13-114535272-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114535272
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 114535272
    reference: chr 13
allele count: 1
allele frequency: 9.56827924066136e-6
allele num: 104512
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000400117
  ensembl transcript: ENST00000418959
  gene symbol: GAS6
  hgvsc: ENST00000418959.3:c.246A>G
  hgvsp: ENST00000418959.3:c.246A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000183087
  ensembl transcript: ENST00000480426
  gene symbol: GAS6
  hgvsc: ENST00000480426.1:n.1298A>G
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000233695
  ensembl transcript: ENST00000458001
  gene symbol: GAS6-AS1
  hgvsc: ENST00000458001.1:n.63-1193T>C
  variant of: http://identifiers.org/hgnc/39826
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000183087
  ensembl transcript: ENST00000610073
  gene symbol: GAS6
  hgvsc: ENST00000610073.1:n.963A>G
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000349962
  ensembl transcript: ENST00000357389
  gene symbol: GAS6
  hgvsc: ENST00000357389.3:c.1272A>G
  hgvsp: ENST00000357389.3:c.1272A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000348003
  ensembl transcript: ENST00000355761
  gene symbol: GAS6
  hgvsc: ENST00000355761.4:c.981A>G
  hgvsp: ENST00000355761.4:c.981A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000331831
  ensembl transcript: ENST00000327773
  gene symbol: GAS6
  hgvsc: ENST00000327773.6:c.1143A>G
  hgvsp: ENST00000327773.6:c.1143A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000416498
  ensembl transcript: ENST00000450766
  gene symbol: GAS6
  hgvsc: ENST00000450766.1:c.324A>G
  hgvsp: ENST00000450766.1:c.324A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/4168
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 947
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1090
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3966
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7921
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6872
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2253
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36724
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1392
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 255
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1421
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 134
  bin: 1.25e1
  variant carriers: 0
hgvs: c.1143A>G
num of homozygotes: 0
population: East Asian
population: Other
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Latino
population: African
reference allele: T
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP

13-114535273-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114535273
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 114535273
    reference: chr 13
allele count: 1
allele frequency: 9.523083955508151e-6
allele num: 105008
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000349962
  ensembl transcript: ENST00000357389
  gene symbol: GAS6
  hgvsc: ENST00000357389.3:c.1271C>T
  hgvsp: ENSP00000349962.3:p.Thr424Ile
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000416498
  ensembl transcript: ENST00000450766
  gene symbol: GAS6
  hgvsc: ENST00000450766.1:c.323C>T
  hgvsp: ENSP00000416498.1:p.Thr108Ile
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000183087
  ensembl transcript: ENST00000480426
  gene symbol: GAS6
  hgvsc: ENST00000480426.1:n.1297C>T
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000348003
  ensembl transcript: ENST00000355761
  gene symbol: GAS6
  hgvsc: ENST00000355761.4:c.980C>T
  hgvsp: ENSP00000348003.4:p.Thr327Ile
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000400117
  ensembl transcript: ENST00000418959
  gene symbol: GAS6
  hgvsc: ENST00000418959.3:c.245C>T
  hgvsp: ENSP00000400117.3:p.Thr82Ile
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000331831
  ensembl transcript: ENST00000327773
  gene symbol: GAS6
  hgvsc: ENST00000327773.6:c.1142C>T
  hgvsp: ENSP00000331831.6:p.Thr381Ile
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000233695
  ensembl transcript: ENST00000458001
  gene symbol: GAS6-AS1
  hgvsc: ENST00000458001.1:n.63-1192G>A
  variant of: http://identifiers.org/hgnc/39826
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000183087
  ensembl transcript: ENST00000610073
  gene symbol: GAS6
  hgvsc: ENST00000610073.1:n.962C>T
  variant of: http://identifiers.org/hgnc/4168
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6607
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2333
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8062
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3739
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 931
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37041
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1053
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 138
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 895
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 252
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1340
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Thr381Ile
num of homozygotes: 0
population: Latino
population: African
population: Other
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: ClippingRankSum

13-114535299-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114535299
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 114535299
    reference: chr 13
allele count: 5
allele frequency: 4.457440359447991e-5
allele num: 112172
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183087
  ensembl transcript: ENST00000480426
  gene symbol: GAS6
  hgvsc: ENST00000480426.1:n.1271G>A
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000331831
  ensembl transcript: ENST00000327773
  gene symbol: GAS6
  hgvsc: ENST00000327773.6:c.1116G>A
  hgvsp: ENST00000327773.6:c.1116G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000233695
  ensembl transcript: ENST00000458001
  gene symbol: GAS6-AS1
  hgvsc: ENST00000458001.1:n.63-1166C>T
  variant of: http://identifiers.org/hgnc/39826
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000400117
  ensembl transcript: ENST00000418959
  gene symbol: GAS6
  hgvsc: ENST00000418959.3:c.219G>A
  hgvsp: ENST00000418959.3:c.219G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183087
  ensembl transcript: ENST00000610073
  gene symbol: GAS6
  hgvsc: ENST00000610073.1:n.936G>A
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000348003
  ensembl transcript: ENST00000355761
  gene symbol: GAS6
  hgvsc: ENST00000355761.4:c.954G>A
  hgvsp: ENST00000355761.4:c.954G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000349962
  ensembl transcript: ENST00000357389
  gene symbol: GAS6
  hgvsc: ENST00000357389.3:c.1245G>A
  hgvsp: ENST00000357389.3:c.1245G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000416498
  ensembl transcript: ENST00000450766
  gene symbol: GAS6
  hgvsc: ENST00000450766.1:c.297G>A
  hgvsp: ENST00000450766.1:c.297G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4168
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3358
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 788
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1834
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 653
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10234
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3486
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39257
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 206
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 143
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 413
  bin: 9.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 339
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 392
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 625
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5939
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Pro372Pro
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum

13-114535300-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114535300
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 114535300
    reference: chr 13
allele count: 6
allele frequency: 5.333902282910177e-5
allele num: 112488
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000349962
  ensembl transcript: ENST00000357389
  gene symbol: GAS6
  hgvsc: ENST00000357389.3:c.1244C>T
  hgvsp: ENSP00000349962.3:p.Pro415Leu
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000348003
  ensembl transcript: ENST00000355761
  gene symbol: GAS6
  hgvsc: ENST00000355761.4:c.953C>T
  hgvsp: ENSP00000348003.4:p.Pro318Leu
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000400117
  ensembl transcript: ENST00000418959
  gene symbol: GAS6
  hgvsc: ENST00000418959.3:c.218C>T
  hgvsp: ENSP00000400117.3:p.Pro73Leu
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000331831
  ensembl transcript: ENST00000327773
  gene symbol: GAS6
  hgvsc: ENST00000327773.6:c.1115C>T
  hgvsp: ENSP00000331831.6:p.Pro372Leu
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000233695
  ensembl transcript: ENST00000458001
  gene symbol: GAS6-AS1
  hgvsc: ENST00000458001.1:n.63-1165G>A
  variant of: http://identifiers.org/hgnc/39826
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183087
  ensembl transcript: ENST00000610073
  gene symbol: GAS6
  hgvsc: ENST00000610073.1:n.935C>T
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000416498
  ensembl transcript: ENST00000450766
  gene symbol: GAS6
  hgvsc: ENST00000450766.1:c.296C>T
  hgvsp: ENSP00000416498.1:p.Pro99Leu
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183087
  ensembl transcript: ENST00000480426
  gene symbol: GAS6
  hgvsc: ENST00000480426.1:n.1270C>T
  variant of: http://identifiers.org/hgnc/4168
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1720
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3211
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 749
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39279
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3586
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 647
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10388
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 619
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 304
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2287
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 549
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 159
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Pro372Leu
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: Other
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: DP

13-114535304-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114535304
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 114535304
    reference: chr 13
allele count: 4
allele frequency: 3.536880824800608e-5
allele num: 113094
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000416498
  ensembl transcript: ENST00000450766
  gene symbol: GAS6
  hgvsc: ENST00000450766.1:c.292G>A
  hgvsp: ENSP00000416498.1:p.Gly98Ser
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000233695
  ensembl transcript: ENST00000458001
  gene symbol: GAS6-AS1
  hgvsc: ENST00000458001.1:n.63-1161C>T
  variant of: http://identifiers.org/hgnc/39826
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000400117
  ensembl transcript: ENST00000418959
  gene symbol: GAS6
  hgvsc: ENST00000418959.3:c.214G>A
  hgvsp: ENSP00000400117.3:p.Gly72Ser
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183087
  ensembl transcript: ENST00000610073
  gene symbol: GAS6
  hgvsc: ENST00000610073.1:n.931G>A
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000349962
  ensembl transcript: ENST00000357389
  gene symbol: GAS6
  hgvsc: ENST00000357389.3:c.1240G>A
  hgvsp: ENSP00000349962.3:p.Gly414Ser
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183087
  ensembl transcript: ENST00000480426
  gene symbol: GAS6
  hgvsc: ENST00000480426.1:n.1266G>A
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000348003
  ensembl transcript: ENST00000355761
  gene symbol: GAS6
  hgvsc: ENST00000355761.4:c.949G>A
  hgvsp: ENSP00000348003.4:p.Gly317Ser
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000331831
  ensembl transcript: ENST00000327773
  gene symbol: GAS6
  hgvsc: ENST00000327773.6:c.1111G>A
  hgvsp: ENSP00000331831.6:p.Gly371Ser
  variant of: http://identifiers.org/hgnc/4168
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2959
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3705
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1671
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 749
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39178
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 632
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10661
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 366
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 290
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3497
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 567
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 564
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 106
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 233
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Gly371Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: Latino
population: Other
reference allele: C
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: MQ

13-114535305-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114535305
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 114535305
    reference: chr 13
allele count: 4
allele frequency: 3.530013943555077e-5
allele num: 113314
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000331831
  ensembl transcript: ENST00000327773
  gene symbol: GAS6
  hgvsc: ENST00000327773.6:c.1110C>T
  hgvsp: ENST00000327773.6:c.1110C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000416498
  ensembl transcript: ENST00000450766
  gene symbol: GAS6
  hgvsc: ENST00000450766.1:c.291C>T
  hgvsp: ENST00000450766.1:c.291C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183087
  ensembl transcript: ENST00000610073
  gene symbol: GAS6
  hgvsc: ENST00000610073.1:n.930C>T
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000348003
  ensembl transcript: ENST00000355761
  gene symbol: GAS6
  hgvsc: ENST00000355761.4:c.948C>T
  hgvsp: ENST00000355761.4:c.948C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183087
  ensembl transcript: ENST00000480426
  gene symbol: GAS6
  hgvsc: ENST00000480426.1:n.1265C>T
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000400117
  ensembl transcript: ENST00000418959
  gene symbol: GAS6
  hgvsc: ENST00000418959.3:c.213C>T
  hgvsp: ENST00000418959.3:c.213C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000233695
  ensembl transcript: ENST00000458001
  gene symbol: GAS6-AS1
  hgvsc: ENST00000458001.1:n.63-1160G>A
  variant of: http://identifiers.org/hgnc/39826
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000349962
  ensembl transcript: ENST00000357389
  gene symbol: GAS6
  hgvsc: ENST00000357389.3:c.1239C>T
  hgvsp: ENST00000357389.3:c.1239C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4168
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3794
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2845
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1621
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 735
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 623
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10751
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 39165
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 163
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2383
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 550
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3390
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 354
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 571
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Ser370Ser
num of homozygotes: 0
population: African
population: Other
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: DP

13-114535311-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114535311
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 114535311
    reference: chr 13
allele count: 97
allele frequency: 8.502805049088359e-4
allele num: 114080
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000400117
  ensembl transcript: ENST00000418959
  gene symbol: GAS6
  hgvsc: ENST00000418959.3:c.207C>T
  hgvsp: ENST00000418959.3:c.207C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000416498
  ensembl transcript: ENST00000450766
  gene symbol: GAS6
  hgvsc: ENST00000450766.1:c.285C>T
  hgvsp: ENST00000450766.1:c.285C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183087
  ensembl transcript: ENST00000480426
  gene symbol: GAS6
  hgvsc: ENST00000480426.1:n.1259C>T
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000349962
  ensembl transcript: ENST00000357389
  gene symbol: GAS6
  hgvsc: ENST00000357389.3:c.1233C>T
  hgvsp: ENST00000357389.3:c.1233C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000348003
  ensembl transcript: ENST00000355761
  gene symbol: GAS6
  hgvsc: ENST00000355761.4:c.942C>T
  hgvsp: ENST00000355761.4:c.942C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000233695
  ensembl transcript: ENST00000458001
  gene symbol: GAS6-AS1
  hgvsc: ENST00000458001.1:n.63-1154G>A
  variant of: http://identifiers.org/hgnc/39826
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000331831
  ensembl transcript: ENST00000327773
  gene symbol: GAS6
  hgvsc: ENST00000327773.6:c.1104C>T
  hgvsp: ENST00000327773.6:c.1104C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183087
  ensembl transcript: ENST00000610073
  gene symbol: GAS6
  hgvsc: ENST00000610073.1:n.924C>T
  variant of: http://identifiers.org/hgnc/4168
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39181
  bin: 2.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 775
  bin: 1.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 2534
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 4.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 10970
  bin: 2.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1500
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3917
  bin: 3.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 3.75e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 5.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 4.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 166
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 276
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 91
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6246
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2119
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 501
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2444
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Thr368Thr
num of homozygotes: 0
population: Other
population: European (Finnish)
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum

13-114535318-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114535318
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 114535318
    reference: chr 13
allele count: 54
allele frequency: 4.718629849702901e-4
allele num: 114440
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000416498
  ensembl transcript: ENST00000450766
  gene symbol: GAS6
  hgvsc: ENST00000450766.1:c.278G>A
  hgvsp: ENSP00000416498.1:p.Arg93His
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000349962
  ensembl transcript: ENST00000357389
  gene symbol: GAS6
  hgvsc: ENST00000357389.3:c.1226G>A
  hgvsp: ENSP00000349962.3:p.Arg409His
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000348003
  ensembl transcript: ENST00000355761
  gene symbol: GAS6
  hgvsc: ENST00000355761.4:c.935G>A
  hgvsp: ENSP00000348003.4:p.Arg312His
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183087
  ensembl transcript: ENST00000480426
  gene symbol: GAS6
  hgvsc: ENST00000480426.1:n.1252G>A
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000400117
  ensembl transcript: ENST00000418959
  gene symbol: GAS6
  hgvsc: ENST00000418959.3:c.200G>A
  hgvsp: ENSP00000400117.3:p.Arg67His
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000331831
  ensembl transcript: ENST00000327773
  gene symbol: GAS6
  hgvsc: ENST00000327773.6:c.1097G>A
  hgvsp: ENSP00000331831.6:p.Arg366His
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000233695
  ensembl transcript: ENST00000458001
  gene symbol: GAS6-AS1
  hgvsc: ENST00000458001.1:n.63-1147C>T
  variant of: http://identifiers.org/hgnc/39826
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183087
  ensembl transcript: ENST00000610073
  gene symbol: GAS6
  hgvsc: ENST00000610073.1:n.917G>A
  variant of: http://identifiers.org/hgnc/4168
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4067
  bin: 3.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 1513
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 11256
  bin: 2.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 948
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 3.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 38688
  bin: 2.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2364
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 5.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 4.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 4.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 377
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2516
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 412
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 362
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 544
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 230
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Arg366His
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
population: East Asian
population: Latino
reference allele: C
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

13-114535322-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114535322
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 114535322
    reference: chr 13
allele count: 1
allele frequency: 8.701099819017123e-6
allele num: 114928
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000348003
  ensembl transcript: ENST00000355761
  gene symbol: GAS6
  hgvsc: ENST00000355761.4:c.931G>A
  hgvsp: ENSP00000348003.4:p.Gly311Ser
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000331831
  ensembl transcript: ENST00000327773
  gene symbol: GAS6
  hgvsc: ENST00000327773.6:c.1093G>A
  hgvsp: ENSP00000331831.6:p.Gly365Ser
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183087
  ensembl transcript: ENST00000610073
  gene symbol: GAS6
  hgvsc: ENST00000610073.1:n.913G>A
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000233695
  ensembl transcript: ENST00000458001
  gene symbol: GAS6-AS1
  hgvsc: ENST00000458001.1:n.63-1143C>T
  variant of: http://identifiers.org/hgnc/39826
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000349962
  ensembl transcript: ENST00000357389
  gene symbol: GAS6
  hgvsc: ENST00000357389.3:c.1222G>A
  hgvsp: ENSP00000349962.3:p.Gly408Ser
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000400117
  ensembl transcript: ENST00000418959
  gene symbol: GAS6
  hgvsc: ENST00000418959.3:c.196G>A
  hgvsp: ENSP00000400117.3:p.Gly66Ser
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000416498
  ensembl transcript: ENST00000450766
  gene symbol: GAS6
  hgvsc: ENST00000450766.1:c.274G>A
  hgvsp: ENSP00000416498.1:p.Gly92Ser
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183087
  ensembl transcript: ENST00000480426
  gene symbol: GAS6
  hgvsc: ENST00000480426.1:n.1248G>A
  variant of: http://identifiers.org/hgnc/4168
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2162
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1437
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38553
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 931
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4223
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11532
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1773
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 487
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 506
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2575
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 556
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Gly365Ser
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
population: East Asian
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD

13-114535323-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114535323
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 114535323
    reference: chr 13
allele count: 2
allele frequency: 1.737498696875977e-5
allele num: 115108
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000331831
  ensembl transcript: ENST00000327773
  gene symbol: GAS6
  hgvsc: ENST00000327773.6:c.1092C>T
  hgvsp: ENST00000327773.6:c.1092C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000233695
  ensembl transcript: ENST00000458001
  gene symbol: GAS6-AS1
  hgvsc: ENST00000458001.1:n.63-1142G>A
  variant of: http://identifiers.org/hgnc/39826
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000348003
  ensembl transcript: ENST00000355761
  gene symbol: GAS6
  hgvsc: ENST00000355761.4:c.930C>T
  hgvsp: ENST00000355761.4:c.930C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000400117
  ensembl transcript: ENST00000418959
  gene symbol: GAS6
  hgvsc: ENST00000418959.3:c.195C>T
  hgvsp: ENST00000418959.3:c.195C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000349962
  ensembl transcript: ENST00000357389
  gene symbol: GAS6
  hgvsc: ENST00000357389.3:c.1221C>T
  hgvsp: ENST00000357389.3:c.1221C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183087
  ensembl transcript: ENST00000480426
  gene symbol: GAS6
  hgvsc: ENST00000480426.1:n.1247C>T
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000416498
  ensembl transcript: ENST00000450766
  gene symbol: GAS6
  hgvsc: ENST00000450766.1:c.273C>T
  hgvsp: ENST00000450766.1:c.273C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183087
  ensembl transcript: ENST00000610073
  gene symbol: GAS6
  hgvsc: ENST00000610073.1:n.912C>T
  variant of: http://identifiers.org/hgnc/4168
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2099
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38558
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 916
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1419
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 501
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4249
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11596
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 501
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 357
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2596
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 484
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 230
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 135
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Val364Val
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
population: African
reference allele: G
site quality: QD
site quality: MQ
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum

http://identifiers.org/exac.variant/13-114535326-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114535326
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 114535326
    reference: chr 13
allele count: 1
allele frequency: 8.664910578122834e-6
allele num: 115408
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000400117
  ensembl transcript: ENST00000418959
  gene symbol: GAS6
  hgvsc: ENST00000418959.3:c.192T>G
  hgvsp: ENST00000418959.3:c.192T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183087
  ensembl transcript: ENST00000480426
  gene symbol: GAS6
  hgvsc: ENST00000480426.1:n.1244T>G
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183087
  ensembl transcript: ENST00000610073
  gene symbol: GAS6
  hgvsc: ENST00000610073.1:n.909T>G
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000348003
  ensembl transcript: ENST00000355761
  gene symbol: GAS6
  hgvsc: ENST00000355761.4:c.927T>G
  hgvsp: ENST00000355761.4:c.927T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000233695
  ensembl transcript: ENST00000458001
  gene symbol: GAS6-AS1
  hgvsc: ENST00000458001.1:n.63-1139A>C
  variant of: http://identifiers.org/hgnc/39826
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000331831
  ensembl transcript: ENST00000327773
  gene symbol: GAS6
  hgvsc: ENST00000327773.6:c.1089T>G
  hgvsp: ENST00000327773.6:c.1089T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000416498
  ensembl transcript: ENST00000450766
  gene symbol: GAS6
  hgvsc: ENST00000450766.1:c.270T>G
  hgvsp: ENST00000450766.1:c.270T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000349962
  ensembl transcript: ENST00000357389
  gene symbol: GAS6
  hgvsc: ENST00000357389.3:c.1218T>G
  hgvsp: ENST00000357389.3:c.1218T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/4168
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4265
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 940
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1387
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38566
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1977
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 606
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11716
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2609
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 154
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39676
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 460
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6535
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Gly363Gly
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: East Asian
reference allele: A
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: VQSLOD

13-114535328-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114535328
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 114535328
    reference: chr 13
allele count: 2
allele frequency: 1.731391865921014e-5
allele num: 115514
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000348003
  ensembl transcript: ENST00000355761
  gene symbol: GAS6
  hgvsc: ENST00000355761.4:c.925G>A
  hgvsp: ENSP00000348003.4:p.Gly309Ser
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183087
  ensembl transcript: ENST00000480426
  gene symbol: GAS6
  hgvsc: ENST00000480426.1:n.1242G>A
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000349962
  ensembl transcript: ENST00000357389
  gene symbol: GAS6
  hgvsc: ENST00000357389.3:c.1216G>A
  hgvsp: ENSP00000349962.3:p.Gly406Ser
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183087
  ensembl transcript: ENST00000610073
  gene symbol: GAS6
  hgvsc: ENST00000610073.1:n.907G>A
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000416498
  ensembl transcript: ENST00000450766
  gene symbol: GAS6
  hgvsc: ENST00000450766.1:c.268G>A
  hgvsp: ENSP00000416498.1:p.Gly90Ser
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000233695
  ensembl transcript: ENST00000458001
  gene symbol: GAS6-AS1
  hgvsc: ENST00000458001.1:n.63-1137C>T
  variant of: http://identifiers.org/hgnc/39826
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000331831
  ensembl transcript: ENST00000327773
  gene symbol: GAS6
  hgvsc: ENST00000327773.6:c.1087G>A
  hgvsp: ENSP00000331831.6:p.Gly363Ser
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000400117
  ensembl transcript: ENST00000418959
  gene symbol: GAS6
  hgvsc: ENST00000418959.3:c.190G>A
  hgvsp: ENSP00000400117.3:p.Gly64Ser
  variant of: http://identifiers.org/hgnc/4168
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1926
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38444
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1370
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11774
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 981
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4338
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 616
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 651
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2632
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 325
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 500
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6535
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Gly363Ser
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Finnish)
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum

13-114535329-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114535329
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 114535329
    reference: chr 13
allele count: 1
allele frequency: 8.646031471554556e-6
allele num: 115660
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183087
  ensembl transcript: ENST00000610073
  gene symbol: GAS6
  hgvsc: ENST00000610073.1:n.906C>A
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000400117
  ensembl transcript: ENST00000418959
  gene symbol: GAS6
  hgvsc: ENST00000418959.3:c.189C>A
  hgvsp: ENSP00000400117.3:p.Asn63Lys
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000331831
  ensembl transcript: ENST00000327773
  gene symbol: GAS6
  hgvsc: ENST00000327773.6:c.1086C>A
  hgvsp: ENSP00000331831.6:p.Asn362Lys
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000349962
  ensembl transcript: ENST00000357389
  gene symbol: GAS6
  hgvsc: ENST00000357389.3:c.1215C>A
  hgvsp: ENSP00000349962.3:p.Asn405Lys
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000233695
  ensembl transcript: ENST00000458001
  gene symbol: GAS6-AS1
  hgvsc: ENST00000458001.1:n.63-1136G>T
  variant of: http://identifiers.org/hgnc/39826
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000348003
  ensembl transcript: ENST00000355761
  gene symbol: GAS6
  hgvsc: ENST00000355761.4:c.924C>A
  hgvsp: ENSP00000348003.4:p.Asn308Lys
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183087
  ensembl transcript: ENST00000480426
  gene symbol: GAS6
  hgvsc: ENST00000480426.1:n.1241C>A
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000416498
  ensembl transcript: ENST00000450766
  gene symbol: GAS6
  hgvsc: ENST00000450766.1:c.267C>A
  hgvsp: ENSP00000416498.1:p.Asn89Lys
  variant of: http://identifiers.org/hgnc/4168
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1882
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1360
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 613
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38461
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4389
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 943
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11807
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6558
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 273
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 451
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 665
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 513
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2529
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Asn362Lys
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP

13-114535330-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114535330
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 114535330
    reference: chr 13
allele count: 5
allele frequency: 4.320251611453851e-5
allele num: 115734
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000331831
  ensembl transcript: ENST00000327773
  gene symbol: GAS6
  hgvsc: ENST00000327773.6:c.1085A>G
  hgvsp: ENSP00000331831.6:p.Asn362Ser
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000416498
  ensembl transcript: ENST00000450766
  gene symbol: GAS6
  hgvsc: ENST00000450766.1:c.266A>G
  hgvsp: ENSP00000416498.1:p.Asn89Ser
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000349962
  ensembl transcript: ENST00000357389
  gene symbol: GAS6
  hgvsc: ENST00000357389.3:c.1214A>G
  hgvsp: ENSP00000349962.3:p.Asn405Ser
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000233695
  ensembl transcript: ENST00000458001
  gene symbol: GAS6-AS1
  hgvsc: ENST00000458001.1:n.63-1135T>C
  variant of: http://identifiers.org/hgnc/39826
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000400117
  ensembl transcript: ENST00000418959
  gene symbol: GAS6
  hgvsc: ENST00000418959.3:c.188A>G
  hgvsp: ENSP00000400117.3:p.Asn63Ser
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183087
  ensembl transcript: ENST00000610073
  gene symbol: GAS6
  hgvsc: ENST00000610073.1:n.905A>G
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183087
  ensembl transcript: ENST00000480426
  gene symbol: GAS6
  hgvsc: ENST00000480426.1:n.1240A>G
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000348003
  ensembl transcript: ENST00000355761
  gene symbol: GAS6
  hgvsc: ENST00000355761.4:c.923A>G
  hgvsp: ENSP00000348003.4:p.Asn308Ser
  variant of: http://identifiers.org/hgnc/4168
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 945
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11837
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38485
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1339
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4373
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1855
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 161
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39685
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 250
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 495
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 246
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 510
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 658
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Asn362Ser
num of homozygotes: 0
population: Other
population: European (Finnish)
population: South Asian
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: T
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum

13-114535336-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114535336
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 114535336
    reference: chr 13
allele count: 26
allele frequency: 2.242075126763478e-4
allele num: 115964
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000416498
  ensembl transcript: ENST00000450766
  gene symbol: GAS6
  hgvsc: ENST00000450766.1:c.260G>A
  hgvsp: ENSP00000416498.1:p.Arg87His
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000233695
  ensembl transcript: ENST00000458001
  gene symbol: GAS6-AS1
  hgvsc: ENST00000458001.1:n.63-1129C>T
  variant of: http://identifiers.org/hgnc/39826
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183087
  ensembl transcript: ENST00000610073
  gene symbol: GAS6
  hgvsc: ENST00000610073.1:n.899G>A
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000331831
  ensembl transcript: ENST00000327773
  gene symbol: GAS6
  hgvsc: ENST00000327773.6:c.1079G>A
  hgvsp: ENSP00000331831.6:p.Arg360His
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000348003
  ensembl transcript: ENST00000355761
  gene symbol: GAS6
  hgvsc: ENST00000355761.4:c.917G>A
  hgvsp: ENSP00000348003.4:p.Arg306His
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000349962
  ensembl transcript: ENST00000357389
  gene symbol: GAS6
  hgvsc: ENST00000357389.3:c.1208G>A
  hgvsp: ENSP00000349962.3:p.Arg403His
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000400117
  ensembl transcript: ENST00000418959
  gene symbol: GAS6
  hgvsc: ENST00000418959.3:c.182G>A
  hgvsp: ENSP00000400117.3:p.Arg61His
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183087
  ensembl transcript: ENST00000480426
  gene symbol: GAS6
  hgvsc: ENST00000480426.1:n.1234G>A
  variant of: http://identifiers.org/hgnc/4168
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 4.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1337
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 38378
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1006
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11893
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1735
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 4467
  bin: 3.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 178
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 296
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 195
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 514
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 519
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 318
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2689
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Arg360His
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: C
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum

13-114535337-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114535337
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 114535337
    reference: chr 13
allele count: 2
allele frequency: 1.724227115195614e-5
allele num: 115994
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183087
  ensembl transcript: ENST00000610073
  gene symbol: GAS6
  hgvsc: ENST00000610073.1:n.898C>T
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000349962
  ensembl transcript: ENST00000357389
  gene symbol: GAS6
  hgvsc: ENST00000357389.3:c.1207C>T
  hgvsp: ENSP00000349962.3:p.Arg403Cys
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000348003
  ensembl transcript: ENST00000355761
  gene symbol: GAS6
  hgvsc: ENST00000355761.4:c.916C>T
  hgvsp: ENSP00000348003.4:p.Arg306Cys
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000416498
  ensembl transcript: ENST00000450766
  gene symbol: GAS6
  hgvsc: ENST00000450766.1:c.259C>T
  hgvsp: ENSP00000416498.1:p.Arg87Cys
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000233695
  ensembl transcript: ENST00000458001
  gene symbol: GAS6-AS1
  hgvsc: ENST00000458001.1:n.63-1128G>A
  variant of: http://identifiers.org/hgnc/39826
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183087
  ensembl transcript: ENST00000480426
  gene symbol: GAS6
  hgvsc: ENST00000480426.1:n.1233C>T
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000331831
  ensembl transcript: ENST00000327773
  gene symbol: GAS6
  hgvsc: ENST00000327773.6:c.1078C>T
  hgvsp: ENSP00000331831.6:p.Arg360Cys
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000400117
  ensembl transcript: ENST00000418959
  gene symbol: GAS6
  hgvsc: ENST00000418959.3:c.181C>T
  hgvsp: ENSP00000400117.3:p.Arg61Cys
  variant of: http://identifiers.org/hgnc/4168
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38249
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4521
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1062
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1347
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1710
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11912
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 654
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 399
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 525
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 400
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 344
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2359
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 666
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 547
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Arg360Cys
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ

13-114535352-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114535352
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 114535352
    reference: chr 13
allele count: 6
allele frequency: 5.137162231583274e-5
allele num: 116796
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183087
  ensembl transcript: ENST00000610073
  gene symbol: GAS6
  hgvsc: ENST00000610073.1:n.883C>A
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000233695
  ensembl transcript: ENST00000458001
  gene symbol: GAS6-AS1
  hgvsc: ENST00000458001.1:n.63-1113G>T
  variant of: http://identifiers.org/hgnc/39826
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000348003
  ensembl transcript: ENST00000355761
  gene symbol: GAS6
  hgvsc: ENST00000355761.4:c.901C>A
  hgvsp: ENSP00000348003.4:p.Leu301Met
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000349962
  ensembl transcript: ENST00000357389
  gene symbol: GAS6
  hgvsc: ENST00000357389.3:c.1192C>A
  hgvsp: ENSP00000349962.3:p.Leu398Met
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000416498
  ensembl transcript: ENST00000450766
  gene symbol: GAS6
  hgvsc: ENST00000450766.1:c.244C>A
  hgvsp: ENSP00000416498.1:p.Leu82Met
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000331831
  ensembl transcript: ENST00000327773
  gene symbol: GAS6
  hgvsc: ENST00000327773.6:c.1063C>A
  hgvsp: ENSP00000331831.6:p.Leu355Met
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000400117
  ensembl transcript: ENST00000418959
  gene symbol: GAS6
  hgvsc: ENST00000418959.3:c.166C>A
  hgvsp: ENSP00000400117.3:p.Leu56Met
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183087
  ensembl transcript: ENST00000480426
  gene symbol: GAS6
  hgvsc: ENST00000480426.1:n.1218C>A
  variant of: http://identifiers.org/hgnc/4168
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4776
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1391
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12430
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38060
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1216
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 927
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 377
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 291
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39376
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 702
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 284
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Leu355Met
num of homozygotes: 0
population: East Asian
population: Other
population: Latino
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: FS

13-114535354-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114535354
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 114535354
    reference: chr 13
allele count: 2
allele frequency: 1.710688381004516e-5
allele num: 116912
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183087
  ensembl transcript: ENST00000480426
  gene symbol: GAS6
  hgvsc: ENST00000480426.1:n.1216G>A
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000233695
  ensembl transcript: ENST00000458001
  gene symbol: GAS6-AS1
  hgvsc: ENST00000458001.1:n.63-1111C>T
  variant of: http://identifiers.org/hgnc/39826
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000416498
  ensembl transcript: ENST00000450766
  gene symbol: GAS6
  hgvsc: ENST00000450766.1:c.242G>A
  hgvsp: ENSP00000416498.1:p.Arg81Gln
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000400117
  ensembl transcript: ENST00000418959
  gene symbol: GAS6
  hgvsc: ENST00000418959.3:c.164G>A
  hgvsp: ENSP00000400117.3:p.Arg55Gln
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000331831
  ensembl transcript: ENST00000327773
  gene symbol: GAS6
  hgvsc: ENST00000327773.6:c.1061G>A
  hgvsp: ENSP00000331831.6:p.Arg354Gln
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000348003
  ensembl transcript: ENST00000355761
  gene symbol: GAS6
  hgvsc: ENST00000355761.4:c.899G>A
  hgvsp: ENSP00000348003.4:p.Arg300Gln
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000349962
  ensembl transcript: ENST00000357389
  gene symbol: GAS6
  hgvsc: ENST00000357389.3:c.1190G>A
  hgvsp: ENSP00000349962.3:p.Arg397Gln
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183087
  ensembl transcript: ENST00000610073
  gene symbol: GAS6
  hgvsc: ENST00000610073.1:n.881G>A
  variant of: http://identifiers.org/hgnc/4168
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1337
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 882
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12553
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4823
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38004
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1186
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 173
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6885
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1942
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 441
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Arg354Gln
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: DP

13-114535356-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114535356
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 114535356
    reference: chr 13
allele count: 95
allele frequency: 8.111615833874108e-4
allele num: 117116
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183087
  ensembl transcript: ENST00000610073
  gene symbol: GAS6
  hgvsc: ENST00000610073.1:n.879C>T
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000416498
  ensembl transcript: ENST00000450766
  gene symbol: GAS6
  hgvsc: ENST00000450766.1:c.240C>T
  hgvsp: ENST00000450766.1:c.240C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183087
  ensembl transcript: ENST00000480426
  gene symbol: GAS6
  hgvsc: ENST00000480426.1:n.1214C>T
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000331831
  ensembl transcript: ENST00000327773
  gene symbol: GAS6
  hgvsc: ENST00000327773.6:c.1059C>T
  hgvsp: ENST00000327773.6:c.1059C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000348003
  ensembl transcript: ENST00000355761
  gene symbol: GAS6
  hgvsc: ENST00000355761.4:c.897C>T
  hgvsp: ENST00000355761.4:c.897C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000349962
  ensembl transcript: ENST00000357389
  gene symbol: GAS6
  hgvsc: ENST00000357389.3:c.1188C>T
  hgvsp: ENST00000357389.3:c.1188C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000233695
  ensembl transcript: ENST00000458001
  gene symbol: GAS6-AS1
  hgvsc: ENST00000458001.1:n.63-1109G>A
  variant of: http://identifiers.org/hgnc/39826
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000400117
  ensembl transcript: ENST00000418959
  gene symbol: GAS6
  hgvsc: ENST00000418959.3:c.162C>T
  hgvsp: ENST00000418959.3:c.162C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4168
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 4.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 714
  bin: 3.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 38009
  bin: 2.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 5.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1160
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1252
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12601
  bin: 2.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 5.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 4926
  bin: 3.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 793
  bin: 1.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 4.75e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 172
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6914
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 364
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2889
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1845
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Gly353Gly
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: QD

13-114535359-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114535359
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 114535359
    reference: chr 13
allele count: 2
allele frequency: 1.704681054174764e-5
allele num: 117324
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000400117
  ensembl transcript: ENST00000418959
  gene symbol: GAS6
  hgvsc: ENST00000418959.3:c.159C>T
  hgvsp: ENST00000418959.3:c.159C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000233695
  ensembl transcript: ENST00000458001
  gene symbol: GAS6-AS1
  hgvsc: ENST00000458001.1:n.63-1106G>A
  variant of: http://identifiers.org/hgnc/39826
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183087
  ensembl transcript: ENST00000480426
  gene symbol: GAS6
  hgvsc: ENST00000480426.1:n.1211C>T
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183087
  ensembl transcript: ENST00000610073
  gene symbol: GAS6
  hgvsc: ENST00000610073.1:n.876C>T
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000349962
  ensembl transcript: ENST00000357389
  gene symbol: GAS6
  hgvsc: ENST00000357389.3:c.1185C>T
  hgvsp: ENST00000357389.3:c.1185C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000348003
  ensembl transcript: ENST00000355761
  gene symbol: GAS6
  hgvsc: ENST00000355761.4:c.894C>T
  hgvsp: ENST00000355761.4:c.894C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000331831
  ensembl transcript: ENST00000327773
  gene symbol: GAS6
  hgvsc: ENST00000327773.6:c.1056C>T
  hgvsp: ENST00000327773.6:c.1056C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000416498
  ensembl transcript: ENST00000450766
  gene symbol: GAS6
  hgvsc: ENST00000450766.1:c.237C>T
  hgvsp: ENST00000450766.1:c.237C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4168
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38104
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12670
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 726
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 697
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1170
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1101
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4998
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 348
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 393
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1720
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 189
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39714
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Ala352Ala
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: South Asian
population: Other
reference allele: G
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: VQSLOD

13-114535362-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114535362
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 114535362
    reference: chr 13
allele count: 1
allele frequency: 8.506149946411256e-6
allele num: 117562
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000400117
  ensembl transcript: ENST00000418959
  gene symbol: GAS6
  hgvsc: ENST00000418959.3:c.156A>G
  hgvsp: ENST00000418959.3:c.156A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000349962
  ensembl transcript: ENST00000357389
  gene symbol: GAS6
  hgvsc: ENST00000357389.3:c.1182A>G
  hgvsp: ENST00000357389.3:c.1182A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000416498
  ensembl transcript: ENST00000450766
  gene symbol: GAS6
  hgvsc: ENST00000450766.1:c.234A>G
  hgvsp: ENST00000450766.1:c.234A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000331831
  ensembl transcript: ENST00000327773
  gene symbol: GAS6
  hgvsc: ENST00000327773.6:c.1053A>G
  hgvsp: ENST00000327773.6:c.1053A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183087
  ensembl transcript: ENST00000610073
  gene symbol: GAS6
  hgvsc: ENST00000610073.1:n.873A>G
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000348003
  ensembl transcript: ENST00000355761
  gene symbol: GAS6
  hgvsc: ENST00000355761.4:c.891A>G
  hgvsp: ENST00000355761.4:c.891A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183087
  ensembl transcript: ENST00000480426
  gene symbol: GAS6
  hgvsc: ENST00000480426.1:n.1208A>G
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000233695
  ensembl transcript: ENST00000458001
  gene symbol: GAS6-AS1
  hgvsc: ENST00000458001.1:n.63-1103T>C
  variant of: http://identifiers.org/hgnc/39826
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5047
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1086
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38243
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 739
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12736
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1037
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 359
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7056
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 116
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3007
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 222
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 323
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Arg351Arg
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
population: European (Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum

13-114535363-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114535363
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 114535363
    reference: chr 13
allele count: 1
allele frequency: 8.50065455040038e-6
allele num: 117638
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183087
  ensembl transcript: ENST00000480426
  gene symbol: GAS6
  hgvsc: ENST00000480426.1:n.1207G>A
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000416498
  ensembl transcript: ENST00000450766
  gene symbol: GAS6
  hgvsc: ENST00000450766.1:c.233G>A
  hgvsp: ENSP00000416498.1:p.Arg78Lys
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000400117
  ensembl transcript: ENST00000418959
  gene symbol: GAS6
  hgvsc: ENST00000418959.3:c.155G>A
  hgvsp: ENSP00000400117.3:p.Arg52Lys
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000348003
  ensembl transcript: ENST00000355761
  gene symbol: GAS6
  hgvsc: ENST00000355761.4:c.890G>A
  hgvsp: ENSP00000348003.4:p.Arg297Lys
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000349962
  ensembl transcript: ENST00000357389
  gene symbol: GAS6
  hgvsc: ENST00000357389.3:c.1181G>A
  hgvsp: ENSP00000349962.3:p.Arg394Lys
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183087
  ensembl transcript: ENST00000610073
  gene symbol: GAS6
  hgvsc: ENST00000610073.1:n.872G>A
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000233695
  ensembl transcript: ENST00000458001
  gene symbol: GAS6-AS1
  hgvsc: ENST00000458001.1:n.63-1102C>T
  variant of: http://identifiers.org/hgnc/39826
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000331831
  ensembl transcript: ENST00000327773
  gene symbol: GAS6
  hgvsc: ENST00000327773.6:c.1052G>A
  hgvsp: ENSP00000331831.6:p.Arg351Lys
  variant of: http://identifiers.org/hgnc/4168
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1050
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 739
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1012
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5070
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38278
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12752
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7066
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 749
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 115
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 129
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 211
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Arg351Lys
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff

13-114535376-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114535376
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 114535376
    reference: chr 13
allele count: 17
allele frequency: 1.440531471375792e-4
allele num: 118012
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000400117
  ensembl transcript: ENST00000418959
  gene symbol: GAS6
  hgvsc: ENST00000418959.3:c.142G>A
  hgvsp: ENSP00000400117.3:p.Val48Met
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000348003
  ensembl transcript: ENST00000355761
  gene symbol: GAS6
  hgvsc: ENST00000355761.4:c.877G>A
  hgvsp: ENSP00000348003.4:p.Val293Met
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000233695
  ensembl transcript: ENST00000458001
  gene symbol: GAS6-AS1
  hgvsc: ENST00000458001.1:n.63-1089C>T
  variant of: http://identifiers.org/hgnc/39826
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000349962
  ensembl transcript: ENST00000357389
  gene symbol: GAS6
  hgvsc: ENST00000357389.3:c.1168G>A
  hgvsp: ENSP00000349962.3:p.Val390Met
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000331831
  ensembl transcript: ENST00000327773
  gene symbol: GAS6
  hgvsc: ENST00000327773.6:c.1039G>A
  hgvsp: ENSP00000331831.6:p.Val347Met
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000416498
  ensembl transcript: ENST00000450766
  gene symbol: GAS6
  hgvsc: ENST00000450766.1:c.220G>A
  hgvsp: ENSP00000416498.1:p.Val74Met
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183087
  ensembl transcript: ENST00000480426
  gene symbol: GAS6
  hgvsc: ENST00000480426.1:n.1194G>A
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183087
  ensembl transcript: ENST00000610073
  gene symbol: GAS6
  hgvsc: ENST00000610073.1:n.859G>A
  variant of: http://identifiers.org/hgnc/4168
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 856
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5236
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 876
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 38221
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 767
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13107
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7143
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2591
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40290
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 107
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Val347Met
num of homozygotes: 0
population: African
population: Other
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: QD

13-114535377-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114535377
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 114535377
    reference: chr 13
allele count: 13
allele frequency: 1.101135016093512e-4
allele num: 118060
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000349962
  ensembl transcript: ENST00000357389
  gene symbol: GAS6
  hgvsc: ENST00000357389.3:c.1167C>T
  hgvsp: ENST00000357389.3:c.1167C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000400117
  ensembl transcript: ENST00000418959
  gene symbol: GAS6
  hgvsc: ENST00000418959.3:c.141C>T
  hgvsp: ENST00000418959.3:c.141C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000348003
  ensembl transcript: ENST00000355761
  gene symbol: GAS6
  hgvsc: ENST00000355761.4:c.876C>T
  hgvsp: ENST00000355761.4:c.876C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183087
  ensembl transcript: ENST00000480426
  gene symbol: GAS6
  hgvsc: ENST00000480426.1:n.1193C>T
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183087
  ensembl transcript: ENST00000610073
  gene symbol: GAS6
  hgvsc: ENST00000610073.1:n.858C>T
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000233695
  ensembl transcript: ENST00000458001
  gene symbol: GAS6-AS1
  hgvsc: ENST00000458001.1:n.63-1088G>A
  variant of: http://identifiers.org/hgnc/39826
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000331831
  ensembl transcript: ENST00000327773
  gene symbol: GAS6
  hgvsc: ENST00000327773.6:c.1038C>T
  hgvsp: ENST00000327773.6:c.1038C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000416498
  ensembl transcript: ENST00000450766
  gene symbol: GAS6
  hgvsc: ENST00000450766.1:c.219C>T
  hgvsp: ENST00000450766.1:c.219C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4168
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 829
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13118
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38268
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5252
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 771
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 852
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 5.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 333
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 205
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3072
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 761
  bin: 9.75e1
  variant carriers: 13
genotype quality: GenotypeQuality
  all individuals: 260
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Ile346Ile
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
population: African
population: European (Non-Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: VQSLOD

13-114535377-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114535377
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 114535377
    reference: chr 13
allele count: 2
allele frequency: 1.694053870913095e-5
allele num: 118060
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000349962
  ensembl transcript: ENST00000357389
  gene symbol: GAS6
  hgvsc: ENST00000357389.3:c.1167C>G
  hgvsp: ENSP00000349962.3:p.Ile389Met
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000348003
  ensembl transcript: ENST00000355761
  gene symbol: GAS6
  hgvsc: ENST00000355761.4:c.876C>G
  hgvsp: ENSP00000348003.4:p.Ile292Met
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000416498
  ensembl transcript: ENST00000450766
  gene symbol: GAS6
  hgvsc: ENST00000450766.1:c.219C>G
  hgvsp: ENSP00000416498.1:p.Ile73Met
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183087
  ensembl transcript: ENST00000610073
  gene symbol: GAS6
  hgvsc: ENST00000610073.1:n.858C>G
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000331831
  ensembl transcript: ENST00000327773
  gene symbol: GAS6
  hgvsc: ENST00000327773.6:c.1038C>G
  hgvsp: ENSP00000331831.6:p.Ile346Met
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000233695
  ensembl transcript: ENST00000458001
  gene symbol: GAS6-AS1
  hgvsc: ENST00000458001.1:n.63-1088G>C
  variant of: http://identifiers.org/hgnc/39826
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000400117
  ensembl transcript: ENST00000418959
  gene symbol: GAS6
  hgvsc: ENST00000418959.3:c.141C>G
  hgvsp: ENSP00000400117.3:p.Ile47Met
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183087
  ensembl transcript: ENST00000480426
  gene symbol: GAS6
  hgvsc: ENST00000480426.1:n.1193C>G
  variant of: http://identifiers.org/hgnc/4168
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5252
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 852
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 771
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38268
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 829
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13118
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 260
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 205
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 133
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40377
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 770
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 761
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 7164
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Ile346Met
num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: QD

13-114535389-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114535389
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 114535389
    reference: chr 13
allele count: 13
allele frequency: 1.100091392207968e-4
allele num: 118172
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183087
  ensembl transcript: ENST00000610073
  gene symbol: GAS6
  hgvsc: ENST00000610073.1:n.846C>T
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000348003
  ensembl transcript: ENST00000355761
  gene symbol: GAS6
  hgvsc: ENST00000355761.4:c.864C>T
  hgvsp: ENST00000355761.4:c.864C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183087
  ensembl transcript: ENST00000480426
  gene symbol: GAS6
  hgvsc: ENST00000480426.1:n.1181C>T
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000233695
  ensembl transcript: ENST00000458001
  gene symbol: GAS6-AS1
  hgvsc: ENST00000458001.1:n.63-1076G>A
  variant of: http://identifiers.org/hgnc/39826
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000349962
  ensembl transcript: ENST00000357389
  gene symbol: GAS6
  hgvsc: ENST00000357389.3:c.1155C>T
  hgvsp: ENST00000357389.3:c.1155C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000416498
  ensembl transcript: ENST00000450766
  gene symbol: GAS6
  hgvsc: ENST00000450766.1:c.207C>T
  hgvsp: ENST00000450766.1:c.207C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000331831
  ensembl transcript: ENST00000327773
  gene symbol: GAS6
  hgvsc: ENST00000327773.6:c.1026C>T
  hgvsp: ENST00000327773.6:c.1026C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000400117
  ensembl transcript: ENST00000418959
  gene symbol: GAS6
  hgvsc: ENST00000418959.3:c.129C>T
  hgvsp: ENST00000418959.3:c.129C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4168
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13204
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5323
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 814
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 812
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38232
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 785
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3092
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 108
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2620
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 181
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Asp342Asp
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: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD

13-114535399-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114535399
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 114535399
    reference: chr 13
allele count: 1
allele frequency: 8.484642796538266e-6
allele num: 117860
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000348003
  ensembl transcript: ENST00000355761
  gene symbol: GAS6
  hgvsc: ENST00000355761.4:c.854G>C
  hgvsp: ENSP00000348003.4:p.Gly285Ala
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000416498
  ensembl transcript: ENST00000450766
  gene symbol: GAS6
  hgvsc: ENST00000450766.1:c.197G>C
  hgvsp: ENSP00000416498.1:p.Gly66Ala
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000331831
  ensembl transcript: ENST00000327773
  gene symbol: GAS6
  hgvsc: ENST00000327773.6:c.1016G>C
  hgvsp: ENSP00000331831.6:p.Gly339Ala
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183087
  ensembl transcript: ENST00000610073
  gene symbol: GAS6
  hgvsc: ENST00000610073.1:n.836G>C
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000400117
  ensembl transcript: ENST00000418959
  gene symbol: GAS6
  hgvsc: ENST00000418959.3:c.119G>C
  hgvsp: ENSP00000400117.3:p.Gly40Ala
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183087
  ensembl transcript: ENST00000480426
  gene symbol: GAS6
  hgvsc: ENST00000480426.1:n.1171G>C
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000349962
  ensembl transcript: ENST00000357389
  gene symbol: GAS6
  hgvsc: ENST00000357389.3:c.1145G>C
  hgvsp: ENSP00000349962.3:p.Gly382Ala
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000233695
  ensembl transcript: ENST00000458001
  gene symbol: GAS6-AS1
  hgvsc: ENST00000458001.1:n.63-1066C>G
  variant of: http://identifiers.org/hgnc/39826
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1081
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37765
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 970
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13159
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 795
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5323
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 111
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 792
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 260
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 377
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 783
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Gly339Ala
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
population: Other
population: East Asian
reference allele: C
site quality: MQ
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum

13-114535404-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114535404
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 114535404
    reference: chr 13
allele count: 29
allele frequency: 2.463849382338448e-4
allele num: 117702
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000416498
  ensembl transcript: ENST00000450766
  gene symbol: GAS6
  hgvsc: ENST00000450766.1:c.192C>T
  hgvsp: ENST00000450766.1:c.192C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183087
  ensembl transcript: ENST00000480426
  gene symbol: GAS6
  hgvsc: ENST00000480426.1:n.1166C>T
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000400117
  ensembl transcript: ENST00000418959
  gene symbol: GAS6
  hgvsc: ENST00000418959.3:c.114C>T
  hgvsp: ENST00000418959.3:c.114C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000348003
  ensembl transcript: ENST00000355761
  gene symbol: GAS6
  hgvsc: ENST00000355761.4:c.849C>T
  hgvsp: ENST00000355761.4:c.849C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000349962
  ensembl transcript: ENST00000357389
  gene symbol: GAS6
  hgvsc: ENST00000357389.3:c.1140C>T
  hgvsp: ENST00000357389.3:c.1140C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000331831
  ensembl transcript: ENST00000327773
  gene symbol: GAS6
  hgvsc: ENST00000327773.6:c.1011C>T
  hgvsp: ENST00000327773.6:c.1011C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183087
  ensembl transcript: ENST00000610073
  gene symbol: GAS6
  hgvsc: ENST00000610073.1:n.831C>T
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000233695
  ensembl transcript: ENST00000458001
  gene symbol: GAS6-AS1
  hgvsc: ENST00000458001.1:n.63-1061G>A
  variant of: http://identifiers.org/hgnc/39826
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 4.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 5347
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 808
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13071
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1033
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1223
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 37527
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2123
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 310
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1751
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 294
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 87
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Ala337Ala
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Other
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: QD

13-114535413-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114535413
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 114535413
    reference: chr 13
allele count: 1
allele frequency: 8.529948649709128e-6
allele num: 117234
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000416498
  ensembl transcript: ENST00000450766
  gene symbol: GAS6
  hgvsc: ENST00000450766.1:c.183C>T
  hgvsp: ENST00000450766.1:c.183C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000349962
  ensembl transcript: ENST00000357389
  gene symbol: GAS6
  hgvsc: ENST00000357389.3:c.1131C>T
  hgvsp: ENST00000357389.3:c.1131C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000348003
  ensembl transcript: ENST00000355761
  gene symbol: GAS6
  hgvsc: ENST00000355761.4:c.840C>T
  hgvsp: ENST00000355761.4:c.840C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183087
  ensembl transcript: ENST00000610073
  gene symbol: GAS6
  hgvsc: ENST00000610073.1:n.822C>T
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000331831
  ensembl transcript: ENST00000327773
  gene symbol: GAS6
  hgvsc: ENST00000327773.6:c.1002C>T
  hgvsp: ENST00000327773.6:c.1002C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000400117
  ensembl transcript: ENST00000418959
  gene symbol: GAS6
  hgvsc: ENST00000418959.3:c.105C>T
  hgvsp: ENST00000418959.3:c.105C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183087
  ensembl transcript: ENST00000480426
  gene symbol: GAS6
  hgvsc: ENST00000480426.1:n.1157C>T
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000233695
  ensembl transcript: ENST00000458001
  gene symbol: GAS6-AS1
  hgvsc: ENST00000458001.1:n.63-1052G>A
  variant of: http://identifiers.org/hgnc/39826
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 36901
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1276
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1651
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 810
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5317
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 496
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12942
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 795
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3112
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2280
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 383
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 815
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Leu334Leu
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
population: European (Finnish)
population: Other
reference allele: G
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum

13-114535418-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114535418
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 114535418
    reference: chr 13
allele count: 6
allele frequency: 5.137250201208966e-5
allele num: 116794
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000416498
  ensembl transcript: ENST00000450766
  gene symbol: GAS6
  hgvsc: ENST00000450766.1:c.178A>G
  hgvsp: ENSP00000416498.1:p.Ile60Val
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000233695
  ensembl transcript: ENST00000458001
  gene symbol: GAS6-AS1
  hgvsc: ENST00000458001.1:n.63-1047T>C
  variant of: http://identifiers.org/hgnc/39826
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000348003
  ensembl transcript: ENST00000355761
  gene symbol: GAS6
  hgvsc: ENST00000355761.4:c.835A>G
  hgvsp: ENSP00000348003.4:p.Ile279Val
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000400117
  ensembl transcript: ENST00000418959
  gene symbol: GAS6
  hgvsc: ENST00000418959.3:c.100A>G
  hgvsp: ENSP00000400117.3:p.Ile34Val
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000331831
  ensembl transcript: ENST00000327773
  gene symbol: GAS6
  hgvsc: ENST00000327773.6:c.997A>G
  hgvsp: ENSP00000331831.6:p.Ile333Val
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183087
  ensembl transcript: ENST00000480426
  gene symbol: GAS6
  hgvsc: ENST00000480426.1:n.1152A>G
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000349962
  ensembl transcript: ENST00000357389
  gene symbol: GAS6
  hgvsc: ENST00000357389.3:c.1126A>G
  hgvsp: ENSP00000349962.3:p.Ile376Val
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183087
  ensembl transcript: ENST00000610073
  gene symbol: GAS6
  hgvsc: ENST00000610073.1:n.817A>G
  variant of: http://identifiers.org/hgnc/4168
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 811
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12684
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36290
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1488
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2125
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 683
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5295
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 118
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 820
  bin: 9.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 785
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 285
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Ile333Val
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
reference allele: T
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: DP
site quality: VQSLOD

13-114535424-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114535424
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 114535424
    reference: chr 13
allele count: 1
allele frequency: 8.602002546192754e-6
allele num: 116252
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000349962
  ensembl transcript: ENST00000357389
  gene symbol: GAS6
  hgvsc: ENST00000357389.3:c.1120G>A
  hgvsp: ENSP00000349962.3:p.Glu374Lys
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183087
  ensembl transcript: ENST00000610073
  gene symbol: GAS6
  hgvsc: ENST00000610073.1:n.811G>A
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000233695
  ensembl transcript: ENST00000458001
  gene symbol: GAS6-AS1
  hgvsc: ENST00000458001.1:n.63-1041C>T
  variant of: http://identifiers.org/hgnc/39826
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000416498
  ensembl transcript: ENST00000450766
  gene symbol: GAS6
  hgvsc: ENST00000450766.1:c.172G>A
  hgvsp: ENSP00000416498.1:p.Glu58Lys
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183087
  ensembl transcript: ENST00000480426
  gene symbol: GAS6
  hgvsc: ENST00000480426.1:n.1146G>A
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000348003
  ensembl transcript: ENST00000355761
  gene symbol: GAS6
  hgvsc: ENST00000355761.4:c.829G>A
  hgvsp: ENSP00000348003.4:p.Glu277Lys
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000331831
  ensembl transcript: ENST00000327773
  gene symbol: GAS6
  hgvsc: ENST00000327773.6:c.991G>A
  hgvsp: ENSP00000331831.6:p.Glu331Lys
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000400117
  ensembl transcript: ENST00000418959
  gene symbol: GAS6
  hgvsc: ENST00000418959.3:c.94G>A
  hgvsp: ENSP00000400117.3:p.Glu32Lys
  variant of: http://identifiers.org/hgnc/4168
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1681
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2449
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35987
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 736
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5273
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12404
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 809
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 595
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2602
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 825
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 125
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Glu331Lys
num of homozygotes: 0
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
population: Latino
reference allele: C
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: MQ

13-114535425-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114535425
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 114535425
    reference: chr 13
allele count: 1
allele frequency: 8.609853115905842e-6
allele num: 116146
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000416498
  ensembl transcript: ENST00000450766
  gene symbol: GAS6
  hgvsc: ENST00000450766.1:c.171C>T
  hgvsp: ENST00000450766.1:c.171C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000348003
  ensembl transcript: ENST00000355761
  gene symbol: GAS6
  hgvsc: ENST00000355761.4:c.828C>T
  hgvsp: ENST00000355761.4:c.828C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000349962
  ensembl transcript: ENST00000357389
  gene symbol: GAS6
  hgvsc: ENST00000357389.3:c.1119C>T
  hgvsp: ENST00000357389.3:c.1119C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000233695
  ensembl transcript: ENST00000458001
  gene symbol: GAS6-AS1
  hgvsc: ENST00000458001.1:n.63-1040G>A
  variant of: http://identifiers.org/hgnc/39826
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000400117
  ensembl transcript: ENST00000418959
  gene symbol: GAS6
  hgvsc: ENST00000418959.3:c.93C>T
  hgvsp: ENST00000418959.3:c.93C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000331831
  ensembl transcript: ENST00000327773
  gene symbol: GAS6
  hgvsc: ENST00000327773.6:c.990C>T
  hgvsp: ENST00000327773.6:c.990C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183087
  ensembl transcript: ENST00000610073
  gene symbol: GAS6
  hgvsc: ENST00000610073.1:n.810C>T
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183087
  ensembl transcript: ENST00000480426
  gene symbol: GAS6
  hgvsc: ENST00000480426.1:n.1145C>T
  variant of: http://identifiers.org/hgnc/4168
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 35892
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5254
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 807
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 766
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1727
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12323
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2553
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 119
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 497
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 135
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3104
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6945
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 322
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Pro330Pro
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD

13-114535438-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114535438
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 114535438
    reference: chr 13
allele count: 1
allele frequency: 8.670019074041962e-6
allele num: 115340
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000348003
  ensembl transcript: ENST00000355761
  gene symbol: GAS6
  hgvsc: ENST00000355761.4:c.815G>A
  hgvsp: ENSP00000348003.4:p.Arg272Gln
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000233695
  ensembl transcript: ENST00000458001
  gene symbol: GAS6-AS1
  hgvsc: ENST00000458001.1:n.63-1027C>T
  variant of: http://identifiers.org/hgnc/39826
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000349962
  ensembl transcript: ENST00000357389
  gene symbol: GAS6
  hgvsc: ENST00000357389.3:c.1106G>A
  hgvsp: ENSP00000349962.3:p.Arg369Gln
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183087
  ensembl transcript: ENST00000610073
  gene symbol: GAS6
  hgvsc: ENST00000610073.1:n.797G>A
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000416498
  ensembl transcript: ENST00000450766
  gene symbol: GAS6
  hgvsc: ENST00000450766.1:c.158G>A
  hgvsp: ENSP00000416498.1:p.Arg53Gln
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183087
  ensembl transcript: ENST00000480426
  gene symbol: GAS6
  hgvsc: ENST00000480426.1:n.1132G>A
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000331831
  ensembl transcript: ENST00000327773
  gene symbol: GAS6
  hgvsc: ENST00000327773.6:c.977G>A
  hgvsp: ENSP00000331831.6:p.Arg326Gln
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000400117
  ensembl transcript: ENST00000418959
  gene symbol: GAS6
  hgvsc: ENST00000418959.3:c.80G>A
  hgvsp: ENSP00000400117.3:p.Arg27Gln
  variant of: http://identifiers.org/hgnc/4168
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5215
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2009
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35486
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2932
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11919
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 810
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 883
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 595
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2597
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 124
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3564
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2121
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36555
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Arg326Gln
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: MQ

13-114535439-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114535439
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 114535439
    reference: chr 13
allele count: 3
allele frequency: 2.602088609790792e-5
allele num: 115292
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183087
  ensembl transcript: ENST00000610073
  gene symbol: GAS6
  hgvsc: ENST00000610073.1:n.796C>T
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000400117
  ensembl transcript: ENST00000418959
  gene symbol: GAS6
  hgvsc: ENST00000418959.3:c.79C>T
  hgvsp: ENSP00000400117.3:p.Arg27Trp
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000348003
  ensembl transcript: ENST00000355761
  gene symbol: GAS6
  hgvsc: ENST00000355761.4:c.814C>T
  hgvsp: ENSP00000348003.4:p.Arg272Trp
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000233695
  ensembl transcript: ENST00000458001
  gene symbol: GAS6-AS1
  hgvsc: ENST00000458001.1:n.63-1026G>A
  variant of: http://identifiers.org/hgnc/39826
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183087
  ensembl transcript: ENST00000480426
  gene symbol: GAS6
  hgvsc: ENST00000480426.1:n.1131C>T
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000416498
  ensembl transcript: ENST00000450766
  gene symbol: GAS6
  hgvsc: ENST00000450766.1:c.157C>T
  hgvsp: ENSP00000416498.1:p.Arg53Trp
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000349962
  ensembl transcript: ENST00000357389
  gene symbol: GAS6
  hgvsc: ENST00000357389.3:c.1105C>T
  hgvsp: ENSP00000349962.3:p.Arg369Trp
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000331831
  ensembl transcript: ENST00000327773
  gene symbol: GAS6
  hgvsc: ENST00000327773.6:c.976C>T
  hgvsp: ENSP00000331831.6:p.Arg326Trp
  variant of: http://identifiers.org/hgnc/4168
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2050
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11900
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 813
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2940
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 856
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35484
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 613
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5212
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 725
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36568
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 119
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 800
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 105
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 621
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 830
  bin: 9.75e1
  variant carriers: 3
hgvs: p.Arg326Trp
num of homozygotes: 0
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
population: East Asian
reference allele: G
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum

13-114535455-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114535455
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 114535455
    reference: chr 13
allele count: 1
allele frequency: 8.751509635412108e-6
allele num: 114266
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000400117
  ensembl transcript: ENST00000418959
  gene symbol: GAS6
  hgvsc: ENST00000418959.3:c.63A>G
  hgvsp: ENST00000418959.3:c.63A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000348003
  ensembl transcript: ENST00000355761
  gene symbol: GAS6
  hgvsc: ENST00000355761.4:c.798A>G
  hgvsp: ENST00000355761.4:c.798A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183087
  ensembl transcript: ENST00000610073
  gene symbol: GAS6
  hgvsc: ENST00000610073.1:n.780A>G
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000331831
  ensembl transcript: ENST00000327773
  gene symbol: GAS6
  hgvsc: ENST00000327773.6:c.960A>G
  hgvsp: ENST00000327773.6:c.960A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000349962
  ensembl transcript: ENST00000357389
  gene symbol: GAS6
  hgvsc: ENST00000357389.3:c.1089A>G
  hgvsp: ENST00000357389.3:c.1089A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183087
  ensembl transcript: ENST00000480426
  gene symbol: GAS6
  hgvsc: ENST00000480426.1:n.1115A>G
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000233695
  ensembl transcript: ENST00000458001
  gene symbol: GAS6-AS1
  hgvsc: ENST00000458001.1:n.63-1010T>C
  variant of: http://identifiers.org/hgnc/39826
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000416498
  ensembl transcript: ENST00000450766
  gene symbol: GAS6
  hgvsc: ENST00000450766.1:c.141A>G
  hgvsp: ENST00000450766.1:c.141A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/4168
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3013
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11688
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2398
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35038
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5216
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 809
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 927
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 779
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 834
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 6865
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 841
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 99
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 786
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 221
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3101
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Val320Val
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: MQ

13-114535455-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114535455
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 114535455
    reference: chr 13
allele count: 5
allele frequency: 4.375754817706054e-5
allele num: 114266
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000349962
  ensembl transcript: ENST00000357389
  gene symbol: GAS6
  hgvsc: ENST00000357389.3:c.1089A>C
  hgvsp: ENST00000357389.3:c.1089A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000331831
  ensembl transcript: ENST00000327773
  gene symbol: GAS6
  hgvsc: ENST00000327773.6:c.960A>C
  hgvsp: ENST00000327773.6:c.960A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000348003
  ensembl transcript: ENST00000355761
  gene symbol: GAS6
  hgvsc: ENST00000355761.4:c.798A>C
  hgvsp: ENST00000355761.4:c.798A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000400117
  ensembl transcript: ENST00000418959
  gene symbol: GAS6
  hgvsc: ENST00000418959.3:c.63A>C
  hgvsp: ENST00000418959.3:c.63A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183087
  ensembl transcript: ENST00000480426
  gene symbol: GAS6
  hgvsc: ENST00000480426.1:n.1115A>C
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000416498
  ensembl transcript: ENST00000450766
  gene symbol: GAS6
  hgvsc: ENST00000450766.1:c.141A>C
  hgvsp: ENST00000450766.1:c.141A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000233695
  ensembl transcript: ENST00000458001
  gene symbol: GAS6-AS1
  hgvsc: ENST00000458001.1:n.63-1010T>G
  variant of: http://identifiers.org/hgnc/39826
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183087
  ensembl transcript: ENST00000610073
  gene symbol: GAS6
  hgvsc: ENST00000610073.1:n.780A>C
  variant of: http://identifiers.org/hgnc/4168
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11688
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 927
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 779
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 809
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 35038
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3013
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5216
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2398
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3624
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 118
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 786
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 221
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3101
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Val320Val
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
population: African
population: European (Finnish)
population: East Asian
reference allele: T
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: ClippingRankSum

13-114535466-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114535466
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 114535466
    reference: chr 13
allele count: 2
allele frequency: 1.760997428943754e-5
allele num: 113572
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000416498
  ensembl transcript: ENST00000450766
  gene symbol: GAS6
  hgvsc: ENST00000450766.1:c.135-5C>G
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183087
  ensembl transcript: ENST00000610073
  gene symbol: GAS6
  hgvsc: ENST00000610073.1:n.774-5C>G
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000331831
  ensembl transcript: ENST00000327773
  gene symbol: GAS6
  hgvsc: ENST00000327773.6:c.954-5C>G
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000233695
  ensembl transcript: ENST00000458001
  gene symbol: GAS6-AS1
  hgvsc: ENST00000458001.1:n.63-999G>C
  variant of: http://identifiers.org/hgnc/39826
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183087
  ensembl transcript: ENST00000480426
  gene symbol: GAS6
  hgvsc: ENST00000480426.1:n.1109-5C>G
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000349962
  ensembl transcript: ENST00000357389
  gene symbol: GAS6
  hgvsc: ENST00000357389.3:c.1083-5C>G
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000400117
  ensembl transcript: ENST00000418959
  gene symbol: GAS6
  hgvsc: ENST00000418959.3:c.57-5C>G
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000348003
  ensembl transcript: ENST00000355761
  gene symbol: GAS6
  hgvsc: ENST00000355761.4:c.792-5C>G
  variant of: http://identifiers.org/hgnc/4168
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5222
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 873
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 894
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2634
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34944
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11632
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 808
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2848
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 801
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 93
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 93
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2120
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2596
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3100
  bin: 7.75e1
  variant carriers: 0
hgvs: c.954-5C>G
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
population: South Asian
population: African
population: East Asian
reference allele: G
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD

http://identifiers.org/exac.variant/13-114535467-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114535467
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 114535467
    reference: chr 13
allele count: 1
allele frequency: 8.815388141539872e-6
allele num: 113438
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000348003
  ensembl transcript: ENST00000355761
  gene symbol: GAS6
  hgvsc: ENST00000355761.4:c.792-6G>T
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000400117
  ensembl transcript: ENST00000418959
  gene symbol: GAS6
  hgvsc: ENST00000418959.3:c.57-6G>T
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183087
  ensembl transcript: ENST00000480426
  gene symbol: GAS6
  hgvsc: ENST00000480426.1:n.1109-6G>T
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000416498
  ensembl transcript: ENST00000450766
  gene symbol: GAS6
  hgvsc: ENST00000450766.1:c.135-6G>T
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000233695
  ensembl transcript: ENST00000458001
  gene symbol: GAS6-AS1
  hgvsc: ENST00000458001.1:n.63-998C>A
  variant of: http://identifiers.org/hgnc/39826
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183087
  ensembl transcript: ENST00000610073
  gene symbol: GAS6
  hgvsc: ENST00000610073.1:n.774-6G>T
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000331831
  ensembl transcript: ENST00000327773
  gene symbol: GAS6
  hgvsc: ENST00000327773.6:c.954-6G>T
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000349962
  ensembl transcript: ENST00000357389
  gene symbol: GAS6
  hgvsc: ENST00000357389.3:c.1083-6G>T
  variant of: http://identifiers.org/hgnc/4168
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 889
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11630
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34955
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2838
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2639
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 875
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5224
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 809
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6874
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 887
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 801
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 814
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2121
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 125
  bin: 2.5e0
  variant carriers: 0
hgvs: c.954-6G>T
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
population: Other
population: African
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQ

13-114535471-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114535471
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 114535471
    reference: chr 13
allele count: 1
allele frequency: 8.821609414421567e-6
allele num: 113358
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000331831
  ensembl transcript: ENST00000327773
  gene symbol: GAS6
  hgvsc: ENST00000327773.6:c.954-10G>C
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000400117
  ensembl transcript: ENST00000418959
  gene symbol: GAS6
  hgvsc: ENST00000418959.3:c.57-10G>C
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000416498
  ensembl transcript: ENST00000450766
  gene symbol: GAS6
  hgvsc: ENST00000450766.1:c.135-10G>C
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183087
  ensembl transcript: ENST00000610073
  gene symbol: GAS6
  hgvsc: ENST00000610073.1:n.774-10G>C
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000349962
  ensembl transcript: ENST00000357389
  gene symbol: GAS6
  hgvsc: ENST00000357389.3:c.1083-10G>C
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183087
  ensembl transcript: ENST00000480426
  gene symbol: GAS6
  hgvsc: ENST00000480426.1:n.1109-10G>C
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000348003
  ensembl transcript: ENST00000355761
  gene symbol: GAS6
  hgvsc: ENST00000355761.4:c.792-10G>C
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000233695
  ensembl transcript: ENST00000458001
  gene symbol: GAS6-AS1
  hgvsc: ENST00000458001.1:n.63-994C>G
  variant of: http://identifiers.org/hgnc/39826
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 34944
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11642
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 817
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2674
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2842
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5220
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 813
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 896
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 275
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 834
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 317
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 802
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2598
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2122
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 141
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
population: South Asian
population: East Asian
population: African
reference allele: C
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum

13-114535473-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114535473
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 114535473
    reference: chr 13
allele count: 5
allele frequency: 4.414075604286951e-5
allele num: 113274
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000416498
  ensembl transcript: ENST00000450766
  gene symbol: GAS6
  hgvsc: ENST00000450766.1:c.135-12G>A
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000349962
  ensembl transcript: ENST00000357389
  gene symbol: GAS6
  hgvsc: ENST00000357389.3:c.1083-12G>A
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183087
  ensembl transcript: ENST00000480426
  gene symbol: GAS6
  hgvsc: ENST00000480426.1:n.1109-12G>A
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183087
  ensembl transcript: ENST00000610073
  gene symbol: GAS6
  hgvsc: ENST00000610073.1:n.774-12G>A
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000400117
  ensembl transcript: ENST00000418959
  gene symbol: GAS6
  hgvsc: ENST00000418959.3:c.57-12G>A
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000331831
  ensembl transcript: ENST00000327773
  gene symbol: GAS6
  hgvsc: ENST00000327773.6:c.954-12G>A
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000233695
  ensembl transcript: ENST00000458001
  gene symbol: GAS6-AS1
  hgvsc: ENST00000458001.1:n.63-992C>T
  variant of: http://identifiers.org/hgnc/39826
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000348003
  ensembl transcript: ENST00000355761
  gene symbol: GAS6
  hgvsc: ENST00000355761.4:c.792-12G>A
  variant of: http://identifiers.org/hgnc/4168
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2701
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 908
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2809
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 815
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 812
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5220
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11640
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34941
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3099
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 283
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 784
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2123
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 787
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3583
  bin: 2.25e1
  variant carriers: 1
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
population: Latino
population: East Asian
reference allele: C
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: DP

13-114535478-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114535478
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 114535478
    reference: chr 13
allele count: 5
allele frequency: 4.416102877532635e-5
allele num: 113222
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183087
  ensembl transcript: ENST00000610073
  gene symbol: GAS6
  hgvsc: ENST00000610073.1:n.774-17C>G
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000400117
  ensembl transcript: ENST00000418959
  gene symbol: GAS6
  hgvsc: ENST00000418959.3:c.57-17C>G
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183087
  ensembl transcript: ENST00000480426
  gene symbol: GAS6
  hgvsc: ENST00000480426.1:n.1109-17C>G
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000348003
  ensembl transcript: ENST00000355761
  gene symbol: GAS6
  hgvsc: ENST00000355761.4:c.792-17C>G
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000349962
  ensembl transcript: ENST00000357389
  gene symbol: GAS6
  hgvsc: ENST00000357389.3:c.1083-17C>G
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000233695
  ensembl transcript: ENST00000458001
  gene symbol: GAS6-AS1
  hgvsc: ENST00000458001.1:n.63-987G>C
  variant of: http://identifiers.org/hgnc/39826
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000331831
  ensembl transcript: ENST00000327773
  gene symbol: GAS6
  hgvsc: ENST00000327773.6:c.954-17C>G
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000416498
  ensembl transcript: ENST00000450766
  gene symbol: GAS6
  hgvsc: ENST00000450766.1:c.135-17C>G
  variant of: http://identifiers.org/hgnc/4168
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2761
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 946
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 812
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 827
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2731
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11610
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34927
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5225
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 935
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 309
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35831
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 772
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 336
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6857
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: DP

http://identifiers.org/exac.variant/13-114535480-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114535480
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 114535480
    reference: chr 13
allele count: 8
allele frequency: 7.067762169802986e-5
allele num: 113190
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183087
  ensembl transcript: ENST00000610073
  gene symbol: GAS6
  hgvsc: ENST00000610073.1:n.774-19T>G
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000233695
  ensembl transcript: ENST00000458001
  gene symbol: GAS6-AS1
  hgvsc: ENST00000458001.1:n.63-985A>C
  variant of: http://identifiers.org/hgnc/39826
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000416498
  ensembl transcript: ENST00000450766
  gene symbol: GAS6
  hgvsc: ENST00000450766.1:c.135-19T>G
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000400117
  ensembl transcript: ENST00000418959
  gene symbol: GAS6
  hgvsc: ENST00000418959.3:c.57-19T>G
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000331831
  ensembl transcript: ENST00000327773
  gene symbol: GAS6
  hgvsc: ENST00000327773.6:c.954-19T>G
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183087
  ensembl transcript: ENST00000480426
  gene symbol: GAS6
  hgvsc: ENST00000480426.1:n.1109-19T>G
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000349962
  ensembl transcript: ENST00000357389
  gene symbol: GAS6
  hgvsc: ENST00000357389.3:c.1083-19T>G
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000348003
  ensembl transcript: ENST00000355761
  gene symbol: GAS6
  hgvsc: ENST00000355761.4:c.792-19T>G
  variant of: http://identifiers.org/hgnc/4168
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 953
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2772
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5226
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11615
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 823
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34922
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 815
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2711
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 851
  bin: 9.75e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 784
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 99
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 354
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 99
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2608
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: African
population: South Asian
population: Latino
reference allele: A
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum

http://identifiers.org/exac.variant/13-114535487-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114535487
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 114535487
    reference: chr 13
allele count: 1
allele frequency: 8.863205289560917e-6
allele num: 112826
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183087
  ensembl transcript: ENST00000610073
  gene symbol: GAS6
  hgvsc: ENST00000610073.1:n.774-26G>T
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000416498
  ensembl transcript: ENST00000450766
  gene symbol: GAS6
  hgvsc: ENST00000450766.1:c.135-26G>T
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183087
  ensembl transcript: ENST00000480426
  gene symbol: GAS6
  hgvsc: ENST00000480426.1:n.1109-26G>T
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000400117
  ensembl transcript: ENST00000418959
  gene symbol: GAS6
  hgvsc: ENST00000418959.3:c.57-26G>T
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000349962
  ensembl transcript: ENST00000357389
  gene symbol: GAS6
  hgvsc: ENST00000357389.3:c.1083-26G>T
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000331831
  ensembl transcript: ENST00000327773
  gene symbol: GAS6
  hgvsc: ENST00000327773.6:c.954-26G>T
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000348003
  ensembl transcript: ENST00000355761
  gene symbol: GAS6
  hgvsc: ENST00000355761.4:c.792-26G>T
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000233695
  ensembl transcript: ENST00000458001
  gene symbol: GAS6-AS1
  hgvsc: ENST00000458001.1:n.63-978C>A
  variant of: http://identifiers.org/hgnc/39826
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2831
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 903
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5229
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2623
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 956
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 813
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11606
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34851
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2607
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 356
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 111
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 784
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2126
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 344
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3258
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 200
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
reference allele: C
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: DP

13-114535492-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114535492
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 114535492
    reference: chr 13
allele count: 1
allele frequency: 8.860692197274451e-6
allele num: 112858
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000416498
  ensembl transcript: ENST00000450766
  gene symbol: GAS6
  hgvsc: ENST00000450766.1:c.135-31G>A
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000348003
  ensembl transcript: ENST00000355761
  gene symbol: GAS6
  hgvsc: ENST00000355761.4:c.792-31G>A
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000400117
  ensembl transcript: ENST00000418959
  gene symbol: GAS6
  hgvsc: ENST00000418959.3:c.57-31G>A
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000349962
  ensembl transcript: ENST00000357389
  gene symbol: GAS6
  hgvsc: ENST00000357389.3:c.1083-31G>A
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183087
  ensembl transcript: ENST00000480426
  gene symbol: GAS6
  hgvsc: ENST00000480426.1:n.1109-31G>A
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183087
  ensembl transcript: ENST00000610073
  gene symbol: GAS6
  hgvsc: ENST00000610073.1:n.774-31G>A
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000233695
  ensembl transcript: ENST00000458001
  gene symbol: GAS6-AS1
  hgvsc: ENST00000458001.1:n.63-973C>T
  variant of: http://identifiers.org/hgnc/39826
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000331831
  ensembl transcript: ENST00000327773
  gene symbol: GAS6
  hgvsc: ENST00000327773.6:c.954-31G>A
  variant of: http://identifiers.org/hgnc/4168
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 816
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34852
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 934
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2841
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5232
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11606
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2573
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 952
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 773
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 120
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 197
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2611
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2126
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 347
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 850
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 934
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
population: Other
population: South Asian
reference allele: C
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum

13-114535496-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114535496
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 114535496
    reference: chr 13
allele count: 1
allele frequency: 8.856768342367236e-6
allele num: 112908
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000416498
  ensembl transcript: ENST00000450766
  gene symbol: GAS6
  hgvsc: ENST00000450766.1:c.135-35C>T
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000348003
  ensembl transcript: ENST00000355761
  gene symbol: GAS6
  hgvsc: ENST00000355761.4:c.792-35C>T
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000349962
  ensembl transcript: ENST00000357389
  gene symbol: GAS6
  hgvsc: ENST00000357389.3:c.1083-35C>T
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183087
  ensembl transcript: ENST00000610073
  gene symbol: GAS6
  hgvsc: ENST00000610073.1:n.774-35C>T
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000233695
  ensembl transcript: ENST00000458001
  gene symbol: GAS6-AS1
  hgvsc: ENST00000458001.1:n.63-969G>A
  variant of: http://identifiers.org/hgnc/39826
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183087
  ensembl transcript: ENST00000480426
  gene symbol: GAS6
  hgvsc: ENST00000480426.1:n.1109-35C>T
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000400117
  ensembl transcript: ENST00000418959
  gene symbol: GAS6
  hgvsc: ENST00000418959.3:c.57-35C>T
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000331831
  ensembl transcript: ENST00000327773
  gene symbol: GAS6
  hgvsc: ENST00000327773.6:c.954-35C>T
  variant of: http://identifiers.org/hgnc/4168
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 976
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11596
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2859
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34796
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 831
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2562
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5238
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 943
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 340
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 421
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 418
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6838
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 906
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3325
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 785
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: European (Finnish)
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

13-114535497-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114535497
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 114535497
    reference: chr 13
allele count: 1
allele frequency: 8.863833785388856e-6
allele num: 112818
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000416498
  ensembl transcript: ENST00000450766
  gene symbol: GAS6
  hgvsc: ENST00000450766.1:c.135-36G>A
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183087
  ensembl transcript: ENST00000480426
  gene symbol: GAS6
  hgvsc: ENST00000480426.1:n.1109-36G>A
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000331831
  ensembl transcript: ENST00000327773
  gene symbol: GAS6
  hgvsc: ENST00000327773.6:c.954-36G>A
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183087
  ensembl transcript: ENST00000610073
  gene symbol: GAS6
  hgvsc: ENST00000610073.1:n.774-36G>A
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000349962
  ensembl transcript: ENST00000357389
  gene symbol: GAS6
  hgvsc: ENST00000357389.3:c.1083-36G>A
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000233695
  ensembl transcript: ENST00000458001
  gene symbol: GAS6-AS1
  hgvsc: ENST00000458001.1:n.63-968C>T
  variant of: http://identifiers.org/hgnc/39826
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000400117
  ensembl transcript: ENST00000418959
  gene symbol: GAS6
  hgvsc: ENST00000418959.3:c.57-36G>A
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000348003
  ensembl transcript: ENST00000355761
  gene symbol: GAS6
  hgvsc: ENST00000355761.4:c.792-36G>A
  variant of: http://identifiers.org/hgnc/4168
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 34794
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2566
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11600
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 935
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5234
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 994
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2850
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 826
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2601
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 805
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6847
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 415
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 774
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2128
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35601
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
population: South Asian
population: Latino
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/13-114535499-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114535499
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 114535499
    reference: chr 13
allele count: 1
allele frequency: 8.862733976176972e-6
allele num: 112832
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183087
  ensembl transcript: ENST00000610073
  gene symbol: GAS6
  hgvsc: ENST00000610073.1:n.774-38G>T
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000348003
  ensembl transcript: ENST00000355761
  gene symbol: GAS6
  hgvsc: ENST00000355761.4:c.792-38G>T
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183087
  ensembl transcript: ENST00000480426
  gene symbol: GAS6
  hgvsc: ENST00000480426.1:n.1109-38G>T
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000416498
  ensembl transcript: ENST00000450766
  gene symbol: GAS6
  hgvsc: ENST00000450766.1:c.135-38G>T
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000400117
  ensembl transcript: ENST00000418959
  gene symbol: GAS6
  hgvsc: ENST00000418959.3:c.57-38G>T
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000233695
  ensembl transcript: ENST00000458001
  gene symbol: GAS6-AS1
  hgvsc: ENST00000458001.1:n.63-966C>A
  variant of: http://identifiers.org/hgnc/39826
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000349962
  ensembl transcript: ENST00000357389
  gene symbol: GAS6
  hgvsc: ENST00000357389.3:c.1083-38G>T
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000331831
  ensembl transcript: ENST00000327773
  gene symbol: GAS6
  hgvsc: ENST00000327773.6:c.954-38G>T
  variant of: http://identifiers.org/hgnc/4168
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5238
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34760
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 924
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 826
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1041
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2867
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2547
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11595
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3201
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 151
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 346
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 500
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 826
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6849
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 449
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 888
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: African
reference allele: C
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: ClippingRankSum

http://identifiers.org/exac.variant/13-114535503-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114535503
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 114535503
    reference: chr 13
allele count: 16
allele frequency: 1.418439716312057e-4
allele num: 112800
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000416498
  ensembl transcript: ENST00000450766
  gene symbol: GAS6
  hgvsc: ENST00000450766.1:c.135-42G>T
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000349962
  ensembl transcript: ENST00000357389
  gene symbol: GAS6
  hgvsc: ENST00000357389.3:c.1083-42G>T
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183087
  ensembl transcript: ENST00000480426
  gene symbol: GAS6
  hgvsc: ENST00000480426.1:n.1109-42G>T
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183087
  ensembl transcript: ENST00000610073
  gene symbol: GAS6
  hgvsc: ENST00000610073.1:n.774-42G>T
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000233695
  ensembl transcript: ENST00000458001
  gene symbol: GAS6-AS1
  hgvsc: ENST00000458001.1:n.63-962C>A
  variant of: http://identifiers.org/hgnc/39826
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000348003
  ensembl transcript: ENST00000355761
  gene symbol: GAS6
  hgvsc: ENST00000355761.4:c.792-42G>T
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000331831
  ensembl transcript: ENST00000327773
  gene symbol: GAS6
  hgvsc: ENST00000327773.6:c.954-42G>T
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000400117
  ensembl transcript: ENST00000418959
  gene symbol: GAS6
  hgvsc: ENST00000418959.3:c.57-42G>T
  variant of: http://identifiers.org/hgnc/4168
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 832
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 11572
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2517
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 5.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 34761
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1055
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5257
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 898
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2891
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2599
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 102
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 340
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 216
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2138
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 195
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35262
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 468
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: South Asian
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ

http://identifiers.org/exac.variant/13-114535511-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114535511
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 114535511
    reference: chr 13
allele count: 2
allele frequency: 1.769754888947881e-5
allele num: 113010
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000400117
  ensembl transcript: ENST00000418959
  gene symbol: GAS6
  hgvsc: ENST00000418959.3:c.57-50G>T
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000349962
  ensembl transcript: ENST00000357389
  gene symbol: GAS6
  hgvsc: ENST00000357389.3:c.1083-50G>T
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000416498
  ensembl transcript: ENST00000450766
  gene symbol: GAS6
  hgvsc: ENST00000450766.1:c.135-50G>T
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183087
  ensembl transcript: ENST00000610073
  gene symbol: GAS6
  hgvsc: ENST00000610073.1:n.774-50G>T
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183087
  ensembl transcript: ENST00000480426
  gene symbol: GAS6
  hgvsc: ENST00000480426.1:n.1109-50G>T
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000348003
  ensembl transcript: ENST00000355761
  gene symbol: GAS6
  hgvsc: ENST00000355761.4:c.792-50G>T
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000331831
  ensembl transcript: ENST00000327773
  gene symbol: GAS6
  hgvsc: ENST00000327773.6:c.954-50G>T
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000233695
  ensembl transcript: ENST00000458001
  gene symbol: GAS6-AS1
  hgvsc: ENST00000458001.1:n.63-954C>A
  variant of: http://identifiers.org/hgnc/39826
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 816
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2867
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1044
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5313
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2516
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 856
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11600
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34756
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 811
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 752
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 765
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 234
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2610
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6840
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 397
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum

13-114535511-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114535511
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 114535511
    reference: chr 13
allele count: 1
allele frequency: 8.848774444739404e-6
allele num: 113010
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183087
  ensembl transcript: ENST00000480426
  gene symbol: GAS6
  hgvsc: ENST00000480426.1:n.1109-50G>A
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000400117
  ensembl transcript: ENST00000418959
  gene symbol: GAS6
  hgvsc: ENST00000418959.3:c.57-50G>A
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000416498
  ensembl transcript: ENST00000450766
  gene symbol: GAS6
  hgvsc: ENST00000450766.1:c.135-50G>A
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000233695
  ensembl transcript: ENST00000458001
  gene symbol: GAS6-AS1
  hgvsc: ENST00000458001.1:n.63-954C>T
  variant of: http://identifiers.org/hgnc/39826
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000331831
  ensembl transcript: ENST00000327773
  gene symbol: GAS6
  hgvsc: ENST00000327773.6:c.954-50G>A
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000349962
  ensembl transcript: ENST00000357389
  gene symbol: GAS6
  hgvsc: ENST00000357389.3:c.1083-50G>A
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000348003
  ensembl transcript: ENST00000355761
  gene symbol: GAS6
  hgvsc: ENST00000355761.4:c.792-50G>A
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183087
  ensembl transcript: ENST00000610073
  gene symbol: GAS6
  hgvsc: ENST00000610073.1:n.774-50G>A
  variant of: http://identifiers.org/hgnc/4168
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1044
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11600
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34756
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2867
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 816
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5313
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2516
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 856
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 752
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 791
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 397
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3190
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35023
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 309
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3131
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 234
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: South Asian
population: Latino
reference allele: C
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD

13-114535562-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114535562
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 114535562
    reference: chr 13
allele count: 1
allele frequency: 8.370302167908262e-6
allele num: 119470
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000348003
  ensembl transcript: ENST00000355761
  gene symbol: GAS6
  hgvsc: ENST00000355761.4:c.791+45G>A
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000400117
  ensembl transcript: ENST00000418959
  gene symbol: GAS6
  hgvsc: ENST00000418959.3:c.56+45G>A
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000349962
  ensembl transcript: ENST00000357389
  gene symbol: GAS6
  hgvsc: ENST00000357389.3:c.1082+45G>A
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000416498
  ensembl transcript: ENST00000450766
  gene symbol: GAS6
  hgvsc: ENST00000450766.1:c.134+45G>A
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000331831
  ensembl transcript: ENST00000327773
  gene symbol: GAS6
  hgvsc: ENST00000327773.6:c.953+45G>A
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183087
  ensembl transcript: ENST00000610073
  gene symbol: GAS6
  hgvsc: ENST00000610073.1:n.773+45G>A
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000233695
  ensembl transcript: ENST00000458001
  gene symbol: GAS6-AS1
  hgvsc: ENST00000458001.1:n.63-903C>T
  variant of: http://identifiers.org/hgnc/39826
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183087
  ensembl transcript: ENST00000480426
  gene symbol: GAS6
  hgvsc: ENST00000480426.1:n.1108+45G>A
  variant of: http://identifiers.org/hgnc/4168
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7371
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18506
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5020
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1270
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24886
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 812
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 906
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 452
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 320
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 980
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 531
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 351
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 126
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 331
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
population: Latino
population: Other
reference allele: C
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum

13-114535570-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114535570
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 114535570
    reference: chr 13
allele count: 1
allele frequency: 8.365820603342981e-6
allele num: 119534
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000233695
  ensembl transcript: ENST00000458001
  gene symbol: GAS6-AS1
  hgvsc: ENST00000458001.1:n.63-895T>G
  variant of: http://identifiers.org/hgnc/39826
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000331831
  ensembl transcript: ENST00000327773
  gene symbol: GAS6
  hgvsc: ENST00000327773.6:c.953+37A>C
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000349962
  ensembl transcript: ENST00000357389
  gene symbol: GAS6
  hgvsc: ENST00000357389.3:c.1082+37A>C
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183087
  ensembl transcript: ENST00000610073
  gene symbol: GAS6
  hgvsc: ENST00000610073.1:n.773+37A>C
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000400117
  ensembl transcript: ENST00000418959
  gene symbol: GAS6
  hgvsc: ENST00000418959.3:c.56+37A>C
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000416498
  ensembl transcript: ENST00000450766
  gene symbol: GAS6
  hgvsc: ENST00000450766.1:c.134+37A>C
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183087
  ensembl transcript: ENST00000480426
  gene symbol: GAS6
  hgvsc: ENST00000480426.1:n.1108+37A>C
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000348003
  ensembl transcript: ENST00000355761
  gene symbol: GAS6
  hgvsc: ENST00000355761.4:c.791+37A>C
  variant of: http://identifiers.org/hgnc/4168
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7942
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 901
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25108
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5015
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18562
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 203
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 145
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 182
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 354
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1560
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 337
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
population: Other
population: European (Finnish)
population: Latino
reference allele: T
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP

13-114535576-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114535576
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 114535576
    reference: chr 13
allele count: 3
allele frequency: 2.509452270217821e-5
allele num: 119548
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000348003
  ensembl transcript: ENST00000355761
  gene symbol: GAS6
  hgvsc: ENST00000355761.4:c.791+31C>T
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183087
  ensembl transcript: ENST00000610073
  gene symbol: GAS6
  hgvsc: ENST00000610073.1:n.773+31C>T
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183087
  ensembl transcript: ENST00000480426
  gene symbol: GAS6
  hgvsc: ENST00000480426.1:n.1108+31C>T
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000331831
  ensembl transcript: ENST00000327773
  gene symbol: GAS6
  hgvsc: ENST00000327773.6:c.953+31C>T
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000349962
  ensembl transcript: ENST00000357389
  gene symbol: GAS6
  hgvsc: ENST00000357389.3:c.1082+31C>T
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000400117
  ensembl transcript: ENST00000418959
  gene symbol: GAS6
  hgvsc: ENST00000418959.3:c.56+31C>T
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000233695
  ensembl transcript: ENST00000458001
  gene symbol: GAS6-AS1
  hgvsc: ENST00000458001.1:n.63-889G>A
  variant of: http://identifiers.org/hgnc/39826
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000416498
  ensembl transcript: ENST00000450766
  gene symbol: GAS6
  hgvsc: ENST00000450766.1:c.134+31C>T
  variant of: http://identifiers.org/hgnc/4168
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8218
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18594
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 899
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5021
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25246
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 213
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 100
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 527
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2025
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 317
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 370
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
population: African
population: Other
reference allele: G
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum

13-114535577-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114535577
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 114535577
    reference: chr 13
allele count: 6
allele frequency: 5.01898850651632e-5
allele num: 119546
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000416498
  ensembl transcript: ENST00000450766
  gene symbol: GAS6
  hgvsc: ENST00000450766.1:c.134+30A>G
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183087
  ensembl transcript: ENST00000480426
  gene symbol: GAS6
  hgvsc: ENST00000480426.1:n.1108+30A>G
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000400117
  ensembl transcript: ENST00000418959
  gene symbol: GAS6
  hgvsc: ENST00000418959.3:c.56+30A>G
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000233695
  ensembl transcript: ENST00000458001
  gene symbol: GAS6-AS1
  hgvsc: ENST00000458001.1:n.63-888T>C
  variant of: http://identifiers.org/hgnc/39826
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183087
  ensembl transcript: ENST00000610073
  gene symbol: GAS6
  hgvsc: ENST00000610073.1:n.773+30A>G
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000331831
  ensembl transcript: ENST00000327773
  gene symbol: GAS6
  hgvsc: ENST00000327773.6:c.953+30A>G
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000349962
  ensembl transcript: ENST00000357389
  gene symbol: GAS6
  hgvsc: ENST00000357389.3:c.1082+30A>G
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000348003
  ensembl transcript: ENST00000355761
  gene symbol: GAS6
  hgvsc: ENST00000355761.4:c.791+30A>G
  variant of: http://identifiers.org/hgnc/4168
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 900
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25259
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8232
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18595
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5022
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 135
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 211
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 313
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1556
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43202
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: Other
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum

13-114535587-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114535587
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 114535587
    reference: chr 13
allele count: 2
allele frequency: 1.671989165510208e-5
allele num: 119618
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000349962
  ensembl transcript: ENST00000357389
  gene symbol: GAS6
  hgvsc: ENST00000357389.3:c.1082+20A>G
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183087
  ensembl transcript: ENST00000480426
  gene symbol: GAS6
  hgvsc: ENST00000480426.1:n.1108+20A>G
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000331831
  ensembl transcript: ENST00000327773
  gene symbol: GAS6
  hgvsc: ENST00000327773.6:c.953+20A>G
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183087
  ensembl transcript: ENST00000610073
  gene symbol: GAS6
  hgvsc: ENST00000610073.1:n.773+20A>G
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000400117
  ensembl transcript: ENST00000418959
  gene symbol: GAS6
  hgvsc: ENST00000418959.3:c.56+20A>G
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000416498
  ensembl transcript: ENST00000450766
  gene symbol: GAS6
  hgvsc: ENST00000450766.1:c.134+20A>G
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000233695
  ensembl transcript: ENST00000458001
  gene symbol: GAS6-AS1
  hgvsc: ENST00000458001.1:n.63-878T>C
  variant of: http://identifiers.org/hgnc/39826
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000348003
  ensembl transcript: ENST00000355761
  gene symbol: GAS6
  hgvsc: ENST00000355761.4:c.791+20A>G
  variant of: http://identifiers.org/hgnc/4168
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18642
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5023
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8361
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 898
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25485
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 140
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 519
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 368
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 277
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43683
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum

13-114535592-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114535592
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 114535592
    reference: chr 13
allele count: 1
allele frequency: 8.357011532675915e-6
allele num: 119660
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183087
  ensembl transcript: ENST00000610073
  gene symbol: GAS6
  hgvsc: ENST00000610073.1:n.773+15A>C
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000348003
  ensembl transcript: ENST00000355761
  gene symbol: GAS6
  hgvsc: ENST00000355761.4:c.791+15A>C
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000400117
  ensembl transcript: ENST00000418959
  gene symbol: GAS6
  hgvsc: ENST00000418959.3:c.56+15A>C
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000349962
  ensembl transcript: ENST00000357389
  gene symbol: GAS6
  hgvsc: ENST00000357389.3:c.1082+15A>C
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183087
  ensembl transcript: ENST00000480426
  gene symbol: GAS6
  hgvsc: ENST00000480426.1:n.1108+15A>C
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000416498
  ensembl transcript: ENST00000450766
  gene symbol: GAS6
  hgvsc: ENST00000450766.1:c.134+15A>C
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000331831
  ensembl transcript: ENST00000327773
  gene symbol: GAS6
  hgvsc: ENST00000327773.6:c.953+15A>C
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000233695
  ensembl transcript: ENST00000458001
  gene symbol: GAS6-AS1
  hgvsc: ENST00000458001.1:n.63-873T>G
  variant of: http://identifiers.org/hgnc/39826
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8409
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 899
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18657
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25548
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5027
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2028
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 957
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
reference allele: T
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: ReadPosRankSum

13-114535614-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114535614
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 114535614
    reference: chr 13
allele count: 3
allele frequency: 2.505637684790779e-5
allele num: 119730
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183087
  ensembl transcript: ENST00000480426
  gene symbol: GAS6
  hgvsc: ENST00000480426.1:n.1101C>G
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000233695
  ensembl transcript: ENST00000458001
  gene symbol: GAS6-AS1
  hgvsc: ENST00000458001.1:n.63-851G>C
  variant of: http://identifiers.org/hgnc/39826
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000416498
  ensembl transcript: ENST00000450766
  gene symbol: GAS6
  hgvsc: ENST00000450766.1:c.127C>G
  hgvsp: ENSP00000416498.1:p.Pro43Ala
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000349962
  ensembl transcript: ENST00000357389
  gene symbol: GAS6
  hgvsc: ENST00000357389.3:c.1075C>G
  hgvsp: ENSP00000349962.3:p.Pro359Ala
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000331831
  ensembl transcript: ENST00000327773
  gene symbol: GAS6
  hgvsc: ENST00000327773.6:c.946C>G
  hgvsp: ENSP00000331831.6:p.Pro316Ala
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000348003
  ensembl transcript: ENST00000355761
  gene symbol: GAS6
  hgvsc: ENST00000355761.4:c.784C>G
  hgvsp: ENSP00000348003.4:p.Pro262Ala
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183087
  ensembl transcript: ENST00000610073
  gene symbol: GAS6
  hgvsc: ENST00000610073.1:n.766C>G
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000400117
  ensembl transcript: ENST00000418959
  gene symbol: GAS6
  hgvsc: ENST00000418959.3:c.49C>G
  hgvsp: ENSP00000400117.3:p.Pro17Ala
  variant of: http://identifiers.org/hgnc/4168
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8347
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25719
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 900
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18706
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5031
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10319
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43998
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Pro316Ala
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: QD

13-114535616-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114535616
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 114535616
    reference: chr 13
allele count: 1
allele frequency: 8.351567589236499e-6
allele num: 119738
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000349962
  ensembl transcript: ENST00000357389
  gene symbol: GAS6
  hgvsc: ENST00000357389.3:c.1073A>G
  hgvsp: ENSP00000349962.3:p.Gln358Arg
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000233695
  ensembl transcript: ENST00000458001
  gene symbol: GAS6-AS1
  hgvsc: ENST00000458001.1:n.63-849T>C
  variant of: http://identifiers.org/hgnc/39826
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000416498
  ensembl transcript: ENST00000450766
  gene symbol: GAS6
  hgvsc: ENST00000450766.1:c.125A>G
  hgvsp: ENSP00000416498.1:p.Gln42Arg
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000331831
  ensembl transcript: ENST00000327773
  gene symbol: GAS6
  hgvsc: ENST00000327773.6:c.944A>G
  hgvsp: ENSP00000331831.6:p.Gln315Arg
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000348003
  ensembl transcript: ENST00000355761
  gene symbol: GAS6
  hgvsc: ENST00000355761.4:c.782A>G
  hgvsp: ENSP00000348003.4:p.Gln261Arg
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183087
  ensembl transcript: ENST00000610073
  gene symbol: GAS6
  hgvsc: ENST00000610073.1:n.764A>G
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183087
  ensembl transcript: ENST00000480426
  gene symbol: GAS6
  hgvsc: ENST00000480426.1:n.1099A>G
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000400117
  ensembl transcript: ENST00000418959
  gene symbol: GAS6
  hgvsc: ENST00000418959.3:c.47A>G
  hgvsp: ENSP00000400117.3:p.Gln16Arg
  variant of: http://identifiers.org/hgnc/4168
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25726
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 900
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8337
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5031
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18716
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 118
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 229
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 518
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Gln315Arg
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
population: Latino
population: European (Finnish)
reference allele: T
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: QD

13-114535628-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114535628
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 114535628
    reference: chr 13
allele count: 1
allele frequency: 8.350312301680083e-6
allele num: 119756
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000349962
  ensembl transcript: ENST00000357389
  gene symbol: GAS6
  hgvsc: ENST00000357389.3:c.1061T>C
  hgvsp: ENSP00000349962.3:p.Phe354Ser
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000233695
  ensembl transcript: ENST00000458001
  gene symbol: GAS6-AS1
  hgvsc: ENST00000458001.1:n.63-837A>G
  variant of: http://identifiers.org/hgnc/39826
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183087
  ensembl transcript: ENST00000610073
  gene symbol: GAS6
  hgvsc: ENST00000610073.1:n.752T>C
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000348003
  ensembl transcript: ENST00000355761
  gene symbol: GAS6
  hgvsc: ENST00000355761.4:c.770T>C
  hgvsp: ENSP00000348003.4:p.Phe257Ser
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000416498
  ensembl transcript: ENST00000450766
  gene symbol: GAS6
  hgvsc: ENST00000450766.1:c.113T>C
  hgvsp: ENSP00000416498.1:p.Phe38Ser
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000331831
  ensembl transcript: ENST00000327773
  gene symbol: GAS6
  hgvsc: ENST00000327773.6:c.932T>C
  hgvsp: ENSP00000331831.6:p.Phe311Ser
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183087
  ensembl transcript: ENST00000480426
  gene symbol: GAS6
  hgvsc: ENST00000480426.1:n.1087T>C
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000400117
  ensembl transcript: ENST00000418959
  gene symbol: GAS6
  hgvsc: ENST00000418959.3:c.35T>C
  hgvsp: ENSP00000400117.3:p.Phe12Ser
  variant of: http://identifiers.org/hgnc/4168
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 900
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18718
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5031
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8345
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25742
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 358
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 252
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Phe311Ser
num of homozygotes: 0
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
population: East Asian
reference allele: A
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ

13-114535631-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114535631
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 114535631
    reference: chr 13
allele count: 2
allele frequency: 1.670062460336017e-5
allele num: 119756
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000400117
  ensembl transcript: ENST00000418959
  gene symbol: GAS6
  hgvsc: ENST00000418959.3:c.32G>A
  hgvsp: ENSP00000400117.3:p.Arg11His
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000348003
  ensembl transcript: ENST00000355761
  gene symbol: GAS6
  hgvsc: ENST00000355761.4:c.767G>A
  hgvsp: ENSP00000348003.4:p.Arg256His
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183087
  ensembl transcript: ENST00000480426
  gene symbol: GAS6
  hgvsc: ENST00000480426.1:n.1084G>A
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000416498
  ensembl transcript: ENST00000450766
  gene symbol: GAS6
  hgvsc: ENST00000450766.1:c.110G>A
  hgvsp: ENSP00000416498.1:p.Arg37His
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000331831
  ensembl transcript: ENST00000327773
  gene symbol: GAS6
  hgvsc: ENST00000327773.6:c.929G>A
  hgvsp: ENSP00000331831.6:p.Arg310His
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000233695
  ensembl transcript: ENST00000458001
  gene symbol: GAS6-AS1
  hgvsc: ENST00000458001.1:n.63-834C>T
  variant of: http://identifiers.org/hgnc/39826
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000349962
  ensembl transcript: ENST00000357389
  gene symbol: GAS6
  hgvsc: ENST00000357389.3:c.1058G>A
  hgvsp: ENSP00000349962.3:p.Arg353His
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183087
  ensembl transcript: ENST00000610073
  gene symbol: GAS6
  hgvsc: ENST00000610073.1:n.749G>A
  variant of: http://identifiers.org/hgnc/4168
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8341
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 900
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18720
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25744
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5030
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10336
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2026
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 350
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Arg310His
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ

13-114535632-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114535632
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 114535632
    reference: chr 13
allele count: 3
allele frequency: 2.505093690504025e-5
allele num: 119756
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000349962
  ensembl transcript: ENST00000357389
  gene symbol: GAS6
  hgvsc: ENST00000357389.3:c.1057C>T
  hgvsp: ENSP00000349962.3:p.Arg353Cys
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000233695
  ensembl transcript: ENST00000458001
  gene symbol: GAS6-AS1
  hgvsc: ENST00000458001.1:n.63-833G>A
  variant of: http://identifiers.org/hgnc/39826
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183087
  ensembl transcript: ENST00000610073
  gene symbol: GAS6
  hgvsc: ENST00000610073.1:n.748C>T
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000400117
  ensembl transcript: ENST00000418959
  gene symbol: GAS6
  hgvsc: ENST00000418959.3:c.31C>T
  hgvsp: ENSP00000400117.3:p.Arg11Cys
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000416498
  ensembl transcript: ENST00000450766
  gene symbol: GAS6
  hgvsc: ENST00000450766.1:c.109C>T
  hgvsp: ENSP00000416498.1:p.Arg37Cys
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000348003
  ensembl transcript: ENST00000355761
  gene symbol: GAS6
  hgvsc: ENST00000355761.4:c.766C>T
  hgvsp: ENSP00000348003.4:p.Arg256Cys
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000331831
  ensembl transcript: ENST00000327773
  gene symbol: GAS6
  hgvsc: ENST00000327773.6:c.928C>T
  hgvsp: ENSP00000331831.6:p.Arg310Cys
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183087
  ensembl transcript: ENST00000480426
  gene symbol: GAS6
  hgvsc: ENST00000480426.1:n.1083C>T
  variant of: http://identifiers.org/hgnc/4168
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 901
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18725
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5032
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8330
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25748
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 136
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1553
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 950
  bin: 9.75e1
  variant carriers: 3
hgvs: p.Arg310Cys
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
reference allele: G
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP

http://identifiers.org/exac.variant/13-114535637-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114535637
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 114535637
    reference: chr 13
allele count: 1
allele frequency: 8.350591221858508e-6
allele num: 119752
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000233695
  ensembl transcript: ENST00000458001
  gene symbol: GAS6-AS1
  hgvsc: ENST00000458001.1:n.63-828C>A
  variant of: http://identifiers.org/hgnc/39826
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000416498
  ensembl transcript: ENST00000450766
  gene symbol: GAS6
  hgvsc: ENST00000450766.1:c.104G>T
  hgvsp: ENSP00000416498.1:p.Arg35Leu
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000400117
  ensembl transcript: ENST00000418959
  gene symbol: GAS6
  hgvsc: ENST00000418959.3:c.26G>T
  hgvsp: ENSP00000400117.3:p.Arg9Leu
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000331831
  ensembl transcript: ENST00000327773
  gene symbol: GAS6
  hgvsc: ENST00000327773.6:c.923G>T
  hgvsp: ENSP00000331831.6:p.Arg308Leu
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000349962
  ensembl transcript: ENST00000357389
  gene symbol: GAS6
  hgvsc: ENST00000357389.3:c.1052G>T
  hgvsp: ENSP00000349962.3:p.Arg351Leu
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000348003
  ensembl transcript: ENST00000355761
  gene symbol: GAS6
  hgvsc: ENST00000355761.4:c.761G>T
  hgvsp: ENSP00000348003.4:p.Arg254Leu
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183087
  ensembl transcript: ENST00000480426
  gene symbol: GAS6
  hgvsc: ENST00000480426.1:n.1078G>T
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183087
  ensembl transcript: ENST00000610073
  gene symbol: GAS6
  hgvsc: ENST00000610073.1:n.743G>T
  variant of: http://identifiers.org/hgnc/4168
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5031
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 900
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25747
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18732
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8333
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 252
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 516
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 135
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44042
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Arg308Leu
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
population: Other
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: ReadPosRankSum

13-114535637-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114535637
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 114535637
    reference: chr 13
allele count: 7
allele frequency: 5.845413855300955e-5
allele num: 119752
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000349962
  ensembl transcript: ENST00000357389
  gene symbol: GAS6
  hgvsc: ENST00000357389.3:c.1052G>A
  hgvsp: ENSP00000349962.3:p.Arg351Gln
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000233695
  ensembl transcript: ENST00000458001
  gene symbol: GAS6-AS1
  hgvsc: ENST00000458001.1:n.63-828C>T
  variant of: http://identifiers.org/hgnc/39826
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183087
  ensembl transcript: ENST00000610073
  gene symbol: GAS6
  hgvsc: ENST00000610073.1:n.743G>A
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000400117
  ensembl transcript: ENST00000418959
  gene symbol: GAS6
  hgvsc: ENST00000418959.3:c.26G>A
  hgvsp: ENSP00000400117.3:p.Arg9Gln
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000348003
  ensembl transcript: ENST00000355761
  gene symbol: GAS6
  hgvsc: ENST00000355761.4:c.761G>A
  hgvsp: ENSP00000348003.4:p.Arg254Gln
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000331831
  ensembl transcript: ENST00000327773
  gene symbol: GAS6
  hgvsc: ENST00000327773.6:c.923G>A
  hgvsp: ENSP00000331831.6:p.Arg308Gln
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000416498
  ensembl transcript: ENST00000450766
  gene symbol: GAS6
  hgvsc: ENST00000450766.1:c.104G>A
  hgvsp: ENSP00000416498.1:p.Arg35Gln
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183087
  ensembl transcript: ENST00000480426
  gene symbol: GAS6
  hgvsc: ENST00000480426.1:n.1078G>A
  variant of: http://identifiers.org/hgnc/4168
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 900
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8333
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25747
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5031
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18732
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 516
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 353
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 118
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Arg308Gln
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ

http://identifiers.org/exac.variant/13-114535640-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114535640
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 114535640
    reference: chr 13
allele count: 1
allele frequency: 8.351288603831571e-6
allele num: 119742
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000331831
  ensembl transcript: ENST00000327773
  gene symbol: GAS6
  hgvsc: ENST00000327773.6:c.920T>G
  hgvsp: ENSP00000331831.6:p.Ile307Ser
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000416498
  ensembl transcript: ENST00000450766
  gene symbol: GAS6
  hgvsc: ENST00000450766.1:c.101T>G
  hgvsp: ENSP00000416498.1:p.Ile34Ser
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183087
  ensembl transcript: ENST00000480426
  gene symbol: GAS6
  hgvsc: ENST00000480426.1:n.1075T>G
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000400117
  ensembl transcript: ENST00000418959
  gene symbol: GAS6
  hgvsc: ENST00000418959.3:c.23T>G
  hgvsp: ENSP00000400117.3:p.Ile8Ser
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000349962
  ensembl transcript: ENST00000357389
  gene symbol: GAS6
  hgvsc: ENST00000357389.3:c.1049T>G
  hgvsp: ENSP00000349962.3:p.Ile350Ser
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000348003
  ensembl transcript: ENST00000355761
  gene symbol: GAS6
  hgvsc: ENST00000355761.4:c.758T>G
  hgvsp: ENSP00000348003.4:p.Ile253Ser
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183087
  ensembl transcript: ENST00000610073
  gene symbol: GAS6
  hgvsc: ENST00000610073.1:n.740T>G
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000233695
  ensembl transcript: ENST00000458001
  gene symbol: GAS6-AS1
  hgvsc: ENST00000458001.1:n.63-825A>C
  variant of: http://identifiers.org/hgnc/39826
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 899
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25768
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5032
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18725
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8327
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2030
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 338
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 255
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Ile307Ser
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
reference allele: A
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum

13-114535644-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114535644
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 114535644
    reference: chr 13
allele count: 1
allele frequency: 8.351428094204109e-6
allele num: 119740
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183087
  ensembl transcript: ENST00000480426
  gene symbol: GAS6
  hgvsc: ENST00000480426.1:n.1071G>A
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000348003
  ensembl transcript: ENST00000355761
  gene symbol: GAS6
  hgvsc: ENST00000355761.4:c.754G>A
  hgvsp: ENSP00000348003.4:p.Val252Met
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000349962
  ensembl transcript: ENST00000357389
  gene symbol: GAS6
  hgvsc: ENST00000357389.3:c.1045G>A
  hgvsp: ENSP00000349962.3:p.Val349Met
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000233695
  ensembl transcript: ENST00000458001
  gene symbol: GAS6-AS1
  hgvsc: ENST00000458001.1:n.63-821C>T
  variant of: http://identifiers.org/hgnc/39826
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000331831
  ensembl transcript: ENST00000327773
  gene symbol: GAS6
  hgvsc: ENST00000327773.6:c.916G>A
  hgvsp: ENSP00000331831.6:p.Val306Met
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000400117
  ensembl transcript: ENST00000418959
  gene symbol: GAS6
  hgvsc: ENST00000418959.3:c.19G>A
  hgvsp: ENSP00000400117.3:p.Val7Met
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183087
  ensembl transcript: ENST00000610073
  gene symbol: GAS6
  hgvsc: ENST00000610073.1:n.736G>A
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000416498
  ensembl transcript: ENST00000450766
  gene symbol: GAS6
  hgvsc: ENST00000450766.1:c.97G>A
  hgvsp: ENSP00000416498.1:p.Val33Met
  variant of: http://identifiers.org/hgnc/4168
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25773
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8326
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5033
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18725
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 899
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 341
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1555
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44071
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Val306Met
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: QD

13-114535645-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114535645
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 114535645
    reference: chr 13
allele count: 1
allele frequency: 8.352265134304423e-6
allele num: 119728
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000349962
  ensembl transcript: ENST00000357389
  gene symbol: GAS6
  hgvsc: ENST00000357389.3:c.1044C>T
  hgvsp: ENST00000357389.3:c.1044C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000331831
  ensembl transcript: ENST00000327773
  gene symbol: GAS6
  hgvsc: ENST00000327773.6:c.915C>T
  hgvsp: ENST00000327773.6:c.915C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183087
  ensembl transcript: ENST00000480426
  gene symbol: GAS6
  hgvsc: ENST00000480426.1:n.1070C>T
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000348003
  ensembl transcript: ENST00000355761
  gene symbol: GAS6
  hgvsc: ENST00000355761.4:c.753C>T
  hgvsp: ENST00000355761.4:c.753C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183087
  ensembl transcript: ENST00000610073
  gene symbol: GAS6
  hgvsc: ENST00000610073.1:n.735C>T
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000416498
  ensembl transcript: ENST00000450766
  gene symbol: GAS6
  hgvsc: ENST00000450766.1:c.96C>T
  hgvsp: ENST00000450766.1:c.96C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000400117
  ensembl transcript: ENST00000418959
  gene symbol: GAS6
  hgvsc: ENST00000418959.3:c.18C>T
  hgvsp: ENST00000418959.3:c.18C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000233695
  ensembl transcript: ENST00000458001
  gene symbol: GAS6-AS1
  hgvsc: ENST00000458001.1:n.63-820G>A
  variant of: http://identifiers.org/hgnc/39826
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8332
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5033
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 899
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18728
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25763
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 135
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 343
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Pro305Pro
num of homozygotes: 0
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: DP

13-114535647-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114535647
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 114535647
    reference: chr 13
allele count: 1
allele frequency: 8.351707088928977e-6
allele num: 119736
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000348003
  ensembl transcript: ENST00000355761
  gene symbol: GAS6
  hgvsc: ENST00000355761.4:c.751C>T
  hgvsp: ENSP00000348003.4:p.Pro251Ser
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183087
  ensembl transcript: ENST00000610073
  gene symbol: GAS6
  hgvsc: ENST00000610073.1:n.733C>T
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000349962
  ensembl transcript: ENST00000357389
  gene symbol: GAS6
  hgvsc: ENST00000357389.3:c.1042C>T
  hgvsp: ENSP00000349962.3:p.Pro348Ser
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000233695
  ensembl transcript: ENST00000458001
  gene symbol: GAS6-AS1
  hgvsc: ENST00000458001.1:n.63-818G>A
  variant of: http://identifiers.org/hgnc/39826
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000331831
  ensembl transcript: ENST00000327773
  gene symbol: GAS6
  hgvsc: ENST00000327773.6:c.913C>T
  hgvsp: ENSP00000331831.6:p.Pro305Ser
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000416498
  ensembl transcript: ENST00000450766
  gene symbol: GAS6
  hgvsc: ENST00000450766.1:c.94C>T
  hgvsp: ENSP00000416498.1:p.Pro32Ser
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000400117
  ensembl transcript: ENST00000418959
  gene symbol: GAS6
  hgvsc: ENST00000418959.3:c.16C>T
  hgvsp: ENSP00000400117.3:p.Pro6Ser
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183087
  ensembl transcript: ENST00000480426
  gene symbol: GAS6
  hgvsc: ENST00000480426.1:n.1068C>T
  variant of: http://identifiers.org/hgnc/4168
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18726
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5033
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8337
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25764
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 900
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 942
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 339
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 116
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Pro305Ser
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum

13-114535652-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114535652
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 114535652
    reference: chr 13
allele count: 2
allele frequency: 1.670257720766314e-5
allele num: 119742
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000416498
  ensembl transcript: ENST00000450766
  gene symbol: GAS6
  hgvsc: ENST00000450766.1:c.89G>A
  hgvsp: ENSP00000416498.1:p.Gly30Glu
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000349962
  ensembl transcript: ENST00000357389
  gene symbol: GAS6
  hgvsc: ENST00000357389.3:c.1037G>A
  hgvsp: ENSP00000349962.3:p.Gly346Glu
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000233695
  ensembl transcript: ENST00000458001
  gene symbol: GAS6-AS1
  hgvsc: ENST00000458001.1:n.63-813C>T
  variant of: http://identifiers.org/hgnc/39826
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183087
  ensembl transcript: ENST00000480426
  gene symbol: GAS6
  hgvsc: ENST00000480426.1:n.1063G>A
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000348003
  ensembl transcript: ENST00000355761
  gene symbol: GAS6
  hgvsc: ENST00000355761.4:c.746G>A
  hgvsp: ENSP00000348003.4:p.Gly249Glu
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183087
  ensembl transcript: ENST00000610073
  gene symbol: GAS6
  hgvsc: ENST00000610073.1:n.728G>A
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000400117
  ensembl transcript: ENST00000418959
  gene symbol: GAS6
  hgvsc: ENST00000418959.3:c.11G>A
  hgvsp: ENSP00000400117.3:p.Gly4Glu
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000331831
  ensembl transcript: ENST00000327773
  gene symbol: GAS6
  hgvsc: ENST00000327773.6:c.908G>A
  hgvsp: ENSP00000331831.6:p.Gly303Glu
  variant of: http://identifiers.org/hgnc/4168
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18721
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5033
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 899
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25764
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8351
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 347
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 514
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 116
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1555
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Gly303Glu
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: QD

13-114535654-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114535654
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 114535654
    reference: chr 13
allele count: 1
allele frequency: 8.351846593281774e-6
allele num: 119734
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000348003
  ensembl transcript: ENST00000355761
  gene symbol: GAS6
  hgvsc: ENST00000355761.4:c.744T>C
  hgvsp: ENST00000355761.4:c.744T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000233695
  ensembl transcript: ENST00000458001
  gene symbol: GAS6-AS1
  hgvsc: ENST00000458001.1:n.63-811A>G
  variant of: http://identifiers.org/hgnc/39826
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183087
  ensembl transcript: ENST00000480426
  gene symbol: GAS6
  hgvsc: ENST00000480426.1:n.1061T>C
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000400117
  ensembl transcript: ENST00000418959
  gene symbol: GAS6
  hgvsc: ENST00000418959.3:c.9T>C
  hgvsp: ENST00000418959.3:c.9T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183087
  ensembl transcript: ENST00000610073
  gene symbol: GAS6
  hgvsc: ENST00000610073.1:n.726T>C
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000349962
  ensembl transcript: ENST00000357389
  gene symbol: GAS6
  hgvsc: ENST00000357389.3:c.1035T>C
  hgvsp: ENST00000357389.3:c.1035T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000331831
  ensembl transcript: ENST00000327773
  gene symbol: GAS6
  hgvsc: ENST00000327773.6:c.906T>C
  hgvsp: ENST00000327773.6:c.906T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000416498
  ensembl transcript: ENST00000450766
  gene symbol: GAS6
  hgvsc: ENST00000450766.1:c.87T>C
  hgvsp: ENST00000450766.1:c.87T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4168
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18722
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8347
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5032
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25769
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 898
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 515
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 135
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1555
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 344
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Ser302Ser
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
reference allele: A
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum

13-114535665-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114535665
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 114535665
    reference: chr 13
allele count: 7
allele frequency: 5.847953216374269e-5
allele num: 119700
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000331831
  ensembl transcript: ENST00000327773
  gene symbol: GAS6
  hgvsc: ENST00000327773.6:c.895C>T
  hgvsp: ENSP00000331831.6:p.Arg299Trp
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183087
  ensembl transcript: ENST00000610073
  gene symbol: GAS6
  hgvsc: ENST00000610073.1:n.715C>T
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000416498
  ensembl transcript: ENST00000450766
  gene symbol: GAS6
  hgvsc: ENST00000450766.1:c.76C>T
  hgvsp: ENSP00000416498.1:p.Arg26Trp
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000348003
  ensembl transcript: ENST00000355761
  gene symbol: GAS6
  hgvsc: ENST00000355761.4:c.733C>T
  hgvsp: ENSP00000348003.4:p.Arg245Trp
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000400117
  ensembl transcript: ENST00000418959
  gene symbol: GAS6
  hgvsc: ENST00000418959.3:c.-3C>T
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000349962
  ensembl transcript: ENST00000357389
  gene symbol: GAS6
  hgvsc: ENST00000357389.3:c.1024C>T
  hgvsp: ENSP00000349962.3:p.Arg342Trp
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183087
  ensembl transcript: ENST00000480426
  gene symbol: GAS6
  hgvsc: ENST00000480426.1:n.1050C>T
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000233695
  ensembl transcript: ENST00000458001
  gene symbol: GAS6-AS1
  hgvsc: ENST00000458001.1:n.63-800G>A
  variant of: http://identifiers.org/hgnc/39826
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5033
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18725
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 898
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25771
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8325
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 333
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 273
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 937
  bin: 9.75e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Arg299Trp
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
population: South Asian
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ

13-114535667-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 114535667
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 114535667
    reference: chr 13
allele count: 1
allele frequency: 8.354498061756449e-6
allele num: 119696
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000416498
  ensembl transcript: ENST00000450766
  gene symbol: GAS6
  hgvsc: ENST00000450766.1:c.74G>C
  hgvsp: ENSP00000416498.1:p.Gly25Ala
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000331831
  ensembl transcript: ENST00000327773
  gene symbol: GAS6
  hgvsc: ENST00000327773.6:c.893G>C
  hgvsp: ENSP00000331831.6:p.Gly298Ala
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000348003
  ensembl transcript: ENST00000355761
  gene symbol: GAS6
  hgvsc: ENST00000355761.4:c.731G>C
  hgvsp: ENSP00000348003.4:p.Gly244Ala
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000349962
  ensembl transcript: ENST00000357389
  gene symbol: GAS6
  hgvsc: ENST00000357389.3:c.1022G>C
  hgvsp: ENSP00000349962.3:p.Gly341Ala
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000183087
  ensembl protein: ENSP00000400117
  ensembl transcript: ENST00000418959
  gene symbol: GAS6
  hgvsc: ENST00000418959.3:c.-5G>C
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000233695
  ensembl transcript: ENST00000458001
  gene symbol: GAS6-AS1
  hgvsc: ENST00000458001.1:n.63-798C>G
  variant of: http://identifiers.org/hgnc/39826
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183087
  ensembl transcript: ENST00000480426
  gene symbol: GAS6
  hgvsc: ENST00000480426.1:n.1048G>C
  variant of: http://identifiers.org/hgnc/4168
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183087
  ensembl transcript: ENST00000610073
  gene symbol: GAS6
  hgvsc: ENST00000610073.1:n.713G>C
  variant of: http://identifiers.org/hgnc/4168
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25771
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 898
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8329
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18722
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Gly298Ala
num of homozygotes: 0
reference allele: C

GenotypeQuality
all individuals: 1442
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 367
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 914
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1633
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4898
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1022
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 729
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 359
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 296
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 7579
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 240
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 488
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 391
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 178
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36333
bin: 6.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7782
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 726
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.729146493290912e-5
allele num: 57832
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15278
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4464
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10392
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8038
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.318e1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.41e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.37e-1

FS
type: SiteQuality
SIO_000300: 9.787000000000001e0

VQSLOD
type: SiteQuality
SIO_000300: -4.241e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.71e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.413e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.7e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.213085e6

GenotypeQuality
all individuals: 7303
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 403
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 500
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36603
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1461
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4924
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1644
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1030
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 176
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 300
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1348
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 362
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 307
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 373
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 708
bin: 3.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10428
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8094
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 732
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7816
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.527415143603133e-5
allele num: 15320
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 58122
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4496
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 6.8e0

VQSLOD
type: SiteQuality
SIO_000300: -4.652e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.34e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.34e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.404e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.221392e6

ClippingRankSum
type: SiteQuality
SIO_000300: 2.0e-1

GenotypeQuality
all individuals: 1963
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 631
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 631
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 373
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 79
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 544
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1513
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 475
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3893
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 537
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2248
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39174
bin: 6.25e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 9.038322487346348e-5
allele num: 11064
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.107665042091272e-4
allele num: 9028
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.241701244813278e-5
allele num: 61696
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.216249087813184e-4
allele num: 8222
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5308
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 786
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16068
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.11e-1

MQRankSum
type: SiteQuality
SIO_000300: -7.7e-2

MQ
type: SiteQuality
SIO_000300: 5.944e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

DP
type: SiteQuality
SIO_000300: 1.320594e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.532e0

FS
type: SiteQuality
SIO_000300: 9.057e0

VQSLOD
type: SiteQuality
SIO_000300: -1.12e0

QD
type: SiteQuality
SIO_000300: 8.029999999999999e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.64e-1

GenotypeQuality
all individuals: 1540
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 99
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3767
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 352
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 594
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39671
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2000
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 598
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 182
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6005
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 432
bin: 9.75e1
variant carriers: 6

GenotypeQuality
all individuals: 341
bin: 3.75e1
variant carriers: 0

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

Latino
type: Population
allele count: 1
allele frequency: 9.022013713460844e-5
allele num: 11084
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.101806963420009e-4
allele num: 9076
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5334
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 796
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.241619071268935e-4
allele num: 16108
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8240
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.233629749393695e-5
allele num: 61850
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.764e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.7e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.2e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.98e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.15e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.08e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.96e0

MQ
type: SiteQuality
SIO_000300: 5.948e1

QD
type: SiteQuality
SIO_000300: 1.114e1

DP
type: SiteQuality
SIO_000300: 1.326894e6

GenotypeQuality
all individuals: 557
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 575
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 350
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39594
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2372
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 597
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 160
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1617
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6107
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 455
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 2062
bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62128
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5442
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8272
num of homozygotes: 0

African
type: Population
allele count: 3
allele frequency: 3.275824415811312e-4
allele num: 9158
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16150
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11142
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.246882793017456e-3
allele num: 802
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.22e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.23e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.04e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.4e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 2.16e-1

FS
type: SiteQuality
SIO_000300: 6.523e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.3e-3

DP
type: SiteQuality
SIO_000300: 1.334786e6

QD
type: SiteQuality
SIO_000300: 1.305e1

MQ
type: SiteQuality
SIO_000300: 5.893e1

GenotypeQuality
all individuals: 585
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 191
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39764
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1634
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 545
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 106
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 312
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2071
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 574
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 462
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 6129
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 281
bin: 4.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9202
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 798
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5476
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8282
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 2.688653880623768e-4
allele num: 11158
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16174
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.607096940087426e-5
allele num: 62224
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.1e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 5.610000000000001e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.0e-2

MQ
type: SiteQuality
SIO_000300: 5.931e1

MQRankSum
type: SiteQuality
SIO_000300: -1.23e-1

QD
type: SiteQuality
SIO_000300: 1.006e1

VQSLOD
type: SiteQuality
SIO_000300: -1.737e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.28e0

FS
type: SiteQuality
SIO_000300: 1.295e1

DP
type: SiteQuality
SIO_000300: 1.339066e6

GenotypeQuality
all individuals: 3098
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 561
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 527
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1679
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 185
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 337
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39871
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 589
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 562
bin: 9.75e1
variant carriers: 97

GenotypeQuality
all individuals: 52
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 260
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 587
bin: 9.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 810
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5634
num of homozygotes: 0

African
type: Population
allele count: 92
allele frequency: 9.877603607472621e-3
allele num: 9314
num of homozygotes: 0

Latino
type: Population
allele count: 5
allele frequency: 4.462691895751518e-4
allele num: 11204
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16228
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62576
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8314
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.7e-3

VQSLOD
type: SiteQuality
SIO_000300: 3.29e0

MQRankSum
type: SiteQuality
SIO_000300: 2.9e-1

MQ
type: SiteQuality
SIO_000300: 5.95e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.31e-1

DP
type: SiteQuality
SIO_000300: 1.349767e6

QD
type: SiteQuality
SIO_000300: 1.233e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.182e0

FS
type: SiteQuality
SIO_000300: 1.147e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.7e-2

GenotypeQuality
all individuals: 1709
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 529
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 131
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2951
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 497
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 607
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2178
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39059
bin: 6.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 54

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5722
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.067691650651292e-4
allele num: 9366
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 50
allele frequency: 7.971176226764022e-4
allele num: 62726
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 816
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.230920728705071e-4
allele num: 16248
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8328
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.901548869503294e-5
allele num: 11234
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.967e1

FS
type: SiteQuality
SIO_000300: 5.42e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.900000000000001e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.98e-1

QD
type: SiteQuality
SIO_000300: 1.232e1

VQSLOD
type: SiteQuality
SIO_000300: 3.69e0

DP
type: SiteQuality
SIO_000300: 1.356726e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.231e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.2e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.35e-1

GenotypeQuality
all individuals: 509
bin: 3.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5822
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62956
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16272
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9446
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.197604790419162e-4
allele num: 8350
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 6.03e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.06e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

QD
type: SiteQuality
SIO_000300: 1.471e1

DP
type: SiteQuality
SIO_000300: 1.365273e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 7.29e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.03e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.312e-1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11270
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63058
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5838
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.195314367678699e-4
allele num: 8366
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.140243153628883e-5
allele num: 16286
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9468
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 2.898e1

MQ
type: SiteQuality
SIO_000300: 5.95e1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.367804e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.18e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.119e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -4.74e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.2e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.379999999999999e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5910
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9540
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.137981831573779e-5
allele num: 16292
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63174
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 826
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11282
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8384
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.951e1

QD
type: SiteQuality
SIO_000300: 8.59e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -4.48e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.17e-1

FS
type: SiteQuality
SIO_000300: 7.408e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.23e0

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.371041e6

VQSLOD
type: SiteQuality
SIO_000300: -2.766e-1

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

GenotypeQuality
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.140243153628883e-5
allele num: 16286
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11292
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5942
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 828
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8394
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9572
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.582278481012658e-5
allele num: 63200
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 6.8e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.373391e6

BaseQRankSum
type: SiteQuality
SIO_000300: 2.08e0

FS
type: SiteQuality
SIO_000300: 7.088e0

QD
type: SiteQuality
SIO_000300: 1.311e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 1.07e0

MQRankSum
type: SiteQuality
SIO_000300: 6.81e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.49e-1

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 570
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variant carriers: 1

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11298
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16288
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9602
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.191043353978085e-4
allele num: 8396
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 830
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63270
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5976
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.135e1

VQSLOD
type: SiteQuality
SIO_000300: -2.369e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.209e0

ReadPosRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: -1.302e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.968e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.04e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.5e-3

DP
type: SiteQuality
SIO_000300: 1.37531e6

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 830
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5998
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16288
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9606
num of homozygotes: 0

East Asian
type: Population
allele count: 5
allele frequency: 5.9509640561771e-4
allele num: 8402
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11302
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63308
num of homozygotes: 0

DP
type: SiteQuality
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QD
type: SiteQuality
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MQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: 1.91e0

MQ
type: SiteQuality
SIO_000300: 5.925e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -4.26e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 26

GenotypeQuality
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variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 838
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9630
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11320
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63402
num of homozygotes: 0

South Asian
type: Population
allele count: 26
allele frequency: 1.595287765369984e-3
allele num: 16298
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6066
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.158e1

ReadPosRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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MQRankSum
type: SiteQuality
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FS
type: SiteQuality
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VQSLOD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.959e1

DP
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11320
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8416
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.154474622251664e-5
allele num: 63402
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 838
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6078
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 8.88e-1

BaseQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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MQRankSum
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FS
type: SiteQuality
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QD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

DP
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
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GenotypeQuality
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bin: 5.75e1
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GenotypeQuality
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bin: 8.75e1
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GenotypeQuality
all individuals: 1939
bin: 8.25e1
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GenotypeQuality
all individuals: 379
bin: 3.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8470
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 842
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11380
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9760
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6254
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16320
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 9.408812921436413e-5
allele num: 63770
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -5.15e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.79e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.39e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.428e0

DP
type: SiteQuality
SIO_000300: 1.395555e6

VQSLOD
type: SiteQuality
SIO_000300: -6.457000000000001e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.4e-3

MQ
type: SiteQuality
SIO_000300: 5.917e1

QD
type: SiteQuality
SIO_000300: 1.255e1

FS
type: SiteQuality
SIO_000300: 8.349e0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1958
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GenotypeQuality
all individuals: 637
bin: 9.75e1
variant carriers: 2

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11380
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6266
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9794
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.566759627737912e-5
allele num: 63826
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 844
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.127450980392157e-5
allele num: 16320
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.41e0

VQSLOD
type: SiteQuality
SIO_000300: 2.24e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.6e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.22e-1

FS
type: SiteQuality
SIO_000300: 5.371e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.4e-3

QD
type: SiteQuality
SIO_000300: 1.296e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.05e-1

DP
type: SiteQuality
SIO_000300: 1.398553e6

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 94

GenotypeQuality
all individuals: 1973
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 5
allele frequency: 4.390586582367404e-4
allele num: 11388
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6296
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16334
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8492
num of homozygotes: 0

African
type: Population
allele count: 90
allele frequency: 9.16310323762981e-3
allele num: 9822
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63938
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.17e-1

MQRankSum
type: SiteQuality
SIO_000300: 8.1e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -2.395e0

VQSLOD
type: SiteQuality
SIO_000300: 3.52e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.69e-1

MQ
type: SiteQuality
SIO_000300: 5.955e1

FS
type: SiteQuality
SIO_000300: 1.127e0

DP
type: SiteQuality
SIO_000300: 1.403686e6

QD
type: SiteQuality
SIO_000300: 1.358e1

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 2016
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GenotypeQuality
all individuals: 737
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variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.561426519268003e-5
allele num: 64044
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: 11410
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9856
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8500
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.12369871402327e-5
allele num: 16330
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 848
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 5.32e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.01e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.08e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.7e-2

QD
type: SiteQuality
SIO_000300: 9.75e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.6e-3

MQ
type: SiteQuality
SIO_000300: 5.946e1

DP
type: SiteQuality
SIO_000300: 1.407755e6

VQSLOD
type: SiteQuality
SIO_000300: 1.48e0

GenotypeQuality
all individuals: 748
bin: 8.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 37
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GenotypeQuality
all individuals: 748
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11430
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9894
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.558749259594102e-5
allele num: 64154
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 860
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16334
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6376
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.23e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.84e0

VQSLOD
type: SiteQuality
SIO_000300: -1.697e0

DP
type: SiteQuality
SIO_000300: 1.411792e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.1e-3

MQRankSum
type: SiteQuality
SIO_000300: -1.79e0

QD
type: SiteQuality
SIO_000300: 1.618e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.303e0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 712
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 310
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GenotypeQuality
all individuals: 360
bin: 2.75e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 1.008471157724889e-4
allele num: 9916
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16332
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6390
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64186
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11436
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8516
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: 1.74e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.91e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.254e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.41291e6

MQRankSum
type: SiteQuality
SIO_000300: 1.03e0

QD
type: SiteQuality
SIO_000300: 4.49e0

FS
type: SiteQuality
SIO_000300: 2.972e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.72e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-3

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 762
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GenotypeQuality
all individuals: 746
bin: 9.75e1
variant carriers: 17

African
type: Population
allele count: 16
allele frequency: 1.603206412825651e-3
allele num: 9980
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 866
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11476
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64432
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6456
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.170686022008897e-4
allele num: 8542
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16260
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.96e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

MQ
type: SiteQuality
SIO_000300: 5.984e1

MQRankSum
type: SiteQuality
SIO_000300: 9.3e-2

DP
type: SiteQuality
SIO_000300: 1.422917e6

BaseQRankSum
type: SiteQuality
SIO_000300: -3.32e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.92e-1

FS
type: SiteQuality
SIO_000300: 1.857e0

VQSLOD
type: SiteQuality
SIO_000300: 3.78e0

QD
type: SiteQuality
SIO_000300: 1.349e1

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1288
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 63
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GenotypeQuality
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GenotypeQuality
all individuals: 767
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 40377
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GenotypeQuality
all individuals: 77
bin: 5.75e1
variant carriers: 0

Latino
type: Population
allele count: 4
allele frequency: 3.483106931382794e-4
allele num: 11484
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6464
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8542
num of homozygotes: 0

South Asian
type: Population
allele count: 6
allele frequency: 3.691399040236249e-4
allele num: 16254
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9994
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.654482266422565e-5
allele num: 64454
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.07e-1

MQRankSum
type: SiteQuality
SIO_000300: -7.000000000000001e-2

MQ
type: SiteQuality
SIO_000300: 5.969e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.2e0

DP
type: SiteQuality
SIO_000300: 1.424556e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.6e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 6.1e-2

FS
type: SiteQuality
SIO_000300: 1.127e0

QD
type: SiteQuality
SIO_000300: 1.305e1

VQSLOD
type: SiteQuality
SIO_000300: 3.33e0

GenotypeQuality
all individuals: 31
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 103
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GenotypeQuality
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GenotypeQuality
all individuals: 333
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GenotypeQuality
all individuals: 34
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GenotypeQuality
all individuals: 2084
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GenotypeQuality
all individuals: 77
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GenotypeQuality
all individuals: 1288
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 63
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GenotypeQuality
all individuals: 767
bin: 8.75e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11484
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6464
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9994
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16254
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8542
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.102988177615043e-5
allele num: 64454
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 3.33e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.2e0

MQRankSum
type: SiteQuality
SIO_000300: -7.000000000000001e-2

MQ
type: SiteQuality
SIO_000300: 5.969e1

DP
type: SiteQuality
SIO_000300: 1.424556e6

ClippingRankSum
type: SiteQuality
SIO_000300: 6.1e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.6e-3

FS
type: SiteQuality
SIO_000300: 1.127e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.07e-1

QD
type: SiteQuality
SIO_000300: 1.305e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 13

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16128
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11502
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10038
num of homozygotes: 0

East Asian
type: Population
allele count: 13
allele frequency: 1.517273576097106e-3
allele num: 8568
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 872
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6520
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 64544
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.157e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.34e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.4282e6

MQRankSum
type: SiteQuality
SIO_000300: -9.7e-2

VQSLOD
type: SiteQuality
SIO_000300: 3.33e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.36e-1

MQ
type: SiteQuality
SIO_000300: 5.948e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.8e-3

QD
type: SiteQuality
SIO_000300: 1.204e1

GenotypeQuality
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variant carriers: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10038
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64476
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.310740880979428e-5
allele num: 15846
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11510
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6546
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8574
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.97e1

QD
type: SiteQuality
SIO_000300: 1.073e1

FS
type: SiteQuality
SIO_000300: 7.531e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.1e-3

VQSLOD
type: SiteQuality
SIO_000300: 3.5e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.56e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -8.8e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.56e-1

DP
type: SiteQuality
SIO_000300: 1.422836e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.98e-1

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6556
num of homozygotes: 0

South Asian
type: Population
allele count: 4
allele frequency: 2.547121752419766e-4
allele num: 15704
num of homozygotes: 0

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

African
type: Population
allele count: 21
allele frequency: 2.088720907101651e-3
allele num: 10054
num of homozygotes: 0

Latino
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allele count: 2
allele frequency: 1.737619461337967e-4
allele num: 11510
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8574
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.103854987894966e-5
allele num: 64436
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 3.73e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.952e1

MQRankSum
type: SiteQuality
SIO_000300: 4.21e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.42e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.27e-1

DP
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SIO_000300: 1.421293e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.88e0

QD
type: SiteQuality
SIO_000300: 1.337e1

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8574
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64346
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11508
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15314
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.946290033817386e-5
allele num: 10054
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 866
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.411949e6

VQSLOD
type: SiteQuality
SIO_000300: -2.406e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 3.8e-2

MQ
type: SiteQuality
SIO_000300: 5.866e1

QD
type: SiteQuality
SIO_000300: 1.263e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.669999999999999e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.701e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.43e-1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11502
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 9.346667912889055e-5
allele num: 64194
num of homozygotes: 0

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15026
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 3.47e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.6e-2

FS
type: SiteQuality
SIO_000300: 5.064e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.03e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

BaseQRankSum
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SIO_000300: 2.47e0

MQ
type: SiteQuality
SIO_000300: 5.969e1

QD
type: SiteQuality
SIO_000300: 1.145e1

DP
type: SiteQuality
SIO_000300: 1.401805e6

VQSLOD
type: SiteQuality
SIO_000300: 2.26e0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6590
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.561719140429785e-5
allele num: 64032
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10038
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14650
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11502
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.003e1

BaseQRankSum
type: SiteQuality
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InbreedingCoeff
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ClippingRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 8.25e-1

MQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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DP
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.953e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 866
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63990
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11498
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.854009595613433e-5
allele num: 14590
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

ClippingRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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MQRankSum
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DP
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 8.832000000000001e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.45e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 3.7e-2

QD
type: SiteQuality
SIO_000300: 1.061e1

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

East Asian
type: Population
allele count: 1
allele frequency: 1.167406023815083e-4
allele num: 8566
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10020
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63814
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
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BaseQRankSum
type: SiteQuality
SIO_000300: -1.679e0

QD
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: -3.62e-1

ClippingRankSum
type: SiteQuality
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DP
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 2.256e0

VQSLOD
type: SiteQuality
SIO_000300: -1.289e0

MQ
type: SiteQuality
SIO_000300: 5.921e1

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10026
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63794
num of homozygotes: 0

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

South Asian
type: Population
allele count: 2
allele frequency: 1.433691756272401e-4
allele num: 13950
num of homozygotes: 0

East Asian
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allele count: 1
allele frequency: 1.167406023815083e-4
allele num: 8566
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.59e-1

MQ
type: SiteQuality
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MQRankSum
type: SiteQuality
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DP
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: 6.19e-1

FS
type: SiteQuality
SIO_000300: 5.172e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.1e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 9.76e-1

QD
type: SiteQuality
SIO_000300: 1.302e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.7e-2

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35922
bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 800
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variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 783
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2122
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 8.695652173913044e-5
allele num: 11500
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13256
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6600
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8562
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9990
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63518
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 840
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.7e-2

DP
type: SiteQuality
SIO_000300: 1.367641e6

MQRankSum
type: SiteQuality
SIO_000300: 4.25e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.2e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.12e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.55e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.9e-3

QD
type: SiteQuality
SIO_000300: 1.142e1

FS
type: SiteQuality
SIO_000300: 6.597e0

MQ
type: SiteQuality
SIO_000300: 5.976e1

GenotypeQuality
all individuals: 6865
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 776
bin: 7.5e0
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 834
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variant carriers: 5

GenotypeQuality
all individuals: 411
bin: 3.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63518
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13256
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11500
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 840
num of homozygotes: 0

African
type: Population
allele count: 5
allele frequency: 5.005005005005005e-4
allele num: 9990
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6600
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8562
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.7e-2

FS
type: SiteQuality
SIO_000300: 6.597e0

QD
type: SiteQuality
SIO_000300: 1.142e1

MQRankSum
type: SiteQuality
SIO_000300: 4.25e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.9e-3

VQSLOD
type: SiteQuality
SIO_000300: 1.55e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.2e0

MQ
type: SiteQuality
SIO_000300: 5.976e1

DP
type: SiteQuality
SIO_000300: 1.367641e6

ClippingRankSum
type: SiteQuality
SIO_000300: 6.12e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 2

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 111
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variant carriers: 0

GenotypeQuality
all individuals: 785
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63316
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6600
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 830
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.562744178777934e-4
allele num: 12798
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9980
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8558
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.7e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -4.59e-1

FS
type: SiteQuality
SIO_000300: 7.35e-1

DP
type: SiteQuality
SIO_000300: 1.363817e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.04e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.94e-1

QD
type: SiteQuality
SIO_000300: 1.269e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-3

VQSLOD
type: SiteQuality
SIO_000300: 8.36e-1

GenotypeQuality
all individuals: 3098
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3540
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2599
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 35814
bin: 6.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8554
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6600
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12694
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11488
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 830
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9980
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.579978512292233e-5
allele num: 63292
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -7.226e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.5e-3

QD
type: SiteQuality
SIO_000300: 1.343e1

DP
type: SiteQuality
SIO_000300: 1.36392e6

ClippingRankSum
type: SiteQuality
SIO_000300: 4.57e-1

MQRankSum
type: SiteQuality
SIO_000300: -6.17e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.805e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.69e-1

FS
type: SiteQuality
SIO_000300: 6.2e0

MQ
type: SiteQuality
SIO_000300: 5.903e1

GenotypeQuality
all individuals: 796
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3098
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3592
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variant carriers: 0

GenotypeQuality
all individuals: 35867
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 88
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variant carriers: 0

GenotypeQuality
all individuals: 6872
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variant carriers: 0

GenotypeQuality
all individuals: 755
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variant carriers: 0

GenotypeQuality
all individuals: 67
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variant carriers: 0

GenotypeQuality
all individuals: 903
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GenotypeQuality
all individuals: 352
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variant carriers: 0

GenotypeQuality
all individuals: 34
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variant carriers: 0

GenotypeQuality
all individuals: 785
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.580378026423921e-5
allele num: 63276
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6602
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 830
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12624
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8552
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9984
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.96e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.2e-3

MQRankSum
type: SiteQuality
SIO_000300: 2.3e-2

FS
type: SiteQuality
SIO_000300: 1.775e0

BaseQRankSum
type: SiteQuality
SIO_000300: 9.23e-1

DP
type: SiteQuality
SIO_000300: 1.363468e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.23e-1

QD
type: SiteQuality
SIO_000300: 9.800000000000001e0

VQSLOD
type: SiteQuality
SIO_000300: 8.42e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.76e0

GenotypeQuality
all individuals: 908
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 802
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variant carriers: 0

GenotypeQuality
all individuals: 839
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variant carriers: 4

GenotypeQuality
all individuals: 332
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variant carriers: 0

GenotypeQuality
all individuals: 151
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variant carriers: 0

GenotypeQuality
all individuals: 62
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variant carriers: 0

GenotypeQuality
all individuals: 91
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variant carriers: 0

GenotypeQuality
all individuals: 345
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variant carriers: 0

GenotypeQuality
all individuals: 35873
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6872
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2600
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 740
bin: 3.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12568
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.580827721394922e-5
allele num: 63258
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6602
num of homozygotes: 0

African
type: Population
allele count: 4
allele frequency: 4.008819402685909e-4
allele num: 9978
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 830
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11486
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8552
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.16e0

MQ
type: SiteQuality
SIO_000300: 5.974e1

VQSLOD
type: SiteQuality
SIO_000300: 9.76e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 4.83e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.44e0

QD
type: SiteQuality
SIO_000300: 1.19e1

FS
type: SiteQuality
SIO_000300: 7.97e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.3e-1

DP
type: SiteQuality
SIO_000300: 1.363179e6

GenotypeQuality
all individuals: 2124
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 85
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variant carriers: 0

GenotypeQuality
all individuals: 3096
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variant carriers: 0

GenotypeQuality
all individuals: 68
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variant carriers: 0

GenotypeQuality
all individuals: 344
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variant carriers: 0

GenotypeQuality
all individuals: 3566
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 56
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variant carriers: 0

GenotypeQuality
all individuals: 843
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 801
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11488
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9982
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63272
num of homozygotes: 0

East Asian
type: Population
allele count: 5
allele frequency: 5.843852267414679e-4
allele num: 8556
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12490
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 832
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6602
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

MQRankSum
type: SiteQuality
SIO_000300: 7.92e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 8.7e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.04e0

MQ
type: SiteQuality
SIO_000300: 5.944e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.23e-1

QD
type: SiteQuality
SIO_000300: 1.315e1

FS
type: SiteQuality
SIO_000300: 2.54e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.64e-1

DP
type: SiteQuality
SIO_000300: 1.362182e6

GenotypeQuality
all individuals: 785
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3096
bin: 7.75e1
variant carriers: 1

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 338
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variant carriers: 0

GenotypeQuality
all individuals: 770
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variant carriers: 0

GenotypeQuality
all individuals: 88
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variant carriers: 0

GenotypeQuality
all individuals: 6863
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variant carriers: 0

GenotypeQuality
all individuals: 801
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variant carriers: 0

GenotypeQuality
all individuals: 2124
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 302
bin: 1.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 830
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63262
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8556
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6602
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9978
num of homozygotes: 0

South Asian
type: Population
allele count: 8
allele frequency: 6.41025641025641e-4
allele num: 12480
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11482
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.362171e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

QD
type: SiteQuality
SIO_000300: 1.237e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.17e-1

MQ
type: SiteQuality
SIO_000300: 5.984e1

FS
type: SiteQuality
SIO_000300: 2.966e0

VQSLOD
type: SiteQuality
SIO_000300: 1.27e0

MQRankSum
type: SiteQuality
SIO_000300: 3.22e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.52e0

GenotypeQuality
all individuals: 116
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 801
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 127
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variant carriers: 0

GenotypeQuality
all individuals: 772
bin: 3.25e1
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GenotypeQuality
all individuals: 495
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variant carriers: 0

GenotypeQuality
all individuals: 3098
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 953
bin: 7.5e0
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GenotypeQuality
all individuals: 849
bin: 9.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 783
bin: 2.75e1
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GenotypeQuality
all individuals: 35644
bin: 6.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9960
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.168497312456181e-4
allele num: 8558
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 826
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63192
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11480
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6602
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12208
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 9.710000000000001e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.22e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -1.039e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.235e0

MQRankSum
type: SiteQuality
SIO_000300: -1.47e-1

FS
type: SiteQuality
SIO_000300: 2.122e0

VQSLOD
type: SiteQuality
SIO_000300: -2.06e-2

DP
type: SiteQuality
SIO_000300: 1.36135e6

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 803
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3098
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9974
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63194
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6602
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.710801393728223e-5
allele num: 11480
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8556
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 826
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12226
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.36179e6

VQSLOD
type: SiteQuality
SIO_000300: 1.18e0

MQRankSum
type: SiteQuality
SIO_000300: -1.33e-1

QD
type: SiteQuality
SIO_000300: 1.504e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.36e-1

MQ
type: SiteQuality
SIO_000300: 5.98e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.414e0

FS
type: SiteQuality
SIO_000300: 1.848e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.78e-1

GenotypeQuality
all individuals: 852
bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 146
bin: 4.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11476
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 826
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6600
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9970
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8558
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12280
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.582328554701098e-5
allele num: 63198
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.504e1

FS
type: SiteQuality
SIO_000300: 3.54e0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.2e-1

MQ
type: SiteQuality
SIO_000300: 5.955e1

VQSLOD
type: SiteQuality
SIO_000300: 4.59e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.158e0

DP
type: SiteQuality
SIO_000300: 1.361948e6

MQRankSum
type: SiteQuality
SIO_000300: 3.35e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.77e-1

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3284
bin: 2.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63162
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: 1
allele frequency: 1.002204850671477e-4
allele num: 9978
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12218
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11482
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6600
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.121e0

VQSLOD
type: SiteQuality
SIO_000300: 1.83e0

MQRankSum
type: SiteQuality
SIO_000300: 4.26e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.13e0

DP
type: SiteQuality
SIO_000300: 1.361995e6

FS
type: SiteQuality
SIO_000300: 4.161e0

QD
type: SiteQuality
SIO_000300: 1.18e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.29e-1

GenotypeQuality
all individuals: 805
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12212
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11486
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8556
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63178
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6602
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 828
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.003009027081244e-4
allele num: 9970
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.642e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.859e0

MQ
type: SiteQuality
SIO_000300: 5.815e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.1e-3

FS
type: SiteQuality
SIO_000300: 1.092e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.96e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.27e0

DP
type: SiteQuality
SIO_000300: 1.361977e6

QD
type: SiteQuality
SIO_000300: 1.133e1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.72e-1

GenotypeQuality
all individuals: 484
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variant carriers: 0

GenotypeQuality
all individuals: 864
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variant carriers: 0

GenotypeQuality
all individuals: 233
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
all individuals: 872
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variant carriers: 16

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 6833
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GenotypeQuality
all individuals: 3113
bin: 7.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 828
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.514692517418964e-4
allele num: 6602
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12190
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8560
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9958
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11488
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 15
allele frequency: 2.374394529395004e-4
allele num: 63174
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.321e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.81e-1

DP
type: SiteQuality
SIO_000300: 1.363297e6

MQRankSum
type: SiteQuality
SIO_000300: 1.27e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.98e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.14e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.991e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

FS
type: SiteQuality
SIO_000300: 5.32e-1

MQ
type: SiteQuality
SIO_000300: 5.962e1

GenotypeQuality
all individuals: 920
bin: 3.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 878
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variant carriers: 2

South Asian
type: Population
allele count: 1
allele frequency: 8.120838070488874e-5
allele num: 12314
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6600
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9958
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8564
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 830
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.58102766798419e-5
allele num: 63250
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 3.73e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.18e-1

FS
type: SiteQuality
SIO_000300: 4.901e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.45e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.18e-1

QD
type: SiteQuality
SIO_000300: 1.356e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.7e-3

DP
type: SiteQuality
SIO_000300: 1.367304e6

ClippingRankSum
type: SiteQuality
SIO_000300: 3.72e-1

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9958
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8564
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 63250
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6600
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 830
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 8.120838070488874e-5
allele num: 12314
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 3.73e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.18e-1

QD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 4.901e0

BaseQRankSum
type: SiteQuality
SIO_000300: 6.45e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.7e-3

DP
type: SiteQuality
SIO_000300: 1.367304e6

ClippingRankSum
type: SiteQuality
SIO_000300: 3.72e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.18e-1

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.532238293699436e-5
allele num: 65264
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16342
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10212
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8610
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: 884
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.08e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.42e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.3e0

ClippingRankSum
type: SiteQuality
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DP
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.948e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.1e-3

QD
type: SiteQuality
SIO_000300: 1.509e1

MQRankSum
type: SiteQuality
SIO_000300: 1.85e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 328
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GenotypeQuality
all individuals: 42709
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GenotypeQuality
all individuals: 123
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 102
bin: 5.75e1
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GenotypeQuality
all individuals: 972
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GenotypeQuality
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GenotypeQuality
all individuals: 88
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variant carriers: 0

GenotypeQuality
all individuals: 10233
bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.531862745098039e-5
allele num: 65280
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16390
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10210
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8610
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 888
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11542
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 5.29e-1

QD
type: SiteQuality
SIO_000300: 1.588e1

MQ
type: SiteQuality
SIO_000300: 5.961e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.7e-3

FS
type: SiteQuality
SIO_000300: 4.54e0

MQRankSum
type: SiteQuality
SIO_000300: 5.87e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.78e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.71e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.36e-1

DP
type: SiteQuality
SIO_000300: 1.757848e6

GenotypeQuality
all individuals: 68
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 203
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 119
bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1554
bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 143
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 139
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43224
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10246
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 971
bin: 9.75e1
variant carriers: 3

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.595588235294118e-5
allele num: 65280
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16402
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11542
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8610
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10212
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 888
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.905e0

DP
type: SiteQuality
SIO_000300: 1.761944e6

BaseQRankSum
type: SiteQuality
SIO_000300: -3.188e0

MQ
type: SiteQuality
SIO_000300: 5.965e1

MQRankSum
type: SiteQuality
SIO_000300: 2.04e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.41e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.6e-3

QD
type: SiteQuality
SIO_000300: 1.275e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.85e-1

GenotypeQuality
all individuals: 64
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 198
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
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GenotypeQuality
all individuals: 74
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 968
bin: 9.75e1
variant carriers: 6

GenotypeQuality
all individuals: 10249
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 119
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2021
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 146
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 108
bin: 4.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 6
allele frequency: 9.071666162685213e-4
allele num: 6614
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11542
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 888
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16404
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10212
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65278
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 5.94e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.42e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.1e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.86e0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.496e1

DP
type: SiteQuality
SIO_000300: 1.762125e6

MQ
type: SiteQuality
SIO_000300: 5.972e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.5e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.4e-2

GenotypeQuality
all individuals: 78
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 120
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2020
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10288
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1562
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 87
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
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variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 119
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 960
bin: 9.75e1
variant carriers: 1

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11542
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16448
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10216
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8610
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.062599534484871e-5
allele num: 65304
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.31e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.7e-2

QD
type: SiteQuality
SIO_000300: 1.315e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.3e-3

FS
type: SiteQuality
SIO_000300: 1.828e0

DP
type: SiteQuality
SIO_000300: 1.766956e6

VQSLOD
type: SiteQuality
SIO_000300: 9.93e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.66e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.37e0

GenotypeQuality
all individuals: 29
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 1.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 90
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43808
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10302
bin: 6.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11540
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10216
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65326
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16472
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.161710037174721e-4
allele num: 8608
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 1.2617e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.4e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.97e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.95e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.563e0

MQRankSum
type: SiteQuality
SIO_000300: 9.12e-1

DP
type: SiteQuality
SIO_000300: 1.768732e6

QD
type: SiteQuality
SIO_000300: 1.148e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.79e-1

GenotypeQuality
all individuals: 362
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 955
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 16
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1555
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 520
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2027
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 118
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 138
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 227
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 2.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 2
allele frequency: 2.322880371660859e-4
allele num: 8610
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11542
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65364
num of homozygotes: 0

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

Other
type: Population
allele count: 1
allele frequency: 1.128668171557562e-3
allele num: 886
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16498
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 4.63e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-3

FS
type: SiteQuality
SIO_000300: 1.152e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.85e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.17e0

MQ
type: SiteQuality
SIO_000300: 5.954e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.0e0

DP
type: SiteQuality
SIO_000300: 1.772027e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.61e-1

QD
type: SiteQuality
SIO_000300: 1.078e1

GenotypeQuality
all individuals: 13
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 139
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10333
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
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variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 349
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variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1557
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variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 953
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2025
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43988
bin: 6.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16500
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65370
num of homozygotes: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.16144018583043e-4
allele num: 8610
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11542
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.898e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.01e0

VQSLOD
type: SiteQuality
SIO_000300: 9.67e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.115e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.45e-1

DP
type: SiteQuality
SIO_000300: 1.771944e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.1e-3

FS
type: SiteQuality
SIO_000300: 1.626e0

MQRankSum
type: SiteQuality
SIO_000300: 1.12e0

QD
type: SiteQuality
SIO_000300: 1.244e1

GenotypeQuality
all individuals: 1553
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 950
bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 138
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10335
bin: 6.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10222
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16504
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65380
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11544
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 1
allele frequency: 1.16144018583043e-4
allele num: 8610
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -2.35e-1

DP
type: SiteQuality
SIO_000300: 1.772414e6

FS
type: SiteQuality
SIO_000300: 1.448e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.58e0

MQRankSum
type: SiteQuality
SIO_000300: -1.288e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.6e-2

QD
type: SiteQuality
SIO_000300: 1.364e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.5e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 4.6e-2

MQ
type: SiteQuality
SIO_000300: 5.916e1

GenotypeQuality
all individuals: 249
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 5.25e1
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GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 518
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1555
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 950
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 137
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11544
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.782821365681862e-5
allele num: 10222
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8610
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.05913717886573e-5
allele num: 16504
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65380
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.306e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.75e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.49e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.4e-2

MQRankSum
type: SiteQuality
SIO_000300: -1.95e-1

FS
type: SiteQuality
SIO_000300: 4.446e0

DP
type: SiteQuality
SIO_000300: 1.77236e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.117e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.7e-3

MQ
type: SiteQuality
SIO_000300: 5.963e1

GenotypeQuality
all individuals: 246
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 354
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GenotypeQuality
all individuals: 30
bin: 2.5e0
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GenotypeQuality
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bin: 6.75e1
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GenotypeQuality
all individuals: 14
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2027
bin: 7.25e1
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GenotypeQuality
all individuals: 22
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GenotypeQuality
all individuals: 24
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variant carriers: 0

GenotypeQuality
all individuals: 8
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variant carriers: 0

GenotypeQuality
all individuals: 44041
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 117
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 518
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11544
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.780907668231612e-5
allele num: 10224
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.059039461609055e-5
allele num: 65380
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16504
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 1.792e0

QD
type: SiteQuality
SIO_000300: 1.34e1

MQRankSum
type: SiteQuality
SIO_000300: 3.97e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.59e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.5e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.01e-1

MQ
type: SiteQuality
SIO_000300: 5.95e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.01e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.33e0

DP
type: SiteQuality
SIO_000300: 1.772519e6

GenotypeQuality
all individuals: 12
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2027
bin: 7.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

East Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele num: 65382
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African
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Latino
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Other
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South Asian
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InbreedingCoeff
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ClippingRankSum
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FS
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MQ
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BaseQRankSum
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VQSLOD
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MQRankSum
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DP
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QD
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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num of homozygotes: 0

South Asian
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East Asian
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Latino
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 3.058945887247255e-5
allele num: 65382
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African
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Other
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ReadPosRankSum
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ClippingRankSum
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BaseQRankSum
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DP
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InbreedingCoeff
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QD
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MQRankSum
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VQSLOD
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FS
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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South Asian
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European (Non-Finnish)
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East Asian
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African
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Other
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allele num: 886
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DP
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VQSLOD
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InbreedingCoeff
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ReadPosRankSum
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MQ
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MQRankSum
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ClippingRankSum
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FS
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QD
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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num of homozygotes: 0

African
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allele frequency: 0.0e0
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South Asian
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allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
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East Asian
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European (Non-Finnish)
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European (Finnish)
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allele num: 6610
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ClippingRankSum
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InbreedingCoeff
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BaseQRankSum
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ReadPosRankSum
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MQ
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VQSLOD
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FS
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MQRankSum
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DP
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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num of homozygotes: 0

European (Finnish)
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allele frequency: 1.51285930408472e-4
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European (Non-Finnish)
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Latino
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African
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East Asian
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South Asian
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ClippingRankSum
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ReadPosRankSum
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QD
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BaseQRankSum
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VQSLOD
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InbreedingCoeff
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MQ
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FS
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MQRankSum
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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East Asian
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South Asian
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Latino
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Other
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European (Non-Finnish)
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European (Finnish)
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MQ
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MQRankSum
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FS
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DP
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InbreedingCoeff
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VQSLOD
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QD
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BaseQRankSum
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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East Asian
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European (Finnish)
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African
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European (Non-Finnish)
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South Asian
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Other
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ReadPosRankSum
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BaseQRankSum
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ClippingRankSum
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InbreedingCoeff
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FS
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VQSLOD
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MQ
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MQRankSum
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DP
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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European (Finnish)
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Latino
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African
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South Asian
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European (Non-Finnish)
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East Asian
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DP
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MQRankSum
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BaseQRankSum
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MQ
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VQSLOD
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QD
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FS
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InbreedingCoeff
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ReadPosRankSum
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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European (Non-Finnish)
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Latino
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African
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East Asian
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South Asian
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QD
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DP
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BaseQRankSum
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VQSLOD
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InbreedingCoeff
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MQRankSum
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FS
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ReadPosRankSum
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MQ
type: SiteQuality
SIO_000300: 5.948e1