENST00000452455
  gene symbol: MYBPC1
  hgvsc: ENST00000452455.2:c.890+27A>G
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000449702
  ensembl transcript: ENST00000550270
  gene symbol: MYBPC1
  hgvsc: ENST00000550270.1:c.890+27A>G
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000388989
  ensembl transcript: ENST00000441232
  gene symbol: MYBPC1
  hgvsc: ENST00000441232.1:c.890+27A>G
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447900
  ensembl transcript: ENST00000553190
  gene symbol: MYBPC1
  hgvsc: ENST00000553190.1:c.890+27A>G
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447660
  ensembl transcript: ENST00000549145
  gene symbol: MYBPC1
  hgvsc: ENST00000549145.1:c.929+27A>G
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000440034
  ensembl transcript: ENST00000545503
  gene symbol: MYBPC1
  hgvsc: ENST00000545503.2:c.890+27A>G
  variant of: http://identifiers.org/hgnc/7549
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 915
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1102
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 971
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16778
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12711
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4709
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2098
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 795
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
population: Other
population: African
reference allele: A
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum

12-102038604-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102038604
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 102038604
    reference: chr 12
allele count: 1
allele frequency: 9.072763563781527e-6
allele num: 110220
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000442847
  ensembl transcript: ENST00000541119
  gene symbol: MYBPC1
  hgvsc: ENST00000541119.1:c.854+30G>A
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447116
  ensembl transcript: ENST00000551300
  gene symbol: MYBPC1
  hgvsc: ENST00000551300.1:c.593+30G>A
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000354845
  ensembl transcript: ENST00000361685
  gene symbol: MYBPC1
  hgvsc: ENST00000361685.2:c.965+30G>A
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000400908
  ensembl transcript: ENST00000452455
  gene symbol: MYBPC1
  hgvsc: ENST00000452455.2:c.890+30G>A
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000354849
  ensembl transcript: ENST00000361466
  gene symbol: MYBPC1
  hgvsc: ENST00000361466.2:c.965+30G>A
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl transcript: ENST00000550501
  gene symbol: MYBPC1
  hgvsc: ENST00000550501.1:n.574+29882G>A
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000446128
  ensembl transcript: ENST00000536007
  gene symbol: MYBPC1
  hgvsc: ENST00000536007.1:c.833+30G>A
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000448175
  ensembl transcript: ENST00000547405
  gene symbol: MYBPC1
  hgvsc: ENST00000547405.1:c.812+30G>A
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447900
  ensembl transcript: ENST00000553190
  gene symbol: MYBPC1
  hgvsc: ENST00000553190.1:c.890+30G>A
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000388989
  ensembl transcript: ENST00000441232
  gene symbol: MYBPC1
  hgvsc: ENST00000441232.1:c.890+30G>A
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000353822
  ensembl transcript: ENST00000360610
  gene symbol: MYBPC1
  hgvsc: ENST00000360610.2:c.890+30G>A
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447362
  ensembl transcript: ENST00000547509
  gene symbol: MYBPC1
  hgvsc: ENST00000547509.1:c.848+30G>A
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447660
  ensembl transcript: ENST00000549145
  gene symbol: MYBPC1
  hgvsc: ENST00000549145.1:c.929+30G>A
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000449702
  ensembl transcript: ENST00000550270
  gene symbol: MYBPC1
  hgvsc: ENST00000550270.1:c.890+30G>A
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000440034
  ensembl transcript: ENST00000545503
  gene symbol: MYBPC1
  hgvsc: ENST00000545503.2:c.890+30G>A
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000376665
  ensembl transcript: ENST00000392934
  gene symbol: MYBPC1
  hgvsc: ENST00000392934.3:c.851+30G>A
  variant of: http://identifiers.org/hgnc/7549
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 978
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17352
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4829
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 985
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 969
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1095
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 795
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: Other
population: South Asian
reference allele: G
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: MQ

12-102038606-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102038606
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 102038606
    reference: chr 12
allele count: 1268
allele frequency: 1.156617714129344e-2
allele num: 109630
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000376665
  ensembl transcript: ENST00000392934
  gene symbol: MYBPC1
  hgvsc: ENST00000392934.3:c.851+32T>C
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000353822
  ensembl transcript: ENST00000360610
  gene symbol: MYBPC1
  hgvsc: ENST00000360610.2:c.890+32T>C
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000354849
  ensembl transcript: ENST00000361466
  gene symbol: MYBPC1
  hgvsc: ENST00000361466.2:c.965+32T>C
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447116
  ensembl transcript: ENST00000551300
  gene symbol: MYBPC1
  hgvsc: ENST00000551300.1:c.593+32T>C
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000449702
  ensembl transcript: ENST00000550270
  gene symbol: MYBPC1
  hgvsc: ENST00000550270.1:c.890+32T>C
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447660
  ensembl transcript: ENST00000549145
  gene symbol: MYBPC1
  hgvsc: ENST00000549145.1:c.929+32T>C
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000354845
  ensembl transcript: ENST00000361685
  gene symbol: MYBPC1
  hgvsc: ENST00000361685.2:c.965+32T>C
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000442847
  ensembl transcript: ENST00000541119
  gene symbol: MYBPC1
  hgvsc: ENST00000541119.1:c.854+32T>C
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447900
  ensembl transcript: ENST00000553190
  gene symbol: MYBPC1
  hgvsc: ENST00000553190.1:c.890+32T>C
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000448175
  ensembl transcript: ENST00000547405
  gene symbol: MYBPC1
  hgvsc: ENST00000547405.1:c.812+32T>C
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000440034
  ensembl transcript: ENST00000545503
  gene symbol: MYBPC1
  hgvsc: ENST00000545503.2:c.890+32T>C
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl transcript: ENST00000550501
  gene symbol: MYBPC1
  hgvsc: ENST00000550501.1:n.574+29884T>C
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000400908
  ensembl transcript: ENST00000452455
  gene symbol: MYBPC1
  hgvsc: ENST00000452455.2:c.890+32T>C
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447362
  ensembl transcript: ENST00000547509
  gene symbol: MYBPC1
  hgvsc: ENST00000547509.1:c.848+32T>C
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000388989
  ensembl transcript: ENST00000441232
  gene symbol: MYBPC1
  hgvsc: ENST00000441232.1:c.890+32T>C
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000446128
  ensembl transcript: ENST00000536007
  gene symbol: MYBPC1
  hgvsc: ENST00000536007.1:c.833+32T>C
  variant of: http://identifiers.org/hgnc/7549
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 9.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 10093
  bin: 2.25e1
  variant carriers: 233
genotype depth: GenotypeDepth
  all individuals: 918
  bin: 4.75e1
  variant carriers: 35
genotype depth: GenotypeDepth
  all individuals: 970
  bin: 4.25e1
  variant carriers: 39
genotype depth: GenotypeDepth
  all individuals: 6573
  bin: 2.75e1
  variant carriers: 167
genotype depth: GenotypeDepth
  all individuals: 823
  bin: 9.75e1
  variant carriers: 116
genotype depth: GenotypeDepth
  all individuals: 1954
  bin: 3.25e1
  variant carriers: 104
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 8.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5010
  bin: 7.5e0
  variant carriers: 21
genotype quality: GenotypeQuality
num of homozygotes: 59
population: Other
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
reference allele: T
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: MQ

12-102038607-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102038607
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 102038607
    reference: chr 12
allele count: 1
allele frequency: 9.16590284142988e-6
allele num: 109100
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447660
  ensembl transcript: ENST00000549145
  gene symbol: MYBPC1
  hgvsc: ENST00000549145.1:c.929+33C>G
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000448175
  ensembl transcript: ENST00000547405
  gene symbol: MYBPC1
  hgvsc: ENST00000547405.1:c.812+33C>G
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000440034
  ensembl transcript: ENST00000545503
  gene symbol: MYBPC1
  hgvsc: ENST00000545503.2:c.890+33C>G
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000354849
  ensembl transcript: ENST00000361466
  gene symbol: MYBPC1
  hgvsc: ENST00000361466.2:c.965+33C>G
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000400908
  ensembl transcript: ENST00000452455
  gene symbol: MYBPC1
  hgvsc: ENST00000452455.2:c.890+33C>G
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447900
  ensembl transcript: ENST00000553190
  gene symbol: MYBPC1
  hgvsc: ENST00000553190.1:c.890+33C>G
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000354845
  ensembl transcript: ENST00000361685
  gene symbol: MYBPC1
  hgvsc: ENST00000361685.2:c.965+33C>G
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000353822
  ensembl transcript: ENST00000360610
  gene symbol: MYBPC1
  hgvsc: ENST00000360610.2:c.890+33C>G
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000442847
  ensembl transcript: ENST00000541119
  gene symbol: MYBPC1
  hgvsc: ENST00000541119.1:c.854+33C>G
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000446128
  ensembl transcript: ENST00000536007
  gene symbol: MYBPC1
  hgvsc: ENST00000536007.1:c.833+33C>G
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl transcript: ENST00000550501
  gene symbol: MYBPC1
  hgvsc: ENST00000550501.1:n.574+29885C>G
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000449702
  ensembl transcript: ENST00000550270
  gene symbol: MYBPC1
  hgvsc: ENST00000550270.1:c.890+33C>G
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000376665
  ensembl transcript: ENST00000392934
  gene symbol: MYBPC1
  hgvsc: ENST00000392934.3:c.851+33C>G
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000388989
  ensembl transcript: ENST00000441232
  gene symbol: MYBPC1
  hgvsc: ENST00000441232.1:c.890+33C>G
  variant of: http://identifiers.org/hgnc/7549
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196091
  ensembl protein: ENSP00000447362
  ensembl transcript: ENST00000547509
  gene symbol: MYBPC1
  hgvsc: ENST00000547509.1:c.848+33C>G
  variant of: http://identifiers.org/hgnc/7549
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
num of homozygotes: 0
reference allele: C

GenotypeDepth
all individuals: 1755
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 353
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 691
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 266
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3164
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 791
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 354
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 262
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1275
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 17350
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 19421
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 940
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2562
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 33
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 2055
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 240
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 614
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6432
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1723
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1013
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 98
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 177
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 130
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 85
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6413
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31286
bin: 6.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 213
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 260
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 845
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12254
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1325
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2168
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2454
bin: 7.75e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.24687656171914e-5
allele num: 16008
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10260
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65884
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6596
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11492
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8608
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 7.16e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.93e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.913e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

QD
type: SiteQuality
SIO_000300: 1.162e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 4.843e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.06e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.645e0

DP
type: SiteQuality
SIO_000300: 2.033871e6

GenotypeDepth
all individuals: 3160
bin: 3.75e1
variant carriers: 1

GenotypeDepth
all individuals: 2056
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1754
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 262
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 552
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 18749
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 941
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 38
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 240
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 17552
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 614
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 266
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1275
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6421
bin: 3.25e1
variant carriers: 1

GenotypeQuality
all individuals: 6372
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2425
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1708
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30882
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 178
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 49
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2120
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 38
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 220
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1231
bin: 2.25e1
variant carriers: 1

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

GenotypeQuality
all individuals: 314
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12250
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 843
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 101
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 235
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 97
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1321
bin: 9.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15970
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11474
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 880
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8592
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6584
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.03573054855651e-5
allele num: 65882
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.021e0

FS
type: SiteQuality
SIO_000300: 9.95e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 2.03116e6

VQSLOD
type: SiteQuality
SIO_000300: -2.128e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 1.8e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.72e0

QD
type: SiteQuality
SIO_000300: 4.75e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.89e-1

GenotypeDepth
all individuals: 6420
bin: 3.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 240
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 18715
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2055
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1671
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 614
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1754
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 38
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 941
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2558
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1275
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 17545
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 354
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 248
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 112
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 178
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 35
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2426
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 107
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1708
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2119
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 217
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1253
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30834
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 301
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6370
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1322
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 318
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12249
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 843
bin: 8.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 880
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6584
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11468
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65882
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.2625250501002e-5
allele num: 15968
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8594
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.159e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.09e0

FS
type: SiteQuality
SIO_000300: 5.084e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

MQ
type: SiteQuality
SIO_000300: 5.986e1

DP
type: SiteQuality
SIO_000300: 2.030686e6

ClippingRankSum
type: SiteQuality
SIO_000300: -5.46e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.7e-1

MQRankSum
type: SiteQuality
SIO_000300: -9.320000000000001e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.297e0

GenotypeDepth
all individuals: 353
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 594
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 18648
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 976
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1671
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2558
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3159
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2056
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 267
bin: 8.25e1
variant carriers: 1

GenotypeDepth
all individuals: 614
bin: 6.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 240
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 262
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1754
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1285
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6361
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 172
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2118
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 94
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1321
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 110
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 313
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 329
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 844
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 255
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1705
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2426
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 12247
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 215
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30807
bin: 6.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15966
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11468
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10242
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8592
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 880
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.036652394400413e-5
allele num: 65862
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.847e0

MQRankSum
type: SiteQuality
SIO_000300: 1.01e0

VQSLOD
type: SiteQuality
SIO_000300: 8.61e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

DP
type: SiteQuality
SIO_000300: 2.030021e6

MQ
type: SiteQuality
SIO_000300: 5.972e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.33e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.506e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.51e-1

QD
type: SiteQuality
SIO_000300: 1.12e1

GenotypeDepth
all individuals: 894
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 2560
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6424
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 744
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 18306
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2056
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 17523
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3162
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1753
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1275
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 266
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 263
bin: 8.75e1
variant carriers: 1

GenotypeDepth
all individuals: 942
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 353
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 843
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 318
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 144
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1321
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12247
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 331
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2416
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1392
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 398
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 410
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 367
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30037
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1702
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2104
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6313
bin: 6.75e1
variant carriers: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 880
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11460
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6570
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65844
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15926
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10228
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.165501165501166e-4
allele num: 8580
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.027279e6

BaseQRankSum
type: SiteQuality
SIO_000300: -3.699e0

VQSLOD
type: SiteQuality
SIO_000300: 8.52e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.21e0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.54e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.17e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

MQ
type: SiteQuality
SIO_000300: 5.974e1

QD
type: SiteQuality
SIO_000300: 1.081e1

GenotypeDepth
all individuals: 976
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1383
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1275
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2559
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 262
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 17469
bin: 2.75e1
variant carriers: 1

GenotypeDepth
all individuals: 891
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3162
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1753
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 266
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 17918
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2057
bin: 4.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 613
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 515
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1696
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 138
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 424
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 842
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 186
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 409
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1600
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 294
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12248
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 29946
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 244
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2399
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1317
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6255
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2094
bin: 7.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 880
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10218
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6548
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.519341213649761e-5
allele num: 65818
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15900
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11432
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 4.19e0

FS
type: SiteQuality
SIO_000300: 5.28e0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.92e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.03e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.8e0

MQRankSum
type: SiteQuality
SIO_000300: 1.78e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.8e-1

DP
type: SiteQuality
SIO_000300: 2.022988e6

GenotypeDepth
all individuals: 263
bin: 8.75e1
variant carriers: 1

GenotypeDepth
all individuals: 1622
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1275
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3156
bin: 3.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 240
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 266
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 38
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 2055
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2558
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1247
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1753
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 353
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1671
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12244
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 42
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 174
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 760
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 850
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2357
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 836
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 646
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1683
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 431
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 408
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 290
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2192
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28336
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6012
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2053
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1316
bin: 9.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6502
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15806
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10156
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.525273786644703e-5
allele num: 65562
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11344
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8544
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 870
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.16e0

DP
type: SiteQuality
SIO_000300: 2.006866e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.139e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.502e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

FS
type: SiteQuality
SIO_000300: 1.898e0

VQSLOD
type: SiteQuality
SIO_000300: 8.22e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.0e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.551e1

GenotypeDepth
all individuals: 6309
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 240
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 613
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 15788
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1444
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 43
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 266
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1276
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1753
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2055
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2297
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 262
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2515
bin: 1.25e1
variant carriers: 1

GenotypeDepth
all individuals: 353
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 357
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 776
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2595
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1315
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 634
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2338
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1038
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 834
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1078
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26769
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2033
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12247
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 5820
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1680
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 616
bin: 4.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8532
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 868
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6478
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10108
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.588559192413582e-5
allele num: 65380
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15738
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11260
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.364e0

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.51e-1

QD
type: SiteQuality
SIO_000300: 1.283e1

FS
type: SiteQuality
SIO_000300: 1.062e0

MQ
type: SiteQuality
SIO_000300: 5.965e1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.78e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

DP
type: SiteQuality
SIO_000300: 1.993792e6

VQSLOD
type: SiteQuality
SIO_000300: 7.87e-1

GenotypeDepth
all individuals: 3160
bin: 3.75e1
variant carriers: 1

GenotypeDepth
all individuals: 15034
bin: 2.25e1
variant carriers: 1

GenotypeDepth
all individuals: 941
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2555
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 44
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 16064
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 266
bin: 8.25e1
variant carriers: 1

GenotypeDepth
all individuals: 239
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1274
bin: 5.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 1757
bin: 9.75e1
variant carriers: 10

GenotypeDepth
all individuals: 613
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 262
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2056
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1328
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 1315
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2315
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 961
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 933
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3046
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1312
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 87
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 579
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 833
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 12245
bin: 9.75e1
variant carriers: 17

GenotypeQuality
all individuals: 463
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5692
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24931
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1672
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2009
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 859
bin: 4.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8510
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65136
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10086
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11160
num of homozygotes: 0

South Asian
type: Population
allele count: 19
allele frequency: 1.215611004478567e-3
allele num: 15630
num of homozygotes: 1

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6450
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 862
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.979615e6

VQSLOD
type: SiteQuality
SIO_000300: 1.04e0

MQRankSum
type: SiteQuality
SIO_000300: -1.67e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.15e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.39e-1

FS
type: SiteQuality
SIO_000300: 4.516e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.669999999999999e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.37e-2

MQ
type: SiteQuality
SIO_000300: 5.976e1

QD
type: SiteQuality
SIO_000300: 1.297e1

GenotypeDepth
all individuals: 46
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 2551
bin: 4.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 352
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2055
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 15534
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3670
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 14613
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3239
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1867
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1274
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 615
bin: 6.75e1
variant carriers: 2

GenotypeDepth
all individuals: 941
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 262
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1504
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1309
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 828
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 24426
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 71
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1001
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 957
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1959
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1670
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1469
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 677
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 707
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3444
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5614
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2302
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 400
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12238
bin: 9.75e1
variant carriers: 4

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10048
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 864
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15576
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6406
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.156119182467373e-5
allele num: 64976
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11090
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.945e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.3e-1

FS
type: SiteQuality
SIO_000300: 1.0578e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.49e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.86e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.4e-3

DP
type: SiteQuality
SIO_000300: 1.967066e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.359e0

QD
type: SiteQuality
SIO_000300: 2.097e1

VQSLOD
type: SiteQuality
SIO_000300: -1.248e0

GenotypeDepth
all individuals: 2032
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 53
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1668
bin: 5.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 4143
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 265
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 942
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6064
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 262
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 612
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2547
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 352
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 239
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2059
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 74
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 790
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23556
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1633
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1308
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 826
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1126
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1670
bin: 8.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 1951
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 442
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1575
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3766
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 682
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12238
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 66
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1073
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5587
bin: 6.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10004
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6384
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11032
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 858
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.542020046260601e-5
allele num: 64850
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15536
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.28e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 4.727e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.29e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.08e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.4e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -4.65e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.75e-1

QD
type: SiteQuality
SIO_000300: 1.288e1

DP
type: SiteQuality
SIO_000300: 1.957578e6

GenotypeDepth
all individuals: 5942
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4168
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 239
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4645
bin: 1.75e1
variant carriers: 1

GenotypeDepth
all individuals: 2727
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 2547
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1669
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 14180
bin: 2.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 352
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3123
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 943
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1757
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1272
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4838
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1303
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1278
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1944
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2245
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1907
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 207
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1651
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 103
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 823
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2122
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5278
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1805
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 966
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12233
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1065
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18916
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1898
bin: 7.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8360
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15380
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10722
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6272
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9898
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.562646498109198e-5
allele num: 63994
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 846
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.930848e6

QD
type: SiteQuality
SIO_000300: 1.944e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.25e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.8e-3

MQ
type: SiteQuality
SIO_000300: 5.967e1

BaseQRankSum
type: SiteQuality
SIO_000300: -8.66e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.26e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.69e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.27e-1

GenotypeDepth
all individuals: 2805
bin: 4.25e1
variant carriers: 2080

GenotypeDepth
all individuals: 333
bin: 7.75e1
variant carriers: 296

GenotypeDepth
all individuals: 6248
bin: 3.25e1
variant carriers: 3115

GenotypeDepth
all individuals: 1274
bin: 5.75e1
variant carriers: 956

GenotypeDepth
all individuals: 3383
bin: 3.75e1
variant carriers: 2464

GenotypeDepth
all individuals: 4745
bin: 1.75e1
variant carriers: 3298

GenotypeDepth
all individuals: 57
bin: 2.5e0
variant carriers: 6

GenotypeDepth
all individuals: 254
bin: 8.25e1
variant carriers: 238

GenotypeDepth
all individuals: 11909
bin: 2.25e1
variant carriers: 4200

GenotypeDepth
all individuals: 4154
bin: 1.25e1
variant carriers: 1434

GenotypeDepth
all individuals: 440
bin: 7.25e1
variant carriers: 380

GenotypeDepth
all individuals: 2828
bin: 9.75e1
variant carriers: 2818

GenotypeDepth
all individuals: 172
bin: 9.25e1
variant carriers: 169

GenotypeDepth
all individuals: 2246
bin: 4.75e1
variant carriers: 1682

GenotypeDepth
all individuals: 612
bin: 6.75e1
variant carriers: 514

GenotypeDepth
all individuals: 13678
bin: 2.75e1
variant carriers: 3753

GenotypeDepth
all individuals: 199
bin: 8.75e1
variant carriers: 192

GenotypeDepth
all individuals: 906
bin: 6.25e1
variant carriers: 697

GenotypeQuality
all individuals: 164
bin: 7.5e0
variant carriers: 54

GenotypeQuality
all individuals: 15042
bin: 6.25e1
variant carriers: 306

GenotypeQuality
all individuals: 164
bin: 1.75e1
variant carriers: 61

GenotypeQuality
all individuals: 714
bin: 4.75e1
variant carriers: 235

GenotypeQuality
all individuals: 818
bin: 5.25e1
variant carriers: 299

GenotypeQuality
all individuals: 846
bin: 3.25e1
variant carriers: 140

GenotypeQuality
all individuals: 122
bin: 1.25e1
variant carriers: 55

GenotypeQuality
all individuals: 753
bin: 2.75e1
variant carriers: 82

GenotypeQuality
all individuals: 1057
bin: 7.75e1
variant carriers: 295

GenotypeQuality
all individuals: 286
bin: 2.5e0
variant carriers: 44

GenotypeQuality
all individuals: 782
bin: 3.75e1
variant carriers: 184

GenotypeQuality
all individuals: 4224
bin: 2.25e1
variant carriers: 73

GenotypeQuality
all individuals: 357
bin: 8.75e1
variant carriers: 172

GenotypeQuality
all individuals: 3564
bin: 6.75e1
variant carriers: 302

GenotypeQuality
all individuals: 476
bin: 4.25e1
variant carriers: 152

GenotypeQuality
all individuals: 1046
bin: 7.25e1
variant carriers: 212

GenotypeQuality
all individuals: 599
bin: 9.25e1
variant carriers: 275

GenotypeQuality
all individuals: 676
bin: 8.25e1
variant carriers: 252

GenotypeQuality
all individuals: 481
bin: 5.75e1
variant carriers: 156

GenotypeQuality
all individuals: 28529
bin: 9.75e1
variant carriers: 26486

European (Non-Finnish)
type: Population
allele count: 19605
allele frequency: 3.079351616247291e-1
allele num: 63666
num of homozygotes: 2883

African
type: Population
allele count: 2970
allele frequency: 3.006681514476615e-1
allele num: 9878
num of homozygotes: 438

South Asian
type: Population
allele count: 3574
allele frequency: 2.315966822187662e-1
allele num: 15432
num of homozygotes: 443

Latino
type: Population
allele count: 2607
allele frequency: 2.464549064095292e-1
allele num: 10578
num of homozygotes: 289

European (Finnish)
type: Population
allele count: 2193
allele frequency: 3.535956143179619e-1
allele num: 6202
num of homozygotes: 369

Other
type: Population
allele count: 229
allele frequency: 2.700471698113208e-1
allele num: 848
num of homozygotes: 28

East Asian
type: Population
allele count: 3295
allele frequency: 4.014376218323586e-1
allele num: 8208
num of homozygotes: 624

BaseQRankSum
type: SiteQuality
SIO_000300: -2.068e0

DP
type: SiteQuality
SIO_000300: 2.120302e6

FS
type: SiteQuality
SIO_000300: 1.375e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.24e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.0e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.78e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.9e-2

VQSLOD
type: SiteQuality
SIO_000300: 3.88e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.709e1

GenotypeDepth
all individuals: 6078
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 51
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 19571
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6694
bin: 1.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 958
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 14
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 176
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 329
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 11
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 23
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 100
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2802
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 461
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 392
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 151
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 10349
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 341
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1111
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1584
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 814
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1559
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 145
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 91
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1644
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 792
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28253
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6742
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 775
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3416
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1512
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 532
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9368
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5746
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14802
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9772
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 794
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7590
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.647989452867502e-5
allele num: 60680
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.9e0

FS
type: SiteQuality
SIO_000300: 4.683e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.467681e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.63e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.52e0

QD
type: SiteQuality
SIO_000300: 1.733e1

MQRankSum
type: SiteQuality
SIO_000300: 2.58e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 8.7e-1

GenotypeDepth
all individuals: 12024
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 10359
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 11
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 14
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 51
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2650
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 786
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4488
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 329
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 953
bin: 4.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 99
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 23
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 453
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1122
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3382
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 82
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1125
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 285
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 130
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 431
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 495
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 435
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2095
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 647
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23864
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 645
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16684
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1945
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 308
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 771
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1131
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4676
bin: 6.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 700
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5070
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8570
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8748
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.776325138553361e-5
allele num: 56296
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14096
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6882
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -4.963e-1

QD
type: SiteQuality
SIO_000300: 1.247e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.8e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -1.688e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.2e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 1.86e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.73e-1

DP
type: SiteQuality
SIO_000300: 1.332219e6

GenotypeDepth
all individuals: 12902
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 11
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3697
bin: 3.25e1
variant carriers: 1

GenotypeDepth
all individuals: 328
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2474
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 10359
bin: 2.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 23
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 99
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 51
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 14
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 176
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 949
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 786
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 482
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 429
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 586
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 344
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3371
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4077
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 719
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 169
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1091
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20673
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2464
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 985
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2318
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 288
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 946
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20190
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 739
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 486
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 314
bin: 4.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6536
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.2811999417504e-5
allele num: 13734
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 53430
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7878
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 668
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8316
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4658
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.53e-1

FS
type: SiteQuality
SIO_000300: 1.585e0

MQRankSum
type: SiteQuality
SIO_000300: 6.14e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.6e-3

VQSLOD
type: SiteQuality
SIO_000300: -1.002e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.5e0

QD
type: SiteQuality
SIO_000300: 1.808e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.25e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.24503e6

GenotypeDepth
all individuals: 176
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 328
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2627
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 948
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 856
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 11
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 51
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 11893
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 785
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 13082
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 14044
bin: 1.25e1
variant carriers: 1

GenotypeDepth
all individuals: 99
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1129
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3524
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18349
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 547
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2479
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 574
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 326
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 916
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 228
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 948
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 22125
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 433
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1178
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3370
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 2670
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3829
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 284
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 412
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 484
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 936
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 554
bin: 5.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7614
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13602
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6424
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.831270832535152e-5
allele num: 52202
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8144
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 648
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4514
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.888e1

MQRankSum
type: SiteQuality
SIO_000300: -7.9e-2

DP
type: SiteQuality
SIO_000300: 1.209765e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.04e0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.97e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.92e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.2e-3

VQSLOD
type: SiteQuality
SIO_000300: 3.56e0

QD
type: SiteQuality
SIO_000300: 1.771e1

GenotypeDepth
all individuals: 1724
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 775
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 176
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 23
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 540
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8231
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7293
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 328
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 15456
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 2403
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 919
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3384
bin: 1.75e1
variant carriers: 1

GenotypeDepth
all individuals: 11
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 51
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 661
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 705
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 485
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25584
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1906
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3193
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 494
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12567
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1509
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2240
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 447
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 617
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1156
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1236
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 177
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2942
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 255
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 454
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3340
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 710
bin: 4.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.087072671870435e-5
allele num: 47914
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 606
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7504
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6900
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13120
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5968
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3992
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.567e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.37e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.65e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.41e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.5e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.089288e6

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -1.299e0

QD
type: SiteQuality
SIO_000300: 1.08e1

GenotypeDepth
all individuals: 775
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 540
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 23
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1737
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 17027
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3259
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 328
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8148
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 11
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1077
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 51
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 14
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 176
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1146
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1924
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 12996
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 481
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 452
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 997
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2929
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 520
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 141
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 685
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 657
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2207
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 614
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3338
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 25840
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1489
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3171
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 487
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 422
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 255
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1074
bin: 5.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6876
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7506
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13124
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.08672426025625e-5
allele num: 47922
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 608
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3964
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5942
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.4e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 6.57e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.014e0

DP
type: SiteQuality
SIO_000300: 1.08698e6

ClippingRankSum
type: SiteQuality
SIO_000300: -2.37e-1

MQRankSum
type: SiteQuality
SIO_000300: -5.49e-1

VQSLOD
type: SiteQuality
SIO_000300: -8.113e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.84e-1

FS
type: SiteQuality
SIO_000300: 2.628e0

GenotypeDepth
all individuals: 877
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 17530
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 11
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 533
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 761
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 326
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3206
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 23
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 51
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 395
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1407
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 420
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3692
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3275
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 807
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1474
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 449
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3420
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1100
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3329
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 248
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 437
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 468
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 9173
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 484
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 511
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28709
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 390
bin: 5.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3390
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5488
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.463271875914545e-4
allele num: 6834
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.963051441312311e-5
allele num: 12558
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6122
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 43450
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 544
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 4.339e0

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.2e-1

DP
type: SiteQuality
SIO_000300: 9.77278e5

VQSLOD
type: SiteQuality
SIO_000300: 1.87e0

QD
type: SiteQuality
SIO_000300: 9.109999999999999e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.1e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 6.929999999999999e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.929999999999999e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
all individuals: 175
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3387
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 2983
bin: 1.75e1
variant carriers: 1

GenotypeDepth
all individuals: 51
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 864
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 14
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 326
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 533
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 99
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9174
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3794
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 200
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 833
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 314
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3338
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29541
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 720
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3328
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 253
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3701
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 247
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 426
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1425
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 399
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 489
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 292
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 348
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1360
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 448
bin: 9.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3352
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 43176
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6790
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12548
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 556
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.647989452867502e-4
allele num: 6068
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5502
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.4e0

VQSLOD
type: SiteQuality
SIO_000300: -7.43e-1

QD
type: SiteQuality
SIO_000300: 9.69e0

DP
type: SiteQuality
SIO_000300: 9.62343e5

MQ
type: SiteQuality
SIO_000300: 5.896e1

MQRankSum
type: SiteQuality
SIO_000300: -1.44e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.261e0

FS
type: SiteQuality
SIO_000300: 5.315e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.800000000000001e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -1.973e0

GenotypeDepth
all individuals: 51
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 24
bin: 8.25e1
variant carriers: 1

GenotypeDepth
all individuals: 4717
bin: 2.25e1
variant carriers: 1

GenotypeDepth
all individuals: 4849
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 10
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 326
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 99
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 760
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 533
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 14
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1366
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 309
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 426
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 800
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3967
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8141
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3542
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 247
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1055
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29500
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 448
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 361
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 389
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 187
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4008
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3328
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 476
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 316
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 315
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1436
bin: 3.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 552
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5984
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3296
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5458
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 2.967359050445104e-4
allele num: 6740
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 42832
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12490
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.53e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.5e-3

VQSLOD
type: SiteQuality
SIO_000300: 4.11e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.72e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.33e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.4e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 9.4619e5

QD
type: SiteQuality
SIO_000300: 1.169e1

GenotypeDepth
all individuals: 3740
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 850
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 100
bin: 7.25e1
variant carriers: 2

GenotypeDepth
all individuals: 760
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 918
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 23
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1461
bin: 3.25e1
variant carriers: 6

GenotypeDepth
all individuals: 325
bin: 6.25e1
variant carriers: 1

GenotypeDepth
all individuals: 176
bin: 6.75e1
variant carriers: 1

GenotypeDepth
all individuals: 534
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 781
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29742
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 428
bin: 8.25e1
variant carriers: 4

GenotypeQuality
all individuals: 908
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4008
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3499
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 146
bin: 5.75e1
variant carriers: 3

GenotypeQuality
all individuals: 1370
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 474
bin: 7.75e1
variant carriers: 2

GenotypeQuality
all individuals: 339
bin: 4.25e1
variant carriers: 1

GenotypeQuality
all individuals: 187
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1362
bin: 6.75e1
variant carriers: 3

GenotypeQuality
all individuals: 248
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3942
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8388
bin: 6.25e1
variant carriers: 2

GenotypeQuality
all individuals: 378
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 279
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3430
bin: 9.75e1
variant carriers: 107

GenotypeQuality
all individuals: 258
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 450
bin: 9.25e1
variant carriers: 3

European (Non-Finnish)
type: Population
allele count: 90
allele frequency: 2.102607232968881e-3
allele num: 42804
num of homozygotes: 2

European (Finnish)
type: Population
allele count: 1
allele frequency: 3.059975520195838e-4
allele num: 3268
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.818181818181818e-3
allele num: 550
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5462
num of homozygotes: 0

Latino
type: Population
allele count: 13
allele frequency: 2.177554438860971e-3
allele num: 5970
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 2.969121140142518e-4
allele num: 6736
num of homozygotes: 0

South Asian
type: Population
allele count: 7
allele frequency: 5.599104143337066e-4
allele num: 12502
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.26e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 1.488e0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.33e-1

QD
type: SiteQuality
SIO_000300: 1.347e1

MQRankSum
type: SiteQuality
SIO_000300: 1.74e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.25e0

DP
type: SiteQuality
SIO_000300: 9.45134e5

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.11e-2

GenotypeDepth
all individuals: 861
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 850
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 14
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 10
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4736
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 49
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1461
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 325
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 760
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 474
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 187
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4008
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1370
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 450
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 339
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 908
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 781
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 428
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 279
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3499
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 378
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29742
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3942
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 258
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 146
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3430
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 248
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8388
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1362
bin: 6.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3268
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5462
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.484560570071259e-4
allele num: 6736
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12502
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5970
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 550
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 42804
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.74e-1

DP
type: SiteQuality
SIO_000300: 9.45134e5

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.11e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -5.33e-1

FS
type: SiteQuality
SIO_000300: 1.488e0

VQSLOD
type: SiteQuality
SIO_000300: 4.25e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.347e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.26e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

GenotypeDepth
all individuals: 6
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 14
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3276
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 324
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 856
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4294
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 99
bin: 7.25e1
variant carriers: 1

GenotypeDepth
all individuals: 918
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 23
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 48
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 248
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 361
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29280
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4522
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 447
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1202
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1330
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 246
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 342
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 971
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1533
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4119
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 389
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 389
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 458
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6933
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3768
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 418
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 310
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3325
bin: 9.75e1
variant carriers: 2

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5370
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3182
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.510574018126888e-4
allele num: 6620
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 42100
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5796
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 8.064516129032258e-5
allele num: 12400
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 532
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.205e1

MQRankSum
type: SiteQuality
SIO_000300: -9.350000000000001e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.016e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.06e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.03e0

FS
type: SiteQuality
SIO_000300: 2.844e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.01e-1

DP
type: SiteQuality
SIO_000300: 9.24658e5

VQSLOD
type: SiteQuality
SIO_000300: 5.69e-1

GenotypeDepth
all individuals: 23
bin: 8.25e1
variant carriers: 1

GenotypeDepth
all individuals: 916
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3854
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 533
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 48
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 14
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 98
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 852
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 10
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 447
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 272
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6893
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 364
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1184
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 342
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 311
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4110
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29580
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 243
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1151
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3322
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1032
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 443
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4758
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3733
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 281
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 225
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 411
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1480
bin: 3.75e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 8.116883116883117e-5
allele num: 12320
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6544
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3146
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5700
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5324
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 41618
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 526
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.87e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.11e-2

FS
type: SiteQuality
SIO_000300: 2.323e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 2.433e1

DP
type: SiteQuality
SIO_000300: 9.16659e5

BaseQRankSum
type: SiteQuality
SIO_000300: -2.451e0

VQSLOD
type: SiteQuality
SIO_000300: -2.334e0

MQRankSum
type: SiteQuality
SIO_000300: 4.23e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.500000000000001e-2

GenotypeDepth
all individuals: 4043
bin: 2.75e1
variant carriers: 4

GenotypeDepth
all individuals: 915
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 174
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 18145
bin: 7.5e0
variant carriers: 7

GenotypeDepth
all individuals: 4572
bin: 2.5e0
variant carriers: 1

GenotypeDepth
all individuals: 21010
bin: 1.25e1
variant carriers: 16

GenotypeDepth
all individuals: 3249
bin: 1.75e1
variant carriers: 24

GenotypeDepth
all individuals: 3620
bin: 2.25e1
variant carriers: 12

GenotypeDepth
all individuals: 6
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 853
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1039
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 412
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 245
bin: 8.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1097
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 225
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6702
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 3378
bin: 9.75e1
variant carriers: 56

GenotypeQuality
all individuals: 225
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4885
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 132
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 339
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29731
bin: 2.25e1
variant carriers: 2

GenotypeQuality
all individuals: 1150
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1512
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3811
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4198
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 448
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 441
bin: 7.75e1
variant carriers: 2

GenotypeQuality
all individuals: 256
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 350
bin: 4.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12314
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 520
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 3.178639542275906e-4
allele num: 3146
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5344
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5680
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6538
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 57
allele frequency: 1.370258185489687e-3
allele num: 41598
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 9.09941e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.44e-1

FS
type: SiteQuality
SIO_000300: 4.532e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.28e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.04e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.99e0

MQRankSum
type: SiteQuality
SIO_000300: 1.43e-1

QD
type: SiteQuality
SIO_000300: 1.265e1

GenotypeDepth
all individuals: 48
bin: 7.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 5140
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 10
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 324
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 915
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 22
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 98
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 847
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 431
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 319
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 447
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 270
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1330
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1567
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5505
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 410
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4338
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4057
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 282
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 385
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1023
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 282
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3324
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 28869
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5501
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1661
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 241
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 308
bin: 5.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5248
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5536
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 8.199409642505739e-5
allele num: 12196
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 510
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6372
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.458814851241701e-5
allele num: 40670
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3008
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 9.051e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.949e0

MQRankSum
type: SiteQuality
SIO_000300: 2.17e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.17e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -2.123e-1

QD
type: SiteQuality
SIO_000300: 1.517e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.22e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -8.149999999999999e-1

DP
type: SiteQuality
SIO_000300: 8.91391e5

GenotypeDepth
all individuals: 21234
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 324
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 533
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 914
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 98
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 851
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 761
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 14
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1151
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 389
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 241
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 300
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 916
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4344
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6555
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1864
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 196
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1758
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 412
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4537
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27752
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 447
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4272
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 407
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 434
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 323
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 229
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1805
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3323
bin: 9.75e1
variant carriers: 1

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12026
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2806
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.549849558876026e-5
allele num: 39218
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5084
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6202
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5206
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 496
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.1e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.06e-1

QD
type: SiteQuality
SIO_000300: 1.544e1

DP
type: SiteQuality
SIO_000300: 8.61738e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.42e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -4.54e-1

MQRankSum
type: SiteQuality
SIO_000300: -4.54e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.28e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.766e1

GenotypeDepth
all individuals: 19016
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 533
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 829
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1871
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 14
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 48
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 22
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 324
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 911
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7617
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4528
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 164
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 273
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1924
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3322
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 26658
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 485
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 315
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 399
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2043
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3406
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 238
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4506
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2369
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 459
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 105
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 447
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 788
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 399
bin: 7.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11792
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 466
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4864
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 37374
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2578
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 2.113271344040575e-4
allele num: 4732
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5948
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.13e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 8.30961e5

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.44e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.77e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.09e-1

QD
type: SiteQuality
SIO_000300: 1.323e1

VQSLOD
type: SiteQuality
SIO_000300: 5.01e0

MQRankSum
type: SiteQuality
SIO_000300: 1.01e-1

GenotypeDepth
all individuals: 533
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 20110
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 174
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 969
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1673
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 22
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 761
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 850
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 48
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4568
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8116
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2009
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 172
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2760
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4518
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2930
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 397
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 583
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 174
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 397
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25421
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2499
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 447
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 496
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 338
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 746
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3322
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 238
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 269
bin: 7.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2440
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4542
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5836
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.757555702625193e-5
allele num: 36264
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11680
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4754
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 456
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.074e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.47e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.74e-2

VQSLOD
type: SiteQuality
SIO_000300: -7.65e-2

MQRankSum
type: SiteQuality
SIO_000300: 5.29e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.435e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 8.19545e5

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.059e0

GenotypeDepth
all individuals: 18333
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 865
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1149
bin: 2.25e1
variant carriers: 1

GenotypeDepth
all individuals: 810
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 850
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 98
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 174
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 22
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 48
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 910
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 139
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4007
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4679
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3322
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 477
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 743
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3189
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 596
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 371
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1990
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22778
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 392
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9420
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 236
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 446
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2232
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4364
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 634
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 241
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 5.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11254
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4466
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5522
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 404
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3976
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.984361943416497e-5
allele num: 33508
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2116
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.98e-1

DP
type: SiteQuality
SIO_000300: 7.83965e5

MQRankSum
type: SiteQuality
SIO_000300: 1.12e0

VQSLOD
type: SiteQuality
SIO_000300: -7.953e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.499e0

MQ
type: SiteQuality
SIO_000300: 5.635e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.96e-2

QD
type: SiteQuality
SIO_000300: 1.69e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.6e-2

GenotypeDepth
all individuals: 14
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 14856
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 10
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 98
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1492
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 24378
bin: 7.5e0
variant carriers: 1

GenotypeDepth
all individuals: 6
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 22
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 48
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2390
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 362
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 445
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 880
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 235
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8104
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4029
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9678
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 823
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4659
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 387
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1244
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 447
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 460
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5932
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15622
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 822
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3319
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 225
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 5.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2930
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1620
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 362
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 28464
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3926
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4848
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10618
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.61e-1

QD
type: SiteQuality
SIO_000300: 1.356e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.29e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.22e0

DP
type: SiteQuality
SIO_000300: 7.4954e5

MQRankSum
type: SiteQuality
SIO_000300: -1.652e0

VQSLOD
type: SiteQuality
SIO_000300: -5.799e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.26e-2

GenotypeDepth
all individuals: 4763
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 174
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1485
bin: 2.25e1
variant carriers: 1

GenotypeDepth
all individuals: 14
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 531
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 324
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 900
bin: 4.25e1
variant carriers: 1

GenotypeDepth
all individuals: 10
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 761
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 448
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3321
bin: 9.75e1
variant carriers: 6

GenotypeQuality
all individuals: 222
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 446
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5890
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 817
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3997
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9717
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 7811
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1414
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2379
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4646
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 236
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 386
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 360
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 891
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15822
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 849
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 438
bin: 6.75e1
variant carriers: 0

South Asian
type: Population
allele count: 6
allele frequency: 5.653976630229929e-4
allele num: 10612
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 360
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2944
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4844
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1618
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3902
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 28372
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.33e-2

VQSLOD
type: SiteQuality
SIO_000300: 6.840000000000001e-1

MQRankSum
type: SiteQuality
SIO_000300: -4.0e-1

FS
type: SiteQuality
SIO_000300: 2.206e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.8e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.17e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.600000000000001e-1

QD
type: SiteQuality
SIO_000300: 1.373e1

DP
type: SiteQuality
SIO_000300: 7.49488e5

GenotypeDepth
all individuals: 174
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 98
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 10
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 790
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4712
bin: 1.75e1
variant carriers: 1

GenotypeDepth
all individuals: 22
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 24549
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 48
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1516
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 846
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4702
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 177
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 447
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14132
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 830
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1511
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 904
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 542
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3996
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 392
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2403
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 359
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5900
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 636
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9369
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 236
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3319
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 221
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 430
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9630
bin: 1.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1594
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2774
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 358
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 27708
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4750
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 5.238344683080147e-4
allele num: 3818
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10536
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 7.48354e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 8.287000000000001e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.32e-2

VQSLOD
type: SiteQuality
SIO_000300: -3.753e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.1e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.66e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.26e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.5e-2

QD
type: SiteQuality
SIO_000300: 1.554e1

GenotypeDepth
all individuals: 985
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 13240
bin: 2.25e1
variant carriers: 1

GenotypeDepth
all individuals: 1135
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 263
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 914
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 165
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 724
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 356
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 796
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 965
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1957
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 303
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1997
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 584
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8392
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 3208
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 140
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4673
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 690
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2960
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2848
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4385
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5612
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 897
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 443
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5482
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14801
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1097
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 168
bin: 1.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16044
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 882
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9724
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8192
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6506
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11182
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.72e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.3e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -7.16e-1

DP
type: SiteQuality
SIO_000300: 1.571386e6

FS
type: SiteQuality
SIO_000300: 2.096e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.74e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 8.21e-1

QD
type: SiteQuality
SIO_000300: 1.29e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.37e0

GenotypeDepth
all individuals: 8435
bin: 2.75e1
variant carriers: 1

GenotypeDepth
all individuals: 724
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 165
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 527
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 796
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 965
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 985
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 916
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 688
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 980
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 584
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5612
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5482
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 690
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2848
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 303
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 897
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1957
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 443
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4385
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2960
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 140
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1997
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 168
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14801
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3208
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1097
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4673
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8392
bin: 9.75e1
variant carriers: 2

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9724
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8192
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11182
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.232859636000998e-5
allele num: 16044
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6506
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 882
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.586697131251587e-5
allele num: 63024
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.571386e6

FS
type: SiteQuality
SIO_000300: 2.096e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.37e0

VQSLOD
type: SiteQuality
SIO_000300: 1.72e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.74e0

QD
type: SiteQuality
SIO_000300: 1.29e1

MQRankSum
type: SiteQuality
SIO_000300: 8.21e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.3e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -7.16e-1

GenotypeDepth
all individuals: 11345
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 263
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 796
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 16171
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 986
bin: 5.75e1
variant carriers: 1

GenotypeDepth
all individuals: 2586
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1132
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 724
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 527
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 165
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19902
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5411
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2601
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3153
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3065
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 845
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 256
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 153
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 440
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 311
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 290
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 148
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4352
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4896
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2891
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1956
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8381
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 631
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 995
bin: 7.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8204
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.027749229188078e-4
allele num: 9730
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63110
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11204
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 882
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16044
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6518
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.11e-1

DP
type: SiteQuality
SIO_000300: 1.587596e6

MQ
type: SiteQuality
SIO_000300: 6.234e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 3.51e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.71e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.1e-3

QD
type: SiteQuality
SIO_000300: 1.896e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.3e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.54e0

GenotypeDepth
all individuals: 17610
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 356
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 145
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 966
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 724
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 917
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 165
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 915
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 263
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8846
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 147
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5288
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1634
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 622
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8382
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 2718
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22179
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4135
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 438
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 831
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3059
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 197
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 141
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 978
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3221
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4299
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 148
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 286
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1942
bin: 2.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63040
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6514
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11196
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8194
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 2.055921052631579e-4
allele num: 9728
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 882
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16038
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 7.17e0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.100000000000001e-1

DP
type: SiteQuality
SIO_000300: 1.596913e6

MQRankSum
type: SiteQuality
SIO_000300: 6.19e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.72e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.858e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.142e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.5e-3

VQSLOD
type: SiteQuality
SIO_000300: 2.96e-1

GenotypeDepth
all individuals: 32
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 10690
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1873
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 528
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4728
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 29393
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 689
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 263
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2483
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 985
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3332
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 594
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 624
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8383
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1186
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1013
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 437
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 874
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1751
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 779
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2616
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35162
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 741
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 600
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2200
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 290
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11308
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63908
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.199628022318661e-5
allele num: 16130
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6550
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9956
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8332
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 3.75e0

MQRankSum
type: SiteQuality
SIO_000300: 1.56e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.44e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.7e-3

FS
type: SiteQuality
SIO_000300: 2.113e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.13e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.97e0

MQ
type: SiteQuality
SIO_000300: 5.847e1

DP
type: SiteQuality
SIO_000300: 1.706275e6

QD
type: SiteQuality
SIO_000300: 1.422e1

GenotypeDepth
all individuals: 2483
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 985
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 263
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 10690
bin: 2.75e1
variant carriers: 1

GenotypeDepth
all individuals: 165
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 689
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 979
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1139
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 356
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 725
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 600
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 624
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2200
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1751
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 437
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2616
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1186
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3332
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 594
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 874
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 290
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 741
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 779
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35162
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8383
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1013
bin: 7.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6550
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8332
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.564749327157789e-5
allele num: 63908
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16130
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11308
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9956
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.847e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.97e0

DP
type: SiteQuality
SIO_000300: 1.706275e6

QD
type: SiteQuality
SIO_000300: 1.422e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.7e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -1.13e-1

FS
type: SiteQuality
SIO_000300: 2.113e0

MQRankSum
type: SiteQuality
SIO_000300: 1.56e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.44e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.75e0

GenotypeDepth
all individuals: 33012
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 970
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 165
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 357
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 528
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2566
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 678
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 264
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 915
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2080
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1055
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 928
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 224
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 617
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 656
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 935
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1656
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 259
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 442
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 40460
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 296
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 315
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 640
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 227
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8385
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3584
bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.539361472861057e-5
allele num: 64962
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10096
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11424
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: 8474
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16250
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.75524e6

MQRankSum
type: SiteQuality
SIO_000300: 1.8e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

QD
type: SiteQuality
SIO_000300: 2.07e1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.39e-1

FS
type: SiteQuality
SIO_000300: 2.663e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.31e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.264e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.209e0

GenotypeDepth
all individuals: 554
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 796
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 969
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 916
bin: 4.75e1
variant carriers: 1

GenotypeDepth
all individuals: 724
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 11718
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 528
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 166
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 357
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 985
bin: 5.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 439
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 533
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3605
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 41092
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1486
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 792
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 930
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 642
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 293
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 190
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 192
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1047
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 285
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8385
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 535
bin: 3.75e1
variant carriers: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.355157795572303e-4
allele num: 8492
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 896
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10134
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11442
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65088
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16276
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 1.12e0

QD
type: SiteQuality
SIO_000300: 1.035e1

MQRankSum
type: SiteQuality
SIO_000300: -5.95e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.39e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.23e-1

DP
type: SiteQuality
SIO_000300: 1.761996e6

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.29e-1

GenotypeDepth
all individuals: 985
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 979
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 34421
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2613
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 796
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 819
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 688
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 332
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 971
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 357
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 528
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 725
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 165
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 971
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 951
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 273
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 301
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 145
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 999
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3703
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 421
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 134
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 295
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8385
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 652
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42501
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 439
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1058
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 234
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 190
bin: 5.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11480
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65610
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8556
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 902
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16350
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.515151515151515e-4
allele num: 6600
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.16e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.09e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.31e0

DP
type: SiteQuality
SIO_000300: 1.779052e6

QD
type: SiteQuality
SIO_000300: 1.17e1

MQRankSum
type: SiteQuality
SIO_000300: -7.18e-1

MQ
type: SiteQuality
SIO_000300: 5.941e1

BaseQRankSum
type: SiteQuality
SIO_000300: -9.16e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

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

GenotypeDepth
all individuals: 973
bin: 4.25e1
variant carriers: 1

GenotypeDepth
all individuals: 688
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2665
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 724
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 35032
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 419
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 182
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 165
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 264
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 796
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 528
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 914
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 979
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8385
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 92
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 999
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 93
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 530
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 149
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3832
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 155
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 653
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 183
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1076
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43681
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 442
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 291
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10320
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8606
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16416
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11522
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.511532996765319e-5
allele num: 66158
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 7.892e0

MQRankSum
type: SiteQuality
SIO_000300: 1.25e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.24e0

DP
type: SiteQuality
SIO_000300: 1.793811e6

QD
type: SiteQuality
SIO_000300: 1.09e1

VQSLOD
type: SiteQuality
SIO_000300: -5.968e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.65e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.63e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
all individuals: 1146
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 165
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 35029
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 917
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 974
bin: 4.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 2695
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 361
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 528
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 264
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 915
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 12706
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 725
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 978
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1002
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 291
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 444
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 439
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 3850
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1083
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 63
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 91
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 88
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 76
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8384
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 110
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 131
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 658
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43850
bin: 6.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11530
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16430
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.678668215253581e-5
allele num: 10332
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66252
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 8.58e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.25e0

VQSLOD
type: SiteQuality
SIO_000300: 7.58e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.635e0

MQ
type: SiteQuality
SIO_000300: 5.982e1

DP
type: SiteQuality
SIO_000300: 1.797371e6

FS
type: SiteQuality
SIO_000300: 2.7e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -3.79e-1

QD
type: SiteQuality
SIO_000300: 1.065e1

GenotypeDepth
all individuals: 12764
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1146
bin: 3.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 688
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2691
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 247
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 264
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 165
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 357
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 978
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 724
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 972
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 528
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 918
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 118
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 44029
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 438
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 367
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3879
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 93
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1091
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 656
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8384
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 99
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 292
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1013
bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10338
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16448
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11542
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.507749834147518e-5
allele num: 66324
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -3.182e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.44e0

MQRankSum
type: SiteQuality
SIO_000300: 1.92e0

QD
type: SiteQuality
SIO_000300: 1.168e1

FS
type: SiteQuality
SIO_000300: 1.9139e1

MQ
type: SiteQuality
SIO_000300: 5.95e1

DP
type: SiteQuality
SIO_000300: 1.799029e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.92e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.37e0

GenotypeDepth
all individuals: 12819
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 978
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1146
bin: 3.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 211
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 725
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 267
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 528
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 688
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 915
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 264
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 165
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 357
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2702
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 85
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 291
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3884
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 44148
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 325
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1094
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 82
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 4.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 1013
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8383
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 109
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 658
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 439
bin: 9.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16460
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66382
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8628
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11542
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.663703131039814e-5
allele num: 10348
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.800414e6

MQRankSum
type: SiteQuality
SIO_000300: -8.33e-1

FS
type: SiteQuality
SIO_000300: 1.636e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.4e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 5.51e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

QD
type: SiteQuality
SIO_000300: 1.436e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.87e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.75e-1

GenotypeDepth
all individuals: 12994
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 985
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 357
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2747
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 528
bin: 7.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 915
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 796
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 76
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1148
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 725
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 688
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 264
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 35169
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8383
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 46
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3914
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 294
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 44353
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 50
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 201
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 441
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1099
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 73
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1023
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 657
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 2.75e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.067961165048543e-5
allele num: 16480
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66510
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11544
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10380
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8640
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.11e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.82e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.31e-1

MQ
type: SiteQuality
SIO_000300: 5.982e1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.29e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

DP
type: SiteQuality
SIO_000300: 1.804859e6

FS
type: SiteQuality
SIO_000300: 1.782e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.11e0

QD
type: SiteQuality
SIO_000300: 1.417e1

GenotypeDepth
all individuals: 528
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 973
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 916
bin: 6.25e1
variant carriers: 1

GenotypeDepth
all individuals: 2746
bin: 3.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 264
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 64
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 986
bin: 5.75e1
variant carriers: 1

GenotypeDepth
all individuals: 166
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 688
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 913
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 13091
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 100
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 796
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 177
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3925
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 441
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1029
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 46
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 292
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 44424
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8386
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 1106
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 659
bin: 8.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16484
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66536
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10388
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 2.596952908587258e-4
allele num: 11552
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.29e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.27e-1

MQRankSum
type: SiteQuality
SIO_000300: -5.12e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.819e0

QD
type: SiteQuality
SIO_000300: 1.174e1

MQ
type: SiteQuality
SIO_000300: 5.933e1

FS
type: SiteQuality
SIO_000300: 4.349e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

DP
type: SiteQuality
SIO_000300: 1.805791e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.011e0

GenotypeDepth
all individuals: 13401
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 75
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 108
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 34830
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1151
bin: 3.75e1
variant carriers: 1

GenotypeDepth
all individuals: 166
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2781
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 986
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 528
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 796
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 724
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 357
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 975
bin: 4.25e1
variant carriers: 1

GenotypeDepth
all individuals: 264
bin: 8.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 44434
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 658
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 291
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 438
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8385
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 28
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 148
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 71
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1107
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3949
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1033
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 4.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8638
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.213444970270598e-4
allele num: 16482
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10396
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11558
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66596
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.444e0

QD
type: SiteQuality
SIO_000300: 7.01e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.379999999999999e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.06e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -2.319e0

FS
type: SiteQuality
SIO_000300: 1.967e0

DP
type: SiteQuality
SIO_000300: 1.808995e6

MQ
type: SiteQuality
SIO_000300: 5.875e1

MQRankSum
type: SiteQuality
SIO_000300: 5.49e-1

GenotypeDepth
all individuals: 1155
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 974
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 13406
bin: 2.75e1
variant carriers: 0

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

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

GenotypeDepth
all individuals: 85
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 357
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 34797
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 915
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 264
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 688
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 166
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 987
bin: 5.75e1
variant carriers: 1

GenotypeDepth
all individuals: 979
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 44416
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 439
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 657
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 157
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 291
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3949
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8385
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1032
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1109
bin: 7.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11560
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8638
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66602
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.620935154897056e-5
allele num: 10394
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16478
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.96e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 2.38e0

MQRankSum
type: SiteQuality
SIO_000300: -2.31e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.27e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.392e1

DP
type: SiteQuality
SIO_000300: 1.809082e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -3.824e0

GenotypeDepth
all individuals: 13435
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 34757
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 166
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 795
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 264
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 975
bin: 4.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 987
bin: 5.75e1
variant carriers: 1

GenotypeDepth
all individuals: 2772
bin: 3.25e1
variant carriers: 1

GenotypeDepth
all individuals: 688
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 914
bin: 4.75e1
variant carriers: 1

GenotypeDepth
all individuals: 1152
bin: 3.75e1
variant carriers: 1

GenotypeDepth
all individuals: 725
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 357
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44360
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 32
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 43
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 439
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8387
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 1
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3947
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 291
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1111
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 658
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 165
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1036
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 79
bin: 5.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11560
num of homozygotes: 0

East Asian
type: Population
allele count: 4
allele frequency: 4.631773969430292e-4
allele num: 8636
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16474
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10394
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501411326647048e-5
allele num: 66604
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 6.929999999999999e-1

FS
type: SiteQuality
SIO_000300: 2.427e0

DP
type: SiteQuality
SIO_000300: 1.809148e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.26e0

MQ
type: SiteQuality
SIO_000300: 5.974e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.271e0

QD
type: SiteQuality
SIO_000300: 1.232e1

VQSLOD
type: SiteQuality
SIO_000300: 1.09e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -2.91e-1

GenotypeDepth
all individuals: 528
bin: 7.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 676
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 918
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 795
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 411
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 985
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 986
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 33236
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 726
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 980
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 357
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 915
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1162
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 190
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 842
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 643
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1070
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 154
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 272
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8385
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3832
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 103
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 197
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 443
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42855
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 217
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 198
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 288
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 999
bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66216
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11510
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.10798924993892e-5
allele num: 16372
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10350
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 896
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8606
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.32e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 2.44e1

MQRankSum
type: SiteQuality
SIO_000300: 1.21e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

FS
type: SiteQuality
SIO_000300: 2.076e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.37e0

VQSLOD
type: SiteQuality
SIO_000300: -2.511e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.75e0

DP
type: SiteQuality
SIO_000300: 1.800025e6

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

GenotypeDepth
all individuals: 1163
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 13590
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 840
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 510
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 166
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 688
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 536
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 987
bin: 5.75e1
variant carriers: 1

GenotypeDepth
all individuals: 2850
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 528
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 264
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 725
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 991
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 402
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 285
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1057
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 42300
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 440
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8384
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1045
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 287
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 221
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 977
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 136
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 640
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 230
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 247
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 233
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3799
bin: 6.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66082
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 896
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16332
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.325040688212044e-4
allele num: 8602
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10336
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6604
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.003e0

FS
type: SiteQuality
SIO_000300: 2.054e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.01e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.255e0

MQRankSum
type: SiteQuality
SIO_000300: -1.202e0

DP
type: SiteQuality
SIO_000300: 1.796354e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

QD
type: SiteQuality
SIO_000300: 1.367e1

VQSLOD
type: SiteQuality
SIO_000300: 1.27e0

MQ
type: SiteQuality
SIO_000300: 5.96e1

GenotypeDepth
all individuals: 264
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 725
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 986
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 528
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 916
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 13529
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1171
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 32060
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 796
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 915
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2825
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 733
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 978
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 302
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 369
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 637
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 206
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 968
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1557
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41528
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8384
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 441
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 294
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 151
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 440
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1045
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 362
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 289
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3693
bin: 6.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8576
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65740
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.730574471800244e-5
allele num: 11454
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16270
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10316
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.7e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -5.54e-1

DP
type: SiteQuality
SIO_000300: 1.78728e6

MQ
type: SiteQuality
SIO_000300: 5.913e1

FS
type: SiteQuality
SIO_000300: 2.79e0

MQRankSum
type: SiteQuality
SIO_000300: 7.02e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -8.54e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -3.7e-2

QD
type: SiteQuality
SIO_000300: 9.17e0

GenotypeDepth
all individuals: 990
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2827
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 915
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 31814
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 357
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 987
bin: 5.75e1
variant carriers: 1

GenotypeDepth
all individuals: 796
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 725
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 916
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 688
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 264
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 13436
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 528
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8384
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 7
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 954
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 412
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3679
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 168
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1051
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1747
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 495
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 288
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 312
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 366
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 635
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 326
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 188
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41222
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 440
bin: 9.25e1
variant carriers: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11446
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.524436720631727e-5
allele num: 65598
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10312
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16250
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.325e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.85e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.72e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 8.56e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.13e-1

QD
type: SiteQuality
SIO_000300: 1.108e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.3e0

DP
type: SiteQuality
SIO_000300: 1.783527e6

GenotypeDepth
all individuals: 912
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 45
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 976
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 166
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8283
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1121
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 528
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 264
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 795
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 985
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 283
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 428
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 500
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2788
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 79
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 402
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30735
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8376
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 88
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 726
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 882
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 495
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2189
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1110
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 586
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8286
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 643
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1985
bin: 2.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8140
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 9.203018590097552e-5
allele num: 10866
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10016
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 852
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15564
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6432
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62080
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.65298e6

MQ
type: SiteQuality
SIO_000300: 5.732e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.1e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.1e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 9.4e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.228e0

VQSLOD
type: SiteQuality
SIO_000300: -9.861e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.1e-2

QD
type: SiteQuality
SIO_000300: 1.537e1

GenotypeDepth
all individuals: 915
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 725
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 688
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4869
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 986
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 9029
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 795
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 166
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 529
bin: 7.75e1
variant carriers: 1

GenotypeDepth
all individuals: 357
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 153
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2252
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 460
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 164
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 422
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12224
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 243
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4583
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8377
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 275
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3646
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 105
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 435
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21865
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 786
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 606
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 556
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 599
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 567
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2388
bin: 3.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7920
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6362
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 836
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.015434606011373e-4
allele num: 9848
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 60620
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15340
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10552
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.3e-3

QD
type: SiteQuality
SIO_000300: 1.501e1

MQRankSum
type: SiteQuality
SIO_000300: 3.13e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.96e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.18e0

VQSLOD
type: SiteQuality
SIO_000300: 8.159999999999999e-1

DP
type: SiteQuality
SIO_000300: 1.547732e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.459e0

MQ
type: SiteQuality
SIO_000300: 5.905e1

FS
type: SiteQuality
SIO_000300: 1.111e0

GenotypeDepth
all individuals: 912
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4634
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 166
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 986
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 795
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2165
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 16054
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8236
bin: 2.75e1
variant carriers: 2

GenotypeDepth
all individuals: 264
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 688
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2936
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 578
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 766
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 464
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2102
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 406
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 207
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8377
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 139
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 327
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 12858
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 738
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 218
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 275
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5430
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 688
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4123
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19101
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 550
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 422
bin: 9.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15286
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9806
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 834
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6336
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 9.52018278750952e-5
allele num: 10504
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.658869977771142e-5
allele num: 60282
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7860
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -3.23e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.062e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.63e-1

FS
type: SiteQuality
SIO_000300: 7.002e0

VQSLOD
type: SiteQuality
SIO_000300: -2.369e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.11e-1

DP
type: SiteQuality
SIO_000300: 1.518588e6

QD
type: SiteQuality
SIO_000300: 2.937e1

MQ
type: SiteQuality
SIO_000300: 5.855e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.4e-3

GenotypeDepth
all individuals: 358
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7037
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 267
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 986
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7718
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 528
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 688
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 977
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 912
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 725
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 550
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4389
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2029
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5976
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17187
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 79
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 13109
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 276
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3385
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 360
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 766
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 260
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 851
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 519
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8378
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 742
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 584
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 188
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 654
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 422
bin: 9.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6352
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.273236567354214e-4
allele num: 7854
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10518
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15308
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 60270
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 834
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9816
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.110000000000001e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.55e0

QD
type: SiteQuality
SIO_000300: 1.444e1

DP
type: SiteQuality
SIO_000300: 1.501376e6

VQSLOD
type: SiteQuality
SIO_000300: 2.76e0

MQ
type: SiteQuality
SIO_000300: 5.962e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.1e-3

MQRankSum
type: SiteQuality
SIO_000300: 5.21e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.74e-1

GenotypeDepth
all individuals: 915
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 166
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7133
bin: 2.75e1
variant carriers: 1

GenotypeDepth
all individuals: 8247
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 11424
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 912
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 528
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 725
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 688
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2019
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 995
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 262
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 557
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15649
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 549
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 338
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 410
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3855
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4626
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8375
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1921
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 463
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 143
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 497
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 274
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6495
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13288
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 845
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 422
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 740
bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.671625823275718e-5
allele num: 59822
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6336
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10430
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9762
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7814
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 828
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15228
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.482873e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.695e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.7e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 1.33e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.2e-3

QD
type: SiteQuality
SIO_000300: 7.38e0

VQSLOD
type: SiteQuality
SIO_000300: 3.45e0

MQRankSum
type: SiteQuality
SIO_000300: -1.673e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.255e1

GenotypeDepth
all individuals: 1104
bin: 3.75e1
variant carriers: 49

GenotypeDepth
all individuals: 539
bin: 7.75e1
variant carriers: 19

GenotypeDepth
all individuals: 975
bin: 5.25e1
variant carriers: 23

GenotypeDepth
all individuals: 17790
bin: 1.25e1
variant carriers: 127

GenotypeDepth
all individuals: 276
bin: 8.75e1
variant carriers: 18

GenotypeDepth
all individuals: 794
bin: 6.75e1
variant carriers: 14

GenotypeDepth
all individuals: 976
bin: 5.75e1
variant carriers: 13

GenotypeDepth
all individuals: 9426
bin: 1.75e1
variant carriers: 221

GenotypeDepth
all individuals: 912
bin: 6.25e1
variant carriers: 11

GenotypeDepth
all individuals: 677
bin: 7.25e1
variant carriers: 6

GenotypeQuality
all individuals: 6900
bin: 3.25e1
variant carriers: 2

GenotypeQuality
all individuals: 415
bin: 9.25e1
variant carriers: 11

GenotypeQuality
all individuals: 4776
bin: 2.75e1
variant carriers: 3

GenotypeQuality
all individuals: 703
bin: 7.75e1
variant carriers: 13

GenotypeQuality
all individuals: 581
bin: 7.5e0
variant carriers: 1

GenotypeQuality
all individuals: 13393
bin: 2.25e1
variant carriers: 3

GenotypeQuality
all individuals: 405
bin: 5.25e1
variant carriers: 4

GenotypeQuality
all individuals: 881
bin: 4.75e1
variant carriers: 6

GenotypeQuality
all individuals: 13745
bin: 6.25e1
variant carriers: 4

GenotypeQuality
all individuals: 1103
bin: 4.25e1
variant carriers: 5

GenotypeQuality
all individuals: 322
bin: 1.25e1
variant carriers: 2

GenotypeQuality
all individuals: 4231
bin: 3.75e1
variant carriers: 4

GenotypeQuality
all individuals: 205
bin: 2.5e0
variant carriers: 2

GenotypeQuality
all individuals: 514
bin: 8.25e1
variant carriers: 6

GenotypeQuality
all individuals: 1767
bin: 6.75e1
variant carriers: 3

GenotypeQuality
all individuals: 501
bin: 7.25e1
variant carriers: 4

GenotypeQuality
all individuals: 264
bin: 8.75e1
variant carriers: 3

GenotypeQuality
all individuals: 9313
bin: 9.75e1
variant carriers: 1152

GenotypeQuality
all individuals: 317
bin: 5.75e1
variant carriers: 7

GenotypeQuality
all individuals: 367
bin: 1.75e1
variant carriers: 1

Other
type: Population
allele count: 3
allele frequency: 3.640776699029126e-3
allele num: 824
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7754
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 1.976284584980237e-4
allele num: 15180
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 51
allele frequency: 8.579214749520574e-4
allele num: 59446
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.580278128950695e-4
allele num: 6328
num of homozygotes: 0

African
type: Population
allele count: 1141
allele frequency: 1.176288659793815e-1
allele num: 9700
num of homozygotes: 59

Latino
type: Population
allele count: 69
allele frequency: 6.635891517599538e-3
allele num: 10398
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.45e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.67e-1

DP
type: SiteQuality
SIO_000300: 1.47767e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.78e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.55e-2

VQSLOD
type: SiteQuality
SIO_000300: 2.47e0

FS
type: SiteQuality
SIO_000300: 9.330000000000001e-1

QD
type: SiteQuality
SIO_000300: 1.545e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.9e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1