4-8089871-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8089871
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 8089871
    reference: chr 4
allele count: 0
allele frequency: 0.0e0
allele num: 49262
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000317020
  ensembl transcript: ENST00000318888
  gene symbol: ABLIM2
  hgvsc: ENST00000318888.4:c.-276+25T>C
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000441255
  ensembl transcript: ENST00000545242
  gene symbol: ABLIM2
  hgvsc: ENST00000545242.1:c.454+25T>C
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000444365
  ensembl transcript: ENST00000546334
  gene symbol: ABLIM2
  hgvsc: ENST00000546334.1:c.454+25T>C
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000389410
  ensembl transcript: ENST00000428004
  gene symbol: ABLIM2
  hgvsc: ENST00000428004.2:c.454+25T>C
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000342813
  ensembl transcript: ENST00000341937
  gene symbol: ABLIM2
  hgvsc: ENST00000341937.5:c.454+25T>C
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000355003
  ensembl transcript: ENST00000361581
  gene symbol: ABLIM2
  hgvsc: ENST00000361581.5:c.454+25T>C
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000421283
  ensembl transcript: ENST00000505872
  gene symbol: ABLIM2
  hgvsc: ENST00000505872.1:c.454+25T>C
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000354887
  ensembl transcript: ENST00000361737
  gene symbol: ABLIM2
  hgvsc: ENST00000361737.5:c.454+25T>C
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000296372
  ensembl transcript: ENST00000296372
  gene symbol: ABLIM2
  hgvsc: ENST00000296372.8:c.454+25T>C
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000393511
  ensembl transcript: ENST00000447017
  gene symbol: ABLIM2
  hgvsc: ENST00000447017.2:c.454+25T>C
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000384658
  ensembl transcript: ENST00000407564
  gene symbol: ABLIM2
  hgvsc: ENST00000407564.3:c.454+25T>C
  variant of: http://identifiers.org/hgnc/19195
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 10289
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3288
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9976
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31917
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1716
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1473
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 191
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: A
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum

http://identifiers.org/exac.variant/4-8089874-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8089874
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 8089874
    reference: chr 4
allele count: 1
allele frequency: 1.894226397939082e-5
allele num: 52792
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000421283
  ensembl transcript: ENST00000505872
  gene symbol: ABLIM2
  hgvsc: ENST00000505872.1:c.454+22G>T
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000317020
  ensembl transcript: ENST00000318888
  gene symbol: ABLIM2
  hgvsc: ENST00000318888.4:c.-276+22G>T
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000441255
  ensembl transcript: ENST00000545242
  gene symbol: ABLIM2
  hgvsc: ENST00000545242.1:c.454+22G>T
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000354887
  ensembl transcript: ENST00000361737
  gene symbol: ABLIM2
  hgvsc: ENST00000361737.5:c.454+22G>T
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000342813
  ensembl transcript: ENST00000341937
  gene symbol: ABLIM2
  hgvsc: ENST00000341937.5:c.454+22G>T
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000384658
  ensembl transcript: ENST00000407564
  gene symbol: ABLIM2
  hgvsc: ENST00000407564.3:c.454+22G>T
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000393511
  ensembl transcript: ENST00000447017
  gene symbol: ABLIM2
  hgvsc: ENST00000447017.2:c.454+22G>T
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000296372
  ensembl transcript: ENST00000296372
  gene symbol: ABLIM2
  hgvsc: ENST00000296372.8:c.454+22G>T
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000389410
  ensembl transcript: ENST00000428004
  gene symbol: ABLIM2
  hgvsc: ENST00000428004.2:c.454+22G>T
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000355003
  ensembl transcript: ENST00000361581
  gene symbol: ABLIM2
  hgvsc: ENST00000361581.5:c.454+22G>T
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000444365
  ensembl transcript: ENST00000546334
  gene symbol: ABLIM2
  hgvsc: ENST00000546334.1:c.454+22G>T
  variant of: http://identifiers.org/hgnc/19195
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2621
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30353
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1729
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9670
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2020
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12225
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: South Asian
population: East Asian
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: MQ
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/4-8089878-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8089878
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 8089878
    reference: chr 4
allele count: 2
allele frequency: 3.307643965203585e-5
allele num: 60466
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000384658
  ensembl transcript: ENST00000407564
  gene symbol: ABLIM2
  hgvsc: ENST00000407564.3:c.454+18G>T
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000421283
  ensembl transcript: ENST00000505872
  gene symbol: ABLIM2
  hgvsc: ENST00000505872.1:c.454+18G>T
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000393511
  ensembl transcript: ENST00000447017
  gene symbol: ABLIM2
  hgvsc: ENST00000447017.2:c.454+18G>T
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000441255
  ensembl transcript: ENST00000545242
  gene symbol: ABLIM2
  hgvsc: ENST00000545242.1:c.454+18G>T
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000389410
  ensembl transcript: ENST00000428004
  gene symbol: ABLIM2
  hgvsc: ENST00000428004.2:c.454+18G>T
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000355003
  ensembl transcript: ENST00000361581
  gene symbol: ABLIM2
  hgvsc: ENST00000361581.5:c.454+18G>T
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000444365
  ensembl transcript: ENST00000546334
  gene symbol: ABLIM2
  hgvsc: ENST00000546334.1:c.454+18G>T
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000296372
  ensembl transcript: ENST00000296372
  gene symbol: ABLIM2
  hgvsc: ENST00000296372.8:c.454+18G>T
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000342813
  ensembl transcript: ENST00000341937
  gene symbol: ABLIM2
  hgvsc: ENST00000341937.5:c.454+18G>T
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000317020
  ensembl transcript: ENST00000318888
  gene symbol: ABLIM2
  hgvsc: ENST00000318888.4:c.-276+18G>T
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000354887
  ensembl transcript: ENST00000361737
  gene symbol: ABLIM2
  hgvsc: ENST00000361737.5:c.454+18G>T
  variant of: http://identifiers.org/hgnc/19195
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2178
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8456
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2063
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1879
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27785
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16208
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3543
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
reference allele: C
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD

4-8089885-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8089885
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 8089885
    reference: chr 4
allele count: 6
allele frequency: 8.342834895297422e-5
allele num: 71918
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000441255
  ensembl transcript: ENST00000545242
  gene symbol: ABLIM2
  hgvsc: ENST00000545242.1:c.454+11G>A
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000317020
  ensembl transcript: ENST00000318888
  gene symbol: ABLIM2
  hgvsc: ENST00000318888.4:c.-276+11G>A
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000389410
  ensembl transcript: ENST00000428004
  gene symbol: ABLIM2
  hgvsc: ENST00000428004.2:c.454+11G>A
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000296372
  ensembl transcript: ENST00000296372
  gene symbol: ABLIM2
  hgvsc: ENST00000296372.8:c.454+11G>A
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000354887
  ensembl transcript: ENST00000361737
  gene symbol: ABLIM2
  hgvsc: ENST00000361737.5:c.454+11G>A
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000355003
  ensembl transcript: ENST00000361581
  gene symbol: ABLIM2
  hgvsc: ENST00000361581.5:c.454+11G>A
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000342813
  ensembl transcript: ENST00000341937
  gene symbol: ABLIM2
  hgvsc: ENST00000341937.5:c.454+11G>A
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000384658
  ensembl transcript: ENST00000407564
  gene symbol: ABLIM2
  hgvsc: ENST00000407564.3:c.454+11G>A
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000393511
  ensembl transcript: ENST00000447017
  gene symbol: ABLIM2
  hgvsc: ENST00000447017.2:c.454+11G>A
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000421283
  ensembl transcript: ENST00000505872
  gene symbol: ABLIM2
  hgvsc: ENST00000505872.1:c.454+11G>A
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000444365
  ensembl transcript: ENST00000546334
  gene symbol: ABLIM2
  hgvsc: ENST00000546334.1:c.454+11G>A
  variant of: http://identifiers.org/hgnc/19195
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6736
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22628
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22611
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3295
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1134
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1954
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 722
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1634
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: South Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum

4-8089886-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8089886
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 8089886
    reference: chr 4
allele count: 2
allele frequency: 2.620819792431072e-5
allele num: 76312
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000421283
  ensembl transcript: ENST00000505872
  gene symbol: ABLIM2
  hgvsc: ENST00000505872.1:c.454+10C>T
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000354887
  ensembl transcript: ENST00000361737
  gene symbol: ABLIM2
  hgvsc: ENST00000361737.5:c.454+10C>T
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000296372
  ensembl transcript: ENST00000296372
  gene symbol: ABLIM2
  hgvsc: ENST00000296372.8:c.454+10C>T
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000342813
  ensembl transcript: ENST00000341937
  gene symbol: ABLIM2
  hgvsc: ENST00000341937.5:c.454+10C>T
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000384658
  ensembl transcript: ENST00000407564
  gene symbol: ABLIM2
  hgvsc: ENST00000407564.3:c.454+10C>T
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000393511
  ensembl transcript: ENST00000447017
  gene symbol: ABLIM2
  hgvsc: ENST00000447017.2:c.454+10C>T
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000441255
  ensembl transcript: ENST00000545242
  gene symbol: ABLIM2
  hgvsc: ENST00000545242.1:c.454+10C>T
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000444365
  ensembl transcript: ENST00000546334
  gene symbol: ABLIM2
  hgvsc: ENST00000546334.1:c.454+10C>T
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000317020
  ensembl transcript: ENST00000318888
  gene symbol: ABLIM2
  hgvsc: ENST00000318888.4:c.-276+10C>T
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000355003
  ensembl transcript: ENST00000361581
  gene symbol: ABLIM2
  hgvsc: ENST00000361581.5:c.454+10C>T
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000389410
  ensembl transcript: ENST00000428004
  gene symbol: ABLIM2
  hgvsc: ENST00000428004.2:c.454+10C>T
  variant of: http://identifiers.org/hgnc/19195
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1855
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3799
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 969
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6104
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24733
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 803
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20822
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24751
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
population: African
population: East Asian
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: DP

4-8089887-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8089887
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 8089887
    reference: chr 4
allele count: 1
allele frequency: 1.263391954720032e-5
allele num: 79152
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000393511
  ensembl transcript: ENST00000447017
  gene symbol: ABLIM2
  hgvsc: ENST00000447017.2:c.454+9G>A
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000444365
  ensembl transcript: ENST00000546334
  gene symbol: ABLIM2
  hgvsc: ENST00000546334.1:c.454+9G>A
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000296372
  ensembl transcript: ENST00000296372
  gene symbol: ABLIM2
  hgvsc: ENST00000296372.8:c.454+9G>A
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000355003
  ensembl transcript: ENST00000361581
  gene symbol: ABLIM2
  hgvsc: ENST00000361581.5:c.454+9G>A
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000354887
  ensembl transcript: ENST00000361737
  gene symbol: ABLIM2
  hgvsc: ENST00000361737.5:c.454+9G>A
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000317020
  ensembl transcript: ENST00000318888
  gene symbol: ABLIM2
  hgvsc: ENST00000318888.4:c.-276+9G>A
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000421283
  ensembl transcript: ENST00000505872
  gene symbol: ABLIM2
  hgvsc: ENST00000505872.1:c.454+9G>A
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000384658
  ensembl transcript: ENST00000407564
  gene symbol: ABLIM2
  hgvsc: ENST00000407564.3:c.454+9G>A
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000441255
  ensembl transcript: ENST00000545242
  gene symbol: ABLIM2
  hgvsc: ENST00000545242.1:c.454+9G>A
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000342813
  ensembl transcript: ENST00000341937
  gene symbol: ABLIM2
  hgvsc: ENST00000341937.5:c.454+9G>A
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000389410
  ensembl transcript: ENST00000428004
  gene symbol: ABLIM2
  hgvsc: ENST00000428004.2:c.454+9G>A
  variant of: http://identifiers.org/hgnc/19195
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5735
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26192
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 896
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3980
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19733
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1746
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1265
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
population: African
population: Latino
reference allele: C
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum

4-8089896-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8089896
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 8089896
    reference: chr 4
allele count: 18
allele frequency: 1.92793796324065e-4
allele num: 93364
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000393511
  ensembl transcript: ENST00000447017
  gene symbol: ABLIM2
  hgvsc: ENST00000447017.2:c.454A>G
  hgvsp: ENSP00000393511.2:p.Ser152Gly
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000296372
  ensembl transcript: ENST00000296372
  gene symbol: ABLIM2
  hgvsc: ENST00000296372.8:c.454A>G
  hgvsp: ENSP00000296372.8:p.Ser152Gly
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000342813
  ensembl transcript: ENST00000341937
  gene symbol: ABLIM2
  hgvsc: ENST00000341937.5:c.454A>G
  hgvsp: ENSP00000342813.5:p.Ser152Gly
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000421283
  ensembl transcript: ENST00000505872
  gene symbol: ABLIM2
  hgvsc: ENST00000505872.1:c.454A>G
  hgvsp: ENSP00000421283.1:p.Ser152Gly
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000441255
  ensembl transcript: ENST00000545242
  gene symbol: ABLIM2
  hgvsc: ENST00000545242.1:c.454A>G
  hgvsp: ENSP00000441255.1:p.Ser152Gly
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000389410
  ensembl transcript: ENST00000428004
  gene symbol: ABLIM2
  hgvsc: ENST00000428004.2:c.454A>G
  hgvsp: ENSP00000389410.2:p.Ser152Gly
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000355003
  ensembl transcript: ENST00000361581
  gene symbol: ABLIM2
  hgvsc: ENST00000361581.5:c.454A>G
  hgvsp: ENSP00000355003.5:p.Ser152Gly
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000444365
  ensembl transcript: ENST00000546334
  gene symbol: ABLIM2
  hgvsc: ENST00000546334.1:c.454A>G
  hgvsp: ENSP00000444365.1:p.Ser152Gly
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000384658
  ensembl transcript: ENST00000407564
  gene symbol: ABLIM2
  hgvsc: ENST00000407564.3:c.454A>G
  hgvsp: ENSP00000384658.3:p.Ser152Gly
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000317020
  ensembl transcript: ENST00000318888
  gene symbol: ABLIM2
  hgvsc: ENST00000318888.4:c.-276A>G
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000354887
  ensembl transcript: ENST00000361737
  gene symbol: ABLIM2
  hgvsc: ENST00000361737.5:c.454A>G
  hgvsp: ENSP00000354887.5:p.Ser152Gly
  variant of: http://identifiers.org/hgnc/19195
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 548
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5291
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1173
  bin: 1.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13141
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3726
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1000
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser152Gly
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
population: South Asian
population: Latino
population: Other
reference allele: T
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: InbreedingCoeff

4-8089898-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8089898
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 8089898
    reference: chr 4
allele count: 22
allele frequency: 2.296834544391548e-4
allele num: 95784
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000354887
  ensembl transcript: ENST00000361737
  gene symbol: ABLIM2
  hgvsc: ENST00000361737.5:c.452G>A
  hgvsp: ENSP00000354887.5:p.Arg151Gln
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000355003
  ensembl transcript: ENST00000361581
  gene symbol: ABLIM2
  hgvsc: ENST00000361581.5:c.452G>A
  hgvsp: ENSP00000355003.5:p.Arg151Gln
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000342813
  ensembl transcript: ENST00000341937
  gene symbol: ABLIM2
  hgvsc: ENST00000341937.5:c.452G>A
  hgvsp: ENSP00000342813.5:p.Arg151Gln
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000389410
  ensembl transcript: ENST00000428004
  gene symbol: ABLIM2
  hgvsc: ENST00000428004.2:c.452G>A
  hgvsp: ENSP00000389410.2:p.Arg151Gln
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000296372
  ensembl transcript: ENST00000296372
  gene symbol: ABLIM2
  hgvsc: ENST00000296372.8:c.452G>A
  hgvsp: ENSP00000296372.8:p.Arg151Gln
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000441255
  ensembl transcript: ENST00000545242
  gene symbol: ABLIM2
  hgvsc: ENST00000545242.1:c.452G>A
  hgvsp: ENSP00000441255.1:p.Arg151Gln
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000317020
  ensembl transcript: ENST00000318888
  gene symbol: ABLIM2
  hgvsc: ENST00000318888.4:c.-278G>A
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000384658
  ensembl transcript: ENST00000407564
  gene symbol: ABLIM2
  hgvsc: ENST00000407564.3:c.452G>A
  hgvsp: ENSP00000384658.3:p.Arg151Gln
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000444365
  ensembl transcript: ENST00000546334
  gene symbol: ABLIM2
  hgvsc: ENST00000546334.1:c.452G>A
  hgvsp: ENSP00000444365.1:p.Arg151Gln
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000421283
  ensembl transcript: ENST00000505872
  gene symbol: ABLIM2
  hgvsc: ENST00000505872.1:c.452G>A
  hgvsp: ENSP00000421283.1:p.Arg151Gln
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000393511
  ensembl transcript: ENST00000447017
  gene symbol: ABLIM2
  hgvsc: ENST00000447017.2:c.452G>A
  hgvsp: ENSP00000393511.2:p.Arg151Gln
  variant of: http://identifiers.org/hgnc/19195
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1125
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1128
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 11847
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3372
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 499
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5707
  bin: 2.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35386
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg151Gln
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: InbreedingCoeff

4-8089909-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8089909
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 8089909
    reference: chr 4
allele count: 1
allele frequency: 9.336196433572962e-6
allele num: 107110
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000296372
  ensembl transcript: ENST00000296372
  gene symbol: ABLIM2
  hgvsc: ENST00000296372.8:c.441C>G
  hgvsp: ENST00000296372.8:c.441C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000342813
  ensembl transcript: ENST00000341937
  gene symbol: ABLIM2
  hgvsc: ENST00000341937.5:c.441C>G
  hgvsp: ENST00000341937.5:c.441C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000393511
  ensembl transcript: ENST00000447017
  gene symbol: ABLIM2
  hgvsc: ENST00000447017.2:c.441C>G
  hgvsp: ENST00000447017.2:c.441C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000355003
  ensembl transcript: ENST00000361581
  gene symbol: ABLIM2
  hgvsc: ENST00000361581.5:c.441C>G
  hgvsp: ENST00000361581.5:c.441C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000384658
  ensembl transcript: ENST00000407564
  gene symbol: ABLIM2
  hgvsc: ENST00000407564.3:c.441C>G
  hgvsp: ENST00000407564.3:c.441C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000441255
  ensembl transcript: ENST00000545242
  gene symbol: ABLIM2
  hgvsc: ENST00000545242.1:c.441C>G
  hgvsp: ENST00000545242.1:c.441C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000421283
  ensembl transcript: ENST00000505872
  gene symbol: ABLIM2
  hgvsc: ENST00000505872.1:c.441C>G
  hgvsp: ENST00000505872.1:c.441C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000444365
  ensembl transcript: ENST00000546334
  gene symbol: ABLIM2
  hgvsc: ENST00000546334.1:c.441C>G
  hgvsp: ENST00000546334.1:c.441C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000389410
  ensembl transcript: ENST00000428004
  gene symbol: ABLIM2
  hgvsc: ENST00000428004.2:c.441C>G
  hgvsp: ENST00000428004.2:c.441C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000354887
  ensembl transcript: ENST00000361737
  gene symbol: ABLIM2
  hgvsc: ENST00000361737.5:c.441C>G
  hgvsp: ENST00000361737.5:c.441C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000317020
  ensembl transcript: ENST00000318888
  gene symbol: ABLIM2
  hgvsc: ENST00000318888.4:c.-289C>G
  variant of: http://identifiers.org/hgnc/19195
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1417
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8051
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6505
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 827
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39989
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1949
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser147Ser
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
reference allele: G
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD

4-8089915-GTGCGCGCTGCT-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8089915
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 8089904
    reference: chr 4
allele count: 1
allele frequency: 9.092727636436378e-6
allele num: 109978
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000296372
  ensembl transcript: ENST00000296372
  gene symbol: ABLIM2
  hgvsp: ENSP00000296372.8:p.Ser142ProfsTer34
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000421283
  ensembl transcript: ENST00000505872
  gene symbol: ABLIM2
  hgvsp: ENSP00000421283.1:p.Ser142ProfsTer34
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000342813
  ensembl transcript: ENST00000341937
  gene symbol: ABLIM2
  hgvsp: ENSP00000342813.5:p.Ser142ProfsTer34
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000354887
  ensembl transcript: ENST00000361737
  gene symbol: ABLIM2
  hgvsp: ENSP00000354887.5:p.Ser142ProfsTer34
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000384658
  ensembl transcript: ENST00000407564
  gene symbol: ABLIM2
  hgvsp: ENSP00000384658.3:p.Ser142ProfsTer34
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000441255
  ensembl transcript: ENST00000545242
  gene symbol: ABLIM2
  hgvsp: ENSP00000441255.1:p.Ser142ProfsTer34
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000317020
  ensembl transcript: ENST00000318888
  gene symbol: ABLIM2
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000389410
  ensembl transcript: ENST00000428004
  gene symbol: ABLIM2
  hgvsp: ENSP00000389410.2:p.Ser142ProfsTer34
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000355003
  ensembl transcript: ENST00000361581
  gene symbol: ABLIM2
  hgvsp: ENSP00000355003.5:p.Ser142ProfsTer34
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000444365
  ensembl transcript: ENST00000546334
  gene symbol: ABLIM2
  hgvsp: ENSP00000444365.1:p.Ser142ProfsTer34
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000393511
  ensembl transcript: ENST00000447017
  gene symbol: ABLIM2
  hgvsp: ENSP00000393511.2:p.Ser142ProfsTer34
  variant of: http://identifiers.org/hgnc/19195
canonical: true
consequence: frameshift
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8732
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41033
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5164
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 742
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1601
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1519
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 715
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 315
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Ser142ProfsTer34
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: Other
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: GTGCGCGCTGCT
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum

4-8089916-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8089916
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 8089916
    reference: chr 4
allele count: 2
allele frequency: 1.816761441055175e-5
allele num: 110086
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000441255
  ensembl transcript: ENST00000545242
  gene symbol: ABLIM2
  hgvsc: ENST00000545242.1:c.434A>G
  hgvsp: ENSP00000441255.1:p.His145Arg
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000393511
  ensembl transcript: ENST00000447017
  gene symbol: ABLIM2
  hgvsc: ENST00000447017.2:c.434A>G
  hgvsp: ENSP00000393511.2:p.His145Arg
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000389410
  ensembl transcript: ENST00000428004
  gene symbol: ABLIM2
  hgvsc: ENST00000428004.2:c.434A>G
  hgvsp: ENSP00000389410.2:p.His145Arg
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000384658
  ensembl transcript: ENST00000407564
  gene symbol: ABLIM2
  hgvsc: ENST00000407564.3:c.434A>G
  hgvsp: ENSP00000384658.3:p.His145Arg
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000342813
  ensembl transcript: ENST00000341937
  gene symbol: ABLIM2
  hgvsc: ENST00000341937.5:c.434A>G
  hgvsp: ENSP00000342813.5:p.His145Arg
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000296372
  ensembl transcript: ENST00000296372
  gene symbol: ABLIM2
  hgvsc: ENST00000296372.8:c.434A>G
  hgvsp: ENSP00000296372.8:p.His145Arg
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000355003
  ensembl transcript: ENST00000361581
  gene symbol: ABLIM2
  hgvsc: ENST00000361581.5:c.434A>G
  hgvsp: ENSP00000355003.5:p.His145Arg
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000421283
  ensembl transcript: ENST00000505872
  gene symbol: ABLIM2
  hgvsc: ENST00000505872.1:c.434A>G
  hgvsp: ENSP00000421283.1:p.His145Arg
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000354887
  ensembl transcript: ENST00000361737
  gene symbol: ABLIM2
  hgvsc: ENST00000361737.5:c.434A>G
  hgvsp: ENSP00000354887.5:p.His145Arg
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000317020
  ensembl transcript: ENST00000318888
  gene symbol: ABLIM2
  hgvsc: ENST00000318888.4:c.-296A>G
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000444365
  ensembl transcript: ENST00000546334
  gene symbol: ABLIM2
  hgvsc: ENST00000546334.1:c.434A>G
  hgvsp: ENSP00000444365.1:p.His145Arg
  variant of: http://identifiers.org/hgnc/19195
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40832
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1535
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8946
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5068
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1604
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His145Arg
num of homozygotes: 0
population: European (Finnish)
population: Other
population: East Asian
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: T
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum

4-8089916-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8089916
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 8089916
    reference: chr 4
allele count: 1
allele frequency: 9.083807205275875e-6
allele num: 110086
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000354887
  ensembl transcript: ENST00000361737
  gene symbol: ABLIM2
  hgvsc: ENST00000361737.5:c.434A>C
  hgvsp: ENSP00000354887.5:p.His145Pro
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000317020
  ensembl transcript: ENST00000318888
  gene symbol: ABLIM2
  hgvsc: ENST00000318888.4:c.-296A>C
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000384658
  ensembl transcript: ENST00000407564
  gene symbol: ABLIM2
  hgvsc: ENST00000407564.3:c.434A>C
  hgvsp: ENSP00000384658.3:p.His145Pro
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000393511
  ensembl transcript: ENST00000447017
  gene symbol: ABLIM2
  hgvsc: ENST00000447017.2:c.434A>C
  hgvsp: ENSP00000393511.2:p.His145Pro
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000389410
  ensembl transcript: ENST00000428004
  gene symbol: ABLIM2
  hgvsc: ENST00000428004.2:c.434A>C
  hgvsp: ENSP00000389410.2:p.His145Pro
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000355003
  ensembl transcript: ENST00000361581
  gene symbol: ABLIM2
  hgvsc: ENST00000361581.5:c.434A>C
  hgvsp: ENSP00000355003.5:p.His145Pro
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000441255
  ensembl transcript: ENST00000545242
  gene symbol: ABLIM2
  hgvsc: ENST00000545242.1:c.434A>C
  hgvsp: ENSP00000441255.1:p.His145Pro
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000444365
  ensembl transcript: ENST00000546334
  gene symbol: ABLIM2
  hgvsc: ENST00000546334.1:c.434A>C
  hgvsp: ENSP00000444365.1:p.His145Pro
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000296372
  ensembl transcript: ENST00000296372
  gene symbol: ABLIM2
  hgvsc: ENST00000296372.8:c.434A>C
  hgvsp: ENSP00000296372.8:p.His145Pro
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000421283
  ensembl transcript: ENST00000505872
  gene symbol: ABLIM2
  hgvsc: ENST00000505872.1:c.434A>C
  hgvsp: ENSP00000421283.1:p.His145Pro
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000342813
  ensembl transcript: ENST00000341937
  gene symbol: ABLIM2
  hgvsc: ENST00000341937.5:c.434A>C
  hgvsp: ENSP00000342813.5:p.His145Pro
  variant of: http://identifiers.org/hgnc/19195
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40832
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8946
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1604
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1535
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5068
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His145Pro
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: QD

4-8089918-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8089918
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 8089918
    reference: chr 4
allele count: 29
allele frequency: 2.619077723389267e-4
allele num: 110726
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000389410
  ensembl transcript: ENST00000428004
  gene symbol: ABLIM2
  hgvsc: ENST00000428004.2:c.432G>A
  hgvsp: ENST00000428004.2:c.432G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000421283
  ensembl transcript: ENST00000505872
  gene symbol: ABLIM2
  hgvsc: ENST00000505872.1:c.432G>A
  hgvsp: ENST00000505872.1:c.432G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000384658
  ensembl transcript: ENST00000407564
  gene symbol: ABLIM2
  hgvsc: ENST00000407564.3:c.432G>A
  hgvsp: ENST00000407564.3:c.432G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000296372
  ensembl transcript: ENST00000296372
  gene symbol: ABLIM2
  hgvsc: ENST00000296372.8:c.432G>A
  hgvsp: ENST00000296372.8:c.432G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000393511
  ensembl transcript: ENST00000447017
  gene symbol: ABLIM2
  hgvsc: ENST00000447017.2:c.432G>A
  hgvsp: ENST00000447017.2:c.432G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000342813
  ensembl transcript: ENST00000341937
  gene symbol: ABLIM2
  hgvsc: ENST00000341937.5:c.432G>A
  hgvsp: ENST00000341937.5:c.432G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000354887
  ensembl transcript: ENST00000361737
  gene symbol: ABLIM2
  hgvsc: ENST00000361737.5:c.432G>A
  hgvsp: ENST00000361737.5:c.432G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000355003
  ensembl transcript: ENST00000361581
  gene symbol: ABLIM2
  hgvsc: ENST00000361581.5:c.432G>A
  hgvsp: ENST00000361581.5:c.432G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000441255
  ensembl transcript: ENST00000545242
  gene symbol: ABLIM2
  hgvsc: ENST00000545242.1:c.432G>A
  hgvsp: ENST00000545242.1:c.432G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000444365
  ensembl transcript: ENST00000546334
  gene symbol: ABLIM2
  hgvsc: ENST00000546334.1:c.432G>A
  hgvsp: ENST00000546334.1:c.432G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000317020
  ensembl transcript: ENST00000318888
  gene symbol: ABLIM2
  hgvsc: ENST00000318888.4:c.-298G>A
  variant of: http://identifiers.org/hgnc/19195
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 40984
  bin: 2.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 765
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1603
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 4759
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 4.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1510
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9144
  bin: 2.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala144Ala
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
population: African
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: MQ
site quality: FS
site quality: VQSLOD

4-8089919-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8089919
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 8089919
    reference: chr 4
allele count: 3
allele frequency: 2.693288325492872e-5
allele num: 111388
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000296372
  ensembl transcript: ENST00000296372
  gene symbol: ABLIM2
  hgvsc: ENST00000296372.8:c.431C>T
  hgvsp: ENSP00000296372.8:p.Ala144Val
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000421283
  ensembl transcript: ENST00000505872
  gene symbol: ABLIM2
  hgvsc: ENST00000505872.1:c.431C>T
  hgvsp: ENSP00000421283.1:p.Ala144Val
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000317020
  ensembl transcript: ENST00000318888
  gene symbol: ABLIM2
  hgvsc: ENST00000318888.4:c.-299C>T
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000384658
  ensembl transcript: ENST00000407564
  gene symbol: ABLIM2
  hgvsc: ENST00000407564.3:c.431C>T
  hgvsp: ENSP00000384658.3:p.Ala144Val
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000441255
  ensembl transcript: ENST00000545242
  gene symbol: ABLIM2
  hgvsc: ENST00000545242.1:c.431C>T
  hgvsp: ENSP00000441255.1:p.Ala144Val
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000444365
  ensembl transcript: ENST00000546334
  gene symbol: ABLIM2
  hgvsc: ENST00000546334.1:c.431C>T
  hgvsp: ENSP00000444365.1:p.Ala144Val
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000389410
  ensembl transcript: ENST00000428004
  gene symbol: ABLIM2
  hgvsc: ENST00000428004.2:c.431C>T
  hgvsp: ENSP00000389410.2:p.Ala144Val
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000354887
  ensembl transcript: ENST00000361737
  gene symbol: ABLIM2
  hgvsc: ENST00000361737.5:c.431C>T
  hgvsp: ENSP00000354887.5:p.Ala144Val
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000342813
  ensembl transcript: ENST00000341937
  gene symbol: ABLIM2
  hgvsc: ENST00000341937.5:c.431C>T
  hgvsp: ENSP00000342813.5:p.Ala144Val
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000355003
  ensembl transcript: ENST00000361581
  gene symbol: ABLIM2
  hgvsc: ENST00000361581.5:c.431C>T
  hgvsp: ENSP00000355003.5:p.Ala144Val
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000393511
  ensembl transcript: ENST00000447017
  gene symbol: ABLIM2
  hgvsc: ENST00000447017.2:c.431C>T
  hgvsp: ENSP00000393511.2:p.Ala144Val
  variant of: http://identifiers.org/hgnc/19195
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41268
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1417
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9304
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4473
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1624
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala144Val
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum

4-8089919-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8089919
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 8089919
    reference: chr 4
allele count: 2
allele frequency: 1.795525550328581e-5
allele num: 111388
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000441255
  ensembl transcript: ENST00000545242
  gene symbol: ABLIM2
  hgvsc: ENST00000545242.1:c.431C>A
  hgvsp: ENSP00000441255.1:p.Ala144Glu
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000354887
  ensembl transcript: ENST00000361737
  gene symbol: ABLIM2
  hgvsc: ENST00000361737.5:c.431C>A
  hgvsp: ENSP00000354887.5:p.Ala144Glu
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000317020
  ensembl transcript: ENST00000318888
  gene symbol: ABLIM2
  hgvsc: ENST00000318888.4:c.-299C>A
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000384658
  ensembl transcript: ENST00000407564
  gene symbol: ABLIM2
  hgvsc: ENST00000407564.3:c.431C>A
  hgvsp: ENSP00000384658.3:p.Ala144Glu
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000393511
  ensembl transcript: ENST00000447017
  gene symbol: ABLIM2
  hgvsc: ENST00000447017.2:c.431C>A
  hgvsp: ENSP00000393511.2:p.Ala144Glu
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000296372
  ensembl transcript: ENST00000296372
  gene symbol: ABLIM2
  hgvsc: ENST00000296372.8:c.431C>A
  hgvsp: ENSP00000296372.8:p.Ala144Glu
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000421283
  ensembl transcript: ENST00000505872
  gene symbol: ABLIM2
  hgvsc: ENST00000505872.1:c.431C>A
  hgvsp: ENSP00000421283.1:p.Ala144Glu
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000355003
  ensembl transcript: ENST00000361581
  gene symbol: ABLIM2
  hgvsc: ENST00000361581.5:c.431C>A
  hgvsp: ENSP00000355003.5:p.Ala144Glu
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000444365
  ensembl transcript: ENST00000546334
  gene symbol: ABLIM2
  hgvsc: ENST00000546334.1:c.431C>A
  hgvsp: ENSP00000444365.1:p.Ala144Glu
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000389410
  ensembl transcript: ENST00000428004
  gene symbol: ABLIM2
  hgvsc: ENST00000428004.2:c.431C>A
  hgvsp: ENSP00000389410.2:p.Ala144Glu
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000342813
  ensembl transcript: ENST00000341937
  gene symbol: ABLIM2
  hgvsc: ENST00000341937.5:c.431C>A
  hgvsp: ENSP00000342813.5:p.Ala144Glu
  variant of: http://identifiers.org/hgnc/19195
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4473
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9304
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1417
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41268
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala144Glu
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Other
population: East Asian
reference allele: G
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum

4-8089920-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8089920
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 8089920
    reference: chr 4
allele count: 10
allele frequency: 8.947104716913607e-5
allele num: 111768
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000354887
  ensembl transcript: ENST00000361737
  gene symbol: ABLIM2
  hgvsc: ENST00000361737.5:c.430G>A
  hgvsp: ENSP00000354887.5:p.Ala144Thr
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000296372
  ensembl transcript: ENST00000296372
  gene symbol: ABLIM2
  hgvsc: ENST00000296372.8:c.430G>A
  hgvsp: ENSP00000296372.8:p.Ala144Thr
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000317020
  ensembl transcript: ENST00000318888
  gene symbol: ABLIM2
  hgvsc: ENST00000318888.4:c.-300G>A
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000342813
  ensembl transcript: ENST00000341937
  gene symbol: ABLIM2
  hgvsc: ENST00000341937.5:c.430G>A
  hgvsp: ENSP00000342813.5:p.Ala144Thr
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000441255
  ensembl transcript: ENST00000545242
  gene symbol: ABLIM2
  hgvsc: ENST00000545242.1:c.430G>A
  hgvsp: ENSP00000441255.1:p.Ala144Thr
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000355003
  ensembl transcript: ENST00000361581
  gene symbol: ABLIM2
  hgvsc: ENST00000361581.5:c.430G>A
  hgvsp: ENSP00000355003.5:p.Ala144Thr
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000389410
  ensembl transcript: ENST00000428004
  gene symbol: ABLIM2
  hgvsc: ENST00000428004.2:c.430G>A
  hgvsp: ENSP00000389410.2:p.Ala144Thr
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000421283
  ensembl transcript: ENST00000505872
  gene symbol: ABLIM2
  hgvsc: ENST00000505872.1:c.430G>A
  hgvsp: ENSP00000421283.1:p.Ala144Thr
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000384658
  ensembl transcript: ENST00000407564
  gene symbol: ABLIM2
  hgvsc: ENST00000407564.3:c.430G>A
  hgvsp: ENSP00000384658.3:p.Ala144Thr
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000444365
  ensembl transcript: ENST00000546334
  gene symbol: ABLIM2
  hgvsc: ENST00000546334.1:c.430G>A
  hgvsp: ENSP00000444365.1:p.Ala144Thr
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000393511
  ensembl transcript: ENST00000447017
  gene symbol: ABLIM2
  hgvsc: ENST00000447017.2:c.430G>A
  hgvsp: ENSP00000393511.2:p.Ala144Thr
  variant of: http://identifiers.org/hgnc/19195
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1382
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 688
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 41388
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9398
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4297
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1632
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala144Thr
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: African
population: Latino
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: DP

4-8089921-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8089921
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 8089921
    reference: chr 4
allele count: 14
allele frequency: 1.246771751714311e-4
allele num: 112290
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000342813
  ensembl transcript: ENST00000341937
  gene symbol: ABLIM2
  hgvsc: ENST00000341937.5:c.429C>T
  hgvsp: ENST00000341937.5:c.429C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000296372
  ensembl transcript: ENST00000296372
  gene symbol: ABLIM2
  hgvsc: ENST00000296372.8:c.429C>T
  hgvsp: ENST00000296372.8:c.429C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000384658
  ensembl transcript: ENST00000407564
  gene symbol: ABLIM2
  hgvsc: ENST00000407564.3:c.429C>T
  hgvsp: ENST00000407564.3:c.429C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000389410
  ensembl transcript: ENST00000428004
  gene symbol: ABLIM2
  hgvsc: ENST00000428004.2:c.429C>T
  hgvsp: ENST00000428004.2:c.429C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000421283
  ensembl transcript: ENST00000505872
  gene symbol: ABLIM2
  hgvsc: ENST00000505872.1:c.429C>T
  hgvsp: ENST00000505872.1:c.429C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000354887
  ensembl transcript: ENST00000361737
  gene symbol: ABLIM2
  hgvsc: ENST00000361737.5:c.429C>T
  hgvsp: ENST00000361737.5:c.429C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000317020
  ensembl transcript: ENST00000318888
  gene symbol: ABLIM2
  hgvsc: ENST00000318888.4:c.-301C>T
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000393511
  ensembl transcript: ENST00000447017
  gene symbol: ABLIM2
  hgvsc: ENST00000447017.2:c.429C>T
  hgvsp: ENST00000447017.2:c.429C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000444365
  ensembl transcript: ENST00000546334
  gene symbol: ABLIM2
  hgvsc: ENST00000546334.1:c.429C>T
  hgvsp: ENST00000546334.1:c.429C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000441255
  ensembl transcript: ENST00000545242
  gene symbol: ABLIM2
  hgvsc: ENST00000545242.1:c.429C>T
  hgvsp: ENST00000545242.1:c.429C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000355003
  ensembl transcript: ENST00000361581
  gene symbol: ABLIM2
  hgvsc: ENST00000361581.5:c.429C>T
  hgvsp: ENST00000361581.5:c.429C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19195
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 9564
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4021
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1692
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41565
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1300
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 3.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser143Ser
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
population: South Asian
population: Latino
reference allele: G
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum

4-8089932-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8089932
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 8089932
    reference: chr 4
allele count: 125
allele frequency: 1.0869376184762e-3
allele num: 115002
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000355003
  ensembl transcript: ENST00000361581
  gene symbol: ABLIM2
  hgvsc: ENST00000361581.5:c.418G>A
  hgvsp: ENSP00000355003.5:p.Val140Met
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000354887
  ensembl transcript: ENST00000361737
  gene symbol: ABLIM2
  hgvsc: ENST00000361737.5:c.418G>A
  hgvsp: ENSP00000354887.5:p.Val140Met
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000384658
  ensembl transcript: ENST00000407564
  gene symbol: ABLIM2
  hgvsc: ENST00000407564.3:c.418G>A
  hgvsp: ENSP00000384658.3:p.Val140Met
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000441255
  ensembl transcript: ENST00000545242
  gene symbol: ABLIM2
  hgvsc: ENST00000545242.1:c.418G>A
  hgvsp: ENSP00000441255.1:p.Val140Met
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000393511
  ensembl transcript: ENST00000447017
  gene symbol: ABLIM2
  hgvsc: ENST00000447017.2:c.418G>A
  hgvsp: ENSP00000393511.2:p.Val140Met
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000444365
  ensembl transcript: ENST00000546334
  gene symbol: ABLIM2
  hgvsc: ENST00000546334.1:c.418G>A
  hgvsp: ENSP00000444365.1:p.Val140Met
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000296372
  ensembl transcript: ENST00000296372
  gene symbol: ABLIM2
  hgvsc: ENST00000296372.8:c.418G>A
  hgvsp: ENSP00000296372.8:p.Val140Met
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000389410
  ensembl transcript: ENST00000428004
  gene symbol: ABLIM2
  hgvsc: ENST00000428004.2:c.418G>A
  hgvsp: ENSP00000389410.2:p.Val140Met
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000342813
  ensembl transcript: ENST00000341937
  gene symbol: ABLIM2
  hgvsc: ENST00000341937.5:c.418G>A
  hgvsp: ENSP00000342813.5:p.Val140Met
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000317020
  ensembl transcript: ENST00000318888
  gene symbol: ABLIM2
  hgvsc: ENST00000318888.4:c.-312G>A
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000421283
  ensembl transcript: ENST00000505872
  gene symbol: ABLIM2
  hgvsc: ENST00000505872.1:c.418G>A
  hgvsp: ENSP00000421283.1:p.Val140Met
  variant of: http://identifiers.org/hgnc/19195
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 1.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 10334
  bin: 2.75e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2738
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 3.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42437
  bin: 2.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1805
  bin: 3.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 954
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 4.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 5.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 4.25e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.25e1
  variant carriers: 5
genotype quality: GenotypeQuality
hgvs: p.Val140Met
num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
reference allele: C
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD

4-8089933-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8089933
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 8089933
    reference: chr 4
allele count: 2
allele frequency: 1.736050831568348e-5
allele num: 115204
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000355003
  ensembl transcript: ENST00000361581
  gene symbol: ABLIM2
  hgvsc: ENST00000361581.5:c.417G>A
  hgvsp: ENST00000361581.5:c.417G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000384658
  ensembl transcript: ENST00000407564
  gene symbol: ABLIM2
  hgvsc: ENST00000407564.3:c.417G>A
  hgvsp: ENST00000407564.3:c.417G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000444365
  ensembl transcript: ENST00000546334
  gene symbol: ABLIM2
  hgvsc: ENST00000546334.1:c.417G>A
  hgvsp: ENST00000546334.1:c.417G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000393511
  ensembl transcript: ENST00000447017
  gene symbol: ABLIM2
  hgvsc: ENST00000447017.2:c.417G>A
  hgvsp: ENST00000447017.2:c.417G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000342813
  ensembl transcript: ENST00000341937
  gene symbol: ABLIM2
  hgvsc: ENST00000341937.5:c.417G>A
  hgvsp: ENST00000341937.5:c.417G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000354887
  ensembl transcript: ENST00000361737
  gene symbol: ABLIM2
  hgvsc: ENST00000361737.5:c.417G>A
  hgvsp: ENST00000361737.5:c.417G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000421283
  ensembl transcript: ENST00000505872
  gene symbol: ABLIM2
  hgvsc: ENST00000505872.1:c.417G>A
  hgvsp: ENST00000505872.1:c.417G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000441255
  ensembl transcript: ENST00000545242
  gene symbol: ABLIM2
  hgvsc: ENST00000545242.1:c.417G>A
  hgvsp: ENST00000545242.1:c.417G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000389410
  ensembl transcript: ENST00000428004
  gene symbol: ABLIM2
  hgvsc: ENST00000428004.2:c.417G>A
  hgvsp: ENST00000428004.2:c.417G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000317020
  ensembl transcript: ENST00000318888
  gene symbol: ABLIM2
  hgvsc: ENST00000318888.4:c.-313G>A
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000296372
  ensembl transcript: ENST00000296372
  gene symbol: ABLIM2
  hgvsc: ENST00000296372.8:c.417G>A
  hgvsp: ENST00000296372.8:c.417G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19195
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42480
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2606
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1855
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 916
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10477
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser139Ser
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP

4-8089936-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8089936
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 8089936
    reference: chr 4
allele count: 2
allele frequency: 1.726996407847472e-5
allele num: 115808
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000444365
  ensembl transcript: ENST00000546334
  gene symbol: ABLIM2
  hgvsc: ENST00000546334.1:c.414A>T
  hgvsp: ENST00000546334.1:c.414A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000441255
  ensembl transcript: ENST00000545242
  gene symbol: ABLIM2
  hgvsc: ENST00000545242.1:c.414A>T
  hgvsp: ENST00000545242.1:c.414A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000317020
  ensembl transcript: ENST00000318888
  gene symbol: ABLIM2
  hgvsc: ENST00000318888.4:c.-316A>T
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000342813
  ensembl transcript: ENST00000341937
  gene symbol: ABLIM2
  hgvsc: ENST00000341937.5:c.414A>T
  hgvsp: ENST00000341937.5:c.414A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000421283
  ensembl transcript: ENST00000505872
  gene symbol: ABLIM2
  hgvsc: ENST00000505872.1:c.414A>T
  hgvsp: ENST00000505872.1:c.414A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000384658
  ensembl transcript: ENST00000407564
  gene symbol: ABLIM2
  hgvsc: ENST00000407564.3:c.414A>T
  hgvsp: ENST00000407564.3:c.414A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000296372
  ensembl transcript: ENST00000296372
  gene symbol: ABLIM2
  hgvsc: ENST00000296372.8:c.414A>T
  hgvsp: ENST00000296372.8:c.414A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000354887
  ensembl transcript: ENST00000361737
  gene symbol: ABLIM2
  hgvsc: ENST00000361737.5:c.414A>T
  hgvsp: ENST00000361737.5:c.414A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000389410
  ensembl transcript: ENST00000428004
  gene symbol: ABLIM2
  hgvsc: ENST00000428004.2:c.414A>T
  hgvsp: ENST00000428004.2:c.414A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000355003
  ensembl transcript: ENST00000361581
  gene symbol: ABLIM2
  hgvsc: ENST00000361581.5:c.414A>T
  hgvsp: ENST00000361581.5:c.414A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000393511
  ensembl transcript: ENST00000447017
  gene symbol: ABLIM2
  hgvsc: ENST00000447017.2:c.414A>T
  hgvsp: ENST00000447017.2:c.414A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19195
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10645
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1834
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42746
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2358
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val138Val
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: QD

4-8089938-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8089938
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 8089938
    reference: chr 4
allele count: 9
allele frequency: 7.756213588886208e-5
allele num: 116036
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000421283
  ensembl transcript: ENST00000505872
  gene symbol: ABLIM2
  hgvsc: ENST00000505872.1:c.412G>A
  hgvsp: ENSP00000421283.1:p.Val138Ile
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000441255
  ensembl transcript: ENST00000545242
  gene symbol: ABLIM2
  hgvsc: ENST00000545242.1:c.412G>A
  hgvsp: ENSP00000441255.1:p.Val138Ile
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000354887
  ensembl transcript: ENST00000361737
  gene symbol: ABLIM2
  hgvsc: ENST00000361737.5:c.412G>A
  hgvsp: ENSP00000354887.5:p.Val138Ile
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000355003
  ensembl transcript: ENST00000361581
  gene symbol: ABLIM2
  hgvsc: ENST00000361581.5:c.412G>A
  hgvsp: ENSP00000355003.5:p.Val138Ile
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000384658
  ensembl transcript: ENST00000407564
  gene symbol: ABLIM2
  hgvsc: ENST00000407564.3:c.412G>A
  hgvsp: ENSP00000384658.3:p.Val138Ile
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000393511
  ensembl transcript: ENST00000447017
  gene symbol: ABLIM2
  hgvsc: ENST00000447017.2:c.412G>A
  hgvsp: ENSP00000393511.2:p.Val138Ile
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000389410
  ensembl transcript: ENST00000428004
  gene symbol: ABLIM2
  hgvsc: ENST00000428004.2:c.412G>A
  hgvsp: ENSP00000389410.2:p.Val138Ile
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000296372
  ensembl transcript: ENST00000296372
  gene symbol: ABLIM2
  hgvsc: ENST00000296372.8:c.412G>A
  hgvsp: ENSP00000296372.8:p.Val138Ile
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000317020
  ensembl transcript: ENST00000318888
  gene symbol: ABLIM2
  hgvsc: ENST00000318888.4:c.-318G>A
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000444365
  ensembl transcript: ENST00000546334
  gene symbol: ABLIM2
  hgvsc: ENST00000546334.1:c.412G>A
  hgvsp: ENSP00000444365.1:p.Val138Ile
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000342813
  ensembl transcript: ENST00000341937
  gene symbol: ABLIM2
  hgvsc: ENST00000341937.5:c.412G>A
  hgvsp: ENSP00000342813.5:p.Val138Ile
  variant of: http://identifiers.org/hgnc/19195
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1901
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10748
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42736
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 806
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2229
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 6.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
hgvs: p.Val138Ile
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Latino
population: African
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP

4-8089939-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8089939
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 8089939
    reference: chr 4
allele count: 1
allele frequency: 8.608222574202878e-6
allele num: 116168
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000342813
  ensembl transcript: ENST00000341937
  gene symbol: ABLIM2
  hgvsc: ENST00000341937.5:c.411C>T
  hgvsp: ENST00000341937.5:c.411C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000355003
  ensembl transcript: ENST00000361581
  gene symbol: ABLIM2
  hgvsc: ENST00000361581.5:c.411C>T
  hgvsp: ENST00000361581.5:c.411C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000389410
  ensembl transcript: ENST00000428004
  gene symbol: ABLIM2
  hgvsc: ENST00000428004.2:c.411C>T
  hgvsp: ENST00000428004.2:c.411C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000317020
  ensembl transcript: ENST00000318888
  gene symbol: ABLIM2
  hgvsc: ENST00000318888.4:c.-319C>T
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000296372
  ensembl transcript: ENST00000296372
  gene symbol: ABLIM2
  hgvsc: ENST00000296372.8:c.411C>T
  hgvsp: ENST00000296372.8:c.411C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000441255
  ensembl transcript: ENST00000545242
  gene symbol: ABLIM2
  hgvsc: ENST00000545242.1:c.411C>T
  hgvsp: ENST00000545242.1:c.411C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000384658
  ensembl transcript: ENST00000407564
  gene symbol: ABLIM2
  hgvsc: ENST00000407564.3:c.411C>T
  hgvsp: ENST00000407564.3:c.411C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000354887
  ensembl transcript: ENST00000361737
  gene symbol: ABLIM2
  hgvsc: ENST00000361737.5:c.411C>T
  hgvsp: ENST00000361737.5:c.411C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000421283
  ensembl transcript: ENST00000505872
  gene symbol: ABLIM2
  hgvsc: ENST00000505872.1:c.411C>T
  hgvsp: ENST00000505872.1:c.411C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000444365
  ensembl transcript: ENST00000546334
  gene symbol: ABLIM2
  hgvsc: ENST00000546334.1:c.411C>T
  hgvsp: ENST00000546334.1:c.411C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000393511
  ensembl transcript: ENST00000447017
  gene symbol: ABLIM2
  hgvsc: ENST00000447017.2:c.411C>T
  hgvsp: ENST00000447017.2:c.411C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19195
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 783
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10839
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2150
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42757
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1899
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro137Pro
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum

4-8089945-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8089945
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 8089945
    reference: chr 4
allele count: 1
allele frequency: 8.564870327863236e-6
allele num: 116756
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000296372
  ensembl transcript: ENST00000296372
  gene symbol: ABLIM2
  hgvsc: ENST00000296372.8:c.405C>T
  hgvsp: ENST00000296372.8:c.405C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000317020
  ensembl transcript: ENST00000318888
  gene symbol: ABLIM2
  hgvsc: ENST00000318888.4:c.-325C>T
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000441255
  ensembl transcript: ENST00000545242
  gene symbol: ABLIM2
  hgvsc: ENST00000545242.1:c.405C>T
  hgvsp: ENST00000545242.1:c.405C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000384658
  ensembl transcript: ENST00000407564
  gene symbol: ABLIM2
  hgvsc: ENST00000407564.3:c.405C>T
  hgvsp: ENST00000407564.3:c.405C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000389410
  ensembl transcript: ENST00000428004
  gene symbol: ABLIM2
  hgvsc: ENST00000428004.2:c.405C>T
  hgvsp: ENST00000428004.2:c.405C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000355003
  ensembl transcript: ENST00000361581
  gene symbol: ABLIM2
  hgvsc: ENST00000361581.5:c.405C>T
  hgvsp: ENST00000361581.5:c.405C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000444365
  ensembl transcript: ENST00000546334
  gene symbol: ABLIM2
  hgvsc: ENST00000546334.1:c.405C>T
  hgvsp: ENST00000546334.1:c.405C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000421283
  ensembl transcript: ENST00000505872
  gene symbol: ABLIM2
  hgvsc: ENST00000505872.1:c.405C>T
  hgvsp: ENST00000505872.1:c.405C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000354887
  ensembl transcript: ENST00000361737
  gene symbol: ABLIM2
  hgvsc: ENST00000361737.5:c.405C>T
  hgvsp: ENST00000361737.5:c.405C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000342813
  ensembl transcript: ENST00000341937
  gene symbol: ABLIM2
  hgvsc: ENST00000341937.5:c.405C>T
  hgvsp: ENST00000341937.5:c.405C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000393511
  ensembl transcript: ENST00000447017
  gene symbol: ABLIM2
  hgvsc: ENST00000447017.2:c.405C>T
  hgvsp: ENST00000447017.2:c.405C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19195
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1928
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 722
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11113
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1885
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 42827
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser135Ser
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Other
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: G
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum

4-8089946-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8089946
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 8089946
    reference: chr 4
allele count: 1
allele frequency: 8.562376915831835e-6
allele num: 116790
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000421283
  ensembl transcript: ENST00000505872
  gene symbol: ABLIM2
  hgvsc: ENST00000505872.1:c.404C>T
  hgvsp: ENSP00000421283.1:p.Ser135Phe
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000296372
  ensembl transcript: ENST00000296372
  gene symbol: ABLIM2
  hgvsc: ENST00000296372.8:c.404C>T
  hgvsp: ENSP00000296372.8:p.Ser135Phe
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000354887
  ensembl transcript: ENST00000361737
  gene symbol: ABLIM2
  hgvsc: ENST00000361737.5:c.404C>T
  hgvsp: ENSP00000354887.5:p.Ser135Phe
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000441255
  ensembl transcript: ENST00000545242
  gene symbol: ABLIM2
  hgvsc: ENST00000545242.1:c.404C>T
  hgvsp: ENSP00000441255.1:p.Ser135Phe
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000393511
  ensembl transcript: ENST00000447017
  gene symbol: ABLIM2
  hgvsc: ENST00000447017.2:c.404C>T
  hgvsp: ENSP00000393511.2:p.Ser135Phe
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000355003
  ensembl transcript: ENST00000361581
  gene symbol: ABLIM2
  hgvsc: ENST00000361581.5:c.404C>T
  hgvsp: ENSP00000355003.5:p.Ser135Phe
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000317020
  ensembl transcript: ENST00000318888
  gene symbol: ABLIM2
  hgvsc: ENST00000318888.4:c.-326C>T
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000384658
  ensembl transcript: ENST00000407564
  gene symbol: ABLIM2
  hgvsc: ENST00000407564.3:c.404C>T
  hgvsp: ENSP00000384658.3:p.Ser135Phe
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000389410
  ensembl transcript: ENST00000428004
  gene symbol: ABLIM2
  hgvsc: ENST00000428004.2:c.404C>T
  hgvsp: ENSP00000389410.2:p.Ser135Phe
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000444365
  ensembl transcript: ENST00000546334
  gene symbol: ABLIM2
  hgvsc: ENST00000546334.1:c.404C>T
  hgvsp: ENSP00000444365.1:p.Ser135Phe
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000342813
  ensembl transcript: ENST00000341937
  gene symbol: ABLIM2
  hgvsc: ENST00000341937.5:c.404C>T
  hgvsp: ENSP00000342813.5:p.Ser135Phe
  variant of: http://identifiers.org/hgnc/19195
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 727
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1874
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1930
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42794
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11140
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser135Phe
num of homozygotes: 0
population: East Asian
population: Other
population: European (Non-Finnish)
population: African
population: South Asian
population: Latino
population: European (Finnish)
reference allele: G
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum

4-8089954-C-CT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8089954
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 8089955
    reference: chr 4
allele count: 1
allele frequency: 8.539272112445135e-6
allele num: 117106
alternate allele: CT
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000389410
  ensembl transcript: ENST00000428004
  gene symbol: ABLIM2
  hgvsc: ENST00000428004.2:c.395dupA
  hgvsp: ENSP00000389410.2:p.Lys133GlufsTer47
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000354887
  ensembl transcript: ENST00000361737
  gene symbol: ABLIM2
  hgvsc: ENST00000361737.5:c.395dupA
  hgvsp: ENSP00000354887.5:p.Lys133GlufsTer47
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000384658
  ensembl transcript: ENST00000407564
  gene symbol: ABLIM2
  hgvsc: ENST00000407564.3:c.395dupA
  hgvsp: ENSP00000384658.3:p.Lys133GlufsTer47
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000355003
  ensembl transcript: ENST00000361581
  gene symbol: ABLIM2
  hgvsc: ENST00000361581.5:c.395dupA
  hgvsp: ENSP00000355003.5:p.Lys133GlufsTer47
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000342813
  ensembl transcript: ENST00000341937
  gene symbol: ABLIM2
  hgvsc: ENST00000341937.5:c.395dupA
  hgvsp: ENSP00000342813.5:p.Lys133GlufsTer47
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000317020
  ensembl transcript: ENST00000318888
  gene symbol: ABLIM2
  hgvsc: ENST00000318888.4:c.-335dupA
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000441255
  ensembl transcript: ENST00000545242
  gene symbol: ABLIM2
  hgvsc: ENST00000545242.1:c.395dupA
  hgvsp: ENSP00000441255.1:p.Lys133GlufsTer47
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000444365
  ensembl transcript: ENST00000546334
  gene symbol: ABLIM2
  hgvsc: ENST00000546334.1:c.395dupA
  hgvsp: ENSP00000444365.1:p.Lys133GlufsTer47
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000421283
  ensembl transcript: ENST00000505872
  gene symbol: ABLIM2
  hgvsc: ENST00000505872.1:c.395dupA
  hgvsp: ENSP00000421283.1:p.Lys133GlufsTer47
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000296372
  ensembl transcript: ENST00000296372
  gene symbol: ABLIM2
  hgvsc: ENST00000296372.8:c.395dupA
  hgvsp: ENSP00000296372.8:p.Lys133GlufsTer47
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000393511
  ensembl transcript: ENST00000447017
  gene symbol: ABLIM2
  hgvsc: ENST00000447017.2:c.395dupA
  hgvsp: ENSP00000393511.2:p.Lys133GlufsTer47
  variant of: http://identifiers.org/hgnc/19195
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 832
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42698
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1721
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11282
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1964
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys133GlufsTer47
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum

4-8089955-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8089955
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 8089955
    reference: chr 4
allele count: 1
allele frequency: 8.535336292249914e-6
allele num: 117160
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000389410
  ensembl transcript: ENST00000428004
  gene symbol: ABLIM2
  hgvsc: ENST00000428004.2:c.395A>G
  hgvsp: ENSP00000389410.2:p.Gln132Arg
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000355003
  ensembl transcript: ENST00000361581
  gene symbol: ABLIM2
  hgvsc: ENST00000361581.5:c.395A>G
  hgvsp: ENSP00000355003.5:p.Gln132Arg
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000342813
  ensembl transcript: ENST00000341937
  gene symbol: ABLIM2
  hgvsc: ENST00000341937.5:c.395A>G
  hgvsp: ENSP00000342813.5:p.Gln132Arg
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000354887
  ensembl transcript: ENST00000361737
  gene symbol: ABLIM2
  hgvsc: ENST00000361737.5:c.395A>G
  hgvsp: ENSP00000354887.5:p.Gln132Arg
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000296372
  ensembl transcript: ENST00000296372
  gene symbol: ABLIM2
  hgvsc: ENST00000296372.8:c.395A>G
  hgvsp: ENSP00000296372.8:p.Gln132Arg
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000441255
  ensembl transcript: ENST00000545242
  gene symbol: ABLIM2
  hgvsc: ENST00000545242.1:c.395A>G
  hgvsp: ENSP00000441255.1:p.Gln132Arg
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000421283
  ensembl transcript: ENST00000505872
  gene symbol: ABLIM2
  hgvsc: ENST00000505872.1:c.395A>G
  hgvsp: ENSP00000421283.1:p.Gln132Arg
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000384658
  ensembl transcript: ENST00000407564
  gene symbol: ABLIM2
  hgvsc: ENST00000407564.3:c.395A>G
  hgvsp: ENSP00000384658.3:p.Gln132Arg
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000317020
  ensembl transcript: ENST00000318888
  gene symbol: ABLIM2
  hgvsc: ENST00000318888.4:c.-335A>G
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000393511
  ensembl transcript: ENST00000447017
  gene symbol: ABLIM2
  hgvsc: ENST00000447017.2:c.395A>G
  hgvsp: ENSP00000393511.2:p.Gln132Arg
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000444365
  ensembl transcript: ENST00000546334
  gene symbol: ABLIM2
  hgvsc: ENST00000546334.1:c.395A>G
  hgvsp: ENSP00000444365.1:p.Gln132Arg
  variant of: http://identifiers.org/hgnc/19195
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1946
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42721
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1702
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11306
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 834
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln132Arg
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: Other
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: T
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: DP

4-8089962-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8089962
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 8089962
    reference: chr 4
allele count: 1
allele frequency: 8.531840829977476e-6
allele num: 117208
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000444365
  ensembl transcript: ENST00000546334
  gene symbol: ABLIM2
  hgvsc: ENST00000546334.1:c.388A>G
  hgvsp: ENSP00000444365.1:p.Met130Val
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000296372
  ensembl transcript: ENST00000296372
  gene symbol: ABLIM2
  hgvsc: ENST00000296372.8:c.388A>G
  hgvsp: ENSP00000296372.8:p.Met130Val
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000384658
  ensembl transcript: ENST00000407564
  gene symbol: ABLIM2
  hgvsc: ENST00000407564.3:c.388A>G
  hgvsp: ENSP00000384658.3:p.Met130Val
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000355003
  ensembl transcript: ENST00000361581
  gene symbol: ABLIM2
  hgvsc: ENST00000361581.5:c.388A>G
  hgvsp: ENSP00000355003.5:p.Met130Val
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000354887
  ensembl transcript: ENST00000361737
  gene symbol: ABLIM2
  hgvsc: ENST00000361737.5:c.388A>G
  hgvsp: ENSP00000354887.5:p.Met130Val
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000342813
  ensembl transcript: ENST00000341937
  gene symbol: ABLIM2
  hgvsc: ENST00000341937.5:c.388A>G
  hgvsp: ENSP00000342813.5:p.Met130Val
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000421283
  ensembl transcript: ENST00000505872
  gene symbol: ABLIM2
  hgvsc: ENST00000505872.1:c.388A>G
  hgvsp: ENSP00000421283.1:p.Met130Val
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000393511
  ensembl transcript: ENST00000447017
  gene symbol: ABLIM2
  hgvsc: ENST00000447017.2:c.388A>G
  hgvsp: ENSP00000393511.2:p.Met130Val
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000389410
  ensembl transcript: ENST00000428004
  gene symbol: ABLIM2
  hgvsc: ENST00000428004.2:c.388A>G
  hgvsp: ENSP00000389410.2:p.Met130Val
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000441255
  ensembl transcript: ENST00000545242
  gene symbol: ABLIM2
  hgvsc: ENST00000545242.1:c.388A>G
  hgvsp: ENSP00000441255.1:p.Met130Val
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000317020
  ensembl transcript: ENST00000318888
  gene symbol: ABLIM2
  hgvsc: ENST00000318888.4:c.-342A>G
  variant of: http://identifiers.org/hgnc/19195
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1671
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 984
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42405
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11450
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Met130Val
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: Other
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum

4-8089970-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8089970
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 8089970
    reference: chr 4
allele count: 1
allele frequency: 8.549054474575111e-6
allele num: 116972
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000317020
  ensembl transcript: ENST00000318888
  gene symbol: ABLIM2
  hgvsc: ENST00000318888.4:c.-350A>G
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000444365
  ensembl transcript: ENST00000546334
  gene symbol: ABLIM2
  hgvsc: ENST00000546334.1:c.380A>G
  hgvsp: ENSP00000444365.1:p.Lys127Arg
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000421283
  ensembl transcript: ENST00000505872
  gene symbol: ABLIM2
  hgvsc: ENST00000505872.1:c.380A>G
  hgvsp: ENSP00000421283.1:p.Lys127Arg
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000441255
  ensembl transcript: ENST00000545242
  gene symbol: ABLIM2
  hgvsc: ENST00000545242.1:c.380A>G
  hgvsp: ENSP00000441255.1:p.Lys127Arg
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000354887
  ensembl transcript: ENST00000361737
  gene symbol: ABLIM2
  hgvsc: ENST00000361737.5:c.380A>G
  hgvsp: ENSP00000354887.5:p.Lys127Arg
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000389410
  ensembl transcript: ENST00000428004
  gene symbol: ABLIM2
  hgvsc: ENST00000428004.2:c.380A>G
  hgvsp: ENSP00000389410.2:p.Lys127Arg
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000355003
  ensembl transcript: ENST00000361581
  gene symbol: ABLIM2
  hgvsc: ENST00000361581.5:c.380A>G
  hgvsp: ENSP00000355003.5:p.Lys127Arg
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000296372
  ensembl transcript: ENST00000296372
  gene symbol: ABLIM2
  hgvsc: ENST00000296372.8:c.380A>G
  hgvsp: ENSP00000296372.8:p.Lys127Arg
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000384658
  ensembl transcript: ENST00000407564
  gene symbol: ABLIM2
  hgvsc: ENST00000407564.3:c.380A>G
  hgvsp: ENSP00000384658.3:p.Lys127Arg
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000393511
  ensembl transcript: ENST00000447017
  gene symbol: ABLIM2
  hgvsc: ENST00000447017.2:c.380A>G
  hgvsp: ENSP00000393511.2:p.Lys127Arg
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000342813
  ensembl transcript: ENST00000341937
  gene symbol: ABLIM2
  hgvsc: ENST00000341937.5:c.380A>G
  hgvsp: ENSP00000342813.5:p.Lys127Arg
  variant of: http://identifiers.org/hgnc/19195
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11596
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41651
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1767
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1928
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1349
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys127Arg
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: South Asian
population: Other
population: European (Non-Finnish)
population: East Asian
reference allele: T
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: QD

4-8089974-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8089974
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 8089974
    reference: chr 4
allele count: 2
allele frequency: 1.71370794989118e-5
allele num: 116706
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000317020
  ensembl transcript: ENST00000318888
  gene symbol: ABLIM2
  hgvsc: ENST00000318888.4:c.-354G>A
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000444365
  ensembl transcript: ENST00000546334
  gene symbol: ABLIM2
  hgvsc: ENST00000546334.1:c.376G>A
  hgvsp: ENSP00000444365.1:p.Gly126Arg
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000421283
  ensembl transcript: ENST00000505872
  gene symbol: ABLIM2
  hgvsc: ENST00000505872.1:c.376G>A
  hgvsp: ENSP00000421283.1:p.Gly126Arg
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000441255
  ensembl transcript: ENST00000545242
  gene symbol: ABLIM2
  hgvsc: ENST00000545242.1:c.376G>A
  hgvsp: ENSP00000441255.1:p.Gly126Arg
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000384658
  ensembl transcript: ENST00000407564
  gene symbol: ABLIM2
  hgvsc: ENST00000407564.3:c.376G>A
  hgvsp: ENSP00000384658.3:p.Gly126Arg
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000296372
  ensembl transcript: ENST00000296372
  gene symbol: ABLIM2
  hgvsc: ENST00000296372.8:c.376G>A
  hgvsp: ENSP00000296372.8:p.Gly126Arg
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000355003
  ensembl transcript: ENST00000361581
  gene symbol: ABLIM2
  hgvsc: ENST00000361581.5:c.376G>A
  hgvsp: ENSP00000355003.5:p.Gly126Arg
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000354887
  ensembl transcript: ENST00000361737
  gene symbol: ABLIM2
  hgvsc: ENST00000361737.5:c.376G>A
  hgvsp: ENSP00000354887.5:p.Gly126Arg
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000389410
  ensembl transcript: ENST00000428004
  gene symbol: ABLIM2
  hgvsc: ENST00000428004.2:c.376G>A
  hgvsp: ENSP00000389410.2:p.Gly126Arg
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000342813
  ensembl transcript: ENST00000341937
  gene symbol: ABLIM2
  hgvsc: ENST00000341937.5:c.376G>A
  hgvsp: ENSP00000342813.5:p.Gly126Arg
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000393511
  ensembl transcript: ENST00000447017
  gene symbol: ABLIM2
  hgvsc: ENST00000447017.2:c.376G>A
  hgvsp: ENSP00000393511.2:p.Gly126Arg
  variant of: http://identifiers.org/hgnc/19195
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11598
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1861
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1993
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1609
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41055
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly126Arg
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: DP

4-8089975-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8089975
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 8089975
    reference: chr 4
allele count: 1
allele frequency: 8.565310492505354e-6
allele num: 116750
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000421283
  ensembl transcript: ENST00000505872
  gene symbol: ABLIM2
  hgvsc: ENST00000505872.1:c.375C>T
  hgvsp: ENST00000505872.1:c.375C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000296372
  ensembl transcript: ENST00000296372
  gene symbol: ABLIM2
  hgvsc: ENST00000296372.8:c.375C>T
  hgvsp: ENST00000296372.8:c.375C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000342813
  ensembl transcript: ENST00000341937
  gene symbol: ABLIM2
  hgvsc: ENST00000341937.5:c.375C>T
  hgvsp: ENST00000341937.5:c.375C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000355003
  ensembl transcript: ENST00000361581
  gene symbol: ABLIM2
  hgvsc: ENST00000361581.5:c.375C>T
  hgvsp: ENST00000361581.5:c.375C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000389410
  ensembl transcript: ENST00000428004
  gene symbol: ABLIM2
  hgvsc: ENST00000428004.2:c.375C>T
  hgvsp: ENST00000428004.2:c.375C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000384658
  ensembl transcript: ENST00000407564
  gene symbol: ABLIM2
  hgvsc: ENST00000407564.3:c.375C>T
  hgvsp: ENST00000407564.3:c.375C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000354887
  ensembl transcript: ENST00000361737
  gene symbol: ABLIM2
  hgvsc: ENST00000361737.5:c.375C>T
  hgvsp: ENST00000361737.5:c.375C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000441255
  ensembl transcript: ENST00000545242
  gene symbol: ABLIM2
  hgvsc: ENST00000545242.1:c.375C>T
  hgvsp: ENST00000545242.1:c.375C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000444365
  ensembl transcript: ENST00000546334
  gene symbol: ABLIM2
  hgvsc: ENST00000546334.1:c.375C>T
  hgvsp: ENST00000546334.1:c.375C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000317020
  ensembl transcript: ENST00000318888
  gene symbol: ABLIM2
  hgvsc: ENST00000318888.4:c.-355C>T
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000393511
  ensembl transcript: ENST00000447017
  gene symbol: ABLIM2
  hgvsc: ENST00000447017.2:c.375C>T
  hgvsp: ENST00000447017.2:c.375C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19195
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1860
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1626
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 659
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41030
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1985
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11652
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn125Asn
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
population: Latino
population: South Asian
reference allele: G
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum

4-8089976-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8089976
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 8089976
    reference: chr 4
allele count: 3
allele frequency: 2.570605977515766e-5
allele num: 116704
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000393511
  ensembl transcript: ENST00000447017
  gene symbol: ABLIM2
  hgvsc: ENST00000447017.2:c.374A>G
  hgvsp: ENSP00000393511.2:p.Asn125Ser
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000421283
  ensembl transcript: ENST00000505872
  gene symbol: ABLIM2
  hgvsc: ENST00000505872.1:c.374A>G
  hgvsp: ENSP00000421283.1:p.Asn125Ser
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000354887
  ensembl transcript: ENST00000361737
  gene symbol: ABLIM2
  hgvsc: ENST00000361737.5:c.374A>G
  hgvsp: ENSP00000354887.5:p.Asn125Ser
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000296372
  ensembl transcript: ENST00000296372
  gene symbol: ABLIM2
  hgvsc: ENST00000296372.8:c.374A>G
  hgvsp: ENSP00000296372.8:p.Asn125Ser
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000444365
  ensembl transcript: ENST00000546334
  gene symbol: ABLIM2
  hgvsc: ENST00000546334.1:c.374A>G
  hgvsp: ENSP00000444365.1:p.Asn125Ser
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000355003
  ensembl transcript: ENST00000361581
  gene symbol: ABLIM2
  hgvsc: ENST00000361581.5:c.374A>G
  hgvsp: ENSP00000355003.5:p.Asn125Ser
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000384658
  ensembl transcript: ENST00000407564
  gene symbol: ABLIM2
  hgvsc: ENST00000407564.3:c.374A>G
  hgvsp: ENSP00000384658.3:p.Asn125Ser
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000342813
  ensembl transcript: ENST00000341937
  gene symbol: ABLIM2
  hgvsc: ENST00000341937.5:c.374A>G
  hgvsp: ENSP00000342813.5:p.Asn125Ser
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000441255
  ensembl transcript: ENST00000545242
  gene symbol: ABLIM2
  hgvsc: ENST00000545242.1:c.374A>G
  hgvsp: ENSP00000441255.1:p.Asn125Ser
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000317020
  ensembl transcript: ENST00000318888
  gene symbol: ABLIM2
  hgvsc: ENST00000318888.4:c.-356A>G
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000389410
  ensembl transcript: ENST00000428004
  gene symbol: ABLIM2
  hgvsc: ENST00000428004.2:c.374A>G
  hgvsp: ENSP00000389410.2:p.Asn125Ser
  variant of: http://identifiers.org/hgnc/19195
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40947
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 680
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11660
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1691
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1899
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1941
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn125Ser
num of homozygotes: 0
population: Other
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: T
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum

4-8089982-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8089982
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 8089982
    reference: chr 4
allele count: 1
allele frequency: 8.611335962661248e-6
allele num: 116126
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000389410
  ensembl transcript: ENST00000428004
  gene symbol: ABLIM2
  hgvsc: ENST00000428004.2:c.368C>A
  hgvsp: ENSP00000389410.2:p.Thr123Asn
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000421283
  ensembl transcript: ENST00000505872
  gene symbol: ABLIM2
  hgvsc: ENST00000505872.1:c.368C>A
  hgvsp: ENSP00000421283.1:p.Thr123Asn
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000393511
  ensembl transcript: ENST00000447017
  gene symbol: ABLIM2
  hgvsc: ENST00000447017.2:c.368C>A
  hgvsp: ENSP00000393511.2:p.Thr123Asn
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000355003
  ensembl transcript: ENST00000361581
  gene symbol: ABLIM2
  hgvsc: ENST00000361581.5:c.368C>A
  hgvsp: ENSP00000355003.5:p.Thr123Asn
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000342813
  ensembl transcript: ENST00000341937
  gene symbol: ABLIM2
  hgvsc: ENST00000341937.5:c.368C>A
  hgvsp: ENSP00000342813.5:p.Thr123Asn
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000444365
  ensembl transcript: ENST00000546334
  gene symbol: ABLIM2
  hgvsc: ENST00000546334.1:c.368C>A
  hgvsp: ENSP00000444365.1:p.Thr123Asn
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000317020
  ensembl transcript: ENST00000318888
  gene symbol: ABLIM2
  hgvsc: ENST00000318888.4:c.-362C>A
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000296372
  ensembl transcript: ENST00000296372
  gene symbol: ABLIM2
  hgvsc: ENST00000296372.8:c.368C>A
  hgvsp: ENSP00000296372.8:p.Thr123Asn
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000384658
  ensembl transcript: ENST00000407564
  gene symbol: ABLIM2
  hgvsc: ENST00000407564.3:c.368C>A
  hgvsp: ENSP00000384658.3:p.Thr123Asn
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000354887
  ensembl transcript: ENST00000361737
  gene symbol: ABLIM2
  hgvsc: ENST00000361737.5:c.368C>A
  hgvsp: ENSP00000354887.5:p.Thr123Asn
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000441255
  ensembl transcript: ENST00000545242
  gene symbol: ABLIM2
  hgvsc: ENST00000545242.1:c.368C>A
  hgvsp: ENSP00000441255.1:p.Thr123Asn
  variant of: http://identifiers.org/hgnc/19195
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 993
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2158
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11481
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2367
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1935
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39857
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr123Asn
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: MQ

4-8089983-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8089983
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 8089983
    reference: chr 4
allele count: 40
allele frequency: 3.444949703734325e-4
allele num: 116112
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000296372
  ensembl transcript: ENST00000296372
  gene symbol: ABLIM2
  hgvsc: ENST00000296372.8:c.367A>T
  hgvsp: ENSP00000296372.8:p.Thr123Ser
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000441255
  ensembl transcript: ENST00000545242
  gene symbol: ABLIM2
  hgvsc: ENST00000545242.1:c.367A>T
  hgvsp: ENSP00000441255.1:p.Thr123Ser
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000384658
  ensembl transcript: ENST00000407564
  gene symbol: ABLIM2
  hgvsc: ENST00000407564.3:c.367A>T
  hgvsp: ENSP00000384658.3:p.Thr123Ser
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000389410
  ensembl transcript: ENST00000428004
  gene symbol: ABLIM2
  hgvsc: ENST00000428004.2:c.367A>T
  hgvsp: ENSP00000389410.2:p.Thr123Ser
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000317020
  ensembl transcript: ENST00000318888
  gene symbol: ABLIM2
  hgvsc: ENST00000318888.4:c.-363A>T
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000421283
  ensembl transcript: ENST00000505872
  gene symbol: ABLIM2
  hgvsc: ENST00000505872.1:c.367A>T
  hgvsp: ENSP00000421283.1:p.Thr123Ser
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000342813
  ensembl transcript: ENST00000341937
  gene symbol: ABLIM2
  hgvsc: ENST00000341937.5:c.367A>T
  hgvsp: ENSP00000342813.5:p.Thr123Ser
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000355003
  ensembl transcript: ENST00000361581
  gene symbol: ABLIM2
  hgvsc: ENST00000361581.5:c.367A>T
  hgvsp: ENSP00000355003.5:p.Thr123Ser
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000444365
  ensembl transcript: ENST00000546334
  gene symbol: ABLIM2
  hgvsc: ENST00000546334.1:c.367A>T
  hgvsp: ENSP00000444365.1:p.Thr123Ser
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000354887
  ensembl transcript: ENST00000361737
  gene symbol: ABLIM2
  hgvsc: ENST00000361737.5:c.367A>T
  hgvsp: ENSP00000354887.5:p.Thr123Ser
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000393511
  ensembl transcript: ENST00000447017
  gene symbol: ABLIM2
  hgvsc: ENST00000447017.2:c.367A>T
  hgvsp: ENSP00000393511.2:p.Thr123Ser
  variant of: http://identifiers.org/hgnc/19195
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11516
  bin: 2.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 4.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 39776
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2380
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 995
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 3.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1938
  bin: 3.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr123Ser
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: African
population: Other
reference allele: T
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: QD

4-8089988-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8089988
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 8089988
    reference: chr 4
allele count: 16
allele frequency: 1.386505831990156e-4
allele num: 115398
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000421283
  ensembl transcript: ENST00000505872
  gene symbol: ABLIM2
  hgvsc: ENST00000505872.1:c.362G>A
  hgvsp: ENSP00000421283.1:p.Arg121Gln
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000342813
  ensembl transcript: ENST00000341937
  gene symbol: ABLIM2
  hgvsc: ENST00000341937.5:c.362G>A
  hgvsp: ENSP00000342813.5:p.Arg121Gln
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000389410
  ensembl transcript: ENST00000428004
  gene symbol: ABLIM2
  hgvsc: ENST00000428004.2:c.362G>A
  hgvsp: ENSP00000389410.2:p.Arg121Gln
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000317020
  ensembl transcript: ENST00000318888
  gene symbol: ABLIM2
  hgvsc: ENST00000318888.4:c.-368G>A
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000444365
  ensembl transcript: ENST00000546334
  gene symbol: ABLIM2
  hgvsc: ENST00000546334.1:c.362G>A
  hgvsp: ENSP00000444365.1:p.Arg121Gln
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000355003
  ensembl transcript: ENST00000361581
  gene symbol: ABLIM2
  hgvsc: ENST00000361581.5:c.362G>A
  hgvsp: ENSP00000355003.5:p.Arg121Gln
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000296372
  ensembl transcript: ENST00000296372
  gene symbol: ABLIM2
  hgvsc: ENST00000296372.8:c.362G>A
  hgvsp: ENSP00000296372.8:p.Arg121Gln
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000441255
  ensembl transcript: ENST00000545242
  gene symbol: ABLIM2
  hgvsc: ENST00000545242.1:c.362G>A
  hgvsp: ENSP00000441255.1:p.Arg121Gln
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000393511
  ensembl transcript: ENST00000447017
  gene symbol: ABLIM2
  hgvsc: ENST00000447017.2:c.362G>A
  hgvsp: ENSP00000393511.2:p.Arg121Gln
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000384658
  ensembl transcript: ENST00000407564
  gene symbol: ABLIM2
  hgvsc: ENST00000407564.3:c.362G>A
  hgvsp: ENSP00000384658.3:p.Arg121Gln
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000354887
  ensembl transcript: ENST00000361737
  gene symbol: ABLIM2
  hgvsc: ENST00000361737.5:c.362G>A
  hgvsp: ENSP00000354887.5:p.Arg121Gln
  variant of: http://identifiers.org/hgnc/19195
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3265
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 38305
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11352
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2015
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2450
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1338
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg121Gln
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
population: African
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum

4-8089989-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8089989
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 8089989
    reference: chr 4
allele count: 1
allele frequency: 8.685984295740394e-6
allele num: 115128
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000355003
  ensembl transcript: ENST00000361581
  gene symbol: ABLIM2
  hgvsc: ENST00000361581.5:c.361C>G
  hgvsp: ENSP00000355003.5:p.Arg121Gly
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000342813
  ensembl transcript: ENST00000341937
  gene symbol: ABLIM2
  hgvsc: ENST00000341937.5:c.361C>G
  hgvsp: ENSP00000342813.5:p.Arg121Gly
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000317020
  ensembl transcript: ENST00000318888
  gene symbol: ABLIM2
  hgvsc: ENST00000318888.4:c.-369C>G
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000393511
  ensembl transcript: ENST00000447017
  gene symbol: ABLIM2
  hgvsc: ENST00000447017.2:c.361C>G
  hgvsp: ENSP00000393511.2:p.Arg121Gly
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000389410
  ensembl transcript: ENST00000428004
  gene symbol: ABLIM2
  hgvsc: ENST00000428004.2:c.361C>G
  hgvsp: ENSP00000389410.2:p.Arg121Gly
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000296372
  ensembl transcript: ENST00000296372
  gene symbol: ABLIM2
  hgvsc: ENST00000296372.8:c.361C>G
  hgvsp: ENSP00000296372.8:p.Arg121Gly
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000421283
  ensembl transcript: ENST00000505872
  gene symbol: ABLIM2
  hgvsc: ENST00000505872.1:c.361C>G
  hgvsp: ENSP00000421283.1:p.Arg121Gly
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000384658
  ensembl transcript: ENST00000407564
  gene symbol: ABLIM2
  hgvsc: ENST00000407564.3:c.361C>G
  hgvsp: ENSP00000384658.3:p.Arg121Gly
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000441255
  ensembl transcript: ENST00000545242
  gene symbol: ABLIM2
  hgvsc: ENST00000545242.1:c.361C>G
  hgvsp: ENSP00000441255.1:p.Arg121Gly
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000444365
  ensembl transcript: ENST00000546334
  gene symbol: ABLIM2
  hgvsc: ENST00000546334.1:c.361C>G
  hgvsp: ENSP00000444365.1:p.Arg121Gly
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000354887
  ensembl transcript: ENST00000361737
  gene symbol: ABLIM2
  hgvsc: ENST00000361737.5:c.361C>G
  hgvsp: ENSP00000354887.5:p.Arg121Gly
  variant of: http://identifiers.org/hgnc/19195
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1986
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3703
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37646
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2590
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11320
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1501
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg121Gly
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: FS
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP

4-8089993-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8089993
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 8089993
    reference: chr 4
allele count: 1
allele frequency: 8.704735376044569e-6
allele num: 114880
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000355003
  ensembl transcript: ENST00000361581
  gene symbol: ABLIM2
  hgvsc: ENST00000361581.5:c.357G>A
  hgvsp: ENST00000361581.5:c.357G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000389410
  ensembl transcript: ENST00000428004
  gene symbol: ABLIM2
  hgvsc: ENST00000428004.2:c.357G>A
  hgvsp: ENST00000428004.2:c.357G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000421283
  ensembl transcript: ENST00000505872
  gene symbol: ABLIM2
  hgvsc: ENST00000505872.1:c.357G>A
  hgvsp: ENST00000505872.1:c.357G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000296372
  ensembl transcript: ENST00000296372
  gene symbol: ABLIM2
  hgvsc: ENST00000296372.8:c.357G>A
  hgvsp: ENST00000296372.8:c.357G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000317020
  ensembl transcript: ENST00000318888
  gene symbol: ABLIM2
  hgvsc: ENST00000318888.4:c.-373G>A
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000444365
  ensembl transcript: ENST00000546334
  gene symbol: ABLIM2
  hgvsc: ENST00000546334.1:c.357G>A
  hgvsp: ENST00000546334.1:c.357G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000393511
  ensembl transcript: ENST00000447017
  gene symbol: ABLIM2
  hgvsc: ENST00000447017.2:c.357G>A
  hgvsp: ENST00000447017.2:c.357G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000384658
  ensembl transcript: ENST00000407564
  gene symbol: ABLIM2
  hgvsc: ENST00000407564.3:c.357G>A
  hgvsp: ENST00000407564.3:c.357G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000354887
  ensembl transcript: ENST00000361737
  gene symbol: ABLIM2
  hgvsc: ENST00000361737.5:c.357G>A
  hgvsp: ENST00000361737.5:c.357G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000342813
  ensembl transcript: ENST00000341937
  gene symbol: ABLIM2
  hgvsc: ENST00000341937.5:c.357G>A
  hgvsp: ENST00000341937.5:c.357G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000441255
  ensembl transcript: ENST00000545242
  gene symbol: ABLIM2
  hgvsc: ENST00000545242.1:c.357G>A
  hgvsp: ENST00000545242.1:c.357G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19195
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1621
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36981
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11318
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1997
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2709
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4104
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly119Gly
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP

4-8089995-C-CG
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8089995
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 8089996
    reference: chr 4
allele count: 29
allele frequency: 2.556417489421721e-4
allele num: 113440
alternate allele: CG
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000342813
  ensembl transcript: ENST00000341937
  gene symbol: ABLIM2
  hgvsc: ENST00000341937.5:c.354dupC
  hgvsp: ENSP00000342813.5:p.Gly119ArgfsTer61
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000384658
  ensembl transcript: ENST00000407564
  gene symbol: ABLIM2
  hgvsc: ENST00000407564.3:c.354dupC
  hgvsp: ENSP00000384658.3:p.Gly119ArgfsTer61
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000444365
  ensembl transcript: ENST00000546334
  gene symbol: ABLIM2
  hgvsc: ENST00000546334.1:c.354dupC
  hgvsp: ENSP00000444365.1:p.Gly119ArgfsTer61
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000421283
  ensembl transcript: ENST00000505872
  gene symbol: ABLIM2
  hgvsc: ENST00000505872.1:c.354dupC
  hgvsp: ENSP00000421283.1:p.Gly119ArgfsTer61
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000317020
  ensembl transcript: ENST00000318888
  gene symbol: ABLIM2
  hgvsc: ENST00000318888.4:c.-376dupC
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000393511
  ensembl transcript: ENST00000447017
  gene symbol: ABLIM2
  hgvsc: ENST00000447017.2:c.354dupC
  hgvsp: ENSP00000393511.2:p.Gly119ArgfsTer61
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000296372
  ensembl transcript: ENST00000296372
  gene symbol: ABLIM2
  hgvsc: ENST00000296372.8:c.354dupC
  hgvsp: ENSP00000296372.8:p.Gly119ArgfsTer61
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000441255
  ensembl transcript: ENST00000545242
  gene symbol: ABLIM2
  hgvsc: ENST00000545242.1:c.354dupC
  hgvsp: ENSP00000441255.1:p.Gly119ArgfsTer61
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000389410
  ensembl transcript: ENST00000428004
  gene symbol: ABLIM2
  hgvsc: ENST00000428004.2:c.354dupC
  hgvsp: ENSP00000389410.2:p.Gly119ArgfsTer61
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000354887
  ensembl transcript: ENST00000361737
  gene symbol: ABLIM2
  hgvsc: ENST00000361737.5:c.354dupC
  hgvsp: ENSP00000354887.5:p.Gly119ArgfsTer61
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000355003
  ensembl transcript: ENST00000361581
  gene symbol: ABLIM2
  hgvsc: ENST00000361581.5:c.354dupC
  hgvsp: ENSP00000355003.5:p.Gly119ArgfsTer61
  variant of: http://identifiers.org/hgnc/19195
canonical: true
consequence: frameshift
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 1874
  bin: 1.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 4679
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2854
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2407
  bin: 3.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 3.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11231
  bin: 2.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Gly119ArgfsTer61
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Other
population: East Asian
reference allele: C
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: ReadPosRankSum

4-8089995-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8089995
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 8089995
    reference: chr 4
allele count: 2
allele frequency: 1.763046544428773e-5
allele num: 113440
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000421283
  ensembl transcript: ENST00000505872
  gene symbol: ABLIM2
  hgvsc: ENST00000505872.1:c.355G>A
  hgvsp: ENSP00000421283.1:p.Gly119Arg
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000296372
  ensembl transcript: ENST00000296372
  gene symbol: ABLIM2
  hgvsc: ENST00000296372.8:c.355G>A
  hgvsp: ENSP00000296372.8:p.Gly119Arg
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000384658
  ensembl transcript: ENST00000407564
  gene symbol: ABLIM2
  hgvsc: ENST00000407564.3:c.355G>A
  hgvsp: ENSP00000384658.3:p.Gly119Arg
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000342813
  ensembl transcript: ENST00000341937
  gene symbol: ABLIM2
  hgvsc: ENST00000341937.5:c.355G>A
  hgvsp: ENSP00000342813.5:p.Gly119Arg
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000441255
  ensembl transcript: ENST00000545242
  gene symbol: ABLIM2
  hgvsc: ENST00000545242.1:c.355G>A
  hgvsp: ENSP00000441255.1:p.Gly119Arg
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000317020
  ensembl transcript: ENST00000318888
  gene symbol: ABLIM2
  hgvsc: ENST00000318888.4:c.-375G>A
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000389410
  ensembl transcript: ENST00000428004
  gene symbol: ABLIM2
  hgvsc: ENST00000428004.2:c.355G>A
  hgvsp: ENSP00000389410.2:p.Gly119Arg
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000444365
  ensembl transcript: ENST00000546334
  gene symbol: ABLIM2
  hgvsc: ENST00000546334.1:c.355G>A
  hgvsp: ENSP00000444365.1:p.Gly119Arg
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000355003
  ensembl transcript: ENST00000361581
  gene symbol: ABLIM2
  hgvsc: ENST00000361581.5:c.355G>A
  hgvsp: ENSP00000355003.5:p.Gly119Arg
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000393511
  ensembl transcript: ENST00000447017
  gene symbol: ABLIM2
  hgvsc: ENST00000447017.2:c.355G>A
  hgvsp: ENSP00000393511.2:p.Gly119Arg
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000354887
  ensembl transcript: ENST00000361737
  gene symbol: ABLIM2
  hgvsc: ENST00000361737.5:c.355G>A
  hgvsp: ENSP00000354887.5:p.Gly119Arg
  variant of: http://identifiers.org/hgnc/19195
canonical: true
consequence: missense
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 2854
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1874
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2407
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4679
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11231
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35066
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly119Arg
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD

4-8089996-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8089996
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 8089996
    reference: chr 4
allele count: 1
allele frequency: 8.8974304220941e-6
allele num: 112392
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000354887
  ensembl transcript: ENST00000361737
  gene symbol: ABLIM2
  hgvsc: ENST00000361737.5:c.354C>T
  hgvsp: ENST00000361737.5:c.354C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000317020
  ensembl transcript: ENST00000318888
  gene symbol: ABLIM2
  hgvsc: ENST00000318888.4:c.-376C>T
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000355003
  ensembl transcript: ENST00000361581
  gene symbol: ABLIM2
  hgvsc: ENST00000361581.5:c.354C>T
  hgvsp: ENST00000361581.5:c.354C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000421283
  ensembl transcript: ENST00000505872
  gene symbol: ABLIM2
  hgvsc: ENST00000505872.1:c.354C>T
  hgvsp: ENST00000505872.1:c.354C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000441255
  ensembl transcript: ENST00000545242
  gene symbol: ABLIM2
  hgvsc: ENST00000545242.1:c.354C>T
  hgvsp: ENST00000545242.1:c.354C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000444365
  ensembl transcript: ENST00000546334
  gene symbol: ABLIM2
  hgvsc: ENST00000546334.1:c.354C>T
  hgvsp: ENST00000546334.1:c.354C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000342813
  ensembl transcript: ENST00000341937
  gene symbol: ABLIM2
  hgvsc: ENST00000341937.5:c.354C>T
  hgvsp: ENST00000341937.5:c.354C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000384658
  ensembl transcript: ENST00000407564
  gene symbol: ABLIM2
  hgvsc: ENST00000407564.3:c.354C>T
  hgvsp: ENST00000407564.3:c.354C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000389410
  ensembl transcript: ENST00000428004
  gene symbol: ABLIM2
  hgvsc: ENST00000428004.2:c.354C>T
  hgvsp: ENST00000428004.2:c.354C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000393511
  ensembl transcript: ENST00000447017
  gene symbol: ABLIM2
  hgvsc: ENST00000447017.2:c.354C>T
  hgvsp: ENST00000447017.2:c.354C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000296372
  ensembl transcript: ENST00000296372
  gene symbol: ABLIM2
  hgvsc: ENST00000296372.8:c.354C>T
  hgvsp: ENST00000296372.8:c.354C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19195
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11099
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2181
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3048
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5296
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2579
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro118Pro
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: Latino
population: African
population: South Asian
reference allele: G
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum

4-8089996-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8089996
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 8089996
    reference: chr 4
allele count: 3
allele frequency: 2.66922912662823e-5
allele num: 112392
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000393511
  ensembl transcript: ENST00000447017
  gene symbol: ABLIM2
  hgvsc: ENST00000447017.2:c.354C>G
  hgvsp: ENST00000447017.2:c.354C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000354887
  ensembl transcript: ENST00000361737
  gene symbol: ABLIM2
  hgvsc: ENST00000361737.5:c.354C>G
  hgvsp: ENST00000361737.5:c.354C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000342813
  ensembl transcript: ENST00000341937
  gene symbol: ABLIM2
  hgvsc: ENST00000341937.5:c.354C>G
  hgvsp: ENST00000341937.5:c.354C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000384658
  ensembl transcript: ENST00000407564
  gene symbol: ABLIM2
  hgvsc: ENST00000407564.3:c.354C>G
  hgvsp: ENST00000407564.3:c.354C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000317020
  ensembl transcript: ENST00000318888
  gene symbol: ABLIM2
  hgvsc: ENST00000318888.4:c.-376C>G
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000421283
  ensembl transcript: ENST00000505872
  gene symbol: ABLIM2
  hgvsc: ENST00000505872.1:c.354C>G
  hgvsp: ENST00000505872.1:c.354C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000444365
  ensembl transcript: ENST00000546334
  gene symbol: ABLIM2
  hgvsc: ENST00000546334.1:c.354C>G
  hgvsp: ENST00000546334.1:c.354C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000389410
  ensembl transcript: ENST00000428004
  gene symbol: ABLIM2
  hgvsc: ENST00000428004.2:c.354C>G
  hgvsp: ENST00000428004.2:c.354C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000441255
  ensembl transcript: ENST00000545242
  gene symbol: ABLIM2
  hgvsc: ENST00000545242.1:c.354C>G
  hgvsp: ENST00000545242.1:c.354C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000355003
  ensembl transcript: ENST00000361581
  gene symbol: ABLIM2
  hgvsc: ENST00000361581.5:c.354C>G
  hgvsp: ENST00000361581.5:c.354C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000296372
  ensembl transcript: ENST00000296372
  gene symbol: ABLIM2
  hgvsc: ENST00000296372.8:c.354C>G
  hgvsp: ENST00000296372.8:c.354C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/19195
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11099
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3048
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2579
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33619
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5296
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro118Pro
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
population: South Asian
population: European (Finnish)
population: African
reference allele: G
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD

4-8089998-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8089998
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 8089998
    reference: chr 4
allele count: 4
allele frequency: 3.516112585925001e-5
allele num: 113762
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000441255
  ensembl transcript: ENST00000545242
  gene symbol: ABLIM2
  hgvsc: ENST00000545242.1:c.352C>G
  hgvsp: ENSP00000441255.1:p.Pro118Ala
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000355003
  ensembl transcript: ENST00000361581
  gene symbol: ABLIM2
  hgvsc: ENST00000361581.5:c.352C>G
  hgvsp: ENSP00000355003.5:p.Pro118Ala
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000444365
  ensembl transcript: ENST00000546334
  gene symbol: ABLIM2
  hgvsc: ENST00000546334.1:c.352C>G
  hgvsp: ENSP00000444365.1:p.Pro118Ala
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000296372
  ensembl transcript: ENST00000296372
  gene symbol: ABLIM2
  hgvsc: ENST00000296372.8:c.352C>G
  hgvsp: ENSP00000296372.8:p.Pro118Ala
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000384658
  ensembl transcript: ENST00000407564
  gene symbol: ABLIM2
  hgvsc: ENST00000407564.3:c.352C>G
  hgvsp: ENSP00000384658.3:p.Pro118Ala
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000342813
  ensembl transcript: ENST00000341937
  gene symbol: ABLIM2
  hgvsc: ENST00000341937.5:c.352C>G
  hgvsp: ENSP00000342813.5:p.Pro118Ala
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000421283
  ensembl transcript: ENST00000505872
  gene symbol: ABLIM2
  hgvsc: ENST00000505872.1:c.352C>G
  hgvsp: ENSP00000421283.1:p.Pro118Ala
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000389410
  ensembl transcript: ENST00000428004
  gene symbol: ABLIM2
  hgvsc: ENST00000428004.2:c.352C>G
  hgvsp: ENSP00000389410.2:p.Pro118Ala
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000393511
  ensembl transcript: ENST00000447017
  gene symbol: ABLIM2
  hgvsc: ENST00000447017.2:c.352C>G
  hgvsp: ENSP00000393511.2:p.Pro118Ala
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000317020
  ensembl transcript: ENST00000318888
  gene symbol: ABLIM2
  hgvsc: ENST00000318888.4:c.-378C>G
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000354887
  ensembl transcript: ENST00000361737
  gene symbol: ABLIM2
  hgvsc: ENST00000361737.5:c.352C>G
  hgvsp: ENSP00000354887.5:p.Pro118Ala
  variant of: http://identifiers.org/hgnc/19195
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11927
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 33996
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2068
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3221
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5472
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1948
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro118Ala
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum

4-8089998-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8089998
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 8089998
    reference: chr 4
allele count: 1
allele frequency: 8.790281464812504e-6
allele num: 113762
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000354887
  ensembl transcript: ENST00000361737
  gene symbol: ABLIM2
  hgvsc: ENST00000361737.5:c.352C>T
  hgvsp: ENSP00000354887.5:p.Pro118Ser
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000393511
  ensembl transcript: ENST00000447017
  gene symbol: ABLIM2
  hgvsc: ENST00000447017.2:c.352C>T
  hgvsp: ENSP00000393511.2:p.Pro118Ser
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000355003
  ensembl transcript: ENST00000361581
  gene symbol: ABLIM2
  hgvsc: ENST00000361581.5:c.352C>T
  hgvsp: ENSP00000355003.5:p.Pro118Ser
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000296372
  ensembl transcript: ENST00000296372
  gene symbol: ABLIM2
  hgvsc: ENST00000296372.8:c.352C>T
  hgvsp: ENSP00000296372.8:p.Pro118Ser
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000342813
  ensembl transcript: ENST00000341937
  gene symbol: ABLIM2
  hgvsc: ENST00000341937.5:c.352C>T
  hgvsp: ENSP00000342813.5:p.Pro118Ser
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000421283
  ensembl transcript: ENST00000505872
  gene symbol: ABLIM2
  hgvsc: ENST00000505872.1:c.352C>T
  hgvsp: ENSP00000421283.1:p.Pro118Ser
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000317020
  ensembl transcript: ENST00000318888
  gene symbol: ABLIM2
  hgvsc: ENST00000318888.4:c.-378C>T
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000384658
  ensembl transcript: ENST00000407564
  gene symbol: ABLIM2
  hgvsc: ENST00000407564.3:c.352C>T
  hgvsp: ENSP00000384658.3:p.Pro118Ser
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000444365
  ensembl transcript: ENST00000546334
  gene symbol: ABLIM2
  hgvsc: ENST00000546334.1:c.352C>T
  hgvsp: ENSP00000444365.1:p.Pro118Ser
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000441255
  ensembl transcript: ENST00000545242
  gene symbol: ABLIM2
  hgvsc: ENST00000545242.1:c.352C>T
  hgvsp: ENSP00000441255.1:p.Pro118Ser
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000389410
  ensembl transcript: ENST00000428004
  gene symbol: ABLIM2
  hgvsc: ENST00000428004.2:c.352C>T
  hgvsp: ENSP00000389410.2:p.Pro118Ser
  variant of: http://identifiers.org/hgnc/19195
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5472
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1948
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11927
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3221
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33996
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2068
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro118Ser
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: Latino
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum

4-8089998-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8089998
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 8089998
    reference: chr 4
allele count: 2
allele frequency: 1.758056292962501e-5
allele num: 113762
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000444365
  ensembl transcript: ENST00000546334
  gene symbol: ABLIM2
  hgvsc: ENST00000546334.1:c.352C>A
  hgvsp: ENSP00000444365.1:p.Pro118Thr
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000441255
  ensembl transcript: ENST00000545242
  gene symbol: ABLIM2
  hgvsc: ENST00000545242.1:c.352C>A
  hgvsp: ENSP00000441255.1:p.Pro118Thr
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000393511
  ensembl transcript: ENST00000447017
  gene symbol: ABLIM2
  hgvsc: ENST00000447017.2:c.352C>A
  hgvsp: ENSP00000393511.2:p.Pro118Thr
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000317020
  ensembl transcript: ENST00000318888
  gene symbol: ABLIM2
  hgvsc: ENST00000318888.4:c.-378C>A
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000342813
  ensembl transcript: ENST00000341937
  gene symbol: ABLIM2
  hgvsc: ENST00000341937.5:c.352C>A
  hgvsp: ENSP00000342813.5:p.Pro118Thr
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000421283
  ensembl transcript: ENST00000505872
  gene symbol: ABLIM2
  hgvsc: ENST00000505872.1:c.352C>A
  hgvsp: ENSP00000421283.1:p.Pro118Thr
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000355003
  ensembl transcript: ENST00000361581
  gene symbol: ABLIM2
  hgvsc: ENST00000361581.5:c.352C>A
  hgvsp: ENSP00000355003.5:p.Pro118Thr
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000384658
  ensembl transcript: ENST00000407564
  gene symbol: ABLIM2
  hgvsc: ENST00000407564.3:c.352C>A
  hgvsp: ENSP00000384658.3:p.Pro118Thr
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000389410
  ensembl transcript: ENST00000428004
  gene symbol: ABLIM2
  hgvsc: ENST00000428004.2:c.352C>A
  hgvsp: ENSP00000389410.2:p.Pro118Thr
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000354887
  ensembl transcript: ENST00000361737
  gene symbol: ABLIM2
  hgvsc: ENST00000361737.5:c.352C>A
  hgvsp: ENSP00000354887.5:p.Pro118Thr
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000296372
  ensembl transcript: ENST00000296372
  gene symbol: ABLIM2
  hgvsc: ENST00000296372.8:c.352C>A
  hgvsp: ENSP00000296372.8:p.Pro118Thr
  variant of: http://identifiers.org/hgnc/19195
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11927
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1948
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3221
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2068
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5472
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33996
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro118Thr
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
reference allele: G
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP

4-8090002-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8090002
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 8090002
    reference: chr 4
allele count: 2
allele frequency: 1.777967427636726e-5
allele num: 112488
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000384658
  ensembl transcript: ENST00000407564
  gene symbol: ABLIM2
  hgvsc: ENST00000407564.3:c.348C>A
  hgvsp: ENSP00000384658.3:p.Phe116Leu
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000389410
  ensembl transcript: ENST00000428004
  gene symbol: ABLIM2
  hgvsc: ENST00000428004.2:c.348C>A
  hgvsp: ENSP00000389410.2:p.Phe116Leu
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000355003
  ensembl transcript: ENST00000361581
  gene symbol: ABLIM2
  hgvsc: ENST00000361581.5:c.348C>A
  hgvsp: ENSP00000355003.5:p.Phe116Leu
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000317020
  ensembl transcript: ENST00000318888
  gene symbol: ABLIM2
  hgvsc: ENST00000318888.4:c.-382C>A
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000342813
  ensembl transcript: ENST00000341937
  gene symbol: ABLIM2
  hgvsc: ENST00000341937.5:c.348C>A
  hgvsp: ENSP00000342813.5:p.Phe116Leu
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000354887
  ensembl transcript: ENST00000361737
  gene symbol: ABLIM2
  hgvsc: ENST00000361737.5:c.348C>A
  hgvsp: ENSP00000354887.5:p.Phe116Leu
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000441255
  ensembl transcript: ENST00000545242
  gene symbol: ABLIM2
  hgvsc: ENST00000545242.1:c.348C>A
  hgvsp: ENSP00000441255.1:p.Phe116Leu
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000421283
  ensembl transcript: ENST00000505872
  gene symbol: ABLIM2
  hgvsc: ENST00000505872.1:c.348C>A
  hgvsp: ENSP00000421283.1:p.Phe116Leu
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000444365
  ensembl transcript: ENST00000546334
  gene symbol: ABLIM2
  hgvsc: ENST00000546334.1:c.348C>A
  hgvsp: ENSP00000444365.1:p.Phe116Leu
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000296372
  ensembl transcript: ENST00000296372
  gene symbol: ABLIM2
  hgvsc: ENST00000296372.8:c.348C>A
  hgvsp: ENSP00000296372.8:p.Phe116Leu
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000393511
  ensembl transcript: ENST00000447017
  gene symbol: ABLIM2
  hgvsc: ENST00000447017.2:c.348C>A
  hgvsp: ENSP00000393511.2:p.Phe116Leu
  variant of: http://identifiers.org/hgnc/19195
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11131
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7064
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2921
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3765
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1986
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31712
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Phe116Leu
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
population: African
reference allele: G
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum

4-8090003-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8090003
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 8090003
    reference: chr 4
allele count: 2
allele frequency: 1.78839688103584e-5
allele num: 111832
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000421283
  ensembl transcript: ENST00000505872
  gene symbol: ABLIM2
  hgvsc: ENST00000505872.1:c.347T>C
  hgvsp: ENSP00000421283.1:p.Phe116Ser
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000296372
  ensembl transcript: ENST00000296372
  gene symbol: ABLIM2
  hgvsc: ENST00000296372.8:c.347T>C
  hgvsp: ENSP00000296372.8:p.Phe116Ser
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000444365
  ensembl transcript: ENST00000546334
  gene symbol: ABLIM2
  hgvsc: ENST00000546334.1:c.347T>C
  hgvsp: ENSP00000444365.1:p.Phe116Ser
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000342813
  ensembl transcript: ENST00000341937
  gene symbol: ABLIM2
  hgvsc: ENST00000341937.5:c.347T>C
  hgvsp: ENSP00000342813.5:p.Phe116Ser
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000389410
  ensembl transcript: ENST00000428004
  gene symbol: ABLIM2
  hgvsc: ENST00000428004.2:c.347T>C
  hgvsp: ENSP00000389410.2:p.Phe116Ser
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000441255
  ensembl transcript: ENST00000545242
  gene symbol: ABLIM2
  hgvsc: ENST00000545242.1:c.347T>C
  hgvsp: ENSP00000441255.1:p.Phe116Ser
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000354887
  ensembl transcript: ENST00000361737
  gene symbol: ABLIM2
  hgvsc: ENST00000361737.5:c.347T>C
  hgvsp: ENSP00000354887.5:p.Phe116Ser
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000355003
  ensembl transcript: ENST00000361581
  gene symbol: ABLIM2
  hgvsc: ENST00000361581.5:c.347T>C
  hgvsp: ENSP00000355003.5:p.Phe116Ser
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000384658
  ensembl transcript: ENST00000407564
  gene symbol: ABLIM2
  hgvsc: ENST00000407564.3:c.347T>C
  hgvsp: ENSP00000384658.3:p.Phe116Ser
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000317020
  ensembl transcript: ENST00000318888
  gene symbol: ABLIM2
  hgvsc: ENST00000318888.4:c.-383T>C
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000393511
  ensembl transcript: ENST00000447017
  gene symbol: ABLIM2
  hgvsc: ENST00000447017.2:c.347T>C
  hgvsp: ENSP00000393511.2:p.Phe116Ser
  variant of: http://identifiers.org/hgnc/19195
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3147
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3867
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30872
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 7392
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11019
  bin: 2.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Phe116Ser
num of homozygotes: 0
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
reference allele: A
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: QD
site quality: DP

http://identifiers.org/exac.variant/4-8090004-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8090004
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 8090004
    reference: chr 4
allele count: 1
allele frequency: 8.931123178050872e-6
allele num: 111968
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000421283
  ensembl transcript: ENST00000505872
  gene symbol: ABLIM2
  hgvsc: ENST00000505872.1:c.346T>G
  hgvsp: ENSP00000421283.1:p.Phe116Val
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000355003
  ensembl transcript: ENST00000361581
  gene symbol: ABLIM2
  hgvsc: ENST00000361581.5:c.346T>G
  hgvsp: ENSP00000355003.5:p.Phe116Val
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000384658
  ensembl transcript: ENST00000407564
  gene symbol: ABLIM2
  hgvsc: ENST00000407564.3:c.346T>G
  hgvsp: ENSP00000384658.3:p.Phe116Val
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000354887
  ensembl transcript: ENST00000361737
  gene symbol: ABLIM2
  hgvsc: ENST00000361737.5:c.346T>G
  hgvsp: ENSP00000354887.5:p.Phe116Val
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000441255
  ensembl transcript: ENST00000545242
  gene symbol: ABLIM2
  hgvsc: ENST00000545242.1:c.346T>G
  hgvsp: ENSP00000441255.1:p.Phe116Val
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000317020
  ensembl transcript: ENST00000318888
  gene symbol: ABLIM2
  hgvsc: ENST00000318888.4:c.-384T>G
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000342813
  ensembl transcript: ENST00000341937
  gene symbol: ABLIM2
  hgvsc: ENST00000341937.5:c.346T>G
  hgvsp: ENSP00000342813.5:p.Phe116Val
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000296372
  ensembl transcript: ENST00000296372
  gene symbol: ABLIM2
  hgvsc: ENST00000296372.8:c.346T>G
  hgvsp: ENSP00000296372.8:p.Phe116Val
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000389410
  ensembl transcript: ENST00000428004
  gene symbol: ABLIM2
  hgvsc: ENST00000428004.2:c.346T>G
  hgvsp: ENSP00000389410.2:p.Phe116Val
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000444365
  ensembl transcript: ENST00000546334
  gene symbol: ABLIM2
  hgvsc: ENST00000546334.1:c.346T>G
  hgvsp: ENSP00000444365.1:p.Phe116Val
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000393511
  ensembl transcript: ENST00000447017
  gene symbol: ABLIM2
  hgvsc: ENST00000447017.2:c.346T>G
  hgvsp: ENSP00000393511.2:p.Phe116Val
  variant of: http://identifiers.org/hgnc/19195
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 30407
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10950
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7902
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1918
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4038
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Phe116Val
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: A
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD

4-8090005-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8090005
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 8090005
    reference: chr 4
allele count: 1
allele frequency: 8.96523282709652e-6
allele num: 111542
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000421283
  ensembl transcript: ENST00000505872
  gene symbol: ABLIM2
  hgvsc: ENST00000505872.1:c.345C>T
  hgvsp: ENST00000505872.1:c.345C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000393511
  ensembl transcript: ENST00000447017
  gene symbol: ABLIM2
  hgvsc: ENST00000447017.2:c.345C>T
  hgvsp: ENST00000447017.2:c.345C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000354887
  ensembl transcript: ENST00000361737
  gene symbol: ABLIM2
  hgvsc: ENST00000361737.5:c.345C>T
  hgvsp: ENST00000361737.5:c.345C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000389410
  ensembl transcript: ENST00000428004
  gene symbol: ABLIM2
  hgvsc: ENST00000428004.2:c.345C>T
  hgvsp: ENST00000428004.2:c.345C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000384658
  ensembl transcript: ENST00000407564
  gene symbol: ABLIM2
  hgvsc: ENST00000407564.3:c.345C>T
  hgvsp: ENST00000407564.3:c.345C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000355003
  ensembl transcript: ENST00000361581
  gene symbol: ABLIM2
  hgvsc: ENST00000361581.5:c.345C>T
  hgvsp: ENST00000361581.5:c.345C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000317020
  ensembl transcript: ENST00000318888
  gene symbol: ABLIM2
  hgvsc: ENST00000318888.4:c.-385C>T
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000441255
  ensembl transcript: ENST00000545242
  gene symbol: ABLIM2
  hgvsc: ENST00000545242.1:c.345C>T
  hgvsp: ENST00000545242.1:c.345C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000444365
  ensembl transcript: ENST00000546334
  gene symbol: ABLIM2
  hgvsc: ENST00000546334.1:c.345C>T
  hgvsp: ENST00000546334.1:c.345C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000342813
  ensembl transcript: ENST00000341937
  gene symbol: ABLIM2
  hgvsc: ENST00000341937.5:c.345C>T
  hgvsp: ENST00000341937.5:c.345C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000296372
  ensembl transcript: ENST00000296372
  gene symbol: ABLIM2
  hgvsc: ENST00000296372.8:c.345C>T
  hgvsp: ENST00000296372.8:c.345C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19195
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8311
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10690
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1873
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29714
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3788
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4209
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro115Pro
num of homozygotes: 0
population: South Asian
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
reference allele: G
site quality: FS
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum

4-8090007-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8090007
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 8090007
    reference: chr 4
allele count: 1
allele frequency: 9.013718880135566e-6
allele num: 110942
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000384658
  ensembl transcript: ENST00000407564
  gene symbol: ABLIM2
  hgvsc: ENST00000407564.3:c.343C>G
  hgvsp: ENSP00000384658.3:p.Pro115Ala
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000421283
  ensembl transcript: ENST00000505872
  gene symbol: ABLIM2
  hgvsc: ENST00000505872.1:c.343C>G
  hgvsp: ENSP00000421283.1:p.Pro115Ala
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000342813
  ensembl transcript: ENST00000341937
  gene symbol: ABLIM2
  hgvsc: ENST00000341937.5:c.343C>G
  hgvsp: ENSP00000342813.5:p.Pro115Ala
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000354887
  ensembl transcript: ENST00000361737
  gene symbol: ABLIM2
  hgvsc: ENST00000361737.5:c.343C>G
  hgvsp: ENSP00000354887.5:p.Pro115Ala
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000296372
  ensembl transcript: ENST00000296372
  gene symbol: ABLIM2
  hgvsc: ENST00000296372.8:c.343C>G
  hgvsp: ENSP00000296372.8:p.Pro115Ala
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000441255
  ensembl transcript: ENST00000545242
  gene symbol: ABLIM2
  hgvsc: ENST00000545242.1:c.343C>G
  hgvsp: ENSP00000441255.1:p.Pro115Ala
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000389410
  ensembl transcript: ENST00000428004
  gene symbol: ABLIM2
  hgvsc: ENST00000428004.2:c.343C>G
  hgvsp: ENSP00000389410.2:p.Pro115Ala
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000355003
  ensembl transcript: ENST00000361581
  gene symbol: ABLIM2
  hgvsc: ENST00000361581.5:c.343C>G
  hgvsp: ENSP00000355003.5:p.Pro115Ala
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000393511
  ensembl transcript: ENST00000447017
  gene symbol: ABLIM2
  hgvsc: ENST00000447017.2:c.343C>G
  hgvsp: ENSP00000393511.2:p.Pro115Ala
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000444365
  ensembl transcript: ENST00000546334
  gene symbol: ABLIM2
  hgvsc: ENST00000546334.1:c.343C>G
  hgvsp: ENSP00000444365.1:p.Pro115Ala
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000317020
  ensembl transcript: ENST00000318888
  gene symbol: ABLIM2
  hgvsc: ENST00000318888.4:c.-387C>G
  variant of: http://identifiers.org/hgnc/19195
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4411
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28670
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1780
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4458
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8984
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10250
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro115Ala
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: South Asian
population: East Asian
reference allele: G
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: FS

http://identifiers.org/exac.variant/4-8090008-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8090008
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 8090008
    reference: chr 4
allele count: 1
allele frequency: 9.090743804658096e-6
allele num: 110002
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000393511
  ensembl transcript: ENST00000447017
  gene symbol: ABLIM2
  hgvsc: ENST00000447017.2:c.342G>T
  hgvsp: ENST00000447017.2:c.342G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000317020
  ensembl transcript: ENST00000318888
  gene symbol: ABLIM2
  hgvsc: ENST00000318888.4:c.-388G>T
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000296372
  ensembl transcript: ENST00000296372
  gene symbol: ABLIM2
  hgvsc: ENST00000296372.8:c.342G>T
  hgvsp: ENST00000296372.8:c.342G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000421283
  ensembl transcript: ENST00000505872
  gene symbol: ABLIM2
  hgvsc: ENST00000505872.1:c.342G>T
  hgvsp: ENST00000505872.1:c.342G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000355003
  ensembl transcript: ENST00000361581
  gene symbol: ABLIM2
  hgvsc: ENST00000361581.5:c.342G>T
  hgvsp: ENST00000361581.5:c.342G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000441255
  ensembl transcript: ENST00000545242
  gene symbol: ABLIM2
  hgvsc: ENST00000545242.1:c.342G>T
  hgvsp: ENST00000545242.1:c.342G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000389410
  ensembl transcript: ENST00000428004
  gene symbol: ABLIM2
  hgvsc: ENST00000428004.2:c.342G>T
  hgvsp: ENST00000428004.2:c.342G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000342813
  ensembl transcript: ENST00000341937
  gene symbol: ABLIM2
  hgvsc: ENST00000341937.5:c.342G>T
  hgvsp: ENST00000341937.5:c.342G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000354887
  ensembl transcript: ENST00000361737
  gene symbol: ABLIM2
  hgvsc: ENST00000361737.5:c.342G>T
  hgvsp: ENST00000361737.5:c.342G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000384658
  ensembl transcript: ENST00000407564
  gene symbol: ABLIM2
  hgvsc: ENST00000407564.3:c.342G>T
  hgvsp: ENST00000407564.3:c.342G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000444365
  ensembl transcript: ENST00000546334
  gene symbol: ABLIM2
  hgvsc: ENST00000546334.1:c.342G>T
  hgvsp: ENST00000546334.1:c.342G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19195
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9881
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1700
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26866
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5551
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4856
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9652
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu114Leu
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: Latino
population: African
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum

4-8090010-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8090010
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 8090010
    reference: chr 4
allele count: 2
allele frequency: 1.819339579732557e-5
allele num: 109930
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000393511
  ensembl transcript: ENST00000447017
  gene symbol: ABLIM2
  hgvsc: ENST00000447017.2:c.340C>A
  hgvsp: ENSP00000393511.2:p.Leu114Met
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000389410
  ensembl transcript: ENST00000428004
  gene symbol: ABLIM2
  hgvsc: ENST00000428004.2:c.340C>A
  hgvsp: ENSP00000389410.2:p.Leu114Met
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000342813
  ensembl transcript: ENST00000341937
  gene symbol: ABLIM2
  hgvsc: ENST00000341937.5:c.340C>A
  hgvsp: ENSP00000342813.5:p.Leu114Met
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000421283
  ensembl transcript: ENST00000505872
  gene symbol: ABLIM2
  hgvsc: ENST00000505872.1:c.340C>A
  hgvsp: ENSP00000421283.1:p.Leu114Met
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000384658
  ensembl transcript: ENST00000407564
  gene symbol: ABLIM2
  hgvsc: ENST00000407564.3:c.340C>A
  hgvsp: ENSP00000384658.3:p.Leu114Met
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000355003
  ensembl transcript: ENST00000361581
  gene symbol: ABLIM2
  hgvsc: ENST00000361581.5:c.340C>A
  hgvsp: ENSP00000355003.5:p.Leu114Met
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000296372
  ensembl transcript: ENST00000296372
  gene symbol: ABLIM2
  hgvsc: ENST00000296372.8:c.340C>A
  hgvsp: ENSP00000296372.8:p.Leu114Met
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000354887
  ensembl transcript: ENST00000361737
  gene symbol: ABLIM2
  hgvsc: ENST00000361737.5:c.340C>A
  hgvsp: ENSP00000354887.5:p.Leu114Met
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000441255
  ensembl transcript: ENST00000545242
  gene symbol: ABLIM2
  hgvsc: ENST00000545242.1:c.340C>A
  hgvsp: ENSP00000441255.1:p.Leu114Met
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000444365
  ensembl transcript: ENST00000546334
  gene symbol: ABLIM2
  hgvsc: ENST00000546334.1:c.340C>A
  hgvsp: ENSP00000444365.1:p.Leu114Met
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000317020
  ensembl transcript: ENST00000318888
  gene symbol: ABLIM2
  hgvsc: ENST00000318888.4:c.-390C>A
  variant of: http://identifiers.org/hgnc/19195
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9933
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9651
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26931
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4888
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5496
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1615
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu114Met
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: African
population: Other
population: Latino
reference allele: G
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum

4-8090011-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8090011
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 8090011
    reference: chr 4
allele count: 1
allele frequency: 9.118762766267872e-6
allele num: 109664
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000389410
  ensembl transcript: ENST00000428004
  gene symbol: ABLIM2
  hgvsc: ENST00000428004.2:c.339G>A
  hgvsp: ENST00000428004.2:c.339G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000421283
  ensembl transcript: ENST00000505872
  gene symbol: ABLIM2
  hgvsc: ENST00000505872.1:c.339G>A
  hgvsp: ENST00000505872.1:c.339G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000317020
  ensembl transcript: ENST00000318888
  gene symbol: ABLIM2
  hgvsc: ENST00000318888.4:c.-391G>A
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000355003
  ensembl transcript: ENST00000361581
  gene symbol: ABLIM2
  hgvsc: ENST00000361581.5:c.339G>A
  hgvsp: ENST00000361581.5:c.339G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000444365
  ensembl transcript: ENST00000546334
  gene symbol: ABLIM2
  hgvsc: ENST00000546334.1:c.339G>A
  hgvsp: ENST00000546334.1:c.339G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000441255
  ensembl transcript: ENST00000545242
  gene symbol: ABLIM2
  hgvsc: ENST00000545242.1:c.339G>A
  hgvsp: ENST00000545242.1:c.339G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000342813
  ensembl transcript: ENST00000341937
  gene symbol: ABLIM2
  hgvsc: ENST00000341937.5:c.339G>A
  hgvsp: ENST00000341937.5:c.339G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000384658
  ensembl transcript: ENST00000407564
  gene symbol: ABLIM2
  hgvsc: ENST00000407564.3:c.339G>A
  hgvsp: ENST00000407564.3:c.339G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000296372
  ensembl transcript: ENST00000296372
  gene symbol: ABLIM2
  hgvsc: ENST00000296372.8:c.339G>A
  hgvsp: ENST00000296372.8:c.339G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000354887
  ensembl transcript: ENST00000361737
  gene symbol: ABLIM2
  hgvsc: ENST00000361737.5:c.339G>A
  hgvsp: ENST00000361737.5:c.339G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000393511
  ensembl transcript: ENST00000447017
  gene symbol: ABLIM2
  hgvsc: ENST00000447017.2:c.339G>A
  hgvsp: ENST00000447017.2:c.339G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19195
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5009
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5797
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9425
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26497
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10197
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.339G>A
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
population: Latino
population: African
reference allele: C
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/4-8090012-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8090012
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 8090012
    reference: chr 4
allele count: 1
allele frequency: 9.149967975112088e-6
allele num: 109290
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000441255
  ensembl transcript: ENST00000545242
  gene symbol: ABLIM2
  hgvsc: ENST00000545242.1:c.339-1G>T
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000296372
  ensembl transcript: ENST00000296372
  gene symbol: ABLIM2
  hgvsc: ENST00000296372.8:c.339-1G>T
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000384658
  ensembl transcript: ENST00000407564
  gene symbol: ABLIM2
  hgvsc: ENST00000407564.3:c.339-1G>T
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000389410
  ensembl transcript: ENST00000428004
  gene symbol: ABLIM2
  hgvsc: ENST00000428004.2:c.339-1G>T
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000355003
  ensembl transcript: ENST00000361581
  gene symbol: ABLIM2
  hgvsc: ENST00000361581.5:c.339-1G>T
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000354887
  ensembl transcript: ENST00000361737
  gene symbol: ABLIM2
  hgvsc: ENST00000361737.5:c.339-1G>T
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000342813
  ensembl transcript: ENST00000341937
  gene symbol: ABLIM2
  hgvsc: ENST00000341937.5:c.339-1G>T
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000444365
  ensembl transcript: ENST00000546334
  gene symbol: ABLIM2
  hgvsc: ENST00000546334.1:c.339-1G>T
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: true
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000393511
  ensembl transcript: ENST00000447017
  gene symbol: ABLIM2
  hgvsc: ENST00000447017.2:c.339-1G>T
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000421283
  ensembl transcript: ENST00000505872
  gene symbol: ABLIM2
  hgvsc: ENST00000505872.1:c.339-1G>T
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000317020
  ensembl transcript: ENST00000318888
  gene symbol: ABLIM2
  hgvsc: ENST00000318888.4:c.-391-1G>T
  variant of: http://identifiers.org/hgnc/19195
canonical: true
consequence: splice acceptor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10504
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1532
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25920
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6153
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5161
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9222
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2442
  bin: 6.75e1
  variant carriers: 0
hgvs: c.339-1G>T
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Other
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD

4-8090022-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8090022
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 8090022
    reference: chr 4
allele count: 7
allele frequency: 6.630294763961507e-5
allele num: 105576
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000393511
  ensembl transcript: ENST00000447017
  gene symbol: ABLIM2
  hgvsc: ENST00000447017.2:c.339-11T>C
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000354887
  ensembl transcript: ENST00000361737
  gene symbol: ABLIM2
  hgvsc: ENST00000361737.5:c.339-11T>C
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000421283
  ensembl transcript: ENST00000505872
  gene symbol: ABLIM2
  hgvsc: ENST00000505872.1:c.339-11T>C
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000355003
  ensembl transcript: ENST00000361581
  gene symbol: ABLIM2
  hgvsc: ENST00000361581.5:c.339-11T>C
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000389410
  ensembl transcript: ENST00000428004
  gene symbol: ABLIM2
  hgvsc: ENST00000428004.2:c.339-11T>C
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000317020
  ensembl transcript: ENST00000318888
  gene symbol: ABLIM2
  hgvsc: ENST00000318888.4:c.-391-11T>C
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000441255
  ensembl transcript: ENST00000545242
  gene symbol: ABLIM2
  hgvsc: ENST00000545242.1:c.339-11T>C
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000342813
  ensembl transcript: ENST00000341937
  gene symbol: ABLIM2
  hgvsc: ENST00000341937.5:c.339-11T>C
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000384658
  ensembl transcript: ENST00000407564
  gene symbol: ABLIM2
  hgvsc: ENST00000407564.3:c.339-11T>C
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000296372
  ensembl transcript: ENST00000296372
  gene symbol: ABLIM2
  hgvsc: ENST00000296372.8:c.339-11T>C
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000444365
  ensembl transcript: ENST00000546334
  gene symbol: ABLIM2
  hgvsc: ENST00000546334.1:c.339-11T>C
  variant of: http://identifiers.org/hgnc/19195
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14926
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8746
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6653
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6353
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 20396
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1167
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 830
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: African
population: East Asian
population: Latino
population: South Asian
reference allele: A
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD

4-8090028-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8090028
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 8090028
    reference: chr 4
allele count: 28012
allele frequency: 2.74191969616883e-1
allele num: 102162
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000355003
  ensembl transcript: ENST00000361581
  gene symbol: ABLIM2
  hgvsc: ENST00000361581.5:c.339-17G>A
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000342813
  ensembl transcript: ENST00000341937
  gene symbol: ABLIM2
  hgvsc: ENST00000341937.5:c.339-17G>A
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000441255
  ensembl transcript: ENST00000545242
  gene symbol: ABLIM2
  hgvsc: ENST00000545242.1:c.339-17G>A
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000317020
  ensembl transcript: ENST00000318888
  gene symbol: ABLIM2
  hgvsc: ENST00000318888.4:c.-391-17G>A
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000384658
  ensembl transcript: ENST00000407564
  gene symbol: ABLIM2
  hgvsc: ENST00000407564.3:c.339-17G>A
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000421283
  ensembl transcript: ENST00000505872
  gene symbol: ABLIM2
  hgvsc: ENST00000505872.1:c.339-17G>A
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000444365
  ensembl transcript: ENST00000546334
  gene symbol: ABLIM2
  hgvsc: ENST00000546334.1:c.339-17G>A
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000389410
  ensembl transcript: ENST00000428004
  gene symbol: ABLIM2
  hgvsc: ENST00000428004.2:c.339-17G>A
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000296372
  ensembl transcript: ENST00000296372
  gene symbol: ABLIM2
  hgvsc: ENST00000296372.8:c.339-17G>A
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000393511
  ensembl transcript: ENST00000447017
  gene symbol: ABLIM2
  hgvsc: ENST00000447017.2:c.339-17G>A
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000354887
  ensembl transcript: ENST00000361737
  gene symbol: ABLIM2
  hgvsc: ENST00000361737.5:c.339-17G>A
  variant of: http://identifiers.org/hgnc/19195
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 842
  bin: 2.5e0
  variant carriers: 38
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 6.75e1
  variant carriers: 48
genotype depth: GenotypeDepth
  all individuals: 2528
  bin: 3.25e1
  variant carriers: 2024
genotype depth: GenotypeDepth
  all individuals: 13094
  bin: 2.25e1
  variant carriers: 5935
genotype depth: GenotypeDepth
  all individuals: 17172
  bin: 1.25e1
  variant carriers: 3964
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 29
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.25e1
  variant carriers: 38
genotype depth: GenotypeDepth
  all individuals: 7107
  bin: 7.5e0
  variant carriers: 1043
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 5.75e1
  variant carriers: 86
genotype depth: GenotypeDepth
  all individuals: 1035
  bin: 3.75e1
  variant carriers: 923
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 4.75e1
  variant carriers: 210
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 4.25e1
  variant carriers: 427
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.75e1
  variant carriers: 28
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 5.25e1
  variant carriers: 118
genotype depth: GenotypeDepth
  all individuals: 658
  bin: 9.75e1
  variant carriers: 477
genotype depth: GenotypeDepth
  all individuals: 9870
  bin: 1.75e1
  variant carriers: 6222
genotype depth: GenotypeDepth
  all individuals: 6478
  bin: 2.75e1
  variant carriers: 3755
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 8.25e1
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 6.25e1
  variant carriers: 69
genotype quality: GenotypeQuality
  all individuals: 540
  bin: 7.75e1
  variant carriers: 440
num of homozygotes: 3860
population: African
population: European (Finnish)
population: Other
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: FS

4-8090029-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8090029
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 8090029
    reference: chr 4
allele count: 2
allele frequency: 2.093188763762716e-5
allele num: 95548
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000421283
  ensembl transcript: ENST00000505872
  gene symbol: ABLIM2
  hgvsc: ENST00000505872.1:c.339-18C>T
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000296372
  ensembl transcript: ENST00000296372
  gene symbol: ABLIM2
  hgvsc: ENST00000296372.8:c.339-18C>T
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000384658
  ensembl transcript: ENST00000407564
  gene symbol: ABLIM2
  hgvsc: ENST00000407564.3:c.339-18C>T
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000389410
  ensembl transcript: ENST00000428004
  gene symbol: ABLIM2
  hgvsc: ENST00000428004.2:c.339-18C>T
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000355003
  ensembl transcript: ENST00000361581
  gene symbol: ABLIM2
  hgvsc: ENST00000361581.5:c.339-18C>T
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000441255
  ensembl transcript: ENST00000545242
  gene symbol: ABLIM2
  hgvsc: ENST00000545242.1:c.339-18C>T
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000317020
  ensembl transcript: ENST00000318888
  gene symbol: ABLIM2
  hgvsc: ENST00000318888.4:c.-391-18C>T
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000393511
  ensembl transcript: ENST00000447017
  gene symbol: ABLIM2
  hgvsc: ENST00000447017.2:c.339-18C>T
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000342813
  ensembl transcript: ENST00000341937
  gene symbol: ABLIM2
  hgvsc: ENST00000341937.5:c.339-18C>T
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000354887
  ensembl transcript: ENST00000361737
  gene symbol: ABLIM2
  hgvsc: ENST00000361737.5:c.339-18C>T
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000444365
  ensembl transcript: ENST00000546334
  gene symbol: ABLIM2
  hgvsc: ENST00000546334.1:c.339-18C>T
  variant of: http://identifiers.org/hgnc/19195
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 23413
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10866
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1359
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9435
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6689
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1370
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5657
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1537
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
population: African
population: Latino
reference allele: G
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff

4-8090030-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8090030
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 8090030
    reference: chr 4
allele count: 1
allele frequency: 1.049846722378533e-5
allele num: 95252
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000355003
  ensembl transcript: ENST00000361581
  gene symbol: ABLIM2
  hgvsc: ENST00000361581.5:c.339-19A>G
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000384658
  ensembl transcript: ENST00000407564
  gene symbol: ABLIM2
  hgvsc: ENST00000407564.3:c.339-19A>G
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000421283
  ensembl transcript: ENST00000505872
  gene symbol: ABLIM2
  hgvsc: ENST00000505872.1:c.339-19A>G
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000441255
  ensembl transcript: ENST00000545242
  gene symbol: ABLIM2
  hgvsc: ENST00000545242.1:c.339-19A>G
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000444365
  ensembl transcript: ENST00000546334
  gene symbol: ABLIM2
  hgvsc: ENST00000546334.1:c.339-19A>G
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000354887
  ensembl transcript: ENST00000361737
  gene symbol: ABLIM2
  hgvsc: ENST00000361737.5:c.339-19A>G
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000342813
  ensembl transcript: ENST00000341937
  gene symbol: ABLIM2
  hgvsc: ENST00000341937.5:c.339-19A>G
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000389410
  ensembl transcript: ENST00000428004
  gene symbol: ABLIM2
  hgvsc: ENST00000428004.2:c.339-19A>G
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000393511
  ensembl transcript: ENST00000447017
  gene symbol: ABLIM2
  hgvsc: ENST00000447017.2:c.339-19A>G
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000296372
  ensembl transcript: ENST00000296372
  gene symbol: ABLIM2
  hgvsc: ENST00000296372.8:c.339-19A>G
  variant of: http://identifiers.org/hgnc/19195
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000163995
  ensembl protein: ENSP00000317020
  ensembl transcript: ENST00000318888
  gene symbol: ABLIM2
  hgvsc: ENST00000318888.4:c.-391-19A>G
  variant of: http://identifiers.org/hgnc/19195
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1455
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6014
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1278
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6153
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23965
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11070
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8866
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1619
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
reference allele: T
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

7-99506259-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 99506259
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 99506259
    reference: chr 7
allele count: 1
allele frequency: 8.238589553468446e-6
allele num: 121380
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000146833
  ensembl protein: ENSP00000348216
  ensembl transcript: ENST00000355947
  gene symbol: TRIM4
  hgvsc: ENST00000355947.2:c.744G>A
  hgvsp: ENST00000355947.2:c.744G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16275
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000146833
  ensembl protein: ENSP00000275736
  ensembl transcript: ENST00000349062
  gene symbol: TRIM4
  hgvsc: ENST00000349062.2:c.666G>A
  hgvsp: ENST00000349062.2:c.666G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16275
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000146833
  ensembl transcript: ENST00000496896
  gene symbol: TRIM4
  hgvsc: ENST00000496896.1:n.211G>A
  variant of: http://identifiers.org/hgnc/16275
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000146833
  ensembl protein: ENSP00000346186
  ensembl transcript: ENST00000354241
  gene symbol: TRIM4
  hgvsc: ENST00000354241.5:c.666G>A
  hgvsp: ENST00000354241.5:c.666G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16275
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000146833
  ensembl protein: ENSP00000396229
  ensembl transcript: ENST00000447480
  gene symbol: TRIM4
  hgvsc: ENST00000447480.1:c.370G>A
  hgvsp: ENST00000447480.1:c.370G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16275
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3971
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7576
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15921
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18378
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2183
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6925
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1202
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1070
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4655
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3240
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3523
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9967
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Lys248Lys
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: South Asian
reference allele: C
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum

7-99506267-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 99506267
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 99506267
    reference: chr 7
allele count: 1
allele frequency: 8.238046594391538e-6
allele num: 121388
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000146833
  ensembl protein: ENSP00000348216
  ensembl transcript: ENST00000355947
  gene symbol: TRIM4
  hgvsc: ENST00000355947.2:c.736T>C
  hgvsp: ENST00000355947.2:c.736T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16275
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000146833
  ensembl protein: ENSP00000275736
  ensembl transcript: ENST00000349062
  gene symbol: TRIM4
  hgvsc: ENST00000349062.2:c.658T>C
  hgvsp: ENST00000349062.2:c.658T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16275
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000146833
  ensembl protein: ENSP00000346186
  ensembl transcript: ENST00000354241
  gene symbol: TRIM4
  hgvsc: ENST00000354241.5:c.658T>C
  hgvsp: ENST00000354241.5:c.658T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16275
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000146833
  ensembl protein: ENSP00000396229
  ensembl transcript: ENST00000447480
  gene symbol: TRIM4
  hgvsc: ENST00000447480.1:c.362T>C
  hgvsp: ENST00000447480.1:c.362T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16275
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000146833
  ensembl transcript: ENST00000496896
  gene symbol: TRIM4
  hgvsc: ENST00000496896.1:n.203T>C
  variant of: http://identifiers.org/hgnc/16275
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6932
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1069
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7577
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15918
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3971
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18388
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1201
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2183
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3242
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3525
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Leu246Leu
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: Other
reference allele: A
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum

7-99506273-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 99506273
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 99506273
    reference: chr 7
allele count: 1
allele frequency: 8.237775141689733e-6
allele num: 121392
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146833
  ensembl protein: ENSP00000346186
  ensembl transcript: ENST00000354241
  gene symbol: TRIM4
  hgvsc: ENST00000354241.5:c.652G>A
  hgvsp: ENSP00000346186.5:p.Ala218Thr
  variant of: http://identifiers.org/hgnc/16275
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146833
  ensembl protein: ENSP00000396229
  ensembl transcript: ENST00000447480
  gene symbol: TRIM4
  hgvsc: ENST00000447480.1:c.356G>A
  hgvsp: ENSP00000396229.1:p.Ala120Thr
  variant of: http://identifiers.org/hgnc/16275
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000146833
  ensembl transcript: ENST00000496896
  gene symbol: TRIM4
  hgvsc: ENST00000496896.1:n.197G>A
  variant of: http://identifiers.org/hgnc/16275
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146833
  ensembl protein: ENSP00000275736
  ensembl transcript: ENST00000349062
  gene symbol: TRIM4
  hgvsc: ENST00000349062.2:c.652G>A
  hgvsp: ENSP00000275736.4:p.Ala218Thr
  variant of: http://identifiers.org/hgnc/16275
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000146833
  ensembl protein: ENSP00000348216
  ensembl transcript: ENST00000355947
  gene symbol: TRIM4
  hgvsc: ENST00000355947.2:c.730G>A
  hgvsp: ENSP00000348216.2:p.Ala244Thr
  variant of: http://identifiers.org/hgnc/16275
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15916
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6935
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3971
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18392
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2183
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1069
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7581
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1201
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8904
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4652
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3242
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26555
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3525
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1544
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9966
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Ala244Thr
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum

7-99506274-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 99506274
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 99506274
    reference: chr 7
allele count: 1
allele frequency: 8.237367996177861e-6
allele num: 121398
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146833
  ensembl protein: ENSP00000346186
  ensembl transcript: ENST00000354241
  gene symbol: TRIM4
  hgvsc: ENST00000354241.5:c.651C>G
  hgvsp: ENSP00000346186.5:p.Ile217Met
  variant of: http://identifiers.org/hgnc/16275
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146833
  ensembl protein: ENSP00000396229
  ensembl transcript: ENST00000447480
  gene symbol: TRIM4
  hgvsc: ENST00000447480.1:c.355C>G
  hgvsp: ENSP00000396229.1:p.Ile119Met
  variant of: http://identifiers.org/hgnc/16275
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146833
  ensembl protein: ENSP00000275736
  ensembl transcript: ENST00000349062
  gene symbol: TRIM4
  hgvsc: ENST00000349062.2:c.651C>G
  hgvsp: ENSP00000275736.4:p.Ile217Met
  variant of: http://identifiers.org/hgnc/16275
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000146833
  ensembl transcript: ENST00000496896
  gene symbol: TRIM4
  hgvsc: ENST00000496896.1:n.196C>G
  variant of: http://identifiers.org/hgnc/16275
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000146833
  ensembl protein: ENSP00000348216
  ensembl transcript: ENST00000355947
  gene symbol: TRIM4
  hgvsc: ENST00000355947.2:c.729C>G
  hgvsp: ENSP00000348216.2:p.Ile243Met
  variant of: http://identifiers.org/hgnc/16275
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7579
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15914
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1201
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3971
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2183
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6935
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18395
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1070
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 770
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9968
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2274
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3525
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26562
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1544
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Ile243Met
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum

7-99506274-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 99506274
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 99506274
    reference: chr 7
allele count: 2
allele frequency: 1.647473599235572e-5
allele num: 121398
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000146833
  ensembl transcript: ENST00000496896
  gene symbol: TRIM4
  hgvsc: ENST00000496896.1:n.196C>A
  variant of: http://identifiers.org/hgnc/16275
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000146833
  ensembl protein: ENSP00000346186
  ensembl transcript: ENST00000354241
  gene symbol: TRIM4
  hgvsc: ENST00000354241.5:c.651C>A
  hgvsp: ENST00000354241.5:c.651C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16275
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000146833
  ensembl protein: ENSP00000396229
  ensembl transcript: ENST00000447480
  gene symbol: TRIM4
  hgvsc: ENST00000447480.1:c.355C>A
  hgvsp: ENST00000447480.1:c.355C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16275
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000146833
  ensembl protein: ENSP00000348216
  ensembl transcript: ENST00000355947
  gene symbol: TRIM4
  hgvsc: ENST00000355947.2:c.729C>A
  hgvsp: ENST00000355947.2:c.729C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16275
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000146833
  ensembl protein: ENSP00000275736
  ensembl transcript: ENST00000349062
  gene symbol: TRIM4
  hgvsc: ENST00000349062.2:c.651C>A
  hgvsp: ENST00000349062.2:c.651C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16275
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 770
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1201
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18395
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3971
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2183
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6935
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15914
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1070
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7579
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9968
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 26562
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3525
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4653
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Ile243Ile
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
population: Latino
population: European (Finnish)
reference allele: G
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: QD

7-99506279-TTTGA-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 99506279
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 99506275
    reference: chr 7
allele count: 1
allele frequency: 8.237503706876667e-6
allele num: 121396
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000146833
  ensembl protein: ENSP00000346186
  ensembl transcript: ENST00000354241
  gene symbol: TRIM4
  hgvsc: ENST00000354241.5:c.642_645delTCAA
  hgvsp: ENSP00000346186.5:p.Asn214LysfsTer6
  variant of: http://identifiers.org/hgnc/16275
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000146833
  ensembl protein: ENSP00000348216
  ensembl transcript: ENST00000355947
  gene symbol: TRIM4
  hgvsc: ENST00000355947.2:c.720_723delTCAA
  hgvsp: ENSP00000348216.2:p.Asn240LysfsTer6
  variant of: http://identifiers.org/hgnc/16275
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000146833
  ensembl transcript: ENST00000496896
  gene symbol: TRIM4
  hgvsc: ENST00000496896.1:n.187_190delTCAA
  variant of: http://identifiers.org/hgnc/16275
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000146833
  ensembl protein: ENSP00000396229
  ensembl transcript: ENST00000447480
  gene symbol: TRIM4
  hgvsc: ENST00000447480.1:c.346_349delTCAA
  hgvsp: ENSP00000396229.1:p.Asn116LysfsTer6
  variant of: http://identifiers.org/hgnc/16275
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000146833
  ensembl protein: ENSP00000275736
  ensembl transcript: ENST00000349062
  gene symbol: TRIM4
  hgvsc: ENST00000349062.2:c.642_645delTCAA
  hgvsp: ENSP00000275736.4:p.Asn214LysfsTer6
  variant of: http://identifiers.org/hgnc/16275
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6934
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3972
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15915
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7578
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2183
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1201
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1069
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18395
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3240
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26564
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4655
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9964
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2274
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Asn240LysfsTer6
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
reference allele: TTTGA
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: VQSLOD

7-99506280-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 99506280
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 99506280
    reference: chr 7
allele count: 2
allele frequency: 1.647555028337947e-5
allele num: 121392
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000146833
  ensembl protein: ENSP00000348216
  ensembl transcript: ENST00000355947
  gene symbol: TRIM4
  hgvsc: ENST00000355947.2:c.723A>G
  hgvsp: ENST00000355947.2:c.723A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16275
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000146833
  ensembl protein: ENSP00000275736
  ensembl transcript: ENST00000349062
  gene symbol: TRIM4
  hgvsc: ENST00000349062.2:c.645A>G
  hgvsp: ENST00000349062.2:c.645A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16275
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000146833
  ensembl protein: ENSP00000346186
  ensembl transcript: ENST00000354241
  gene symbol: TRIM4
  hgvsc: ENST00000354241.5:c.645A>G
  hgvsp: ENST00000354241.5:c.645A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16275
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000146833
  ensembl protein: ENSP00000396229
  ensembl transcript: ENST00000447480
  gene symbol: TRIM4
  hgvsc: ENST00000447480.1:c.349A>G
  hgvsp: ENST00000447480.1:c.349A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16275
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000146833
  ensembl transcript: ENST00000496896
  gene symbol: TRIM4
  hgvsc: ENST00000496896.1:n.190A>G
  variant of: http://identifiers.org/hgnc/16275
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2183
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1069
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3972
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18394
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7578
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6935
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1201
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15915
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4655
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1544
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8907
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2274
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26564
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Gln241Gln
num of homozygotes: 0
population: Latino
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
reference allele: T
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum

7-99506284-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 99506284
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 99506284
    reference: chr 7
allele count: 4
allele frequency: 3.295055768818887e-5
allele num: 121394
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146833
  ensembl protein: ENSP00000275736
  ensembl transcript: ENST00000349062
  gene symbol: TRIM4
  hgvsc: ENST00000349062.2:c.641A>G
  hgvsp: ENSP00000275736.4:p.Asn214Ser
  variant of: http://identifiers.org/hgnc/16275
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146833
  ensembl protein: ENSP00000396229
  ensembl transcript: ENST00000447480
  gene symbol: TRIM4
  hgvsc: ENST00000447480.1:c.345A>G
  hgvsp: ENSP00000396229.1:p.Asn116Ser
  variant of: http://identifiers.org/hgnc/16275
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000146833
  ensembl protein: ENSP00000348216
  ensembl transcript: ENST00000355947
  gene symbol: TRIM4
  hgvsc: ENST00000355947.2:c.719A>G
  hgvsp: ENSP00000348216.2:p.Asn240Ser
  variant of: http://identifiers.org/hgnc/16275
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000146833
  ensembl transcript: ENST00000496896
  gene symbol: TRIM4
  hgvsc: ENST00000496896.1:n.186A>G
  variant of: http://identifiers.org/hgnc/16275
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146833
  ensembl protein: ENSP00000346186
  ensembl transcript: ENST00000354241
  gene symbol: TRIM4
  hgvsc: ENST00000354241.5:c.641A>G
  hgvsp: ENSP00000346186.5:p.Asn214Ser
  variant of: http://identifiers.org/hgnc/16275
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6933
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1070
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3973
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7576
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2183
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18399
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15913
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1201
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4656
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3239
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9964
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3525
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2274
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Asn240Ser
num of homozygotes: 0
population: Latino
population: Other
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum

7-99506295-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 99506295
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 99506295
    reference: chr 7
allele count: 2
allele frequency: 1.647500741375333e-5
allele num: 121396
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000146833
  ensembl protein: ENSP00000275736
  ensembl transcript: ENST00000349062
  gene symbol: TRIM4
  hgvsc: ENST00000349062.2:c.630G>A
  hgvsp: ENST00000349062.2:c.630G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16275
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000146833
  ensembl transcript: ENST00000496896
  gene symbol: TRIM4
  hgvsc: ENST00000496896.1:n.175G>A
  variant of: http://identifiers.org/hgnc/16275
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000146833
  ensembl protein: ENSP00000346186
  ensembl transcript: ENST00000354241
  gene symbol: TRIM4
  hgvsc: ENST00000354241.5:c.630G>A
  hgvsp: ENST00000354241.5:c.630G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16275
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000146833
  ensembl protein: ENSP00000396229
  ensembl transcript: ENST00000447480
  gene symbol: TRIM4
  hgvsc: ENST00000447480.1:c.334G>A
  hgvsp: ENST00000447480.1:c.334G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16275
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000146833
  ensembl protein: ENSP00000348216
  ensembl transcript: ENST00000355947
  gene symbol: TRIM4
  hgvsc: ENST00000355947.2:c.708G>A
  hgvsp: ENST00000355947.2:c.708G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16275
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1068
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1202
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7577
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2184
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18396
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15917
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6935
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3972
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3238
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26566
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8903
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3526
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Thr236Thr
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
population: Other
reference allele: C
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD

7-99506296-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 99506296
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 99506296
    reference: chr 7
allele count: 2
allele frequency: 1.647473599235572e-5
allele num: 121398
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000146833
  ensembl protein: ENSP00000348216
  ensembl transcript: ENST00000355947
  gene symbol: TRIM4
  hgvsc: ENST00000355947.2:c.707C>T
  hgvsp: ENSP00000348216.2:p.Thr236Met
  variant of: http://identifiers.org/hgnc/16275
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146833
  ensembl protein: ENSP00000275736
  ensembl transcript: ENST00000349062
  gene symbol: TRIM4
  hgvsc: ENST00000349062.2:c.629C>T
  hgvsp: ENSP00000275736.4:p.Thr210Met
  variant of: http://identifiers.org/hgnc/16275
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146833
  ensembl protein: ENSP00000346186
  ensembl transcript: ENST00000354241
  gene symbol: TRIM4
  hgvsc: ENST00000354241.5:c.629C>T
  hgvsp: ENSP00000346186.5:p.Thr210Met
  variant of: http://identifiers.org/hgnc/16275
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146833
  ensembl protein: ENSP00000396229
  ensembl transcript: ENST00000447480
  gene symbol: TRIM4
  hgvsc: ENST00000447480.1:c.333C>T
  hgvsp: ENSP00000396229.1:p.Thr112Met
  variant of: http://identifiers.org/hgnc/16275
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000146833
  ensembl transcript: ENST00000496896
  gene symbol: TRIM4
  hgvsc: ENST00000496896.1:n.174C>T
  variant of: http://identifiers.org/hgnc/16275
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18399
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1067
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7576
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2184
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15916
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6936
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3972
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1202
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4655
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9959
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1544
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2273
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26572
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Thr236Met
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
population: Other
reference allele: G
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD

7-99506298-GT-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 99506298
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 99506297
    reference: chr 7
allele count: 1
allele frequency: 8.237096588194593e-6
allele num: 121402
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000146833
  ensembl protein: ENSP00000396229
  ensembl transcript: ENST00000447480
  gene symbol: TRIM4
  hgvsc: ENST00000447480.1:c.330delA
  hgvsp: ENSP00000396229.1:p.Asn111ThrfsTer3
  variant of: http://identifiers.org/hgnc/16275
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000146833
  ensembl transcript: ENST00000496896
  gene symbol: TRIM4
  hgvsc: ENST00000496896.1:n.171delA
  variant of: http://identifiers.org/hgnc/16275
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000146833
  ensembl protein: ENSP00000275736
  ensembl transcript: ENST00000349062
  gene symbol: TRIM4
  hgvsc: ENST00000349062.2:c.626delA
  hgvsp: ENSP00000275736.4:p.Asn209ThrfsTer3
  variant of: http://identifiers.org/hgnc/16275
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000146833
  ensembl protein: ENSP00000346186
  ensembl transcript: ENST00000354241
  gene symbol: TRIM4
  hgvsc: ENST00000354241.5:c.626delA
  hgvsp: ENSP00000346186.5:p.Asn209ThrfsTer3
  variant of: http://identifiers.org/hgnc/16275
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000146833
  ensembl protein: ENSP00000348216
  ensembl transcript: ENST00000355947
  gene symbol: TRIM4
  hgvsc: ENST00000355947.2:c.704delA
  hgvsp: ENSP00000348216.2:p.Asn235ThrfsTer3
  variant of: http://identifiers.org/hgnc/16275
canonical: true
consequence: frameshift
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 18403
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7576
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2183
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3972
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1202
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1067
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6936
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15916
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26573
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2273
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8904
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1544
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Asn235ThrfsTer3
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: GT
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ

7-99506299-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 99506299
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 99506299
    reference: chr 7
allele count: 1
allele frequency: 8.237367996177861e-6
allele num: 121398
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146833
  ensembl protein: ENSP00000396229
  ensembl transcript: ENST00000447480
  gene symbol: TRIM4
  hgvsc: ENST00000447480.1:c.330A>G
  hgvsp: ENSP00000396229.1:p.Asn111Ser
  variant of: http://identifiers.org/hgnc/16275
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000146833
  ensembl transcript: ENST00000496896
  gene symbol: TRIM4
  hgvsc: ENST00000496896.1:n.171A>G
  variant of: http://identifiers.org/hgnc/16275
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000146833
  ensembl protein: ENSP00000348216
  ensembl transcript: ENST00000355947
  gene symbol: TRIM4
  hgvsc: ENST00000355947.2:c.704A>G
  hgvsp: ENSP00000348216.2:p.Asn235Ser
  variant of: http://identifiers.org/hgnc/16275
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146833
  ensembl protein: ENSP00000346186
  ensembl transcript: ENST00000354241
  gene symbol: TRIM4
  hgvsc: ENST00000354241.5:c.626A>G
  hgvsp: ENSP00000346186.5:p.Asn209Ser
  variant of: http://identifiers.org/hgnc/16275
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000146833
  ensembl protein: ENSP00000275736
  ensembl transcript: ENST00000349062
  gene symbol: TRIM4
  hgvsc: ENST00000349062.2:c.626A>G
  hgvsp: ENSP00000275736.4:p.Asn209Ser
  variant of: http://identifiers.org/hgnc/16275
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7574
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15916
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6937
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1066
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1202
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3972
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2183
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18404
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1544
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26575
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4655
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2273
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3240
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Asn235Ser
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: African
reference allele: T
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: QD

7-99506304-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 99506304
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 99506304
    reference: chr 7
allele count: 241
allele frequency: 1.985140277754897e-3
allele num: 121402
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000146833
  ensembl protein: ENSP00000348216
  ensembl transcript: ENST00000355947
  gene symbol: TRIM4
  hgvsc: ENST00000355947.2:c.699T>C
  hgvsp: ENST00000355947.2:c.699T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16275
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000146833
  ensembl transcript: ENST00000496896
  gene symbol: TRIM4
  hgvsc: ENST00000496896.1:n.166T>C
  variant of: http://identifiers.org/hgnc/16275
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000146833
  ensembl protein: ENSP00000396229
  ensembl transcript: ENST00000447480
  gene symbol: TRIM4
  hgvsc: ENST00000447480.1:c.325T>C
  hgvsp: ENST00000447480.1:c.325T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16275
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000146833
  ensembl protein: ENSP00000275736
  ensembl transcript: ENST00000349062
  gene symbol: TRIM4
  hgvsc: ENST00000349062.2:c.621T>C
  hgvsp: ENST00000349062.2:c.621T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16275
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000146833
  ensembl protein: ENSP00000346186
  ensembl transcript: ENST00000354241
  gene symbol: TRIM4
  hgvsc: ENST00000354241.5:c.621T>C
  hgvsp: ENST00000354241.5:c.621T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16275
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6933
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 9.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 7565
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1194
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 6.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 2168
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1184
  bin: 9.75e1
  variant carriers: 167
genotype depth: GenotypeDepth
  all individuals: 15902
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 8.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18401
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 6.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 7.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 760
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 8.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 7.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 3954
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9985
  bin: 9.75e1
  variant carriers: 238
genotype quality: GenotypeQuality
  all individuals: 2269
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1541
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Asn233Asn
num of homozygotes: 3
reference allele: A

GenotypeQuality
all individuals: 666
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 391
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3015
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4465
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 339
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 254
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 676
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 580
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1252
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 656
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 76
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 263
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2002
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9538
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30320
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 133
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 957
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 73
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4562
bin: 3.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 348
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2494
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3358
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4266
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 27952
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3550
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7294
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.399999999999999e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -9.22e-1

QD
type: SiteQuality
SIO_000300: 5.72e0

MQ
type: SiteQuality
SIO_000300: 5.739e1

MQRankSum
type: SiteQuality
SIO_000300: -9.22e-1

DP
type: SiteQuality
SIO_000300: 7.57675e5

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.22e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.913e0

BaseQRankSum
type: SiteQuality
SIO_000300: -9.22e-1

GenotypeQuality
all individuals: 616
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 643
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 138
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4238
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 244
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11587
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2590
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 553
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 698
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 357
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29058
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1870
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4152
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 283
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1252
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1091
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 611
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 282
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 80
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 29970
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2706
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 2.198768689533861e-4
allele num: 4548
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3906
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7630
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3664
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 368
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.733e0

QD
type: SiteQuality
SIO_000300: 1.243e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.33e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.45e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.68e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.86e-1

FS
type: SiteQuality
SIO_000300: 3.119e0

DP
type: SiteQuality
SIO_000300: 7.98339e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.800000000000001e-3

GenotypeQuality
all individuals: 26905
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1810
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 281
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 464
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 261
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 782
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 630
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 456
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3728
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1819
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 348
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1325
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 162
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 345
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 387
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1256
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 82
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15764
bin: 6.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5038
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 430
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 34374
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3038
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 4.595588235294118e-4
allele num: 4352
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4752
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.283e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.7e-3

DP
type: SiteQuality
SIO_000300: 8.61761e5

MQ
type: SiteQuality
SIO_000300: 5.93e1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.07e0

FS
type: SiteQuality
SIO_000300: 2.553e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.17e0

MQRankSum
type: SiteQuality
SIO_000300: -6.37e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.8e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.51e-2

GenotypeQuality
all individuals: 345
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 183
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 840
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 573
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 722
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 91
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21229
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1575
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2958
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1197
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2741
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 290
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 916
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 950
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22029
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1263
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 92
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 405
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 410
bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 1.725923369002416e-4
allele num: 5794
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5286
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6226
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 2.053809817210926e-4
allele num: 9738
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 500
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 7.354383212394588e-5
allele num: 40792
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3582
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.923e1

QD
type: SiteQuality
SIO_000300: 1.104e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.8e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.733e0

VQSLOD
type: SiteQuality
SIO_000300: 1.05e0

DP
type: SiteQuality
SIO_000300: 9.73707e5

MQRankSum
type: SiteQuality
SIO_000300: -7.52e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.6e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 3.03e-1

GenotypeQuality
all individuals: 351
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 204
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 20445
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 239
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1015
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 290
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2030
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 454
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 727
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2543
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 453
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 625
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 536
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2679
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1432
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1264
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 98
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 217
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 93
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 4.625132972572962e-5
allele num: 43242
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10230
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6766
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 534
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6106
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5644
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3790
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.4e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.7e-1

VQSLOD
type: SiteQuality
SIO_000300: -5.117e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.2e-2

QD
type: SiteQuality
SIO_000300: 1.443e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.6e0

MQ
type: SiteQuality
SIO_000300: 5.87e1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.02e-1

FS
type: SiteQuality
SIO_000300: 9.266999999999999e0

DP
type: SiteQuality
SIO_000300: 1.013032e6

GenotypeQuality
all individuals: 2351
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 893
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 19392
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 580
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 492
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 101
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2509
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 101
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 171
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 700
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 218
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 127
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1335
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26447
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 474
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 270
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2139
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 519
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 364
bin: 5.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.227766886472999e-5
allele num: 44888
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5892
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10532
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3918
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 556
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6282
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7084
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.33e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.33e-1

MQRankSum
type: SiteQuality
SIO_000300: -9.78e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.035069e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.4e-3

QD
type: SiteQuality
SIO_000300: 1.182e1

VQSLOD
type: SiteQuality
SIO_000300: 2.73e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.96e-1

GenotypeDepth
all individuals: 57
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 40
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 370
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 34204
bin: 2.25e1
variant carriers: 5

GenotypeQuality
all individuals: 584
bin: 7.25e1
variant carriers: 1

GenotypeQuality
all individuals: 541
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 93
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13056
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1607
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1564
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1281
bin: 9.75e1
variant carriers: 17

GenotypeQuality
all individuals: 35339
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 515
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 899
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 490
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 326
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 539
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 381
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2552
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 247
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 109
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 52962
num of homozygotes: 0

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

African
type: Population
allele count: 17
allele frequency: 2.363080344731721e-3
allele num: 7194
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7036
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12054
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.135073779795687e-4
allele num: 8810
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 650
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 6.12e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.18e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.3e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.4e-2

QD
type: SiteQuality
SIO_000300: 1.339e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.04e-1

FS
type: SiteQuality
SIO_000300: 7.02e-1

DP
type: SiteQuality
SIO_000300: 1.168137e6

MQ
type: SiteQuality
SIO_000300: 5.911e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-3

GenotypeDepth
all individuals: 40
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 96
bin: 4.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 57
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 106
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 91
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 220
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 416
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1428
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 513
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1515
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 383
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 110
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 249
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11807
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 36548
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1285
bin: 9.75e1
variant carriers: 22

GenotypeQuality
all individuals: 568
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2589
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 581
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 845
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 542
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 557
bin: 5.25e1
variant carriers: 0

Latino
type: Population
allele count: 3
allele frequency: 3.298153034300791e-4
allele num: 9096
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.384274640088594e-4
allele num: 7224
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4786
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7380
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12346
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.501501501501501e-3
allele num: 666
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 17
allele frequency: 3.131562465460708e-4
allele num: 54286
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.96e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.195529e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.145e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.59e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.3e-2

VQSLOD
type: SiteQuality
SIO_000300: 3.48e0

FS
type: SiteQuality
SIO_000300: 6.22e-1

QD
type: SiteQuality
SIO_000300: 1.248e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.1e-3

GenotypeDepth
all individuals: 40
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 360
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 312
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 498
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 401
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43108
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3371
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 318
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 113
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 242
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 754
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 843
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 677
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 407
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 785
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 116
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6657
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 123
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1277
bin: 9.75e1
variant carriers: 1

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5550
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8218
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8036
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.662123529020677e-5
allele num: 60164
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10412
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13968
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 762
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.883e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.88e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.71e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 2.71e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.307959e6

VQSLOD
type: SiteQuality
SIO_000300: -1.693e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.88e-1

QD
type: SiteQuality
SIO_000300: 7.66e0

GenotypeQuality
all individuals: 672
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5346
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 803
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 627
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 408
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44939
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3536
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 259
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 84
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 203
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1276
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 125
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 328
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 412
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 115
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 233
bin: 5.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8480
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10690
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8194
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 784
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14454
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5798
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.623956607879438e-5
allele num: 61578
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.71e-1

QD
type: SiteQuality
SIO_000300: 2.95e0

BaseQRankSum
type: SiteQuality
SIO_000300: 8.149999999999999e-1

DP
type: SiteQuality
SIO_000300: 1.337223e6

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -3.532e0

VQSLOD
type: SiteQuality
SIO_000300: -1.9e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

MQ
type: SiteQuality
SIO_000300: 4.768e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.992e0

GenotypeDepth
all individuals: 57
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 831
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 114
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 729
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43959
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 679
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3492
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1277
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 54
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 437
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 716
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 146
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 431
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 255
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5188
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 637
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 795
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 314
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 122
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 233
bin: 4.25e1
variant carriers: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 784
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8196
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8478
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.380452788514633e-4
allele num: 14488
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10698
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61624
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.68e0

FS
type: SiteQuality
SIO_000300: 2.402e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.340341e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.9e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -1.53e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 8.72e-1

QD
type: SiteQuality
SIO_000300: 1.47e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.51e-1

GenotypeDepth
all individuals: 40
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 637
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 431
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 437
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5188
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 146
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 114
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 255
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1277
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 729
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 122
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 679
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 314
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 795
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 716
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 831
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 233
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43959
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3492
bin: 6.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10698
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14488
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8196
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 784
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.179523472517103e-4
allele num: 8478
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61624
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.53e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.68e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.51e-1

FS
type: SiteQuality
SIO_000300: 2.402e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.9e-3

DP
type: SiteQuality
SIO_000300: 1.340341e6

BaseQRankSum
type: SiteQuality
SIO_000300: 8.72e-1

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.47e1

GenotypeDepth
all individuals: 242
bin: 3.75e1
variant carriers: 4

GenotypeQuality
all individuals: 3579
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 226
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4940
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1302
bin: 9.75e1
variant carriers: 27

GenotypeQuality
all individuals: 71
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 597
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 417
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 115
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 365
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 248
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 823
bin: 7.25e1
variant carriers: 1

GenotypeQuality
all individuals: 663
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 322
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 727
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 520
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44963
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 325
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 122
bin: 8.75e1
variant carriers: 1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8222
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5866
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.856665428889714e-4
allele num: 10772
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.458279514337381e-5
allele num: 61936
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 790
num of homozygotes: 0

African
type: Population
allele count: 23
allele frequency: 2.690058479532164e-3
allele num: 8550
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14590
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.12e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.15e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.203e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.92e-1

DP
type: SiteQuality
SIO_000300: 1.348912e6

QD
type: SiteQuality
SIO_000300: 1.157e1

MQ
type: SiteQuality
SIO_000300: 5.925e1

FS
type: SiteQuality
SIO_000300: 2.669e0

VQSLOD
type: SiteQuality
SIO_000300: 1.62e0

GenotypeDepth
all individuals: 74
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 187
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 612
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 123
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 370
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 744
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 330
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 841
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 384
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4672
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 149
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 252
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3645
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45744
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 326
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1283
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 113
bin: 9.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8260
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.797172376291462e-5
allele num: 14712
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.846040243677312e-4
allele num: 10834
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5920
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8634
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62234
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 1.82e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.6e-1

DP
type: SiteQuality
SIO_000300: 1.354934e6

MQRankSum
type: SiteQuality
SIO_000300: 1.06e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.37e-1

FS
type: SiteQuality
SIO_000300: 2.13e0

QD
type: SiteQuality
SIO_000300: 1.17e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.6e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 9.88e-1

GenotypeDepth
all individuals: 1624
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 612
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 370
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 123
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 252
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1283
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 45744
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 326
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 187
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 149
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3645
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 841
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 330
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 384
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 113
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4672
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 744
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8634
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10834
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62234
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5920
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.359434475258292e-4
allele num: 14712
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8260
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.37e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.6e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.354934e6

FS
type: SiteQuality
SIO_000300: 2.13e0

MQRankSum
type: SiteQuality
SIO_000300: 1.06e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 9.88e-1

QD
type: SiteQuality
SIO_000300: 1.17e1

VQSLOD
type: SiteQuality
SIO_000300: 1.82e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.6e-1

GenotypeDepth
all individuals: 370
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 392
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45729
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 841
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3674
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 361
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 167
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1287
bin: 9.75e1
variant carriers: 10

GenotypeQuality
all individuals: 588
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 524
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 329
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 248
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 69
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 749
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 115
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4505
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 124
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 339
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 360
bin: 5.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 9.614460148062687e-5
allele num: 62406
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 3
allele frequency: 5.043712172158709e-4
allele num: 5948
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 1.152870647913304e-4
allele num: 8674
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10860
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14806
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.2e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 1.35e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.07e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -8.88e-1

QD
type: SiteQuality
SIO_000300: 1.189e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -5.5e-2

MQ
type: SiteQuality
SIO_000300: 5.93e1

DP
type: SiteQuality
SIO_000300: 1.358821e6

GenotypeDepth
all individuals: 80
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 357
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 253
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 116
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 194
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 317
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 123
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 839
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 46271
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4241
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 324
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 545
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 181
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3693
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1292
bin: 9.75e1
variant carriers: 14

GenotypeQuality
all individuals: 754
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 502
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 335
bin: 3.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5986
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.144426642252232e-4
allele num: 8738
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8318
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 800
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 12
allele frequency: 1.915647648542511e-4
allele num: 62642
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14902
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 9.170946441672781e-5
allele num: 10904
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.26e0

BaseQRankSum
type: SiteQuality
SIO_000300: 8.26e-1

DP
type: SiteQuality
SIO_000300: 1.365654e6

MQ
type: SiteQuality
SIO_000300: 5.943e1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.9e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.0e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

QD
type: SiteQuality
SIO_000300: 1.183e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.7e-2

GenotypeDepth
all individuals: 97
bin: 5.25e1
variant carriers: 8

GenotypeQuality
all individuals: 1394
bin: 9.75e1
variant carriers: 121

GenotypeQuality
all individuals: 26
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 303
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 47841
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 224
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 202
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 386
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 140
bin: 4.25e1
variant carriers: 1

GenotypeQuality
all individuals: 27
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 324
bin: 3.25e1
variant carriers: 1

GenotypeQuality
all individuals: 2963
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 206
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 123
bin: 9.25e1
variant carriers: 2

GenotypeQuality
all individuals: 769
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 131
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3857
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 341
bin: 8.25e1
variant carriers: 2

GenotypeQuality
all individuals: 876
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 298
bin: 5.75e1
variant carriers: 0

Latino
type: Population
allele count: 9
allele frequency: 8.111031002162941e-4
allele num: 11096
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8442
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: 39
allele frequency: 6.098895943452288e-4
allele num: 63946
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: 6214
num of homozygotes: 0

South Asian
type: Population
allele count: 76
allele frequency: 4.935705935835823e-3
allele num: 15398
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.934e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 4.15e-1

FS
type: SiteQuality
SIO_000300: 5.56e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.452e0

DP
type: SiteQuality
SIO_000300: 1.397289e6

ClippingRankSum
type: SiteQuality
SIO_000300: -2.06e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.72e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.15e-1

QD
type: SiteQuality
SIO_000300: 1.063e1

GenotypeDepth
all individuals: 78
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 121
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 206
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 770
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 878
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 313
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2851
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 48142
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 209
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1282
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 311
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 148
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 132
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 220
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3862
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 337
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 215
bin: 5.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8442
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.099384344766931e-4
allele num: 9096
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11118
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.561524047470331e-5
allele num: 64040
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 834
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15442
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6232
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 3.11e-1

QD
type: SiteQuality
SIO_000300: 5.55e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.25e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.1e-3

FS
type: SiteQuality
SIO_000300: 8.53e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -1.42e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.559e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.89e-1

DP
type: SiteQuality
SIO_000300: 1.399278e6

GenotypeDepth
all individuals: 245
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 318
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 208
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 164
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 807
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 48731
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2598
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 134
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3921
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 202
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 157
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 350
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 82
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1285
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 268
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 899
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 171
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 124
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9158
num of homozygotes: 0

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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 836
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15554
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64356
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 2
allele frequency: 3.18775900541919e-4
allele num: 6274
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.22e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.44e0

FS
type: SiteQuality
SIO_000300: 4.904e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.0e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.83e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.27e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

DP
type: SiteQuality
SIO_000300: 1.404474e6

QD
type: SiteQuality
SIO_000300: 1.233e1

GenotypeDepth
all individuals: 100
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1291
bin: 9.75e1
variant carriers: 9

GenotypeQuality
all individuals: 182
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 179
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 345
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 132
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 201
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 196
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2481
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 889
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3909
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 308
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 813
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 236
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 267
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 113
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 122
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 48737
bin: 6.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6290
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 9.307231719045698e-5
allele num: 64466
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8474
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.282873636946761e-4
allele num: 15590
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.957362952346828e-5
allele num: 11164
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9210
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: 9.5e-2

VQSLOD
type: SiteQuality
SIO_000300: 2.13e0

FS
type: SiteQuality
SIO_000300: 1.796e0

MQRankSum
type: SiteQuality
SIO_000300: 1.82e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-3

QD
type: SiteQuality
SIO_000300: 1.181e1

MQ
type: SiteQuality
SIO_000300: 5.948e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.67e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.0e-1

DP
type: SiteQuality
SIO_000300: 1.408722e6

GenotypeDepth
all individuals: 260
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1282
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 155
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 130
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 288
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 894
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 203
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 263
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 216
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 154
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 346
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2410
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 122
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3912
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 817
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 48909
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 121
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9228
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11180
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8478
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.550147263990079e-5
allele num: 64510
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6306
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15622
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 8.99e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.06e-1

MQ
type: SiteQuality
SIO_000300: 5.945e1

DP
type: SiteQuality
SIO_000300: 1.410774e6

QD
type: SiteQuality
SIO_000300: 1.355e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.54e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.18e-1

FS
type: SiteQuality
SIO_000300: 6.44e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -9.62e-1

GenotypeDepth
all individuals: 372
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 133
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 236
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 122
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 917
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2189
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 27
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 140
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 192
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 78
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 158
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 245
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 209
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 49263
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1282
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 347
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3947
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 133
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 829
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9284
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.543257507947776e-5
allele num: 64798
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11234
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8498
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6354
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15740
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 3.493e0

DP
type: SiteQuality
SIO_000300: 1.416902e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.93e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.59e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.861e0

VQSLOD
type: SiteQuality
SIO_000300: -1.379e0

QD
type: SiteQuality
SIO_000300: 5.53e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.93e-1

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

GenotypeQuality
all individuals: 122
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3968
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 918
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 211
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 244
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1282
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 49212
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 76
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2176
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 821
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 244
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 221
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 190
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 132
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 128
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 126
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 346
bin: 8.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8498
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64812
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9292
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.350012700025399e-5
allele num: 15748
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11236
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6356
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.417192e6

ClippingRankSum
type: SiteQuality
SIO_000300: -4.19e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.19e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.17e-1

QD
type: SiteQuality
SIO_000300: 7.87e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.2e-3

VQSLOD
type: SiteQuality
SIO_000300: 2.26e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 2.71e-1

GenotypeDepth
all individuals: 372
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2119
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 132
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 186
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 270
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1282
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 216
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 242
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 121
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 149
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 49263
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 911
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 805
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 211
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 105
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3982
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 347
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9306
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8508
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15840
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.539361472861057e-5
allele num: 64962
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 850
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11246
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6394
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.34e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.4e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.420022e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.485e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.8e-3

QD
type: SiteQuality
SIO_000300: 5.74e0

VQSLOD
type: SiteQuality
SIO_000300: 4.02e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.099999999999999e-2

GenotypeDepth
all individuals: 39
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 146
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 225
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 242
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 49414
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1282
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3979
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 183
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 147
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2100
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 348
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 806
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 916
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 100
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 133
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 209
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 121
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9308
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.538792970793709e-5
allele num: 64986
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11254
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 850
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15856
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6392
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.321e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.73e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.45e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-3

MQRankSum
type: SiteQuality
SIO_000300: -2.325e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.374e0

FS
type: SiteQuality
SIO_000300: 1.054e0

VQSLOD
type: SiteQuality
SIO_000300: -8.004e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.420339e6

GenotypeDepth
all individuals: 1949
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2206
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 233
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 208
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 123
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1281
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 132
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 192
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 898
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 159
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 97
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 265
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 342
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 802
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3990
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 133
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 49298
bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65002
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11256
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9328
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 852
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.175088131609871e-4
allele num: 8510
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15856
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6404
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -6.75e-1

DP
type: SiteQuality
SIO_000300: 1.419973e6

MQ
type: SiteQuality
SIO_000300: 5.911e1

MQRankSum
type: SiteQuality
SIO_000300: 3.2e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.1e-3

VQSLOD
type: SiteQuality
SIO_000300: -6.5e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 1.6e0

QD
type: SiteQuality
SIO_000300: 1.024e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.97e0

GenotypeDepth
all individuals: 372
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 371
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 209
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 274
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 332
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1283
bin: 9.75e1
variant carriers: 1

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

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

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

GenotypeQuality
all individuals: 84
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 197
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 159
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2545
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 48665
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 785
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3913
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 128
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 878
bin: 7.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9292
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6408
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11232
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15786
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 850
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.540784567501772e-5
allele num: 64902
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 1.55e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.4e-3

VQSLOD
type: SiteQuality
SIO_000300: 6.900000000000001e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.99e-1

MQ
type: SiteQuality
SIO_000300: 5.839e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.21e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.09e-1

DP
type: SiteQuality
SIO_000300: 1.414852e6

QD
type: SiteQuality
SIO_000300: 1.471e1

GenotypeDepth
all individuals: 87
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1282
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 858
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 200
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 125
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 198
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 448
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 756
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 251
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 315
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 401
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2845
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 47839
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 367
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 374
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 127
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3848
bin: 6.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 850
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9262
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6400
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8488
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.08794466403162e-5
allele num: 64768
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11206
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15732
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 7.0e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 8.28e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.47e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.21e-1

QD
type: SiteQuality
SIO_000300: 2.01e1

MQRankSum
type: SiteQuality
SIO_000300: 1.63e-1

MQ
type: SiteQuality
SIO_000300: 5.95e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.21e-1

DP
type: SiteQuality
SIO_000300: 1.411597e6

GenotypeDepth
all individuals: 372
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 251
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 216
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 405
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 326
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 181
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 855
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 201
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 445
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 48101
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2845
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 115
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1280
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 126
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 312
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 752
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3850
bin: 6.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8488
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64804
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9264
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 850
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.925383791503035e-5
allele num: 11204
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15734
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.683e0

QD
type: SiteQuality
SIO_000300: 8.140000000000001e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.202e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.9e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.03e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.64e-1

DP
type: SiteQuality
SIO_000300: 1.411376e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

MQ
type: SiteQuality
SIO_000300: 5.963e1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.51e-1

GenotypeDepth
all individuals: 372
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 418
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 255
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 195
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 256
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1282
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 27
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 180
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 100
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3865
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 48142
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 449
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2933
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 855
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 751
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 153
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 311
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 126
bin: 8.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.178967224711153e-4
allele num: 8482
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6404
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11204
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.543591010125957e-5
allele num: 64784
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.080146899978397e-4
allele num: 9258
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15728
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.119e0

DP
type: SiteQuality
SIO_000300: 1.409444e6

VQSLOD
type: SiteQuality
SIO_000300: 9.48e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 1.46e-1

MQ
type: SiteQuality
SIO_000300: 5.95e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.33e-1

QD
type: SiteQuality
SIO_000300: 1.332e1

BaseQRankSum
type: SiteQuality
SIO_000300: 9.74e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.27e-1

GenotypeDepth
all individuals: 372
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 149
bin: 4.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 219
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 298
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 216
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1280
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3658
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 125
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 46778
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 607
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 383
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 615
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 326
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 717
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 303
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3732
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 841
bin: 7.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11152
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15606
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9178
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8442
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.549666821633349e-5
allele num: 64530
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.396501e6

MQRankSum
type: SiteQuality
SIO_000300: 1.22e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.025e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.74e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.826e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.89e-1

QD
type: SiteQuality
SIO_000300: 6.1e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.734e1

GenotypeDepth
all individuals: 2159
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 610
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 211
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 305
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 384
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 46888
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 301
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 222
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3722
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 609
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 32
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3666
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 839
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 712
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 125
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 186
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1319
bin: 9.75e1
variant carriers: 40

Latino
type: Population
allele count: 40
allele frequency: 3.586800573888092e-3
allele num: 11152
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15610
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64520
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8440
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9172
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -4.5e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

VQSLOD
type: SiteQuality
SIO_000300: 1.11e0

DP
type: SiteQuality
SIO_000300: 1.397057e6

MQRankSum
type: SiteQuality
SIO_000300: 2.06e-1

FS
type: SiteQuality
SIO_000300: 1.154e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.0e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 1.84e-1

MQ
type: SiteQuality
SIO_000300: 5.948e1

QD
type: SiteQuality
SIO_000300: 1.067e1

GenotypeDepth
all individuals: 90
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 890
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 82
bin: 1.75e1
variant carriers: 1

GenotypeQuality
all individuals: 293
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4482
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44973
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3574
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 262
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1295
bin: 9.75e1
variant carriers: 16

GenotypeQuality
all individuals: 553
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 804
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 232
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 684
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 350
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 305
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 857
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 124
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 470
bin: 5.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64198
num of homozygotes: 0

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

Latino
type: Population
allele count: 3
allele frequency: 2.708559046587215e-4
allele num: 11076
num of homozygotes: 0

South Asian
type: Population
allele count: 12
allele frequency: 7.763975155279503e-4
allele num: 15456
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8392
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6332
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.098177026136613e-4
allele num: 9106
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.674e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.69e-1

DP
type: SiteQuality
SIO_000300: 1.382722e6

QD
type: SiteQuality
SIO_000300: 1.015e1

MQ
type: SiteQuality
SIO_000300: 5.962e1

VQSLOD
type: SiteQuality
SIO_000300: 9.05e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.1e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.17e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 8.0e-1

GenotypeDepth
all individuals: 39
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1280
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 242
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 631
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1026
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 799
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 125
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4868
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 980
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 674
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 291
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 90
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 374
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 595
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43862
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 270
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 646
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3485
bin: 6.75e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.500260010400417e-5
allele num: 15384
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11036
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9088
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8388
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64066
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6328
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.05e0

FS
type: SiteQuality
SIO_000300: 5.089e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.265e1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.27e-1

MQRankSum
type: SiteQuality
SIO_000300: -5.6e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.91e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.46e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

DP
type: SiteQuality
SIO_000300: 1.374293e6

GenotypeDepth
all individuals: 86
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 62
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 351
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 115
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43702
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 295
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 123
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 321
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5250
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 90
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 787
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1067
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1280
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 247
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 433
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 286
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3475
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1163
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 696
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 672
bin: 7.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 836
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8372
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10990
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6326
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.103022281050077e-4
allele num: 9066
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15346
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63944
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -2.802e0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.87e-1

QD
type: SiteQuality
SIO_000300: 7.49e0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.049e0

MQ
type: SiteQuality
SIO_000300: 5.825e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.024e0

MQRankSum
type: SiteQuality
SIO_000300: 1.59e-1

DP
type: SiteQuality
SIO_000300: 1.368366e6

GenotypeDepth
all individuals: 35066
bin: 2.25e1
variant carriers: 8

GenotypeQuality
all individuals: 973
bin: 3.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1482
bin: 3.25e1
variant carriers: 2

GenotypeQuality
all individuals: 371
bin: 7.5e0
variant carriers: 2

GenotypeQuality
all individuals: 472
bin: 5.75e1
variant carriers: 2

GenotypeQuality
all individuals: 282
bin: 2.5e0
variant carriers: 4

GenotypeQuality
all individuals: 578
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 193
bin: 1.75e1
variant carriers: 5

GenotypeQuality
all individuals: 711
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 108
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5778
bin: 2.25e1
variant carriers: 4

GenotypeQuality
all individuals: 1324
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1287
bin: 2.75e1
variant carriers: 5

GenotypeQuality
all individuals: 116
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 251
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 195
bin: 1.25e1
variant carriers: 1

GenotypeQuality
all individuals: 670
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 622
bin: 4.25e1
variant carriers: 5

GenotypeQuality
all individuals: 3133
bin: 6.75e1
variant carriers: 3

GenotypeQuality
all individuals: 41265
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 636
bin: 4.75e1
variant carriers: 2

Latino
type: Population
allele count: 1
allele frequency: 9.219988936013277e-5
allele num: 10846
num of homozygotes: 0

African
type: Population
allele count: 5
allele frequency: 5.604124635731899e-4
allele num: 8922
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.597954618088846e-4
allele num: 6258
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 1.983602221634488e-4
allele num: 15124
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 16
allele frequency: 2.531725687521757e-4
allele num: 63198
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.207729468599034e-3
allele num: 828
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.420135527589545e-4
allele num: 8264
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 8.7e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.04e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.7e-3

VQSLOD
type: SiteQuality
SIO_000300: 1.42e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.5e-2

MQRankSum
type: SiteQuality
SIO_000300: 4.62e-1

MQ
type: SiteQuality
SIO_000300: 5.941e1

FS
type: SiteQuality
SIO_000300: 1.673e0

DP
type: SiteQuality
SIO_000300: 1.377081e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.34e-1

GenotypeDepth
all individuals: 61
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 371
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 251
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1287
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 622
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 282
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 670
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 711
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 195
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1482
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 108
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5778
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 193
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 636
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 116
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3133
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 472
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 973
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41265
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 578
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1324
bin: 9.75e1
variant carriers: 2

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15124
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10846
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8264
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8922
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6258
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.164657109402196e-5
allele num: 63198
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.377081e6

MQ
type: SiteQuality
SIO_000300: 5.941e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.7e-3

FS
type: SiteQuality
SIO_000300: 1.673e0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.04e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.34e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.62e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.42e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.5e-2

QD
type: SiteQuality
SIO_000300: 8.7e-1

GenotypeDepth
all individuals: 33619
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1407
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1280
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2975
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1022
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 295
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 409
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6248
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 661
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 240
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1666
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 644
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 108
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 727
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 237
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39355
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 405
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 552
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 963
bin: 5.25e1
variant carriers: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.22040517451794e-4
allele num: 8194
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6206
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62670
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10720
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8816
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14958
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.769e0

QD
type: SiteQuality
SIO_000300: 1.595e1

FS
type: SiteQuality
SIO_000300: 6.5e-1

DP
type: SiteQuality
SIO_000300: 1.372144e6

VQSLOD
type: SiteQuality
SIO_000300: 1.87e0

MQRankSum
type: SiteQuality
SIO_000300: -4.5e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.1e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -9.8e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.9e-2

GenotypeDepth
all individuals: 2181
bin: 1.75e1
variant carriers: 2

GenotypeQuality
all individuals: 240
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39355
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 963
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 295
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 237
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1407
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6248
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 405
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 409
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 661
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 644
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2975
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1022
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1280
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 552
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1666
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 727
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 108
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.595659805329504e-5
allele num: 62670
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8194
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.865671641791045e-4
allele num: 10720
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14958
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6206
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8816
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -4.5e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.1e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -1.769e0

FS
type: SiteQuality
SIO_000300: 6.5e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.8e-2

DP
type: SiteQuality
SIO_000300: 1.372144e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.9e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.87e0

QD
type: SiteQuality
SIO_000300: 1.595e1

GenotypeDepth
all individuals: 60
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1480
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 307
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1308
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 114
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 603
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6535
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 307
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 357
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 179
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42253
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1310
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3311
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 699
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 300
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 849
bin: 3.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8950
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.589351607801793e-5
allele num: 15176
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10834
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8270
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6270
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: 3
allele frequency: 4.729474082482028e-5
allele num: 63432
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.351862e6

QD
type: SiteQuality
SIO_000300: 9.529999999999999e0

MQRankSum
type: SiteQuality
SIO_000300: 3.87e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.04e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 4.77e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.3e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.44e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.96e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.48e-1

GenotypeDepth
all individuals: 104
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 300
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3311
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 114
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1480
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 603
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6535
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1310
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 357
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 307
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 42253
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 849
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 179
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1308
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 307
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 699
bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8950
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.589351607801793e-5
allele num: 15176
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8270
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10834
num of homozygotes: 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: 6270
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63432
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 3.87e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.96e0

VQSLOD
type: SiteQuality
SIO_000300: 6.04e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.3e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.351862e6

FS
type: SiteQuality
SIO_000300: 4.77e-1

QD
type: SiteQuality
SIO_000300: 9.529999999999999e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.48e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.44e-1

GenotypeDepth
all individuals: 104
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6535
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42253
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 300
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 1.25e1
variant carriers: 1

GenotypeQuality
all individuals: 699
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 849
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 114
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 307
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1480
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1308
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 307
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3311
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 179
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 357
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 603
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1310
bin: 2.75e1
variant carriers: 1

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10834
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6270
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: 1.576491360827343e-5
allele num: 63432
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8950
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.589351607801793e-5
allele num: 15176
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8270
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 4.77e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 3.87e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.3e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 3.48e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.96e0

QD
type: SiteQuality
SIO_000300: 9.529999999999999e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.44e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.04e-1

DP
type: SiteQuality
SIO_000300: 1.351862e6

GenotypeDepth
all individuals: 57
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7948
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2163
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 247
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 85
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38963
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 474
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 112
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 463
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 559
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 110
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1248
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1303
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1697
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 361
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 422
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3047
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 639
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 133
bin: 1.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14970
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6204
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10626
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.454590083456063e-4
allele num: 8148
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62890
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8836
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.318197e6

FS
type: SiteQuality
SIO_000300: 7.039e0

MQRankSum
type: SiteQuality
SIO_000300: -5.53e-1

MQ
type: SiteQuality
SIO_000300: 5.932e1

QD
type: SiteQuality
SIO_000300: 5.06e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.94e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.95e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.053e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -1.457e0

GenotypeDepth
all individuals: 2197
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37955
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 154
bin: 1.25e1
variant carriers: 2

GenotypeQuality
all individuals: 1784
bin: 2.75e1
variant carriers: 1

GenotypeQuality
all individuals: 543
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 107
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 572
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8248
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1360
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 416
bin: 7.5e0
variant carriers: 1

GenotypeQuality
all individuals: 513
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 233
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 110
bin: 2.5e0
variant carriers: 2

GenotypeQuality
all individuals: 2301
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 186
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 591
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 511
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2911
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1303
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 107
bin: 9.25e1
variant carriers: 0

East Asian
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: 804
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6150
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.597597213790459e-5
allele num: 62594
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10548
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.734006734006734e-5
allele num: 14850
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8792
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.61e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -8.03e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.62e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.8e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -1.67e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.195e0

FS
type: SiteQuality
SIO_000300: 1.771e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 3.3e-1

DP
type: SiteQuality
SIO_000300: 1.315545e6

GenotypeDepth
all individuals: 3372
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 355
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8698
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 420
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2441
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 109
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1875
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 456
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37759
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 388
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 93
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2977
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 521
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 137
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 108
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 598
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1473
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 235
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 475
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1302
bin: 9.75e1
variant carriers: 1

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10544
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14876
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8096
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8780
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.595252528475258e-5
allele num: 62686
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6172
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.925e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.884e0

FS
type: SiteQuality
SIO_000300: 5.704e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.942e0

DP
type: SiteQuality
SIO_000300: 1.301643e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.2e-3

MQRankSum
type: SiteQuality
SIO_000300: -8.699999999999999e-2

VQSLOD
type: SiteQuality
SIO_000300: -6.38e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.95e0

QD
type: SiteQuality
SIO_000300: 2.66e0

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

GenotypeQuality
all individuals: 1624
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36613
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 554
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 108
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1302
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 490
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 96
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 405
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 506
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 508
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2615
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 230
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1990
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 107
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 577
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2924
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9102
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 486
bin: 5.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14812
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8046
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10480
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.600307258993727e-5
allele num: 62488
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8756
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6146
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.769e0

QD
type: SiteQuality
SIO_000300: 1.424e1

MQ
type: SiteQuality
SIO_000300: 5.901e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.4e-3

DP
type: SiteQuality
SIO_000300: 1.291325e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.523e0

MQRankSum
type: SiteQuality
SIO_000300: 3.3e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.15e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.24e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.41e-1

GenotypeDepth
all individuals: 57
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 340
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1845
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 643
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35246
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 565
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2929
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 229
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 430
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 123
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 107
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 187
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9742
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 520
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2856
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 106
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 491
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 565
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1302
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2176
bin: 2.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8686
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10388
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62240
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6132
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 802
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.792555359326178e-5
allele num: 14722
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7972
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -9.689e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.5e-3

DP
type: SiteQuality
SIO_000300: 1.274813e6

MQRankSum
type: SiteQuality
SIO_000300: -7.000000000000001e-2

MQ
type: SiteQuality
SIO_000300: 5.866e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.495e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.63e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.75e-1

QD
type: SiteQuality
SIO_000300: 1.083e1

FS
type: SiteQuality
SIO_000300: 3.091e0

GenotypeDepth
all individuals: 39
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31830
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2315
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3410
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 149
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10575
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 789
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2435
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 850
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 481
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 227
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1185
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 275
bin: 1.75e1
variant carriers: 1

GenotypeQuality
all individuals: 533
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 780
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2562
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1302
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 106
bin: 8.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7880
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6096
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61828
num of homozygotes: 0

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14576
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.39e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.16e-1

QD
type: SiteQuality
SIO_000300: 5.19e0

MQ
type: SiteQuality
SIO_000300: 5.942e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.821e0

DP
type: SiteQuality
SIO_000300: 1.250766e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -7.870000000000001e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 3.64e-1

GenotypeDepth
all individuals: 96
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 40
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 89
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 39
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 492
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32729
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2434
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 209
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 627
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2284
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10672
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 843
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3398
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 162
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 479
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 525
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 106
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1302
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 765
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2534
bin: 6.75e1
variant carriers: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7862
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.618384851917786e-5
allele num: 61790
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.868131868131868e-5
allele num: 14560
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6096
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8606
num of homozygotes: 0

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: -2.022e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.56e-1

MQ
type: SiteQuality
SIO_000300: 5.901e1

DP
type: SiteQuality
SIO_000300: 1.249119e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-3

FS
type: SiteQuality
SIO_000300: 9.13e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.65e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.27e-1

QD
type: SiteQuality
SIO_000300: 1.034e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.99e-1

GenotypeDepth
all individuals: 372
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 89
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1576
bin: 3.25e1
variant carriers: 1

GenotypeDepth
all individuals: 254
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1301
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 220
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 170
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 888
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 223
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2402
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 815
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10951
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3523
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 105
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 606
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2478
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 515
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2512
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 502
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 32113
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 487
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 471
bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61702
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7842
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.890848952590959e-5
allele num: 14512
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6074
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10172
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -2.328e0

MQRankSum
type: SiteQuality
SIO_000300: 8.87e-1

DP
type: SiteQuality
SIO_000300: 1.241933e6

MQ
type: SiteQuality
SIO_000300: 5.914e1

VQSLOD
type: SiteQuality
SIO_000300: -8.057e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.381e0

FS
type: SiteQuality
SIO_000300: 3.691e0

QD
type: SiteQuality
SIO_000300: 1.727e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.05e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

GenotypeQuality
all individuals: 971
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 186
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 511
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2585
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2517
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 104
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3658
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 474
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 465
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 529
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 570
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 233
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1301
bin: 9.75e1
variant carriers: 1

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

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

GenotypeQuality
all individuals: 11271
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 890
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31349
bin: 6.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14424
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6064
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 790
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7788
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10120
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.624431448992852e-5
allele num: 61560
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.105e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.000000000000001e-2

DP
type: SiteQuality
SIO_000300: 1.233317e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 4.38e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.63e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.67e-1

QD
type: SiteQuality
SIO_000300: 1.282e1

GenotypeQuality
all individuals: 215
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 349
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 701
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 435
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4113
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1910
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 830
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 472
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5221
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1860
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14713
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18709
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3776
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 62
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1308
bin: 9.75e1
variant carriers: 7

GenotypeQuality
all individuals: 2830
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 103
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1881
bin: 5.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5916
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.671458180116333e-5
allele num: 59828
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 770
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8234
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7386
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9584
num of homozygotes: 0

South Asian
type: Population
allele count: 6
allele frequency: 4.329629095107519e-4
allele num: 13858
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 7.149e0

VQSLOD
type: SiteQuality
SIO_000300: 4.28e-1

DP
type: SiteQuality
SIO_000300: 1.134222e6

ClippingRankSum
type: SiteQuality
SIO_000300: 2.07e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.6e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.3e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 2.65e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.97e-1

MQ
type: SiteQuality
SIO_000300: 5.958e1

QD
type: SiteQuality
SIO_000300: 1.464e1

GenotypeQuality
all individuals: 8482
bin: 6.25e1
variant carriers: 480

GenotypeQuality
all individuals: 821
bin: 2.5e0
variant carriers: 55

GenotypeQuality
all individuals: 410
bin: 8.25e1
variant carriers: 360

GenotypeQuality
all individuals: 3056
bin: 2.75e1
variant carriers: 141

GenotypeQuality
all individuals: 531
bin: 1.25e1
variant carriers: 107

GenotypeQuality
all individuals: 1048
bin: 7.5e0
variant carriers: 82

GenotypeQuality
all individuals: 3420
bin: 3.25e1
variant carriers: 285

GenotypeQuality
all individuals: 20702
bin: 9.75e1
variant carriers: 20022

GenotypeQuality
all individuals: 304
bin: 8.75e1
variant carriers: 272

GenotypeQuality
all individuals: 328
bin: 9.25e1
variant carriers: 298

GenotypeQuality
all individuals: 754
bin: 1.75e1
variant carriers: 133

GenotypeQuality
all individuals: 1925
bin: 3.75e1
variant carriers: 377

GenotypeQuality
all individuals: 826
bin: 5.25e1
variant carriers: 476

GenotypeQuality
all individuals: 825
bin: 4.75e1
variant carriers: 456

GenotypeQuality
all individuals: 13435
bin: 2.25e1
variant carriers: 173

GenotypeQuality
all individuals: 692
bin: 4.25e1
variant carriers: 238

GenotypeQuality
all individuals: 1083
bin: 6.75e1
variant carriers: 448

GenotypeQuality
all individuals: 734
bin: 5.75e1
variant carriers: 308

GenotypeQuality
all individuals: 450
bin: 7.25e1
variant carriers: 323

African
type: Population
allele count: 1709
allele frequency: 2.129860418743769e-1
allele num: 8024
num of homozygotes: 159

European (Finnish)
type: Population
allele count: 2047
allele frequency: 3.595012293642431e-1
allele num: 5694
num of homozygotes: 328

Other
type: Population
allele count: 207
allele frequency: 2.774798927613941e-1
allele num: 746
num of homozygotes: 27

East Asian
type: Population
allele count: 512
allele frequency: 7.225515100197573e-2
allele num: 7086
num of homozygotes: 20

Latino
type: Population
allele count: 1459
allele frequency: 1.585524885894371e-1
allele num: 9202
num of homozygotes: 98

South Asian
type: Population
allele count: 2307
allele frequency: 1.704343971631206e-1
allele num: 13536
num of homozygotes: 195

European (Non-Finnish)
type: Population
allele count: 19771
allele frequency: 3.416214535024363e-1
allele num: 57874
num of homozygotes: 3033

BaseQRankSum
type: SiteQuality
SIO_000300: 1.73e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.99e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.01e-2

VQSLOD
type: SiteQuality
SIO_000300: 3.54e0

QD
type: SiteQuality
SIO_000300: 1.752e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.76e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.5e-2

DP
type: SiteQuality
SIO_000300: 1.19925e6

FS
type: SiteQuality
SIO_000300: 1.564e0

GenotypeQuality
all individuals: 5686
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 529
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 689
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 704
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 380
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 264
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5147
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 153
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 24110
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 487
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1335
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 434
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 114
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14180
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 302
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1561
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2667
bin: 3.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5222
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 53432
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12876
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7018
num of homozygotes: 0

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

African
type: Population
allele count: 2
allele frequency: 2.635740643120717e-4
allele num: 7588
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8712
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.36e0

BaseQRankSum
type: SiteQuality
SIO_000300: -8.99e-1

QD
type: SiteQuality
SIO_000300: 1.003e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -7.75e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.536e-1

DP
type: SiteQuality
SIO_000300: 1.011682e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.27e0

FS
type: SiteQuality
SIO_000300: 4.005e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-3

GenotypeQuality
all individuals: 297
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 360
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2838
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 477
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 109
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 24446
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 495
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1334
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1528
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5347
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6011
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 735
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13069
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 702
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 258
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 543
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 110
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8696
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5200
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7570
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.877793217410899e-5
allele num: 53254
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 690
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6994
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12848
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-3

QD
type: SiteQuality
SIO_000300: 1.103e1

DP
type: SiteQuality
SIO_000300: 9.95886e5

ClippingRankSum
type: SiteQuality
SIO_000300: -5.91e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 8.54e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.139e0

VQSLOD
type: SiteQuality
SIO_000300: 2.31e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.6e-1

GenotypeQuality
all individuals: 26524
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2274
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8904
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1544
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66714
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.155535012710885e-4
allele num: 8654
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

FS
type: SiteQuality
SIO_000300: 5.912e0

VQSLOD
type: SiteQuality
SIO_000300: -1.12e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -4.948e0

MQ
type: SiteQuality
SIO_000300: 5.947e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.526e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.04e0

DP
type: SiteQuality
SIO_000300: 2.157991e6

MQRankSum
type: SiteQuality
SIO_000300: 1.8e-2

GenotypeQuality
all individuals: 9967
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2274
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4653
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26555
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1544
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8906
bin: 6.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498800959232614e-5
allele num: 66720
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.46e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.979e1

DP
type: SiteQuality
SIO_000300: 2.158071e6

QD
type: SiteQuality
SIO_000300: 1.461e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.889999999999999e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.72e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 3.21e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.14e-1

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

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

GenotypeQuality
all individuals: 5
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2274
bin: 9.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
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: 8654
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498756032493031e-5
allele num: 66722
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.938e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.77e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.743e0

QD
type: SiteQuality
SIO_000300: 1.37e1

FS
type: SiteQuality
SIO_000300: 3.863e0

VQSLOD
type: SiteQuality
SIO_000300: -1.746e-1

MQRankSum
type: SiteQuality
SIO_000300: 8.03e-1

DP
type: SiteQuality
SIO_000300: 2.15819e6

BaseQRankSum
type: SiteQuality
SIO_000300: 5.81e0

GenotypeQuality
all individuals: 1
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8908
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4653
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3241
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 5.75e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 8.637070305752289e-5
allele num: 11578
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66726
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.77e0

FS
type: SiteQuality
SIO_000300: 8.144e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.78e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.19e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 2.158121e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 5.6e-2

QD
type: SiteQuality
SIO_000300: 1.276e1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.07e-1

GenotypeQuality
all individuals: 1544
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3241
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8908
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2274
bin: 9.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66726
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.727414061150458e-4
allele num: 11578
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 8.144e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.07e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.78e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.6e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.19e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 2.158121e6

BaseQRankSum
type: SiteQuality
SIO_000300: 2.77e0

QD
type: SiteQuality
SIO_000300: 1.276e1

GenotypeQuality
all individuals: 3525
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8907
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1544
bin: 8.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66726
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.157947e6

ClippingRankSum
type: SiteQuality
SIO_000300: -2.175e0

MQ
type: SiteQuality
SIO_000300: 5.706e1

FS
type: SiteQuality
SIO_000300: 6.870000000000001e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.79e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.61e0

QD
type: SiteQuality
SIO_000300: 1.192e1

MQRankSum
type: SiteQuality
SIO_000300: -2.398e0

VQSLOD
type: SiteQuality
SIO_000300: 1.44e0

GenotypeQuality
all individuals: 2
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3240
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9963
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 2
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3526
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 2
allele frequency: 1.728011059270779e-4
allele num: 11574
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66726
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: 8654
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 4.04e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 9.65e-1

FS
type: SiteQuality
SIO_000300: 2.517e0

DP
type: SiteQuality
SIO_000300: 2.157925e6

BaseQRankSum
type: SiteQuality
SIO_000300: 5.33e0

MQ
type: SiteQuality
SIO_000300: 5.974e1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.13e-1

QD
type: SiteQuality
SIO_000300: 1.677e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.86e0

GenotypeQuality
all individuals: 1545
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26566
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8906
bin: 6.75e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11574
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.056935190793458e-5
allele num: 16510
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.495863805299125e-5
allele num: 66728
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.237e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 1.11e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.47e-1

DP
type: SiteQuality
SIO_000300: 2.158067e6

MQ
type: SiteQuality
SIO_000300: 5.975e1

VQSLOD
type: SiteQuality
SIO_000300: 5.2e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.62e-1

MQRankSum
type: SiteQuality
SIO_000300: 9.1e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.06e0

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

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

GenotypeQuality
all individuals: 1544
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4655
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2273
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9962
bin: 9.75e1
variant carriers: 2

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498666187093487e-5
allele num: 66726
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.511944360447536e-4
allele num: 6614
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 8.37e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.64e0

FS
type: SiteQuality
SIO_000300: 1.3633e1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.32e-1

DP
type: SiteQuality
SIO_000300: 2.157771e6

MQ
type: SiteQuality
SIO_000300: 5.979e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 9.83e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.058e0

QD
type: SiteQuality
SIO_000300: 1.603e1

GenotypeQuality
all individuals: 8903
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3238
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3526
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 9.609840476648087e-5
allele num: 10406
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498621268433042e-5
allele num: 66728
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 5.04e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.157648e6

BaseQRankSum
type: SiteQuality
SIO_000300: 2.4e-2

MQRankSum
type: SiteQuality
SIO_000300: 6.2e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.01e-1

MQ
type: SiteQuality
SIO_000300: 5.977e1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.7e-1

QD
type: SiteQuality
SIO_000300: 1.453e1

GenotypeQuality
all individuals: 1
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3527
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4654
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3238
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9957
bin: 9.75e1
variant carriers: 1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498576352465158e-5
allele num: 66730
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 3.05e-1

DP
type: SiteQuality
SIO_000300: 2.157564e6

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.73e0

VQSLOD
type: SiteQuality
SIO_000300: 7.58e-1

QD
type: SiteQuality
SIO_000300: 1.541e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.461e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.21e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 6.024e1

GenotypeQuality
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 9956
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 6
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3526
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8904
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 5.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498621268433042e-5
allele num: 66728
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -2.96e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.11e-1

MQ
type: SiteQuality
SIO_000300: 5.839e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.24e-1

FS
type: SiteQuality
SIO_000300: 9.09e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.76e0

DP
type: SiteQuality
SIO_000300: 2.157468e6

VQSLOD
type: SiteQuality
SIO_000300: -1.52e0

QD
type: SiteQuality
SIO_000300: 1.361e1