19-19162862-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 19162862
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 19162862
    reference: chr 19
allele count: 4
allele frequency: 3.321652189799206e-5
allele num: 120422
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444317
  ensembl transcript: ENST00000545091
  gene symbol: ARMC6
  hgvsc: ENST00000545091.1:c.*421C>T
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000446037
  ensembl transcript: ENST00000541898
  gene symbol: ARMC6
  hgvsc: ENST00000541898.1:c.636C>T
  hgvsp: ENST00000541898.1:c.636C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000376148
  ensembl transcript: ENST00000392336
  gene symbol: ARMC6
  hgvsc: ENST00000392336.3:c.711C>T
  hgvsp: ENST00000392336.3:c.711C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444341
  ensembl transcript: ENST00000546344
  gene symbol: ARMC6
  hgvsc: ENST00000546344.1:c.432C>T
  hgvsp: ENST00000546344.1:c.432C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000441420
  ensembl transcript: ENST00000539985
  gene symbol: ARMC6
  hgvsc: ENST00000539985.1:c.*723C>T
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000441948
  ensembl transcript: ENST00000537263
  gene symbol: ARMC6
  hgvsc: ENST00000537263.1:c.636C>T
  hgvsp: ENST00000537263.1:c.636C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000437580
  ensembl transcript: ENST00000535288
  gene symbol: ARMC6
  hgvsc: ENST00000535288.1:c.432C>T
  hgvsp: ENST00000535288.1:c.432C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444156
  ensembl transcript: ENST00000535612
  gene symbol: ARMC6
  hgvsc: ENST00000535612.1:c.711C>T
  hgvsp: ENST00000535612.1:c.711C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000269932
  ensembl transcript: ENST00000269932
  gene symbol: ARMC6
  hgvsc: ENST00000269932.6:c.636C>T
  hgvsp: ENST00000269932.6:c.636C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000376147
  ensembl transcript: ENST00000392335
  gene symbol: ARMC6
  hgvsc: ENST00000392335.2:c.636C>T
  hgvsp: ENST00000392335.2:c.636C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25049
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 817
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 31310
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 657
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8131
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 876
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18193
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 417
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Asp237Asp
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: Other
population: East Asian
reference allele: C
site quality: MQ
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum

19-19162863-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 19162863
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 19162863
    reference: chr 19
allele count: 1
allele frequency: 8.305233958440609e-6
allele num: 120406
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000437580
  ensembl transcript: ENST00000535288
  gene symbol: ARMC6
  hgvsc: ENST00000535288.1:c.433G>A
  hgvsp: ENSP00000437580.1:p.Val145Met
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444317
  ensembl transcript: ENST00000545091
  gene symbol: ARMC6
  hgvsc: ENST00000545091.1:c.*422G>A
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000441948
  ensembl transcript: ENST00000537263
  gene symbol: ARMC6
  hgvsc: ENST00000537263.1:c.637G>A
  hgvsp: ENSP00000441948.1:p.Val213Met
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000441420
  ensembl transcript: ENST00000539985
  gene symbol: ARMC6
  hgvsc: ENST00000539985.1:c.*724G>A
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444156
  ensembl transcript: ENST00000535612
  gene symbol: ARMC6
  hgvsc: ENST00000535612.1:c.712G>A
  hgvsp: ENSP00000444156.1:p.Val238Met
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000376147
  ensembl transcript: ENST00000392335
  gene symbol: ARMC6
  hgvsc: ENST00000392335.2:c.637G>A
  hgvsp: ENSP00000376147.2:p.Val213Met
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444341
  ensembl transcript: ENST00000546344
  gene symbol: ARMC6
  hgvsc: ENST00000546344.1:c.433G>A
  hgvsp: ENSP00000444341.1:p.Val145Met
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000446037
  ensembl transcript: ENST00000541898
  gene symbol: ARMC6
  hgvsc: ENST00000541898.1:c.637G>A
  hgvsp: ENSP00000446037.1:p.Val213Met
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000269932
  ensembl transcript: ENST00000269932
  gene symbol: ARMC6
  hgvsc: ENST00000269932.6:c.637G>A
  hgvsp: ENSP00000269932.6:p.Val213Met
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000376148
  ensembl transcript: ENST00000392336
  gene symbol: ARMC6
  hgvsc: ENST00000392336.3:c.712G>A
  hgvsp: ENSP00000376148.3:p.Val238Met
  variant of: http://identifiers.org/hgnc/25049
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 31294
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 813
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 659
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18227
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8116
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 872
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 123
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Val238Met
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum

19-19162866-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 19162866
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 19162866
    reference: chr 19
allele count: 1
allele frequency: 8.304682179812978e-6
allele num: 120414
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000437580
  ensembl transcript: ENST00000535288
  gene symbol: ARMC6
  hgvsc: ENST00000535288.1:c.436G>C
  hgvsp: ENSP00000437580.1:p.Val146Leu
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000376147
  ensembl transcript: ENST00000392335
  gene symbol: ARMC6
  hgvsc: ENST00000392335.2:c.640G>C
  hgvsp: ENSP00000376147.2:p.Val214Leu
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444341
  ensembl transcript: ENST00000546344
  gene symbol: ARMC6
  hgvsc: ENST00000546344.1:c.436G>C
  hgvsp: ENSP00000444341.1:p.Val146Leu
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444317
  ensembl transcript: ENST00000545091
  gene symbol: ARMC6
  hgvsc: ENST00000545091.1:c.*425G>C
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000441948
  ensembl transcript: ENST00000537263
  gene symbol: ARMC6
  hgvsc: ENST00000537263.1:c.640G>C
  hgvsp: ENSP00000441948.1:p.Val214Leu
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000446037
  ensembl transcript: ENST00000541898
  gene symbol: ARMC6
  hgvsc: ENST00000541898.1:c.640G>C
  hgvsp: ENSP00000446037.1:p.Val214Leu
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000441420
  ensembl transcript: ENST00000539985
  gene symbol: ARMC6
  hgvsc: ENST00000539985.1:c.*727G>C
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444156
  ensembl transcript: ENST00000535612
  gene symbol: ARMC6
  hgvsc: ENST00000535612.1:c.715G>C
  hgvsp: ENSP00000444156.1:p.Val239Leu
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000269932
  ensembl transcript: ENST00000269932
  gene symbol: ARMC6
  hgvsc: ENST00000269932.6:c.640G>C
  hgvsp: ENSP00000269932.6:p.Val214Leu
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000376148
  ensembl transcript: ENST00000392336
  gene symbol: ARMC6
  hgvsc: ENST00000392336.3:c.715G>C
  hgvsp: ENSP00000376148.3:p.Val239Leu
  variant of: http://identifiers.org/hgnc/25049
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31289
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18249
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8104
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 868
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 795
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 667
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7687
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Val239Leu
num of homozygotes: 0
population: East Asian
population: Other
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum

19-19162876-CCTG-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 19162876
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 19162873
    reference: chr 19
allele count: 1
allele frequency: 8.315178526882972e-6
allele num: 120262
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000376147
  ensembl transcript: ENST00000392335
  gene symbol: ARMC6
  hgvsc: ENST00000392335.2:c.654_656delCTG
  hgvsp: ENSP00000376147.2:p.Cys218del
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: true
  consequence: inframe_deletion
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444156
  ensembl transcript: ENST00000535612
  gene symbol: ARMC6
  hgvsc: ENST00000535612.1:c.729_731delCTG
  hgvsp: ENSP00000444156.1:p.Cys243del
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000446037
  ensembl transcript: ENST00000541898
  gene symbol: ARMC6
  hgvsc: ENST00000541898.1:c.654_656delCTG
  hgvsp: ENSP00000446037.1:p.Cys218del
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000437580
  ensembl transcript: ENST00000535288
  gene symbol: ARMC6
  hgvsc: ENST00000535288.1:c.450_452delCTG
  hgvsp: ENSP00000437580.1:p.Cys150del
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000269932
  ensembl transcript: ENST00000269932
  gene symbol: ARMC6
  hgvsc: ENST00000269932.6:c.654_656delCTG
  hgvsp: ENSP00000269932.6:p.Cys218del
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000441948
  ensembl transcript: ENST00000537263
  gene symbol: ARMC6
  hgvsc: ENST00000537263.1:c.654_656delCTG
  hgvsp: ENSP00000441948.1:p.Cys218del
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444341
  ensembl transcript: ENST00000546344
  gene symbol: ARMC6
  hgvsc: ENST00000546344.1:c.450_452delCTG
  hgvsp: ENSP00000444341.1:p.Cys150del
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000376148
  ensembl transcript: ENST00000392336
  gene symbol: ARMC6
  hgvsc: ENST00000392336.3:c.729_731delCTG
  hgvsp: ENSP00000376148.3:p.Cys243del
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000441420
  ensembl transcript: ENST00000539985
  gene symbol: ARMC6
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444317
  ensembl transcript: ENST00000545091
  gene symbol: ARMC6
  hgvsc: ENST00000545091.1:c.*439_*441delCTG
  variant of: http://identifiers.org/hgnc/25049
canonical: true
consequence: inframe deletion
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 863
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 729
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 965
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8083
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31280
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17988
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7526
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Cys243del
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: CCTG
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: QD

19-19162879-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 19162879
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 19162879
    reference: chr 19
allele count: 2
allele frequency: 1.663146340246478e-5
allele num: 120254
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000376148
  ensembl transcript: ENST00000392336
  gene symbol: ARMC6
  hgvsc: ENST00000392336.3:c.728G>C
  hgvsp: ENSP00000376148.3:p.Cys243Ser
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000441948
  ensembl transcript: ENST00000537263
  gene symbol: ARMC6
  hgvsc: ENST00000537263.1:c.653G>C
  hgvsp: ENSP00000441948.1:p.Cys218Ser
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444156
  ensembl transcript: ENST00000535612
  gene symbol: ARMC6
  hgvsc: ENST00000535612.1:c.728G>C
  hgvsp: ENSP00000444156.1:p.Cys243Ser
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000376147
  ensembl transcript: ENST00000392335
  gene symbol: ARMC6
  hgvsc: ENST00000392335.2:c.653G>C
  hgvsp: ENSP00000376147.2:p.Cys218Ser
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000437580
  ensembl transcript: ENST00000535288
  gene symbol: ARMC6
  hgvsc: ENST00000535288.1:c.449G>C
  hgvsp: ENSP00000437580.1:p.Cys150Ser
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000269932
  ensembl transcript: ENST00000269932
  gene symbol: ARMC6
  hgvsc: ENST00000269932.6:c.653G>C
  hgvsp: ENSP00000269932.6:p.Cys218Ser
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000446037
  ensembl transcript: ENST00000541898
  gene symbol: ARMC6
  hgvsc: ENST00000541898.1:c.653G>C
  hgvsp: ENSP00000446037.1:p.Cys218Ser
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444341
  ensembl transcript: ENST00000546344
  gene symbol: ARMC6
  hgvsc: ENST00000546344.1:c.449G>C
  hgvsp: ENSP00000444341.1:p.Cys150Ser
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444317
  ensembl transcript: ENST00000545091
  gene symbol: ARMC6
  hgvsc: ENST00000545091.1:c.*438G>C
  variant of: http://identifiers.org/hgnc/25049
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 933
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8032
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 726
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31267
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18077
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 868
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7523
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1447
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1193
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Cys243Ser
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ

19-19162900-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 19162900
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 19162900
    reference: chr 19
allele count: 1
allele frequency: 8.335556148306214e-6
allele num: 119968
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000376147
  ensembl transcript: ENST00000392335
  gene symbol: ARMC6
  hgvsc: ENST00000392335.2:c.674C>T
  hgvsp: ENSP00000376147.2:p.Thr225Ile
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000269932
  ensembl transcript: ENST00000269932
  gene symbol: ARMC6
  hgvsc: ENST00000269932.6:c.674C>T
  hgvsp: ENSP00000269932.6:p.Thr225Ile
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444156
  ensembl transcript: ENST00000535612
  gene symbol: ARMC6
  hgvsc: ENST00000535612.1:c.749C>T
  hgvsp: ENSP00000444156.1:p.Thr250Ile
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444317
  ensembl transcript: ENST00000545091
  gene symbol: ARMC6
  hgvsc: ENST00000545091.1:c.*459C>T
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000441948
  ensembl transcript: ENST00000537263
  gene symbol: ARMC6
  hgvsc: ENST00000537263.1:c.674C>T
  hgvsp: ENSP00000441948.1:p.Thr225Ile
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000376148
  ensembl transcript: ENST00000392336
  gene symbol: ARMC6
  hgvsc: ENST00000392336.3:c.749C>T
  hgvsp: ENSP00000376148.3:p.Thr250Ile
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444341
  ensembl transcript: ENST00000546344
  gene symbol: ARMC6
  hgvsc: ENST00000546344.1:c.470C>T
  hgvsp: ENSP00000444341.1:p.Thr157Ile
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000446037
  ensembl transcript: ENST00000541898
  gene symbol: ARMC6
  hgvsc: ENST00000541898.1:c.674C>T
  hgvsp: ENSP00000446037.1:p.Thr225Ile
  variant of: http://identifiers.org/hgnc/25049
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 906
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31045
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 665
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18309
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7865
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 829
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 124
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 441
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 383
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 337
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Thr250Ile
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: DP

19-19162904-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 19162904
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 19162904
    reference: chr 19
allele count: 3
allele frequency: 2.501709501492687e-5
allele num: 119918
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444156
  ensembl transcript: ENST00000535612
  gene symbol: ARMC6
  hgvsc: ENST00000535612.1:c.753C>T
  hgvsp: ENST00000535612.1:c.753C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444341
  ensembl transcript: ENST00000546344
  gene symbol: ARMC6
  hgvsc: ENST00000546344.1:c.474C>T
  hgvsp: ENST00000546344.1:c.474C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444317
  ensembl transcript: ENST00000545091
  gene symbol: ARMC6
  hgvsc: ENST00000545091.1:c.*463C>T
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000269932
  ensembl transcript: ENST00000269932
  gene symbol: ARMC6
  hgvsc: ENST00000269932.6:c.678C>T
  hgvsp: ENST00000269932.6:c.678C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000376147
  ensembl transcript: ENST00000392335
  gene symbol: ARMC6
  hgvsc: ENST00000392335.2:c.678C>T
  hgvsp: ENST00000392335.2:c.678C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000441948
  ensembl transcript: ENST00000537263
  gene symbol: ARMC6
  hgvsc: ENST00000537263.1:c.678C>T
  hgvsp: ENST00000537263.1:c.678C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000376148
  ensembl transcript: ENST00000392336
  gene symbol: ARMC6
  hgvsc: ENST00000392336.3:c.753C>T
  hgvsp: ENST00000392336.3:c.753C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000446037
  ensembl transcript: ENST00000541898
  gene symbol: ARMC6
  hgvsc: ENST00000541898.1:c.678C>T
  hgvsp: ENST00000541898.1:c.678C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25049
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30966
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18417
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 826
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 697
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7828
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 879
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1141
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7318
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 378
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 328
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Phe251Phe
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ

19-19162910-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 19162910
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 19162910
    reference: chr 19
allele count: 1
allele frequency: 8.348639171814994e-6
allele num: 119780
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000376148
  ensembl transcript: ENST00000392336
  gene symbol: ARMC6
  hgvsc: ENST00000392336.3:c.759C>T
  hgvsp: ENST00000392336.3:c.759C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444156
  ensembl transcript: ENST00000535612
  gene symbol: ARMC6
  hgvsc: ENST00000535612.1:c.759C>T
  hgvsp: ENST00000535612.1:c.759C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000269932
  ensembl transcript: ENST00000269932
  gene symbol: ARMC6
  hgvsc: ENST00000269932.6:c.684C>T
  hgvsp: ENST00000269932.6:c.684C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000441948
  ensembl transcript: ENST00000537263
  gene symbol: ARMC6
  hgvsc: ENST00000537263.1:c.684C>T
  hgvsp: ENST00000537263.1:c.684C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444341
  ensembl transcript: ENST00000546344
  gene symbol: ARMC6
  hgvsc: ENST00000546344.1:c.480C>T
  hgvsp: ENST00000546344.1:c.480C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000446037
  ensembl transcript: ENST00000541898
  gene symbol: ARMC6
  hgvsc: ENST00000541898.1:c.684C>T
  hgvsp: ENST00000541898.1:c.684C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444317
  ensembl transcript: ENST00000545091
  gene symbol: ARMC6
  hgvsc: ENST00000545091.1:c.*469C>T
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000376147
  ensembl transcript: ENST00000392335
  gene symbol: ARMC6
  hgvsc: ENST00000392335.2:c.684C>T
  hgvsp: ENST00000392335.2:c.684C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25049
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 30831
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7768
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 759
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 869
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 838
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18558
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 818
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 306
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 296
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46881
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 312
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Asp253Asp
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: Latino
population: East Asian
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP

19-19162913-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 19162913
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 19162913
    reference: chr 19
allele count: 1
allele frequency: 8.353241893178742e-6
allele num: 119714
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000376147
  ensembl transcript: ENST00000392335
  gene symbol: ARMC6
  hgvsc: ENST00000392335.2:c.687C>T
  hgvsp: ENST00000392335.2:c.687C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000441948
  ensembl transcript: ENST00000537263
  gene symbol: ARMC6
  hgvsc: ENST00000537263.1:c.687C>T
  hgvsp: ENST00000537263.1:c.687C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000269932
  ensembl transcript: ENST00000269932
  gene symbol: ARMC6
  hgvsc: ENST00000269932.6:c.687C>T
  hgvsp: ENST00000269932.6:c.687C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000446037
  ensembl transcript: ENST00000541898
  gene symbol: ARMC6
  hgvsc: ENST00000541898.1:c.687C>T
  hgvsp: ENST00000541898.1:c.687C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444341
  ensembl transcript: ENST00000546344
  gene symbol: ARMC6
  hgvsc: ENST00000546344.1:c.483C>T
  hgvsp: ENST00000546344.1:c.483C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000376148
  ensembl transcript: ENST00000392336
  gene symbol: ARMC6
  hgvsc: ENST00000392336.3:c.762C>T
  hgvsp: ENST00000392336.3:c.762C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444156
  ensembl transcript: ENST00000535612
  gene symbol: ARMC6
  hgvsc: ENST00000535612.1:c.762C>T
  hgvsp: ENST00000535612.1:c.762C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444317
  ensembl transcript: ENST00000545091
  gene symbol: ARMC6
  hgvsc: ENST00000545091.1:c.*472C>T
  variant of: http://identifiers.org/hgnc/25049
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 803
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30779
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 900
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 826
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18618
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7714
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 810
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1329
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 109
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 97
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Asp254Asp
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: C
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: QD

19-19162914-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 19162914
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 19162914
    reference: chr 19
allele count: 1
allele frequency: 8.353800143685363e-6
allele num: 119706
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000441948
  ensembl transcript: ENST00000537263
  gene symbol: ARMC6
  hgvsc: ENST00000537263.1:c.688A>G
  hgvsp: ENSP00000441948.1:p.Ile230Val
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444156
  ensembl transcript: ENST00000535612
  gene symbol: ARMC6
  hgvsc: ENST00000535612.1:c.763A>G
  hgvsp: ENSP00000444156.1:p.Ile255Val
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444341
  ensembl transcript: ENST00000546344
  gene symbol: ARMC6
  hgvsc: ENST00000546344.1:c.484A>G
  hgvsp: ENSP00000444341.1:p.Ile162Val
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000376148
  ensembl transcript: ENST00000392336
  gene symbol: ARMC6
  hgvsc: ENST00000392336.3:c.763A>G
  hgvsp: ENSP00000376148.3:p.Ile255Val
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000269932
  ensembl transcript: ENST00000269932
  gene symbol: ARMC6
  hgvsc: ENST00000269932.6:c.688A>G
  hgvsp: ENSP00000269932.6:p.Ile230Val
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000446037
  ensembl transcript: ENST00000541898
  gene symbol: ARMC6
  hgvsc: ENST00000541898.1:c.688A>G
  hgvsp: ENSP00000446037.1:p.Ile230Val
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444317
  ensembl transcript: ENST00000545091
  gene symbol: ARMC6
  hgvsc: ENST00000545091.1:c.*473A>G
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000376147
  ensembl transcript: ENST00000392335
  gene symbol: ARMC6
  hgvsc: ENST00000392335.2:c.688A>G
  hgvsp: ENSP00000376147.2:p.Ile230Val
  variant of: http://identifiers.org/hgnc/25049
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18659
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 897
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7692
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 806
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 801
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 807
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30792
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1139
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 338
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 316
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1325
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Ile255Val
num of homozygotes: 0
population: Other
population: East Asian
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
reference allele: A
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: DP

19-19162917-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 19162917
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 19162917
    reference: chr 19
allele count: 2
allele frequency: 1.672100994900092e-5
allele num: 119610
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000376148
  ensembl transcript: ENST00000392336
  gene symbol: ARMC6
  hgvsc: ENST00000392336.3:c.766C>T
  hgvsp: ENSP00000376148.3:p.Arg256Cys
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000446037
  ensembl transcript: ENST00000541898
  gene symbol: ARMC6
  hgvsc: ENST00000541898.1:c.691C>T
  hgvsp: ENSP00000446037.1:p.Arg231Cys
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444317
  ensembl transcript: ENST00000545091
  gene symbol: ARMC6
  hgvsc: ENST00000545091.1:c.*476C>T
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444341
  ensembl transcript: ENST00000546344
  gene symbol: ARMC6
  hgvsc: ENST00000546344.1:c.487C>T
  hgvsp: ENSP00000444341.1:p.Arg163Cys
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444156
  ensembl transcript: ENST00000535612
  gene symbol: ARMC6
  hgvsc: ENST00000535612.1:c.766C>T
  hgvsp: ENSP00000444156.1:p.Arg256Cys
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000441948
  ensembl transcript: ENST00000537263
  gene symbol: ARMC6
  hgvsc: ENST00000537263.1:c.691C>T
  hgvsp: ENSP00000441948.1:p.Arg231Cys
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000269932
  ensembl transcript: ENST00000269932
  gene symbol: ARMC6
  hgvsc: ENST00000269932.6:c.691C>T
  hgvsp: ENSP00000269932.6:p.Arg231Cys
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000376147
  ensembl transcript: ENST00000392335
  gene symbol: ARMC6
  hgvsc: ENST00000392335.2:c.691C>T
  hgvsp: ENSP00000376147.2:p.Arg231Cys
  variant of: http://identifiers.org/hgnc/25049
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18706
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 907
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7737
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 809
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 837
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30698
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 753
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7290
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1310
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 162
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Arg256Cys
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
population: Other
population: African
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum

19-19162918-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 19162918
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 19162918
    reference: chr 19
allele count: 1
allele frequency: 8.36456102783726e-6
allele num: 119552
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444156
  ensembl transcript: ENST00000535612
  gene symbol: ARMC6
  hgvsc: ENST00000535612.1:c.767G>A
  hgvsp: ENSP00000444156.1:p.Arg256His
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444317
  ensembl transcript: ENST00000545091
  gene symbol: ARMC6
  hgvsc: ENST00000545091.1:c.*477G>A
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000376148
  ensembl transcript: ENST00000392336
  gene symbol: ARMC6
  hgvsc: ENST00000392336.3:c.767G>A
  hgvsp: ENSP00000376148.3:p.Arg256His
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000441948
  ensembl transcript: ENST00000537263
  gene symbol: ARMC6
  hgvsc: ENST00000537263.1:c.692G>A
  hgvsp: ENSP00000441948.1:p.Arg231His
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000376147
  ensembl transcript: ENST00000392335
  gene symbol: ARMC6
  hgvsc: ENST00000392335.2:c.692G>A
  hgvsp: ENSP00000376147.2:p.Arg231His
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000446037
  ensembl transcript: ENST00000541898
  gene symbol: ARMC6
  hgvsc: ENST00000541898.1:c.692G>A
  hgvsp: ENSP00000446037.1:p.Arg231His
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444341
  ensembl transcript: ENST00000546344
  gene symbol: ARMC6
  hgvsc: ENST00000546344.1:c.488G>A
  hgvsp: ENSP00000444341.1:p.Arg163His
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000269932
  ensembl transcript: ENST00000269932
  gene symbol: ARMC6
  hgvsc: ENST00000269932.6:c.692G>A
  hgvsp: ENSP00000269932.6:p.Arg231His
  variant of: http://identifiers.org/hgnc/25049
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18747
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7712
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 909
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30681
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 862
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 730
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 807
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 246
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 147
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1389
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Arg256His
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: ReadPosRankSum

19-19162933-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 19162933
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 19162933
    reference: chr 19
allele count: 1
allele frequency: 8.420768984623676e-6
allele num: 118754
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000376148
  ensembl transcript: ENST00000392336
  gene symbol: ARMC6
  hgvsc: ENST00000392336.3:c.782A>T
  hgvsp: ENSP00000376148.3:p.His261Leu
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000446037
  ensembl transcript: ENST00000541898
  gene symbol: ARMC6
  hgvsc: ENST00000541898.1:c.707A>T
  hgvsp: ENSP00000446037.1:p.His236Leu
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000269932
  ensembl transcript: ENST00000269932
  gene symbol: ARMC6
  hgvsc: ENST00000269932.6:c.707A>T
  hgvsp: ENSP00000269932.6:p.His236Leu
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444156
  ensembl transcript: ENST00000535612
  gene symbol: ARMC6
  hgvsc: ENST00000535612.1:c.782A>T
  hgvsp: ENSP00000444156.1:p.His261Leu
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444341
  ensembl transcript: ENST00000546344
  gene symbol: ARMC6
  hgvsc: ENST00000546344.1:c.503A>T
  hgvsp: ENSP00000444341.1:p.His168Leu
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444317
  ensembl transcript: ENST00000545091
  gene symbol: ARMC6
  hgvsc: ENST00000545091.1:c.*492A>T
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000441948
  ensembl transcript: ENST00000537263
  gene symbol: ARMC6
  hgvsc: ENST00000537263.1:c.707A>T
  hgvsp: ENSP00000441948.1:p.His236Leu
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000376147
  ensembl transcript: ENST00000392335
  gene symbol: ARMC6
  hgvsc: ENST00000392335.2:c.707A>T
  hgvsp: ENSP00000376147.2:p.His236Leu
  variant of: http://identifiers.org/hgnc/25049
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18658
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1246
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 760
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1296
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30281
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7447
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 752
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 352
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2068
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 324
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 146
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 105
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
hgvs: p.His261Leu
num of homozygotes: 0
population: European (Finnish)
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: A
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: QD

19-19162934-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 19162934
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 19162934
    reference: chr 19
allele count: 2
allele frequency: 1.685232309273833e-5
allele num: 118678
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444317
  ensembl transcript: ENST00000545091
  gene symbol: ARMC6
  hgvsc: ENST00000545091.1:c.*493T>C
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444341
  ensembl transcript: ENST00000546344
  gene symbol: ARMC6
  hgvsc: ENST00000546344.1:c.504T>C
  hgvsp: ENST00000546344.1:c.504T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000376147
  ensembl transcript: ENST00000392335
  gene symbol: ARMC6
  hgvsc: ENST00000392335.2:c.708T>C
  hgvsp: ENST00000392335.2:c.708T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000376148
  ensembl transcript: ENST00000392336
  gene symbol: ARMC6
  hgvsc: ENST00000392336.3:c.783T>C
  hgvsp: ENST00000392336.3:c.783T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000441948
  ensembl transcript: ENST00000537263
  gene symbol: ARMC6
  hgvsc: ENST00000537263.1:c.708T>C
  hgvsp: ENST00000537263.1:c.708T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000269932
  ensembl transcript: ENST00000269932
  gene symbol: ARMC6
  hgvsc: ENST00000269932.6:c.708T>C
  hgvsp: ENST00000269932.6:c.708T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000446037
  ensembl transcript: ENST00000541898
  gene symbol: ARMC6
  hgvsc: ENST00000541898.1:c.708T>C
  hgvsp: ENST00000541898.1:c.708T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444156
  ensembl transcript: ENST00000535612
  gene symbol: ARMC6
  hgvsc: ENST00000535612.1:c.783T>C
  hgvsp: ENST00000535612.1:c.783T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25049
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 761
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1290
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7434
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30232
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1334
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18639
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 750
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7076
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 337
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 106
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 362
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
hgvs: p.His261His
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: South Asian
reference allele: T
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ

http://identifiers.org/exac.variant/19-19162938-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 19162938
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 19162938
    reference: chr 19
allele count: 3
allele frequency: 2.539360081259523e-5
allele num: 118140
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444156
  ensembl transcript: ENST00000535612
  gene symbol: ARMC6
  hgvsc: ENST00000535612.1:c.787C>A
  hgvsp: ENSP00000444156.1:p.His263Asn
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444317
  ensembl transcript: ENST00000545091
  gene symbol: ARMC6
  hgvsc: ENST00000545091.1:c.*497C>A
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000441948
  ensembl transcript: ENST00000537263
  gene symbol: ARMC6
  hgvsc: ENST00000537263.1:c.712C>A
  hgvsp: ENSP00000441948.1:p.His238Asn
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000376148
  ensembl transcript: ENST00000392336
  gene symbol: ARMC6
  hgvsc: ENST00000392336.3:c.787C>A
  hgvsp: ENSP00000376148.3:p.His263Asn
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000269932
  ensembl transcript: ENST00000269932
  gene symbol: ARMC6
  hgvsc: ENST00000269932.6:c.712C>A
  hgvsp: ENSP00000269932.6:p.His238Asn
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444341
  ensembl transcript: ENST00000546344
  gene symbol: ARMC6
  hgvsc: ENST00000546344.1:c.508C>A
  hgvsp: ENSP00000444341.1:p.His170Asn
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000446037
  ensembl transcript: ENST00000541898
  gene symbol: ARMC6
  hgvsc: ENST00000541898.1:c.712C>A
  hgvsp: ENSP00000446037.1:p.His238Asn
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000376147
  ensembl transcript: ENST00000392335
  gene symbol: ARMC6
  hgvsc: ENST00000392335.2:c.712C>A
  hgvsp: ENSP00000376147.2:p.His238Asn
  variant of: http://identifiers.org/hgnc/25049
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18331
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1523
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30102
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7374
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 779
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1568
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 743
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 376
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 103
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45930
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 451
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 7.5e0
  variant carriers: 0
hgvs: p.His263Asn
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: Other
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: BaseQRankSum

19-19162942-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 19162942
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 19162942
    reference: chr 19
allele count: 7
allele frequency: 5.938443788387797e-5
allele num: 117876
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000446037
  ensembl transcript: ENST00000541898
  gene symbol: ARMC6
  hgvsc: ENST00000541898.1:c.716A>G
  hgvsp: ENSP00000446037.1:p.Asn239Ser
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000441948
  ensembl transcript: ENST00000537263
  gene symbol: ARMC6
  hgvsc: ENST00000537263.1:c.716A>G
  hgvsp: ENSP00000441948.1:p.Asn239Ser
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444156
  ensembl transcript: ENST00000535612
  gene symbol: ARMC6
  hgvsc: ENST00000535612.1:c.791A>G
  hgvsp: ENSP00000444156.1:p.Asn264Ser
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444341
  ensembl transcript: ENST00000546344
  gene symbol: ARMC6
  hgvsc: ENST00000546344.1:c.512A>G
  hgvsp: ENSP00000444341.1:p.Asn171Ser
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000376148
  ensembl transcript: ENST00000392336
  gene symbol: ARMC6
  hgvsc: ENST00000392336.3:c.791A>G
  hgvsp: ENSP00000376148.3:p.Asn264Ser
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000269932
  ensembl transcript: ENST00000269932
  gene symbol: ARMC6
  hgvsc: ENST00000269932.6:c.716A>G
  hgvsp: ENSP00000269932.6:p.Asn239Ser
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000376147
  ensembl transcript: ENST00000392335
  gene symbol: ARMC6
  hgvsc: ENST00000392335.2:c.716A>G
  hgvsp: ENSP00000376147.2:p.Asn239Ser
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444317
  ensembl transcript: ENST00000545091
  gene symbol: ARMC6
  hgvsc: ENST00000545091.1:c.*501A>G
  variant of: http://identifiers.org/hgnc/25049
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29966
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18349
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1708
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7282
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1657
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 735
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 726
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 4.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 144
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 272
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Asn264Ser
num of homozygotes: 0
population: Other
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
reference allele: A
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQ

19-19162948-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 19162948
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 19162948
    reference: chr 19
allele count: 1
allele frequency: 8.539709649871904e-6
allele num: 117100
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000376147
  ensembl transcript: ENST00000392335
  gene symbol: ARMC6
  hgvsc: ENST00000392335.2:c.722C>G
  hgvsp: ENSP00000376147.2:p.Ala241Gly
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000269932
  ensembl transcript: ENST00000269932
  gene symbol: ARMC6
  hgvsc: ENST00000269932.6:c.722C>G
  hgvsp: ENSP00000269932.6:p.Ala241Gly
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444156
  ensembl transcript: ENST00000535612
  gene symbol: ARMC6
  hgvsc: ENST00000535612.1:c.797C>G
  hgvsp: ENSP00000444156.1:p.Ala266Gly
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444341
  ensembl transcript: ENST00000546344
  gene symbol: ARMC6
  hgvsc: ENST00000546344.1:c.518C>G
  hgvsp: ENSP00000444341.1:p.Ala173Gly
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000376148
  ensembl transcript: ENST00000392336
  gene symbol: ARMC6
  hgvsc: ENST00000392336.3:c.797C>G
  hgvsp: ENSP00000376148.3:p.Ala266Gly
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000441948
  ensembl transcript: ENST00000537263
  gene symbol: ARMC6
  hgvsc: ENST00000537263.1:c.722C>G
  hgvsp: ENSP00000441948.1:p.Ala241Gly
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444317
  ensembl transcript: ENST00000545091
  gene symbol: ARMC6
  hgvsc: ENST00000545091.1:c.*507C>G
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000446037
  ensembl transcript: ENST00000541898
  gene symbol: ARMC6
  hgvsc: ENST00000541898.1:c.722C>G
  hgvsp: ENSP00000446037.1:p.Ala241Gly
  variant of: http://identifiers.org/hgnc/25049
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 713
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1995
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18057
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29649
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 715
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7224
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2056
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 235
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 434
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 350
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Ala266Gly
num of homozygotes: 0
population: South Asian
population: Other
population: Latino
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD

19-19162949-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 19162949
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 19162949
    reference: chr 19
allele count: 1
allele frequency: 8.548762139242238e-6
allele num: 116976
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000269932
  ensembl transcript: ENST00000269932
  gene symbol: ARMC6
  hgvsc: ENST00000269932.6:c.723C>G
  hgvsp: ENST00000269932.6:c.723C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000446037
  ensembl transcript: ENST00000541898
  gene symbol: ARMC6
  hgvsc: ENST00000541898.1:c.723C>G
  hgvsp: ENST00000541898.1:c.723C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000376148
  ensembl transcript: ENST00000392336
  gene symbol: ARMC6
  hgvsc: ENST00000392336.3:c.798C>G
  hgvsp: ENST00000392336.3:c.798C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000376147
  ensembl transcript: ENST00000392335
  gene symbol: ARMC6
  hgvsc: ENST00000392335.2:c.723C>G
  hgvsp: ENST00000392335.2:c.723C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000441948
  ensembl transcript: ENST00000537263
  gene symbol: ARMC6
  hgvsc: ENST00000537263.1:c.723C>G
  hgvsp: ENST00000537263.1:c.723C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444156
  ensembl transcript: ENST00000535612
  gene symbol: ARMC6
  hgvsc: ENST00000535612.1:c.798C>G
  hgvsp: ENST00000535612.1:c.798C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444317
  ensembl transcript: ENST00000545091
  gene symbol: ARMC6
  hgvsc: ENST00000545091.1:c.*508C>G
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444341
  ensembl transcript: ENST00000546344
  gene symbol: ARMC6
  hgvsc: ENST00000546344.1:c.519C>G
  hgvsp: ENST00000546344.1:c.519C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25049
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29599
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7190
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 699
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18009
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2065
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2141
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 115
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 346
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1119
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Ala266Ala
num of homozygotes: 0
population: East Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
population: South Asian
reference allele: C
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: DP

http://identifiers.org/exac.variant/19-19162951-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 19162951
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 19162951
    reference: chr 19
allele count: 1
allele frequency: 8.566631257924135e-6
allele num: 116732
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444341
  ensembl transcript: ENST00000546344
  gene symbol: ARMC6
  hgvsc: ENST00000546344.1:c.521A>C
  hgvsp: ENSP00000444341.1:p.Lys174Thr
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444156
  ensembl transcript: ENST00000535612
  gene symbol: ARMC6
  hgvsc: ENST00000535612.1:c.800A>C
  hgvsp: ENSP00000444156.1:p.Lys267Thr
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000376147
  ensembl transcript: ENST00000392335
  gene symbol: ARMC6
  hgvsc: ENST00000392335.2:c.725A>C
  hgvsp: ENSP00000376147.2:p.Lys242Thr
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444317
  ensembl transcript: ENST00000545091
  gene symbol: ARMC6
  hgvsc: ENST00000545091.1:c.*510A>C
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000446037
  ensembl transcript: ENST00000541898
  gene symbol: ARMC6
  hgvsc: ENST00000541898.1:c.725A>C
  hgvsp: ENSP00000446037.1:p.Lys242Thr
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000441948
  ensembl transcript: ENST00000537263
  gene symbol: ARMC6
  hgvsc: ENST00000537263.1:c.725A>C
  hgvsp: ENSP00000441948.1:p.Lys242Thr
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000376148
  ensembl transcript: ENST00000392336
  gene symbol: ARMC6
  hgvsc: ENST00000392336.3:c.800A>C
  hgvsp: ENSP00000376148.3:p.Lys267Thr
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000269932
  ensembl transcript: ENST00000269932
  gene symbol: ARMC6
  hgvsc: ENST00000269932.6:c.725A>C
  hgvsp: ENSP00000269932.6:p.Lys242Thr
  variant of: http://identifiers.org/hgnc/25049
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17866
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29515
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7117
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2323
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2208
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 680
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 699
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 115
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 942
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6681
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 219
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Lys267Thr
num of homozygotes: 0
population: South Asian
population: Other
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum

19-19162965-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 19162965
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 19162965
    reference: chr 19
allele count: 15
allele frequency: 1.327128271371189e-4
allele num: 113026
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000441948
  ensembl transcript: ENST00000537263
  gene symbol: ARMC6
  hgvsc: ENST00000537263.1:c.739G>C
  hgvsp: ENSP00000441948.1:p.Glu247Gln
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000376148
  ensembl transcript: ENST00000392336
  gene symbol: ARMC6
  hgvsc: ENST00000392336.3:c.814G>C
  hgvsp: ENSP00000376148.3:p.Glu272Gln
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000269932
  ensembl transcript: ENST00000269932
  gene symbol: ARMC6
  hgvsc: ENST00000269932.6:c.739G>C
  hgvsp: ENSP00000269932.6:p.Glu247Gln
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444317
  ensembl transcript: ENST00000545091
  gene symbol: ARMC6
  hgvsc: ENST00000545091.1:c.*524G>C
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444341
  ensembl transcript: ENST00000546344
  gene symbol: ARMC6
  hgvsc: ENST00000546344.1:c.535G>C
  hgvsp: ENSP00000444341.1:p.Glu179Gln
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444156
  ensembl transcript: ENST00000535612
  gene symbol: ARMC6
  hgvsc: ENST00000535612.1:c.814G>C
  hgvsp: ENSP00000444156.1:p.Glu272Gln
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000446037
  ensembl transcript: ENST00000541898
  gene symbol: ARMC6
  hgvsc: ENST00000541898.1:c.739G>C
  hgvsp: ENSP00000446037.1:p.Glu247Gln
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000376147
  ensembl transcript: ENST00000392335
  gene symbol: ARMC6
  hgvsc: ENST00000392335.2:c.739G>C
  hgvsp: ENSP00000376147.2:p.Glu247Gln
  variant of: http://identifiers.org/hgnc/25049
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4562
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15755
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27693
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3923
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 653
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 999
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6735
  bin: 3.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 9.75e1
  variant carriers: 15
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 386
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 222
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 759
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Glu272Gln
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
population: East Asian
population: Other
population: European (Finnish)
reference allele: G
site quality: DP
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum

19-19162971-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 19162971
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 19162971
    reference: chr 19
allele count: 1
allele frequency: 9.040773890245005e-6
allele num: 110610
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000446037
  ensembl transcript: ENST00000541898
  gene symbol: ARMC6
  hgvsc: ENST00000541898.1:c.745A>G
  hgvsp: ENSP00000446037.1:p.Lys249Glu
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000376147
  ensembl transcript: ENST00000392335
  gene symbol: ARMC6
  hgvsc: ENST00000392335.2:c.745A>G
  hgvsp: ENSP00000376147.2:p.Lys249Glu
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000441948
  ensembl transcript: ENST00000537263
  gene symbol: ARMC6
  hgvsc: ENST00000537263.1:c.745A>G
  hgvsp: ENSP00000441948.1:p.Lys249Glu
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444341
  ensembl transcript: ENST00000546344
  gene symbol: ARMC6
  hgvsc: ENST00000546344.1:c.541A>G
  hgvsp: ENSP00000444341.1:p.Lys181Glu
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000269932
  ensembl transcript: ENST00000269932
  gene symbol: ARMC6
  hgvsc: ENST00000269932.6:c.745A>G
  hgvsp: ENSP00000269932.6:p.Lys249Glu
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444156
  ensembl transcript: ENST00000535612
  gene symbol: ARMC6
  hgvsc: ENST00000535612.1:c.820A>G
  hgvsp: ENSP00000444156.1:p.Lys274Glu
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000376148
  ensembl transcript: ENST00000392336
  gene symbol: ARMC6
  hgvsc: ENST00000392336.3:c.820A>G
  hgvsp: ENSP00000376148.3:p.Lys274Glu
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444317
  ensembl transcript: ENST00000545091
  gene symbol: ARMC6
  hgvsc: ENST00000545091.1:c.*530A>G
  variant of: http://identifiers.org/hgnc/25049
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6428
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1266
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6253
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5027
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14375
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26255
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5700
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 168
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 732
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 230
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Lys274Glu
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: Latino
population: African
reference allele: A
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum

19-19162978-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 19162978
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 19162978
    reference: chr 19
allele count: 2
allele frequency: 1.856079588692763e-5
allele num: 107754
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000376147
  ensembl transcript: ENST00000392335
  gene symbol: ARMC6
  hgvsc: ENST00000392335.2:c.752T>C
  hgvsp: ENSP00000376147.2:p.Leu251Ser
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000376148
  ensembl transcript: ENST00000392336
  gene symbol: ARMC6
  hgvsc: ENST00000392336.3:c.827T>C
  hgvsp: ENSP00000376148.3:p.Leu276Ser
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000269932
  ensembl transcript: ENST00000269932
  gene symbol: ARMC6
  hgvsc: ENST00000269932.6:c.752T>C
  hgvsp: ENSP00000269932.6:p.Leu251Ser
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000446037
  ensembl transcript: ENST00000541898
  gene symbol: ARMC6
  hgvsc: ENST00000541898.1:c.752T>C
  hgvsp: ENSP00000446037.1:p.Leu251Ser
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444341
  ensembl transcript: ENST00000546344
  gene symbol: ARMC6
  hgvsc: ENST00000546344.1:c.548T>C
  hgvsp: ENSP00000444341.1:p.Leu183Ser
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444317
  ensembl transcript: ENST00000545091
  gene symbol: ARMC6
  hgvsc: ENST00000545091.1:c.*537T>C
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000441948
  ensembl transcript: ENST00000537263
  gene symbol: ARMC6
  hgvsc: ENST00000537263.1:c.752T>C
  hgvsp: ENSP00000441948.1:p.Leu251Ser
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444156
  ensembl transcript: ENST00000535612
  gene symbol: ARMC6
  hgvsc: ENST00000535612.1:c.827T>C
  hgvsp: ENSP00000444156.1:p.Leu276Ser
  variant of: http://identifiers.org/hgnc/25049
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6306
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24248
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13393
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8200
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5789
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1599
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 339
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 126
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 223
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 629
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 250
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Leu276Ser
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum

19-19162987-TCATCGAAGCCAC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 19162987
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 19162975
    reference: chr 19
allele count: 1
allele frequency: 9.974266392706816e-6
allele num: 100258
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000376147
  ensembl transcript: ENST00000392335
  gene symbol: ARMC6
  hgvsp: ENSP00000376147.2:p.Ile255_Thr258del
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000446037
  ensembl transcript: ENST00000541898
  gene symbol: ARMC6
  hgvsp: ENSP00000446037.1:p.Ile255_Thr258del
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000376148
  ensembl transcript: ENST00000392336
  gene symbol: ARMC6
  hgvsp: ENSP00000376148.3:p.Ile280_Thr283del
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000269932
  ensembl transcript: ENST00000269932
  gene symbol: ARMC6
  hgvsp: ENSP00000269932.6:p.Ile255_Thr258del
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444317
  ensembl transcript: ENST00000545091
  gene symbol: ARMC6
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: true
  consequence: inframe_deletion
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444156
  ensembl transcript: ENST00000535612
  gene symbol: ARMC6
  hgvsp: ENSP00000444156.1:p.Ile280_Thr283del
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444341
  ensembl transcript: ENST00000546344
  gene symbol: ARMC6
  hgvsp: ENSP00000444341.1:p.Ile187_Thr190del
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: coding_sequence_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000441948
  ensembl transcript: ENST00000537263
  gene symbol: ARMC6
  variant of: http://identifiers.org/hgnc/25049
canonical: true
consequence: inframe deletion
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3986
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2779
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11260
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13521
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 953
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9432
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18169
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1055
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2000
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27743
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 563
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 365
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 997
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 191
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 432
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Ile280_Thr283del
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
population: Other
population: African
reference allele: TCATCGAAGCCAC
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: VQSLOD

19-19162991-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 19162991
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 19162991
    reference: chr 19
allele count: 5
allele frequency: 5.135790295410658e-5
allele num: 97356
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444317
  ensembl transcript: ENST00000545091
  gene symbol: ARMC6
  hgvsc: ENST00000545091.1:c.*550C>T
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000376147
  ensembl transcript: ENST00000392335
  gene symbol: ARMC6
  hgvsc: ENST00000392335.2:c.765C>T
  hgvsp: ENST00000392335.2:c.765C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444341
  ensembl transcript: ENST00000546344
  gene symbol: ARMC6
  hgvsc: ENST00000546344.1:c.561C>T
  hgvsp: ENST00000546344.1:c.561C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444156
  ensembl transcript: ENST00000535612
  gene symbol: ARMC6
  hgvsc: ENST00000535612.1:c.840C>T
  hgvsp: ENST00000535612.1:c.840C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000441948
  ensembl transcript: ENST00000537263
  gene symbol: ARMC6
  hgvsc: ENST00000537263.1:c.765C>T
  hgvsp: ENST00000537263.1:c.765C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000376148
  ensembl transcript: ENST00000392336
  gene symbol: ARMC6
  hgvsc: ENST00000392336.3:c.840C>T
  hgvsp: ENST00000392336.3:c.840C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000269932
  ensembl transcript: ENST00000269932
  gene symbol: ARMC6
  hgvsc: ENST00000269932.6:c.765C>T
  hgvsp: ENST00000269932.6:c.765C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000446037
  ensembl transcript: ENST00000541898
  gene symbol: ARMC6
  hgvsc: ENST00000541898.1:c.765C>T
  hgvsp: ENST00000541898.1:c.765C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25049
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10487
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11113
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3079
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15974
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1152
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3365
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 14960
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 410
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 487
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 158
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 450
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 397
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2207
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Ile280Ile
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum

19-19162992-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 19162992
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 19162992
    reference: chr 19
allele count: 4
allele frequency: 4.14696856597827e-5
allele num: 96456
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000441948
  ensembl transcript: ENST00000537263
  gene symbol: ARMC6
  hgvsc: ENST00000537263.1:c.766G>A
  hgvsp: ENSP00000441948.1:p.Glu256Lys
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000269932
  ensembl transcript: ENST00000269932
  gene symbol: ARMC6
  hgvsc: ENST00000269932.6:c.766G>A
  hgvsp: ENSP00000269932.6:p.Glu256Lys
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444156
  ensembl transcript: ENST00000535612
  gene symbol: ARMC6
  hgvsc: ENST00000535612.1:c.841G>A
  hgvsp: ENSP00000444156.1:p.Glu281Lys
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444341
  ensembl transcript: ENST00000546344
  gene symbol: ARMC6
  hgvsc: ENST00000546344.1:c.562G>A
  hgvsp: ENSP00000444341.1:p.Glu188Lys
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000376148
  ensembl transcript: ENST00000392336
  gene symbol: ARMC6
  hgvsc: ENST00000392336.3:c.841G>A
  hgvsp: ENSP00000376148.3:p.Glu281Lys
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000446037
  ensembl transcript: ENST00000541898
  gene symbol: ARMC6
  hgvsc: ENST00000541898.1:c.766G>A
  hgvsp: ENSP00000446037.1:p.Glu256Lys
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000376147
  ensembl transcript: ENST00000392335
  gene symbol: ARMC6
  hgvsc: ENST00000392335.2:c.766G>A
  hgvsp: ENSP00000376147.2:p.Glu256Lys
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444317
  ensembl transcript: ENST00000545091
  gene symbol: ARMC6
  hgvsc: ENST00000545091.1:c.*551G>A
  variant of: http://identifiers.org/hgnc/25049
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3130
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15358
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1230
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11060
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10797
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3093
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15465
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2725
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 200
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 381
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 504
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21781
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 529
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Glu281Lys
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum

19-19163007-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 19163007
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 19163007
    reference: chr 19
allele count: 4
allele frequency: 4.684608718056824e-5
allele num: 85386
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000376147
  ensembl transcript: ENST00000392335
  gene symbol: ARMC6
  hgvsc: ENST00000392335.2:c.778+3A>G
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444341
  ensembl transcript: ENST00000546344
  gene symbol: ARMC6
  hgvsc: ENST00000546344.1:c.574+3A>G
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000376148
  ensembl transcript: ENST00000392336
  gene symbol: ARMC6
  hgvsc: ENST00000392336.3:c.853+3A>G
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000269932
  ensembl transcript: ENST00000269932
  gene symbol: ARMC6
  hgvsc: ENST00000269932.6:c.778+3A>G
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444317
  ensembl transcript: ENST00000545091
  gene symbol: ARMC6
  hgvsc: ENST00000545091.1:c.*563+3A>G
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444156
  ensembl transcript: ENST00000535612
  gene symbol: ARMC6
  hgvsc: ENST00000535612.1:c.853+3A>G
  variant of: http://identifiers.org/hgnc/25049
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2789
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21813
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4296
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14953
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8485
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5909
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1969
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13686
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 324
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 123
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 583
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1648
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4004
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 514
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 8.25e1
  variant carriers: 0
hgvs: c.853+3A>G
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Other
population: African
population: East Asian
population: European (Finnish)
population: Latino
reference allele: A
site quality: FS
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

19-19163014-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 19163014
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 19163014
    reference: chr 19
allele count: 1
allele frequency: 1.283730005905158e-5
allele num: 77898
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000376147
  ensembl transcript: ENST00000392335
  gene symbol: ARMC6
  hgvsc: ENST00000392335.2:c.778+10G>A
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444156
  ensembl transcript: ENST00000535612
  gene symbol: ARMC6
  hgvsc: ENST00000535612.1:c.853+10G>A
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000376148
  ensembl transcript: ENST00000392336
  gene symbol: ARMC6
  hgvsc: ENST00000392336.3:c.853+10G>A
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444341
  ensembl transcript: ENST00000546344
  gene symbol: ARMC6
  hgvsc: ENST00000546344.1:c.574+10G>A
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444317
  ensembl transcript: ENST00000545091
  gene symbol: ARMC6
  hgvsc: ENST00000545091.1:c.*563+10G>A
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000269932
  ensembl transcript: ENST00000269932
  gene symbol: ARMC6
  hgvsc: ENST00000269932.6:c.778+10G>A
  variant of: http://identifiers.org/hgnc/25049
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24425
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1397
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5183
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4160
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4682
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3466
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16894
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32989
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 894
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7948
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 236
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4881
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1481
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 151
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3926
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 261
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1151
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4631
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
population: African
population: European (Non-Finnish)
population: Latino
reference allele: G
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: QD

19-19163016-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 19163016
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 19163016
    reference: chr 19
allele count: 60
allele frequency: 8.08996035919424e-4
allele num: 74166
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000376147
  ensembl transcript: ENST00000392335
  gene symbol: ARMC6
  hgvsc: ENST00000392335.2:c.778+12G>A
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444341
  ensembl transcript: ENST00000546344
  gene symbol: ARMC6
  hgvsc: ENST00000546344.1:c.574+12G>A
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444156
  ensembl transcript: ENST00000535612
  gene symbol: ARMC6
  hgvsc: ENST00000535612.1:c.853+12G>A
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444317
  ensembl transcript: ENST00000545091
  gene symbol: ARMC6
  hgvsc: ENST00000545091.1:c.*563+12G>A
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000269932
  ensembl transcript: ENST00000269932
  gene symbol: ARMC6
  hgvsc: ENST00000269932.6:c.778+12G>A
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000376148
  ensembl transcript: ENST00000392336
  gene symbol: ARMC6
  hgvsc: ENST00000392336.3:c.853+12G>A
  variant of: http://identifiers.org/hgnc/25049
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3587
  bin: 2.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5039
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4966
  bin: 1.75e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 2663
  bin: 2.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 25127
  bin: 1.25e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17717
  bin: 7.5e0
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1074
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1261
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 126
  bin: 7.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 362
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4907
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 120
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1707
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 417
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 253
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 279
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4329
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5312
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 856
  bin: 6.75e1
  variant carriers: 1
num of homozygotes: 1
population: European (Finnish)
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
reference allele: G
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD

19-19163020-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 19163020
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 19163020
    reference: chr 19
allele count: 30
allele frequency: 4.395218002812939e-4
allele num: 68256
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444317
  ensembl transcript: ENST00000545091
  gene symbol: ARMC6
  hgvsc: ENST00000545091.1:c.*563+16C>T
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444341
  ensembl transcript: ENST00000546344
  gene symbol: ARMC6
  hgvsc: ENST00000546344.1:c.574+16C>T
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000269932
  ensembl transcript: ENST00000269932
  gene symbol: ARMC6
  hgvsc: ENST00000269932.6:c.778+16C>T
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000376148
  ensembl transcript: ENST00000392336
  gene symbol: ARMC6
  hgvsc: ENST00000392336.3:c.853+16C>T
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000376147
  ensembl transcript: ENST00000392335
  gene symbol: ARMC6
  hgvsc: ENST00000392335.2:c.778+16C>T
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444156
  ensembl transcript: ENST00000535612
  gene symbol: ARMC6
  hgvsc: ENST00000535612.1:c.853+16C>T
  variant of: http://identifiers.org/hgnc/25049
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2472
  bin: 2.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18983
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5924
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4583
  bin: 1.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2588
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25020
  bin: 1.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4695
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1730
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 456
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3800
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 31916
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1719
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 467
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 223
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2402
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 442
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4244
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: African
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum

19-19163021-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 19163021
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 19163021
    reference: chr 19
allele count: 3
allele frequency: 4.433672262946323e-5
allele num: 67664
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444156
  ensembl transcript: ENST00000535612
  gene symbol: ARMC6
  hgvsc: ENST00000535612.1:c.853+17G>A
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000269932
  ensembl transcript: ENST00000269932
  gene symbol: ARMC6
  hgvsc: ENST00000269932.6:c.778+17G>A
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000376147
  ensembl transcript: ENST00000392335
  gene symbol: ARMC6
  hgvsc: ENST00000392335.2:c.778+17G>A
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444341
  ensembl transcript: ENST00000546344
  gene symbol: ARMC6
  hgvsc: ENST00000546344.1:c.574+17G>A
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000376148
  ensembl transcript: ENST00000392336
  gene symbol: ARMC6
  hgvsc: ENST00000392336.3:c.853+17G>A
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444317
  ensembl transcript: ENST00000545091
  gene symbol: ARMC6
  hgvsc: ENST00000545091.1:c.*563+17G>A
  variant of: http://identifiers.org/hgnc/25049
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5990
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19173
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25014
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4401
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2577
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2440
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4118
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1736
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2100
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 733
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 111
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32335
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 363
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 419
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 420
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
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: G
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum

19-19163022-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 19163022
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 19163022
    reference: chr 19
allele count: 2
allele frequency: 2.994818963193675e-5
allele num: 66782
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444341
  ensembl transcript: ENST00000546344
  gene symbol: ARMC6
  hgvsc: ENST00000546344.1:c.574+18A>G
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444156
  ensembl transcript: ENST00000535612
  gene symbol: ARMC6
  hgvsc: ENST00000535612.1:c.853+18A>G
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000376147
  ensembl transcript: ENST00000392335
  gene symbol: ARMC6
  hgvsc: ENST00000392335.2:c.778+18A>G
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444317
  ensembl transcript: ENST00000545091
  gene symbol: ARMC6
  hgvsc: ENST00000545091.1:c.*563+18A>G
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000269932
  ensembl transcript: ENST00000269932
  gene symbol: ARMC6
  hgvsc: ENST00000269932.6:c.778+18A>G
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000376148
  ensembl transcript: ENST00000392336
  gene symbol: ARMC6
  hgvsc: ENST00000392336.3:c.853+18A>G
  variant of: http://identifiers.org/hgnc/25049
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2284
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6389
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19507
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24894
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2266
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4317
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1714
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 510
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 87
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 438
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7309
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 413
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4729
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1822
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Other
population: European (Non-Finnish)
population: South Asian
population: African
population: European (Finnish)
population: Latino
reference allele: A
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum

http://identifiers.org/exac.variant/19-19163025-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 19163025
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 19163025
    reference: chr 19
allele count: 1
allele frequency: 1.633666601320003e-5
allele num: 61212
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000376147
  ensembl transcript: ENST00000392335
  gene symbol: ARMC6
  hgvsc: ENST00000392335.2:c.778+21C>A
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000269932
  ensembl transcript: ENST00000269932
  gene symbol: ARMC6
  hgvsc: ENST00000269932.6:c.778+21C>A
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444156
  ensembl transcript: ENST00000535612
  gene symbol: ARMC6
  hgvsc: ENST00000535612.1:c.853+21C>A
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444341
  ensembl transcript: ENST00000546344
  gene symbol: ARMC6
  hgvsc: ENST00000546344.1:c.574+21C>A
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000376148
  ensembl transcript: ENST00000392336
  gene symbol: ARMC6
  hgvsc: ENST00000392336.3:c.853+21C>A
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444317
  ensembl transcript: ENST00000545091
  gene symbol: ARMC6
  hgvsc: ENST00000545091.1:c.*563+21C>A
  variant of: http://identifiers.org/hgnc/25049
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1815
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2088
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7299
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20279
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24016
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4233
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 340
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 454
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1691
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8248
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1046
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4191
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3457
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 538
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
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: C
site quality: QD
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP

19-19163025-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 19163025
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 19163025
    reference: chr 19
allele count: 2
allele frequency: 3.267333202640005e-5
allele num: 61212
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000376147
  ensembl transcript: ENST00000392335
  gene symbol: ARMC6
  hgvsc: ENST00000392335.2:c.778+21C>G
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444156
  ensembl transcript: ENST00000535612
  gene symbol: ARMC6
  hgvsc: ENST00000535612.1:c.853+21C>G
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000269932
  ensembl transcript: ENST00000269932
  gene symbol: ARMC6
  hgvsc: ENST00000269932.6:c.778+21C>G
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444341
  ensembl transcript: ENST00000546344
  gene symbol: ARMC6
  hgvsc: ENST00000546344.1:c.574+21C>G
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444317
  ensembl transcript: ENST00000545091
  gene symbol: ARMC6
  hgvsc: ENST00000545091.1:c.*563+21C>G
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000376148
  ensembl transcript: ENST00000392336
  gene symbol: ARMC6
  hgvsc: ENST00000392336.3:c.853+21C>G
  variant of: http://identifiers.org/hgnc/25049
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 24016
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7299
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20279
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4233
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2088
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1815
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8248
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3457
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4607
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 538
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2420
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1691
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30042
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2233
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD

19-19163025-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 19163025
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 19163025
    reference: chr 19
allele count: 1
allele frequency: 1.633666601320003e-5
allele num: 61212
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444317
  ensembl transcript: ENST00000545091
  gene symbol: ARMC6
  hgvsc: ENST00000545091.1:c.*563+21C>T
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000376147
  ensembl transcript: ENST00000392335
  gene symbol: ARMC6
  hgvsc: ENST00000392335.2:c.778+21C>T
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444341
  ensembl transcript: ENST00000546344
  gene symbol: ARMC6
  hgvsc: ENST00000546344.1:c.574+21C>T
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444156
  ensembl transcript: ENST00000535612
  gene symbol: ARMC6
  hgvsc: ENST00000535612.1:c.853+21C>T
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000269932
  ensembl transcript: ENST00000269932
  gene symbol: ARMC6
  hgvsc: ENST00000269932.6:c.778+21C>T
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000376148
  ensembl transcript: ENST00000392336
  gene symbol: ARMC6
  hgvsc: ENST00000392336.3:c.853+21C>T
  variant of: http://identifiers.org/hgnc/25049
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20279
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2088
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24016
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4233
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7299
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1815
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 454
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2420
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4191
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3457
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30042
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1046
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 538
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 287
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 340
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
population: East Asian
population: Latino
reference allele: C
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: QD

19-19163034-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 19163034
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 19163034
    reference: chr 19
allele count: 3
allele frequency: 5.366342301087579e-5
allele num: 55904
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444341
  ensembl transcript: ENST00000546344
  gene symbol: ARMC6
  hgvsc: ENST00000546344.1:c.574+30G>A
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000376148
  ensembl transcript: ENST00000392336
  gene symbol: ARMC6
  hgvsc: ENST00000392336.3:c.853+30G>A
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000376147
  ensembl transcript: ENST00000392335
  gene symbol: ARMC6
  hgvsc: ENST00000392335.2:c.778+30G>A
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444317
  ensembl transcript: ENST00000545091
  gene symbol: ARMC6
  hgvsc: ENST00000545091.1:c.*563+30G>A
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000269932
  ensembl transcript: ENST00000269932
  gene symbol: ARMC6
  hgvsc: ENST00000269932.6:c.778+30G>A
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444156
  ensembl transcript: ENST00000535612
  gene symbol: ARMC6
  hgvsc: ENST00000535612.1:c.853+30G>A
  variant of: http://identifiers.org/hgnc/25049
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21906
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22226
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3962
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1041
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1481
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9150
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10123
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 379
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1708
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2524
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 235
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 861
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4672
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2757
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 124
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: QD
site quality: BaseQRankSum

http://identifiers.org/exac.variant/19-19163037-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 19163037
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 19163037
    reference: chr 19
allele count: 1
allele frequency: 1.84304618673744e-5
allele num: 54258
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444341
  ensembl transcript: ENST00000546344
  gene symbol: ARMC6
  hgvsc: ENST00000546344.1:c.574+33C>A
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000269932
  ensembl transcript: ENST00000269932
  gene symbol: ARMC6
  hgvsc: ENST00000269932.6:c.778+33C>A
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000376147
  ensembl transcript: ENST00000392335
  gene symbol: ARMC6
  hgvsc: ENST00000392335.2:c.778+33C>A
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444317
  ensembl transcript: ENST00000545091
  gene symbol: ARMC6
  hgvsc: ENST00000545091.1:c.*563+33C>A
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000376148
  ensembl transcript: ENST00000392336
  gene symbol: ARMC6
  hgvsc: ENST00000392336.3:c.853+33C>A
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444156
  ensembl transcript: ENST00000535612
  gene symbol: ARMC6
  hgvsc: ENST00000535612.1:c.853+33C>A
  variant of: http://identifiers.org/hgnc/25049
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4089
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22674
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1285
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21196
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9613
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 857
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4669
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1642
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28425
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 134
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1798
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 410
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10701
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3243
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Other
population: African
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD

19-19163042-TG-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 19163042
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 19163041
    reference: chr 19
allele count: 1
allele frequency: 1.970288056113804e-5
allele num: 50754
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444317
  ensembl transcript: ENST00000545091
  gene symbol: ARMC6
  hgvsc: ENST00000545091.1:c.*563+41delG
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000269932
  ensembl transcript: ENST00000269932
  gene symbol: ARMC6
  hgvsc: ENST00000269932.6:c.778+41delG
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444341
  ensembl transcript: ENST00000546344
  gene symbol: ARMC6
  hgvsc: ENST00000546344.1:c.574+41delG
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000376148
  ensembl transcript: ENST00000392336
  gene symbol: ARMC6
  hgvsc: ENST00000392336.3:c.853+41delG
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444156
  ensembl transcript: ENST00000535612
  gene symbol: ARMC6
  hgvsc: ENST00000535612.1:c.853+41delG
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000376147
  ensembl transcript: ENST00000392335
  gene symbol: ARMC6
  hgvsc: ENST00000392335.2:c.778+41delG
  variant of: http://identifiers.org/hgnc/25049
canonical: true
consequence: intron
filter: VQSRTrancheINDEL96.00to97.00
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4352
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23887
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19663
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 636
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10043
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1043
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 352
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11519
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1914
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1012
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 127
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 203
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1197
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 464
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4207
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Other
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: TG
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: QD

19-19163045-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 19163045
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 19163045
    reference: chr 19
allele count: 1
allele frequency: 2.054738226349963e-5
allele num: 48668
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000376147
  ensembl transcript: ENST00000392335
  gene symbol: ARMC6
  hgvsc: ENST00000392335.2:c.778+41G>T
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000376148
  ensembl transcript: ENST00000392336
  gene symbol: ARMC6
  hgvsc: ENST00000392336.3:c.853+41G>T
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444156
  ensembl transcript: ENST00000535612
  gene symbol: ARMC6
  hgvsc: ENST00000535612.1:c.853+41G>T
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444341
  ensembl transcript: ENST00000546344
  gene symbol: ARMC6
  hgvsc: ENST00000546344.1:c.574+41G>T
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000269932
  ensembl transcript: ENST00000269932
  gene symbol: ARMC6
  hgvsc: ENST00000269932.6:c.778+41G>T
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444317
  ensembl transcript: ENST00000545091
  gene symbol: ARMC6
  hgvsc: ENST00000545091.1:c.*563+41G>T
  variant of: http://identifiers.org/hgnc/25049
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 987
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24901
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10138
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18624
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4369
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11835
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24376
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4592
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4791
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1109
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4272
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 190
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1934
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 123
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 477
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: African
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum

http://identifiers.org/exac.variant/19-19163046-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 19163046
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 19163046
    reference: chr 19
allele count: 1
allele frequency: 2.129834724825354e-5
allele num: 46952
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444317
  ensembl transcript: ENST00000545091
  gene symbol: ARMC6
  hgvsc: ENST00000545091.1:c.*563+42C>A
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000376147
  ensembl transcript: ENST00000392335
  gene symbol: ARMC6
  hgvsc: ENST00000392335.2:c.778+42C>A
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000376148
  ensembl transcript: ENST00000392336
  gene symbol: ARMC6
  hgvsc: ENST00000392336.3:c.853+42C>A
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444341
  ensembl transcript: ENST00000546344
  gene symbol: ARMC6
  hgvsc: ENST00000546344.1:c.574+42C>A
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444156
  ensembl transcript: ENST00000535612
  gene symbol: ARMC6
  hgvsc: ENST00000535612.1:c.853+42C>A
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000269932
  ensembl transcript: ENST00000269932
  gene symbol: ARMC6
  hgvsc: ENST00000269932.6:c.778+42C>A
  variant of: http://identifiers.org/hgnc/25049
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18247
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25285
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4384
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 975
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10128
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4796
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 181
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11899
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 893
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1742
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 473
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4486
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5059
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
population: Other
population: African
population: South Asian
reference allele: C
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum

19-19163046-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 19163046
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 19163046
    reference: chr 19
allele count: 4
allele frequency: 8.519338899301415e-5
allele num: 46952
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444317
  ensembl transcript: ENST00000545091
  gene symbol: ARMC6
  hgvsc: ENST00000545091.1:c.*563+42C>T
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444341
  ensembl transcript: ENST00000546344
  gene symbol: ARMC6
  hgvsc: ENST00000546344.1:c.574+42C>T
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444156
  ensembl transcript: ENST00000535612
  gene symbol: ARMC6
  hgvsc: ENST00000535612.1:c.853+42C>T
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000376147
  ensembl transcript: ENST00000392335
  gene symbol: ARMC6
  hgvsc: ENST00000392335.2:c.778+42C>T
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000269932
  ensembl transcript: ENST00000269932
  gene symbol: ARMC6
  hgvsc: ENST00000269932.6:c.778+42C>T
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000376148
  ensembl transcript: ENST00000392336
  gene symbol: ARMC6
  hgvsc: ENST00000392336.3:c.853+42C>T
  variant of: http://identifiers.org/hgnc/25049
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 975
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25285
  bin: 7.5e0
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4384
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 18247
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10128
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1742
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4486
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 893
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4796
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11899
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 473
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Other
population: East Asian
population: Latino
population: European (Finnish)
population: African
reference allele: C
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ

19-19163047-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 19163047
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 19163047
    reference: chr 19
allele count: 1
allele frequency: 2.154429507066529e-5
allele num: 46416
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444156
  ensembl transcript: ENST00000535612
  gene symbol: ARMC6
  hgvsc: ENST00000535612.1:c.853+43G>A
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444341
  ensembl transcript: ENST00000546344
  gene symbol: ARMC6
  hgvsc: ENST00000546344.1:c.574+43G>A
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444317
  ensembl transcript: ENST00000545091
  gene symbol: ARMC6
  hgvsc: ENST00000545091.1:c.*563+43G>A
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000376148
  ensembl transcript: ENST00000392336
  gene symbol: ARMC6
  hgvsc: ENST00000392336.3:c.853+43G>A
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000376147
  ensembl transcript: ENST00000392335
  gene symbol: ARMC6
  hgvsc: ENST00000392335.2:c.778+43G>A
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000269932
  ensembl transcript: ENST00000269932
  gene symbol: ARMC6
  hgvsc: ENST00000269932.6:c.778+43G>A
  variant of: http://identifiers.org/hgnc/25049
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10162
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25660
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17946
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 995
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4273
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4321
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 848
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5166
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1913
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22625
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5300
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 140
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 179
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4476
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11980
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
population: European (Finnish)
population: African
reference allele: G
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum

http://identifiers.org/exac.variant/19-19163052-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 19163052
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 19163052
    reference: chr 19
allele count: 3
allele frequency: 7.087172218284904e-5
allele num: 42330
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444341
  ensembl transcript: ENST00000546344
  gene symbol: ARMC6
  hgvsc: ENST00000546344.1:c.574+48A>C
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444156
  ensembl transcript: ENST00000535612
  gene symbol: ARMC6
  hgvsc: ENST00000535612.1:c.853+48A>C
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000376148
  ensembl transcript: ENST00000392336
  gene symbol: ARMC6
  hgvsc: ENST00000392336.3:c.853+48A>C
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000376147
  ensembl transcript: ENST00000392335
  gene symbol: ARMC6
  hgvsc: ENST00000392335.2:c.778+48A>C
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000269932
  ensembl transcript: ENST00000269932
  gene symbol: ARMC6
  hgvsc: ENST00000269932.6:c.778+48A>C
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444317
  ensembl transcript: ENST00000545091
  gene symbol: ARMC6
  hgvsc: ENST00000545091.1:c.*563+48A>C
  variant of: http://identifiers.org/hgnc/25049
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1141
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16290
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27299
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4098
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10208
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 543
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1833
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 456
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 18231
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6411
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4300
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 309
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
population: African
reference allele: A
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD

19-19163055-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 19163055
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 19163055
    reference: chr 19
allele count: 3
allele frequency: 6.988120195667365e-5
allele num: 42930
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444317
  ensembl transcript: ENST00000545091
  gene symbol: ARMC6
  hgvsc: ENST00000545091.1:c.*563+51T>G
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444341
  ensembl transcript: ENST00000546344
  gene symbol: ARMC6
  hgvsc: ENST00000546344.1:c.574+51T>G
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000376148
  ensembl transcript: ENST00000392336
  gene symbol: ARMC6
  hgvsc: ENST00000392336.3:c.853+51T>G
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000269932
  ensembl transcript: ENST00000269932
  gene symbol: ARMC6
  hgvsc: ENST00000269932.6:c.778+51T>G
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000376147
  ensembl transcript: ENST00000392335
  gene symbol: ARMC6
  hgvsc: ENST00000392335.2:c.778+51T>G
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444156
  ensembl transcript: ENST00000535612
  gene symbol: ARMC6
  hgvsc: ENST00000535612.1:c.853+51T>G
  variant of: http://identifiers.org/hgnc/25049
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27253
  bin: 7.5e0
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 10208
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16372
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1141
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4071
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1959
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 7511
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 6326
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 541
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4328
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1686
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4298
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: T
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD

19-19164914-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 19164914
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 19164914
    reference: chr 19
allele count: 2
allele frequency: 1.810380723066061e-5
allele num: 110474
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444341
  ensembl transcript: ENST00000546344
  gene symbol: ARMC6
  hgvsc: ENST00000546344.1:c.575-47C>T
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000269932
  ensembl transcript: ENST00000269932
  gene symbol: ARMC6
  hgvsc: ENST00000269932.6:c.779-47C>T
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000376147
  ensembl transcript: ENST00000392335
  gene symbol: ARMC6
  hgvsc: ENST00000392335.2:c.779-47C>T
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000376148
  ensembl transcript: ENST00000392336
  gene symbol: ARMC6
  hgvsc: ENST00000392336.3:c.854-47C>T
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444317
  ensembl transcript: ENST00000545091
  gene symbol: ARMC6
  hgvsc: ENST00000545091.1:c.*564-47C>T
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444156
  ensembl transcript: ENST00000535612
  gene symbol: ARMC6
  hgvsc: ENST00000535612.1:c.854-47C>T
  variant of: http://identifiers.org/hgnc/25049
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1010
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1658
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5174
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3674
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1296
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21401
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 920
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2862
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6971
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12950
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 702
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3321
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2684
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 713
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 596
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2614
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 714
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 188
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 447
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 237
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 338
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27657
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 318
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
population: African
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: MQRankSum

19-19164915-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 19164915
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 19164915
    reference: chr 19
allele count: 2
allele frequency: 1.809692714177133e-5
allele num: 110516
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000269932
  ensembl transcript: ENST00000269932
  gene symbol: ARMC6
  hgvsc: ENST00000269932.6:c.779-46G>A
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444156
  ensembl transcript: ENST00000535612
  gene symbol: ARMC6
  hgvsc: ENST00000535612.1:c.854-46G>A
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444317
  ensembl transcript: ENST00000545091
  gene symbol: ARMC6
  hgvsc: ENST00000545091.1:c.*564-46G>A
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444341
  ensembl transcript: ENST00000546344
  gene symbol: ARMC6
  hgvsc: ENST00000546344.1:c.575-46G>A
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000376148
  ensembl transcript: ENST00000392336
  gene symbol: ARMC6
  hgvsc: ENST00000392336.3:c.854-46G>A
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000376147
  ensembl transcript: ENST00000392335
  gene symbol: ARMC6
  hgvsc: ENST00000392335.2:c.779-46G>A
  variant of: http://identifiers.org/hgnc/25049
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1668
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1011
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1328
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21497
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 729
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3660
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13020
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5183
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6997
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2857
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1390
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 382
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 244
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2768
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2273
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 223
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 353
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2720
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 765
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 311
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 229
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
population: East Asian
reference allele: G
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD

19-19164921-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 19164921
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 19164921
    reference: chr 19
allele count: 223
allele frequency: 2.076543439798864e-3
allele num: 107390
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000269932
  ensembl transcript: ENST00000269932
  gene symbol: ARMC6
  hgvsc: ENST00000269932.6:c.779-40T>G
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000376148
  ensembl transcript: ENST00000392336
  gene symbol: ARMC6
  hgvsc: ENST00000392336.3:c.854-40T>G
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000376147
  ensembl transcript: ENST00000392335
  gene symbol: ARMC6
  hgvsc: ENST00000392335.2:c.779-40T>G
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444317
  ensembl transcript: ENST00000545091
  gene symbol: ARMC6
  hgvsc: ENST00000545091.1:c.*564-40T>G
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444341
  ensembl transcript: ENST00000546344
  gene symbol: ARMC6
  hgvsc: ENST00000546344.1:c.575-40T>G
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444156
  ensembl transcript: ENST00000535612
  gene symbol: ARMC6
  hgvsc: ENST00000535612.1:c.854-40T>G
  variant of: http://identifiers.org/hgnc/25049
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7339
  bin: 2.25e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 1623
  bin: 4.75e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3576
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2763
  bin: 4.25e1
  variant carriers: 28
genotype depth: GenotypeDepth
  all individuals: 13012
  bin: 3.25e1
  variant carriers: 36
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 1.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 7.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 7.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 1.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 948
  bin: 5.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21875
  bin: 2.75e1
  variant carriers: 42
genotype depth: GenotypeDepth
  all individuals: 1458
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5122
  bin: 3.75e1
  variant carriers: 32
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 647
  bin: 5.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 334
  bin: 4.25e1
  variant carriers: 12
genotype quality: GenotypeQuality
  all individuals: 27911
  bin: 6.25e1
  variant carriers: 10
genotype quality: GenotypeQuality
  all individuals: 315
  bin: 4.75e1
  variant carriers: 10
genotype quality: GenotypeQuality
  all individuals: 363
  bin: 5.75e1
  variant carriers: 15
genotype quality: GenotypeQuality
  all individuals: 544
  bin: 1.75e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 2562
  bin: 7.25e1
  variant carriers: 13
genotype quality: GenotypeQuality
  all individuals: 349
  bin: 2.75e1
  variant carriers: 9
genotype quality: GenotypeQuality
  all individuals: 1035
  bin: 2.25e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 5169
  bin: 9.75e1
  variant carriers: 74
genotype quality: GenotypeQuality
  all individuals: 812
  bin: 1.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 3015
  bin: 7.5e0
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 362
  bin: 3.75e1
  variant carriers: 8
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: European (Finnish)
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum

19-19164925-TC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 19164925
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 19164924
    reference: chr 19
allele count: 1
allele frequency: 9.039466309909063e-6
allele num: 110626
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000376148
  ensembl transcript: ENST00000392336
  gene symbol: ARMC6
  hgvsc: ENST00000392336.3:c.854-33delC
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000376147
  ensembl transcript: ENST00000392335
  gene symbol: ARMC6
  hgvsc: ENST00000392335.2:c.779-33delC
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444156
  ensembl transcript: ENST00000535612
  gene symbol: ARMC6
  hgvsc: ENST00000535612.1:c.854-33delC
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444317
  ensembl transcript: ENST00000545091
  gene symbol: ARMC6
  hgvsc: ENST00000545091.1:c.*564-33delC
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000269932
  ensembl transcript: ENST00000269932
  gene symbol: ARMC6
  hgvsc: ENST00000269932.6:c.779-33delC
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444341
  ensembl transcript: ENST00000546344
  gene symbol: ARMC6
  hgvsc: ENST00000546344.1:c.575-33delC
  variant of: http://identifiers.org/hgnc/25049
canonical: true
consequence: intron
filter: VQSRTrancheINDEL95.00to96.00
genotype depth: GenotypeDepth
  all individuals: 866
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3492
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7410
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22596
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1455
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13275
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4995
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1551
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2605
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2843
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 585
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 155
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1009
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3275
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2746
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 156
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30023
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 91
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 369
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 174
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
reference allele: TC
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ

19-19164929-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 19164929
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 19164929
    reference: chr 19
allele count: 6
allele frequency: 5.420543861234077e-5
allele num: 110690
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000269932
  ensembl transcript: ENST00000269932
  gene symbol: ARMC6
  hgvsc: ENST00000269932.6:c.779-32G>A
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000376147
  ensembl transcript: ENST00000392335
  gene symbol: ARMC6
  hgvsc: ENST00000392335.2:c.779-32G>A
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000376148
  ensembl transcript: ENST00000392336
  gene symbol: ARMC6
  hgvsc: ENST00000392336.3:c.854-32G>A
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444156
  ensembl transcript: ENST00000535612
  gene symbol: ARMC6
  hgvsc: ENST00000535612.1:c.854-32G>A
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444341
  ensembl transcript: ENST00000546344
  gene symbol: ARMC6
  hgvsc: ENST00000546344.1:c.575-32G>A
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444317
  ensembl transcript: ENST00000545091
  gene symbol: ARMC6
  hgvsc: ENST00000545091.1:c.*564-32G>A
  variant of: http://identifiers.org/hgnc/25049
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7364
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1826
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13279
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1453
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22768
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3245
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2609
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5017
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 863
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1282
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 278
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 133
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 502
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5340
  bin: 9.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 279
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2123
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2776
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30274
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1344
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 106
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
reference allele: G
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD

19-19164930-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 19164930
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 19164930
    reference: chr 19
allele count: 2
allele frequency: 1.80606476548249e-5
allele num: 110738
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000376147
  ensembl transcript: ENST00000392335
  gene symbol: ARMC6
  hgvsc: ENST00000392335.2:c.779-31C>T
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444156
  ensembl transcript: ENST00000535612
  gene symbol: ARMC6
  hgvsc: ENST00000535612.1:c.854-31C>T
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444341
  ensembl transcript: ENST00000546344
  gene symbol: ARMC6
  hgvsc: ENST00000546344.1:c.575-31C>T
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000376148
  ensembl transcript: ENST00000392336
  gene symbol: ARMC6
  hgvsc: ENST00000392336.3:c.854-31C>T
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000269932
  ensembl transcript: ENST00000269932
  gene symbol: ARMC6
  hgvsc: ENST00000269932.6:c.779-31C>T
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444317
  ensembl transcript: ENST00000545091
  gene symbol: ARMC6
  hgvsc: ENST00000545091.1:c.*564-31C>T
  variant of: http://identifiers.org/hgnc/25049
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13292
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7378
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2600
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3186
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 859
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1452
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4989
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22829
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1891
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3255
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5341
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 141
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 472
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2746
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1281
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 261
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 131
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30377
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1396
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: MQ

19-19164940-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 19164940
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 19164940
    reference: chr 19
allele count: 2
allele frequency: 1.800698671084381e-5
allele num: 111068
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444341
  ensembl transcript: ENST00000546344
  gene symbol: ARMC6
  hgvsc: ENST00000546344.1:c.575-21C>T
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444156
  ensembl transcript: ENST00000535612
  gene symbol: ARMC6
  hgvsc: ENST00000535612.1:c.854-21C>T
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000376148
  ensembl transcript: ENST00000392336
  gene symbol: ARMC6
  hgvsc: ENST00000392336.3:c.854-21C>T
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444317
  ensembl transcript: ENST00000545091
  gene symbol: ARMC6
  hgvsc: ENST00000545091.1:c.*564-21C>T
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000376147
  ensembl transcript: ENST00000392335
  gene symbol: ARMC6
  hgvsc: ENST00000392335.2:c.779-21C>T
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000269932
  ensembl transcript: ENST00000269932
  gene symbol: ARMC6
  hgvsc: ENST00000269932.6:c.779-21C>T
  variant of: http://identifiers.org/hgnc/25049
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2744
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13311
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2584
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1447
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7471
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2264
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 862
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23026
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4987
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 575
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2075
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2124
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 129
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8610
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 135
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 943
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 287
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 218
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2354
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Non-Finnish)
population: Other
population: East Asian
population: African
population: European (Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: DP

19-19164941-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 19164941
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 19164941
    reference: chr 19
allele count: 6
allele frequency: 5.398596364945114e-5
allele num: 111140
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000376147
  ensembl transcript: ENST00000392335
  gene symbol: ARMC6
  hgvsc: ENST00000392335.2:c.779-20G>A
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000269932
  ensembl transcript: ENST00000269932
  gene symbol: ARMC6
  hgvsc: ENST00000269932.6:c.779-20G>A
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444156
  ensembl transcript: ENST00000535612
  gene symbol: ARMC6
  hgvsc: ENST00000535612.1:c.854-20G>A
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444341
  ensembl transcript: ENST00000546344
  gene symbol: ARMC6
  hgvsc: ENST00000546344.1:c.575-20G>A
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444317
  ensembl transcript: ENST00000545091
  gene symbol: ARMC6
  hgvsc: ENST00000545091.1:c.*564-20G>A
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000376148
  ensembl transcript: ENST00000392336
  gene symbol: ARMC6
  hgvsc: ENST00000392336.3:c.854-20G>A
  variant of: http://identifiers.org/hgnc/25049
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2888
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 575
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1446
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4985
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 858
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7492
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2100
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23038
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13308
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2584
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 8607
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 147
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 261
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 123
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1941
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 217
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30831
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: African
reference allele: G
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum

19-19164945-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 19164945
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 19164945
    reference: chr 19
allele count: 4
allele frequency: 3.593051039290013e-5
allele num: 111326
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000269932
  ensembl transcript: ENST00000269932
  gene symbol: ARMC6
  hgvsc: ENST00000269932.6:c.779-16C>T
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444317
  ensembl transcript: ENST00000545091
  gene symbol: ARMC6
  hgvsc: ENST00000545091.1:c.*564-16C>T
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000376148
  ensembl transcript: ENST00000392336
  gene symbol: ARMC6
  hgvsc: ENST00000392336.3:c.854-16C>T
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444341
  ensembl transcript: ENST00000546344
  gene symbol: ARMC6
  hgvsc: ENST00000546344.1:c.575-16C>T
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444156
  ensembl transcript: ENST00000535612
  gene symbol: ARMC6
  hgvsc: ENST00000535612.1:c.854-16C>T
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000376147
  ensembl transcript: ENST00000392335
  gene symbol: ARMC6
  hgvsc: ENST00000392335.2:c.779-16C>T
  variant of: http://identifiers.org/hgnc/25049
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4990
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7501
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3180
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23072
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1747
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2582
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 857
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1444
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13305
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2742
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30885
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 162
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5331
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 3269
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1632
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 95
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum

http://identifiers.org/exac.variant/19-19164951-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 19164951
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 19164951
    reference: chr 19
allele count: 106
allele frequency: 9.501443143722773e-4
allele num: 111562
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000269932
  ensembl transcript: ENST00000269932
  gene symbol: ARMC6
  hgvsc: ENST00000269932.6:c.779-10C>A
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444156
  ensembl transcript: ENST00000535612
  gene symbol: ARMC6
  hgvsc: ENST00000535612.1:c.854-10C>A
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000376147
  ensembl transcript: ENST00000392335
  gene symbol: ARMC6
  hgvsc: ENST00000392335.2:c.779-10C>A
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444317
  ensembl transcript: ENST00000545091
  gene symbol: ARMC6
  hgvsc: ENST00000545091.1:c.*564-10C>A
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000376148
  ensembl transcript: ENST00000392336
  gene symbol: ARMC6
  hgvsc: ENST00000392336.3:c.854-10C>A
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444341
  ensembl transcript: ENST00000546344
  gene symbol: ARMC6
  hgvsc: ENST00000546344.1:c.575-10C>A
  variant of: http://identifiers.org/hgnc/25049
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13297
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 1.25e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 1287
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 9.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 3521
  bin: 7.5e0
  variant carriers: 33
genotype depth: GenotypeDepth
  all individuals: 4973
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 1.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 7.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 7538
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 7.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 861
  bin: 5.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 5.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 1447
  bin: 4.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 23074
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 6.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 2580
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 180
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 170
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2126
  bin: 8.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 3186
  bin: 2.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 8611
  bin: 6.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 149
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 942
  bin: 8.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 1218
  bin: 7.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2748
  bin: 7.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 118
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 1
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
population: European (Finnish)
population: African
population: Latino
reference allele: C
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum

19-19164955-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 19164955
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 19164955
    reference: chr 19
allele count: 2
allele frequency: 1.788173023621766e-5
allele num: 111846
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444317
  ensembl transcript: ENST00000545091
  gene symbol: ARMC6
  hgvsc: ENST00000545091.1:c.*564-6C>T
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444341
  ensembl transcript: ENST00000546344
  gene symbol: ARMC6
  hgvsc: ENST00000546344.1:c.575-6C>T
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000376148
  ensembl transcript: ENST00000392336
  gene symbol: ARMC6
  hgvsc: ENST00000392336.3:c.854-6C>T
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444156
  ensembl transcript: ENST00000535612
  gene symbol: ARMC6
  hgvsc: ENST00000535612.1:c.854-6C>T
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000376147
  ensembl transcript: ENST00000392335
  gene symbol: ARMC6
  hgvsc: ENST00000392335.2:c.779-6C>T
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000269932
  ensembl transcript: ENST00000269932
  gene symbol: ARMC6
  hgvsc: ENST00000269932.6:c.779-6C>T
  variant of: http://identifiers.org/hgnc/25049
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13316
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1441
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23123
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2578
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7578
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1057
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4982
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3630
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 555
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 856
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5300
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 3268
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3364
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2751
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 181
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 230
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8634
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 112
  bin: 1.25e1
  variant carriers: 0
hgvs: c.854-6C>T
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Other
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP

19-19164956-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 19164956
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 19164956
    reference: chr 19
allele count: 26
allele frequency: 2.322216466301066e-4
allele num: 111962
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000376147
  ensembl transcript: ENST00000392335
  gene symbol: ARMC6
  hgvsc: ENST00000392335.2:c.779-5T>C
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000376148
  ensembl transcript: ENST00000392336
  gene symbol: ARMC6
  hgvsc: ENST00000392336.3:c.854-5T>C
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000269932
  ensembl transcript: ENST00000269932
  gene symbol: ARMC6
  hgvsc: ENST00000269932.6:c.779-5T>C
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444156
  ensembl transcript: ENST00000535612
  gene symbol: ARMC6
  hgvsc: ENST00000535612.1:c.854-5T>C
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444341
  ensembl transcript: ENST00000546344
  gene symbol: ARMC6
  hgvsc: ENST00000546344.1:c.575-5T>C
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444317
  ensembl transcript: ENST00000545091
  gene symbol: ARMC6
  hgvsc: ENST00000545091.1:c.*564-5T>C
  variant of: http://identifiers.org/hgnc/25049
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1440
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 1.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 6.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 23129
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13314
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1000
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2578
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3645
  bin: 7.5e0
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 7584
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4980
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 853
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2128
  bin: 8.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 241
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 149
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 961
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 111
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 940
  bin: 8.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2752
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 5.25e1
  variant carriers: 1
hgvs: c.854-5T>C
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
reference allele: T
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: QD

19-19164957-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 19164957
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 19164957
    reference: chr 19
allele count: 1
allele frequency: 8.926658573162893e-6
allele num: 112024
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000376148
  ensembl transcript: ENST00000392336
  gene symbol: ARMC6
  hgvsc: ENST00000392336.3:c.854-4G>A
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444156
  ensembl transcript: ENST00000535612
  gene symbol: ARMC6
  hgvsc: ENST00000535612.1:c.854-4G>A
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000269932
  ensembl transcript: ENST00000269932
  gene symbol: ARMC6
  hgvsc: ENST00000269932.6:c.779-4G>A
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444317
  ensembl transcript: ENST00000545091
  gene symbol: ARMC6
  hgvsc: ENST00000545091.1:c.*564-4G>A
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000376147
  ensembl transcript: ENST00000392335
  gene symbol: ARMC6
  hgvsc: ENST00000392335.2:c.779-4G>A
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444341
  ensembl transcript: ENST00000546344
  gene symbol: ARMC6
  hgvsc: ENST00000546344.1:c.575-4G>A
  variant of: http://identifiers.org/hgnc/25049
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 853
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13319
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 943
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23137
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1441
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3666
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7594
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4983
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2576
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8637
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 107
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 219
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3453
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 157
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3271
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 2.5e0
  variant carriers: 0
hgvs: c.854-4G>A
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: Other
reference allele: G
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum

19-19164958-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 19164958
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 19164958
    reference: chr 19
allele count: 2
allele frequency: 1.784726312220021e-5
allele num: 112062
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444341
  ensembl transcript: ENST00000546344
  gene symbol: ARMC6
  hgvsc: ENST00000546344.1:c.575-3C>G
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000376147
  ensembl transcript: ENST00000392335
  gene symbol: ARMC6
  hgvsc: ENST00000392335.2:c.779-3C>G
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000269932
  ensembl transcript: ENST00000269932
  gene symbol: ARMC6
  hgvsc: ENST00000269932.6:c.779-3C>G
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000376148
  ensembl transcript: ENST00000392336
  gene symbol: ARMC6
  hgvsc: ENST00000392336.3:c.854-3C>G
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444317
  ensembl transcript: ENST00000545091
  gene symbol: ARMC6
  hgvsc: ENST00000545091.1:c.*564-3C>G
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444156
  ensembl transcript: ENST00000535612
  gene symbol: ARMC6
  hgvsc: ENST00000535612.1:c.854-3C>G
  variant of: http://identifiers.org/hgnc/25049
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7603
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2576
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 887
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23140
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 641
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4984
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13320
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3643
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 852
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1440
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8640
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 93
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 867
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 219
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 157
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 108
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 125
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2128
  bin: 8.25e1
  variant carriers: 0
hgvs: c.854-3C>G
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
population: Other
population: East Asian
reference allele: C
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD

19-19164959-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 19164959
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 19164959
    reference: chr 19
allele count: 1
allele frequency: 8.907733694393473e-6
allele num: 112262
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444317
  ensembl transcript: ENST00000545091
  gene symbol: ARMC6
  hgvsc: ENST00000545091.1:c.*564-2A>G
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444341
  ensembl transcript: ENST00000546344
  gene symbol: ARMC6
  hgvsc: ENST00000546344.1:c.575-2A>G
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000376148
  ensembl transcript: ENST00000392336
  gene symbol: ARMC6
  hgvsc: ENST00000392336.3:c.854-2A>G
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000376147
  ensembl transcript: ENST00000392335
  gene symbol: ARMC6
  hgvsc: ENST00000392335.2:c.779-2A>G
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: true
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444156
  ensembl transcript: ENST00000535612
  gene symbol: ARMC6
  hgvsc: ENST00000535612.1:c.854-2A>G
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000269932
  ensembl transcript: ENST00000269932
  gene symbol: ARMC6
  hgvsc: ENST00000269932.6:c.779-2A>G
  variant of: http://identifiers.org/hgnc/25049
canonical: true
consequence: splice acceptor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 822
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4983
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3671
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7619
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2575
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 852
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23144
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 655
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13324
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1441
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 791
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3474
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 275
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 155
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 99
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8641
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 113
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 232
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2129
  bin: 8.25e1
  variant carriers: 0
hgvs: c.854-2A>G
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: African
population: South Asian
population: East Asian
reference allele: A
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum

19-19164962-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 19164962
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 19164962
    reference: chr 19
allele count: 4
allele frequency: 3.5503798906483e-5
allele num: 112664
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000376148
  ensembl transcript: ENST00000392336
  gene symbol: ARMC6
  hgvsc: ENST00000392336.3:c.855G>A
  hgvsp: ENST00000392336.3:c.855G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444156
  ensembl transcript: ENST00000535612
  gene symbol: ARMC6
  hgvsc: ENST00000535612.1:c.855G>A
  hgvsp: ENST00000535612.1:c.855G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000269932
  ensembl transcript: ENST00000269932
  gene symbol: ARMC6
  hgvsc: ENST00000269932.6:c.780G>A
  hgvsp: ENST00000269932.6:c.780G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444341
  ensembl transcript: ENST00000546344
  gene symbol: ARMC6
  hgvsc: ENST00000546344.1:c.576G>A
  hgvsp: ENST00000546344.1:c.576G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444317
  ensembl transcript: ENST00000545091
  gene symbol: ARMC6
  hgvsc: ENST00000545091.1:c.*565G>A
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000376147
  ensembl transcript: ENST00000392335
  gene symbol: ARMC6
  hgvsc: ENST00000392335.2:c.780G>A
  hgvsp: ENST00000392335.2:c.780G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25049
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 23150
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1440
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13326
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4985
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3667
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7714
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 719
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 852
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2577
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 129
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5292
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 255
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 610
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31172
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8654
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3541
  bin: 2.25e1
  variant carriers: 0
hgvs: c.855G>A
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: MQ

19-19164969-GATA-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 19164969
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 19164966
    reference: chr 19
allele count: 2
allele frequency: 1.765910856819948e-5
allele num: 113256
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444317
  ensembl transcript: ENST00000545091
  gene symbol: ARMC6
  hgvsc: ENST00000545091.1:c.*574_*576delTAA
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: true
  consequence: inframe_deletion
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444156
  ensembl transcript: ENST00000535612
  gene symbol: ARMC6
  hgvsc: ENST00000535612.1:c.864_866delTAA
  hgvsp: ENSP00000444156.1:p.Asn289del
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000376148
  ensembl transcript: ENST00000392336
  gene symbol: ARMC6
  hgvsc: ENST00000392336.3:c.864_866delTAA
  hgvsp: ENSP00000376148.3:p.Asn289del
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000376147
  ensembl transcript: ENST00000392335
  gene symbol: ARMC6
  hgvsc: ENST00000392335.2:c.789_791delTAA
  hgvsp: ENSP00000376147.2:p.Asn264del
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444341
  ensembl transcript: ENST00000546344
  gene symbol: ARMC6
  hgvsc: ENST00000546344.1:c.585_587delTAA
  hgvsp: ENSP00000444341.1:p.Asn196del
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000269932
  ensembl transcript: ENST00000269932
  gene symbol: ARMC6
  hgvsc: ENST00000269932.6:c.789_791delTAA
  hgvsp: ENSP00000269932.6:p.Asn264del
  variant of: http://identifiers.org/hgnc/25049
canonical: true
consequence: inframe deletion
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3627
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2576
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1440
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13331
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7924
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23163
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4985
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 851
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 320
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8662
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3537
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3275
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 270
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2131
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2754
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1273
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 95
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Asn289del
num of homozygotes: 0
population: European (Finnish)
population: Other
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
reference allele: GATA
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: FS

19-19164970-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 19164970
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 19164970
    reference: chr 19
allele count: 1
allele frequency: 8.825657952800381e-6
allele num: 113306
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444156
  ensembl transcript: ENST00000535612
  gene symbol: ARMC6
  hgvsc: ENST00000535612.1:c.863A>G
  hgvsp: ENSP00000444156.1:p.Asp288Gly
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000269932
  ensembl transcript: ENST00000269932
  gene symbol: ARMC6
  hgvsc: ENST00000269932.6:c.788A>G
  hgvsp: ENSP00000269932.6:p.Asp263Gly
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444341
  ensembl transcript: ENST00000546344
  gene symbol: ARMC6
  hgvsc: ENST00000546344.1:c.584A>G
  hgvsp: ENSP00000444341.1:p.Asp195Gly
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000376147
  ensembl transcript: ENST00000392335
  gene symbol: ARMC6
  hgvsc: ENST00000392335.2:c.788A>G
  hgvsp: ENSP00000376147.2:p.Asp263Gly
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000376148
  ensembl transcript: ENST00000392336
  gene symbol: ARMC6
  hgvsc: ENST00000392336.3:c.863A>G
  hgvsp: ENSP00000376148.3:p.Asp288Gly
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444317
  ensembl transcript: ENST00000545091
  gene symbol: ARMC6
  hgvsc: ENST00000545091.1:c.*573A>G
  variant of: http://identifiers.org/hgnc/25049
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 850
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4985
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 763
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3605
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7967
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23166
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13329
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1441
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2576
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 265
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2755
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 381
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3276
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 939
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Asp288Gly
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: A
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: DP

19-19164971-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 19164971
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 19164971
    reference: chr 19
allele count: 1
allele frequency: 8.815854432611609e-6
allele num: 113432
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444156
  ensembl transcript: ENST00000535612
  gene symbol: ARMC6
  hgvsc: ENST00000535612.1:c.864T>C
  hgvsp: ENST00000535612.1:c.864T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444317
  ensembl transcript: ENST00000545091
  gene symbol: ARMC6
  hgvsc: ENST00000545091.1:c.*574T>C
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000269932
  ensembl transcript: ENST00000269932
  gene symbol: ARMC6
  hgvsc: ENST00000269932.6:c.789T>C
  hgvsp: ENST00000269932.6:c.789T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000376148
  ensembl transcript: ENST00000392336
  gene symbol: ARMC6
  hgvsc: ENST00000392336.3:c.864T>C
  hgvsp: ENST00000392336.3:c.864T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444341
  ensembl transcript: ENST00000546344
  gene symbol: ARMC6
  hgvsc: ENST00000546344.1:c.585T>C
  hgvsp: ENST00000546344.1:c.585T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000376147
  ensembl transcript: ENST00000392335
  gene symbol: ARMC6
  hgvsc: ENST00000392335.2:c.789T>C
  hgvsp: ENST00000392335.2:c.789T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25049
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1440
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4986
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 850
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2576
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8020
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 752
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23167
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13329
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3606
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 305
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 337
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 147
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 270
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31476
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3275
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5286
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Asp288Asp
num of homozygotes: 0
population: East Asian
population: Latino
population: Other
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: DP

http://identifiers.org/exac.variant/19-19164975-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 19164975
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 19164975
    reference: chr 19
allele count: 1
allele frequency: 8.771775933755548e-6
allele num: 114002
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444341
  ensembl transcript: ENST00000546344
  gene symbol: ARMC6
  hgvsc: ENST00000546344.1:c.589C>A
  hgvsp: ENSP00000444341.1:p.Pro197Thr
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000376148
  ensembl transcript: ENST00000392336
  gene symbol: ARMC6
  hgvsc: ENST00000392336.3:c.868C>A
  hgvsp: ENSP00000376148.3:p.Pro290Thr
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444317
  ensembl transcript: ENST00000545091
  gene symbol: ARMC6
  hgvsc: ENST00000545091.1:c.*578C>A
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000376147
  ensembl transcript: ENST00000392335
  gene symbol: ARMC6
  hgvsc: ENST00000392335.2:c.793C>A
  hgvsp: ENSP00000376147.2:p.Pro265Thr
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444156
  ensembl transcript: ENST00000535612
  gene symbol: ARMC6
  hgvsc: ENST00000535612.1:c.868C>A
  hgvsp: ENSP00000444156.1:p.Pro290Thr
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000269932
  ensembl transcript: ENST00000269932
  gene symbol: ARMC6
  hgvsc: ENST00000269932.6:c.793C>A
  hgvsp: ENSP00000269932.6:p.Pro265Thr
  variant of: http://identifiers.org/hgnc/25049
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3356
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 781
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23204
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2576
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4987
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13327
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8262
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1441
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 850
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31650
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 101
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 162
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2754
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3299
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 272
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 253
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 313
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Pro290Thr
num of homozygotes: 0
population: European (Finnish)
population: Other
population: African
population: Latino
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum

19-19164977-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 19164977
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 19164977
    reference: chr 19
allele count: 1
allele frequency: 8.741105924721597e-6
allele num: 114402
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444341
  ensembl transcript: ENST00000546344
  gene symbol: ARMC6
  hgvsc: ENST00000546344.1:c.591T>C
  hgvsp: ENST00000546344.1:c.591T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000376147
  ensembl transcript: ENST00000392335
  gene symbol: ARMC6
  hgvsc: ENST00000392335.2:c.795T>C
  hgvsp: ENST00000392335.2:c.795T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000376148
  ensembl transcript: ENST00000392336
  gene symbol: ARMC6
  hgvsc: ENST00000392336.3:c.870T>C
  hgvsp: ENST00000392336.3:c.870T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000269932
  ensembl transcript: ENST00000269932
  gene symbol: ARMC6
  hgvsc: ENST00000269932.6:c.795T>C
  hgvsp: ENST00000269932.6:c.795T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444317
  ensembl transcript: ENST00000545091
  gene symbol: ARMC6
  hgvsc: ENST00000545091.1:c.*580T>C
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444156
  ensembl transcript: ENST00000535612
  gene symbol: ARMC6
  hgvsc: ENST00000535612.1:c.870T>C
  hgvsp: ENST00000535612.1:c.870T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25049
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 850
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23225
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13328
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3232
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 777
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4986
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2577
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1441
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8391
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2129
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31840
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 217
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 317
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 153
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1274
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Pro290Pro
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Other
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
reference allele: T
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP

19-19164982-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 19164982
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 19164982
    reference: chr 19
allele count: 1
allele frequency: 8.679199430644517e-6
allele num: 115218
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000376148
  ensembl transcript: ENST00000392336
  gene symbol: ARMC6
  hgvsc: ENST00000392336.3:c.875T>A
  hgvsp: ENSP00000376148.3:p.Ile292Asn
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000376147
  ensembl transcript: ENST00000392335
  gene symbol: ARMC6
  hgvsc: ENST00000392335.2:c.800T>A
  hgvsp: ENSP00000376147.2:p.Ile267Asn
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444317
  ensembl transcript: ENST00000545091
  gene symbol: ARMC6
  hgvsc: ENST00000545091.1:c.*585T>A
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444156
  ensembl transcript: ENST00000535612
  gene symbol: ARMC6
  hgvsc: ENST00000535612.1:c.875T>A
  hgvsp: ENSP00000444156.1:p.Ile292Asn
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444341
  ensembl transcript: ENST00000546344
  gene symbol: ARMC6
  hgvsc: ENST00000546344.1:c.596T>A
  hgvsp: ENSP00000444341.1:p.Ile199Asn
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000269932
  ensembl transcript: ENST00000269932
  gene symbol: ARMC6
  hgvsc: ENST00000269932.6:c.800T>A
  hgvsp: ENSP00000269932.6:p.Ile267Asn
  variant of: http://identifiers.org/hgnc/25049
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 850
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8767
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1441
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13333
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 728
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23272
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2894
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4986
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2576
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2895
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1273
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5285
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 292
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 158
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32203
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 267
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Ile292Asn
num of homozygotes: 0
population: South Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
population: European (Finnish)
reference allele: T
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP

19-19164983-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 19164983
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 19164983
    reference: chr 19
allele count: 1888
allele frequency: 1.635821723157968e-2
allele num: 115416
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000269932
  ensembl transcript: ENST00000269932
  gene symbol: ARMC6
  hgvsc: ENST00000269932.6:c.801C>T
  hgvsp: ENST00000269932.6:c.801C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000376148
  ensembl transcript: ENST00000392336
  gene symbol: ARMC6
  hgvsc: ENST00000392336.3:c.876C>T
  hgvsp: ENST00000392336.3:c.876C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444156
  ensembl transcript: ENST00000535612
  gene symbol: ARMC6
  hgvsc: ENST00000535612.1:c.876C>T
  hgvsp: ENST00000535612.1:c.876C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444341
  ensembl transcript: ENST00000546344
  gene symbol: ARMC6
  hgvsc: ENST00000546344.1:c.597C>T
  hgvsp: ENST00000546344.1:c.597C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000376147
  ensembl transcript: ENST00000392335
  gene symbol: ARMC6
  hgvsc: ENST00000392335.2:c.801C>T
  hgvsp: ENST00000392335.2:c.801C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444317
  ensembl transcript: ENST00000545091
  gene symbol: ARMC6
  hgvsc: ENST00000545091.1:c.*586C>T
  variant of: http://identifiers.org/hgnc/25049
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2759
  bin: 7.5e0
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 4701
  bin: 3.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 1148
  bin: 9.75e1
  variant carriers: 1102
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 6.75e1
  variant carriers: 64
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 6.25e1
  variant carriers: 61
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 8.75e1
  variant carriers: 103
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 7.75e1
  variant carriers: 86
genotype depth: GenotypeDepth
  all individuals: 23118
  bin: 2.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 1.75e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 13102
  bin: 3.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 738
  bin: 1.25e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 7.25e1
  variant carriers: 75
genotype depth: GenotypeDepth
  all individuals: 8753
  bin: 2.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 721
  bin: 5.25e1
  variant carriers: 28
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.25e1
  variant carriers: 98
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 8.25e1
  variant carriers: 91
genotype depth: GenotypeDepth
  all individuals: 2356
  bin: 4.25e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 1247
  bin: 4.75e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 5.75e1
  variant carriers: 40
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 162
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 282
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3169
  bin: 7.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 887
  bin: 8.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 256
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6013
  bin: 9.75e1
  variant carriers: 1861
hgvs: p.Ile292Ile
num of homozygotes: 23
population: Latino
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: C
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ

19-19164988-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 19164988
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 19164988
    reference: chr 19
allele count: 1
allele frequency: 8.597121683660311e-6
allele num: 116318
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444341
  ensembl transcript: ENST00000546344
  gene symbol: ARMC6
  hgvsc: ENST00000546344.1:c.602G>C
  hgvsp: ENSP00000444341.1:p.Ser201Thr
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000376147
  ensembl transcript: ENST00000392335
  gene symbol: ARMC6
  hgvsc: ENST00000392335.2:c.806G>C
  hgvsp: ENSP00000376147.2:p.Ser269Thr
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000376148
  ensembl transcript: ENST00000392336
  gene symbol: ARMC6
  hgvsc: ENST00000392336.3:c.881G>C
  hgvsp: ENSP00000376148.3:p.Ser294Thr
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000269932
  ensembl transcript: ENST00000269932
  gene symbol: ARMC6
  hgvsc: ENST00000269932.6:c.806G>C
  hgvsp: ENSP00000269932.6:p.Ser269Thr
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444156
  ensembl transcript: ENST00000535612
  gene symbol: ARMC6
  hgvsc: ENST00000535612.1:c.881G>C
  hgvsp: ENSP00000444156.1:p.Ser294Thr
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444317
  ensembl transcript: ENST00000545091
  gene symbol: ARMC6
  hgvsc: ENST00000545091.1:c.*591G>C
  variant of: http://identifiers.org/hgnc/25049
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2396
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4879
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23925
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 715
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1260
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2412
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9390
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13587
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2405
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 125
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3274
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33662
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 164
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 249
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4269
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 275
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Ser294Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Latino
population: Other
population: European (Finnish)
population: African
reference allele: G
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: DP

19-19164989-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 19164989
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 19164989
    reference: chr 19
allele count: 2
allele frequency: 1.718094976290289e-5
allele num: 116408
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000376148
  ensembl transcript: ENST00000392336
  gene symbol: ARMC6
  hgvsc: ENST00000392336.3:c.882C>T
  hgvsp: ENST00000392336.3:c.882C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000269932
  ensembl transcript: ENST00000269932
  gene symbol: ARMC6
  hgvsc: ENST00000269932.6:c.807C>T
  hgvsp: ENST00000269932.6:c.807C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444317
  ensembl transcript: ENST00000545091
  gene symbol: ARMC6
  hgvsc: ENST00000545091.1:c.*592C>T
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000376147
  ensembl transcript: ENST00000392335
  gene symbol: ARMC6
  hgvsc: ENST00000392335.2:c.807C>T
  hgvsp: ENST00000392335.2:c.807C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444341
  ensembl transcript: ENST00000546344
  gene symbol: ARMC6
  hgvsc: ENST00000546344.1:c.603C>T
  hgvsp: ENST00000546344.1:c.603C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444156
  ensembl transcript: ENST00000535612
  gene symbol: ARMC6
  hgvsc: ENST00000535612.1:c.882C>T
  hgvsp: ENST00000535612.1:c.882C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25049
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1260
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2413
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13593
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23969
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4879
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9425
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 666
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2281
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 715
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1213
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4269
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 136
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 172
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 106
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 914
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 249
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 276
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2292
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Ser294Ser
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum

19-19164995-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 19164995
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 19164995
    reference: chr 19
allele count: 1
allele frequency: 8.503690601721147e-6
allele num: 117596
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000269932
  ensembl transcript: ENST00000269932
  gene symbol: ARMC6
  hgvsc: ENST00000269932.6:c.813C>T
  hgvsp: ENST00000269932.6:c.813C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444317
  ensembl transcript: ENST00000545091
  gene symbol: ARMC6
  hgvsc: ENST00000545091.1:c.*598C>T
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000376148
  ensembl transcript: ENST00000392336
  gene symbol: ARMC6
  hgvsc: ENST00000392336.3:c.888C>T
  hgvsp: ENST00000392336.3:c.888C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000376147
  ensembl transcript: ENST00000392335
  gene symbol: ARMC6
  hgvsc: ENST00000392335.2:c.813C>T
  hgvsp: ENST00000392335.2:c.813C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444156
  ensembl transcript: ENST00000535612
  gene symbol: ARMC6
  hgvsc: ENST00000535612.1:c.888C>T
  hgvsp: ENST00000535612.1:c.888C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444341
  ensembl transcript: ENST00000546344
  gene symbol: ARMC6
  hgvsc: ENST00000546344.1:c.609C>T
  hgvsp: ENST00000546344.1:c.609C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25049
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1260
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2412
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 716
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13601
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24059
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4880
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1806
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9989
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4270
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3280
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 202
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1214
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 168
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34067
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2788
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 159
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Leu296Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP

19-19165011-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 19165011
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 19165011
    reference: chr 19
allele count: 1
allele frequency: 8.394050297149381e-6
allele num: 119132
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444341
  ensembl transcript: ENST00000546344
  gene symbol: ARMC6
  hgvsc: ENST00000546344.1:c.625C>T
  hgvsp: ENSP00000444341.1:p.Arg209Cys
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000269932
  ensembl transcript: ENST00000269932
  gene symbol: ARMC6
  hgvsc: ENST00000269932.6:c.829C>T
  hgvsp: ENSP00000269932.6:p.Arg277Cys
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000376148
  ensembl transcript: ENST00000392336
  gene symbol: ARMC6
  hgvsc: ENST00000392336.3:c.904C>T
  hgvsp: ENSP00000376148.3:p.Arg302Cys
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444317
  ensembl transcript: ENST00000545091
  gene symbol: ARMC6
  hgvsc: ENST00000545091.1:c.*614C>T
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444156
  ensembl transcript: ENST00000535612
  gene symbol: ARMC6
  hgvsc: ENST00000535612.1:c.904C>T
  hgvsp: ENSP00000444156.1:p.Arg302Cys
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000376147
  ensembl transcript: ENST00000392335
  gene symbol: ARMC6
  hgvsc: ENST00000392335.2:c.829C>T
  hgvsp: ENSP00000376147.2:p.Arg277Cys
  variant of: http://identifiers.org/hgnc/25049
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4880
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2413
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1064
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 716
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24426
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13631
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10613
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1261
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1119
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2797
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35167
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 95
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 119
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 102
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Arg302Cys
num of homozygotes: 0
population: Other
population: South Asian
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP

19-19165012-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 19165012
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 19165012
    reference: chr 19
allele count: 1
allele frequency: 8.381808123648433e-6
allele num: 119306
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000376148
  ensembl transcript: ENST00000392336
  gene symbol: ARMC6
  hgvsc: ENST00000392336.3:c.905G>T
  hgvsp: ENSP00000376148.3:p.Arg302Leu
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000269932
  ensembl transcript: ENST00000269932
  gene symbol: ARMC6
  hgvsc: ENST00000269932.6:c.830G>T
  hgvsp: ENSP00000269932.6:p.Arg277Leu
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444341
  ensembl transcript: ENST00000546344
  gene symbol: ARMC6
  hgvsc: ENST00000546344.1:c.626G>T
  hgvsp: ENSP00000444341.1:p.Arg209Leu
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444317
  ensembl transcript: ENST00000545091
  gene symbol: ARMC6
  hgvsc: ENST00000545091.1:c.*615G>T
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444156
  ensembl transcript: ENST00000535612
  gene symbol: ARMC6
  hgvsc: ENST00000535612.1:c.905G>T
  hgvsp: ENSP00000444156.1:p.Arg302Leu
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000376147
  ensembl transcript: ENST00000392335
  gene symbol: ARMC6
  hgvsc: ENST00000392335.2:c.830G>T
  hgvsp: ENSP00000376147.2:p.Arg277Leu
  variant of: http://identifiers.org/hgnc/25049
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4877
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 992
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2411
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10702
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1260
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 715
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13635
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24455
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1050
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 115
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 127
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3293
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1212
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Arg302Leu
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: MQ
site quality: BaseQRankSum

19-19165013-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 19165013
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 19165013
    reference: chr 19
allele count: 3
allele frequency: 2.511805485783181e-5
allele num: 119436
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000269932
  ensembl transcript: ENST00000269932
  gene symbol: ARMC6
  hgvsc: ENST00000269932.6:c.831C>T
  hgvsp: ENST00000269932.6:c.831C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444317
  ensembl transcript: ENST00000545091
  gene symbol: ARMC6
  hgvsc: ENST00000545091.1:c.*616C>T
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000376148
  ensembl transcript: ENST00000392336
  gene symbol: ARMC6
  hgvsc: ENST00000392336.3:c.906C>T
  hgvsp: ENST00000392336.3:c.906C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444156
  ensembl transcript: ENST00000535612
  gene symbol: ARMC6
  hgvsc: ENST00000535612.1:c.906C>T
  hgvsp: ENST00000535612.1:c.906C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000444341
  ensembl transcript: ENST00000546344
  gene symbol: ARMC6
  hgvsc: ENST00000546344.1:c.627C>T
  hgvsp: ENST00000546344.1:c.627C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25049
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105676
  ensembl protein: ENSP00000376147
  ensembl transcript: ENST00000392335
  gene symbol: ARMC6
  hgvsc: ENST00000392335.2:c.831C>T
  hgvsp: ENST00000392335.2:c.831C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25049
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24477
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1260
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 715
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13634
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10777
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 937
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4872
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2411
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 997
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 118
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9108
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 914
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Arg302Arg
num of homozygotes: 0
reference allele: C

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

GenotypeQuality
all individuals: 164
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 135
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1516
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 277
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 317
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 304
bin: 3.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 268
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1235
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 126
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 792
bin: 2.25e1
variant carriers: 1

GenotypeQuality
all individuals: 104
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7691
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 46952
bin: 6.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6558
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 9.769441187964049e-5
allele num: 10236
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.535421643032081e-5
allele num: 66146
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16480
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8600
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.983e1

FS
type: SiteQuality
SIO_000300: 8.537000000000001e0

QD
type: SiteQuality
SIO_000300: 1.24e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.2e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.53e-1

DP
type: SiteQuality
SIO_000300: 1.574435e6

VQSLOD
type: SiteQuality
SIO_000300: 1.21e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -7.4e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 1.07e0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
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GenotypeQuality
all individuals: 47031
bin: 6.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6564
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16478
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11506
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8598
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.512264464809606e-5
allele num: 66126
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 892
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 7.45e-1

DP
type: SiteQuality
SIO_000300: 1.573953e6

QD
type: SiteQuality
SIO_000300: 1.097e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.2e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 7.54e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.31e-1

FS
type: SiteQuality
SIO_000300: 4.984e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.33e0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.162790697674419e-4
allele num: 8600
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16476
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10244
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66132
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6560
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.217e0

VQSLOD
type: SiteQuality
SIO_000300: -6.485e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.689e0

QD
type: SiteQuality
SIO_000300: 1.526e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.79e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.84e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

DP
type: SiteQuality
SIO_000300: 1.573523e6

MQRankSum
type: SiteQuality
SIO_000300: -5.08e-1

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1447
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GenotypeQuality
all individuals: 220
bin: 4.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10234
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6562
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8600
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 892
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16440
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.514233797698365e-5
allele num: 66040
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.493e1

VQSLOD
type: SiteQuality
SIO_000300: 2.28e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.163e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.029e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

DP
type: SiteQuality
SIO_000300: 1.570487e6

MQRankSum
type: SiteQuality
SIO_000300: -6.55e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 9.9e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.953e1

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
all individuals: 161
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GenotypeQuality
all individuals: 311
bin: 2.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16440
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8604
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6562
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.778994719342852e-5
allele num: 10226
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 890
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.514142087093453e-5
allele num: 66044
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 4.58e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.570288e6

MQRankSum
type: SiteQuality
SIO_000300: -7.51e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.837e0

QD
type: SiteQuality
SIO_000300: 1.173e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.76e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.76e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

MQ
type: SiteQuality
SIO_000300: 5.938e1

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6544
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16384
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.162790697674419e-4
allele num: 8600
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65896
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10192
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 884
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BaseQRankSum
type: SiteQuality
SIO_000300: -5.183e0

MQRankSum
type: SiteQuality
SIO_000300: -1.47e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.27e0

VQSLOD
type: SiteQuality
SIO_000300: 1.82e-1

FS
type: SiteQuality
SIO_000300: 5.254e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.14e-1

QD
type: SiteQuality
SIO_000300: 1.569e1

MQ
type: SiteQuality
SIO_000300: 5.944e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

DP
type: SiteQuality
SIO_000300: 1.563683e6

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10194
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8596
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11466
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.222344456667889e-4
allele num: 16362
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.518233990222573e-5
allele num: 65866
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6550
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.848e0

QD
type: SiteQuality
SIO_000300: 1.489e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.87e-1

DP
type: SiteQuality
SIO_000300: 1.562657e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.7e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 3.52e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.91e0

MQRankSum
type: SiteQuality
SIO_000300: 1.23e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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bin: 1.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10174
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.519710647092794e-5
allele num: 65802
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11456
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16322
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

VQSLOD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: 1.86e0

QD
type: SiteQuality
SIO_000300: 2.984e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.59e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.51e-1

DP
type: SiteQuality
SIO_000300: 1.55991e6

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

GenotypeQuality
all individuals: 323
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GenotypeQuality
all individuals: 380
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11444
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16290
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 9.83671060397403e-5
allele num: 10166
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65792
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6544
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.557922e6

BaseQRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: -7.7e-1

ReadPosRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: -6.815e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.172e0

MQ
type: SiteQuality
SIO_000300: 5.006e1

FS
type: SiteQuality
SIO_000300: 2.387e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

QD
type: SiteQuality
SIO_000300: 1.162e1

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 7.25e1
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 377
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 98
bin: 8.75e1
variant carriers: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16292
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10164
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6544
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.52012647452268e-5
allele num: 65784
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11444
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.72e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.45e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.555e0

MQRankSum
type: SiteQuality
SIO_000300: 3.14e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.41e-1

MQ
type: SiteQuality
SIO_000300: 5.883e1

FS
type: SiteQuality
SIO_000300: 3.965e0

QD
type: SiteQuality
SIO_000300: 1.005e1

DP
type: SiteQuality
SIO_000300: 1.557702e6

GenotypeQuality
all individuals: 232
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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variant carriers: 2

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8586
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11442
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.229256299938537e-4
allele num: 16270
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65726
num of homozygotes: 0

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6544
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.34e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.38e0

QD
type: SiteQuality
SIO_000300: 1.407e1

FS
type: SiteQuality
SIO_000300: 7.46e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.91e-1

MQ
type: SiteQuality
SIO_000300: 5.911e1

DP
type: SiteQuality
SIO_000300: 1.557546e6

VQSLOD
type: SiteQuality
SIO_000300: 1.58e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.9e-1

GenotypeQuality
all individuals: 285
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 70
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GenotypeQuality
all individuals: 7288
bin: 6.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.521977352976988e-5
allele num: 65704
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11434
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6534
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10148
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -8.86e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.9e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.556844e6

ClippingRankSum
type: SiteQuality
SIO_000300: 3.2e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -9.2e-1

QD
type: SiteQuality
SIO_000300: 9.57e0

FS
type: SiteQuality
SIO_000300: 3.729e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.11e-1

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6516
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10088
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8580
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65342
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11406
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.275100401606425e-5
allele num: 15936
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.6e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.17e-1

DP
type: SiteQuality
SIO_000300: 1.540932e6

ClippingRankSum
type: SiteQuality
SIO_000300: 4.88e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.35e-1

FS
type: SiteQuality
SIO_000300: 1.384e0

VQSLOD
type: SiteQuality
SIO_000300: 1.78e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.4e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.529e1

GenotypeQuality
all individuals: 46536
bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 87
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GenotypeQuality
all individuals: 266
bin: 4.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10080
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8580
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11402
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6516
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15910
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.539394e6

VQSLOD
type: SiteQuality
SIO_000300: 8.090000000000001e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.583e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.2e-3

FS
type: SiteQuality
SIO_000300: 2.907e0

QD
type: SiteQuality
SIO_000300: 1.208e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.09e0

MQRankSum
type: SiteQuality
SIO_000300: 6.21e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.45e0

MQ
type: SiteQuality
SIO_000300: 5.936e1

GenotypeQuality
all individuals: 1029
bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 171
bin: 4.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11366
num of homozygotes: 0

East Asian
type: Population
allele count: 3
allele frequency: 3.497318722312894e-4
allele num: 8578
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6496
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 878
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10060
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65098
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15664
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.032e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.1e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -9.28e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.94e-1

DP
type: SiteQuality
SIO_000300: 1.532163e6

VQSLOD
type: SiteQuality
SIO_000300: 8.6e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.84e-1

QD
type: SiteQuality
SIO_000300: 9.94e0

MQ
type: SiteQuality
SIO_000300: 5.944e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.749e0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 7

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 874
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11354
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15532
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 7
allele frequency: 1.076790548855525e-4
allele num: 65008
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6488
num of homozygotes: 0

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

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

QD
type: SiteQuality
SIO_000300: 1.279e1

MQRankSum
type: SiteQuality
SIO_000300: -4.87e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.23e-1

FS
type: SiteQuality
SIO_000300: 9.09e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.2e-3

VQSLOD
type: SiteQuality
SIO_000300: 7.94e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.07e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.83e0

DP
type: SiteQuality
SIO_000300: 1.526891e6

MQ
type: SiteQuality
SIO_000300: 5.936e1

GenotypeQuality
all individuals: 3364
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 311
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variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15180
num of homozygotes: 0

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6468
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9968
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.544735541275334e-5
allele num: 64736
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.8e-3

FS
type: SiteQuality
SIO_000300: 4.625e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.182e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.01e0

DP
type: SiteQuality
SIO_000300: 1.515789e6

VQSLOD
type: SiteQuality
SIO_000300: -1.199e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.42e0

MQRankSum
type: SiteQuality
SIO_000300: 2.06e-1

QD
type: SiteQuality
SIO_000300: 5.81e0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6683
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 306
bin: 8.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8566
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64658
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11322
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9966
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.606765327695561e-5
allele num: 15136
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.42e0

MQRankSum
type: SiteQuality
SIO_000300: -1.278e0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 1.52e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.17e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.9e-1

QD
type: SiteQuality
SIO_000300: 1.422e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

DP
type: SiteQuality
SIO_000300: 1.513206e6

GenotypeQuality
all individuals: 12
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 92
bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45544
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 259
bin: 3.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15028
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9946
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11310
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.548658861426005e-5
allele num: 64572
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6458
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 7.2e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.246e0

DP
type: SiteQuality
SIO_000300: 1.508045e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.27e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.719e0

QD
type: SiteQuality
SIO_000300: 1.222e1

MQRankSum
type: SiteQuality
SIO_000300: -5.659999999999999e-1

GenotypeQuality
all individuals: 75
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variant carriers: 0

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

GenotypeQuality
all individuals: 41850
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variant carriers: 0

GenotypeQuality
all individuals: 878
bin: 2.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 15
allele frequency: 2.378762409210568e-4
allele num: 63058
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13658
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11058
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9670
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8486
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6274
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.443146e6

FS
type: SiteQuality
SIO_000300: 5.69e-1

MQ
type: SiteQuality
SIO_000300: 5.956e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.2e-3

MQRankSum
type: SiteQuality
SIO_000300: 6.820000000000001e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.83e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.66e-1

QD
type: SiteQuality
SIO_000300: 1.202e1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.18e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.17e-1

GenotypeQuality
all individuals: 9577
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
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GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 318
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variant carriers: 0

GenotypeQuality
all individuals: 908
bin: 7.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8390
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13006
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61944
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6126
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 804
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 9.199632014719411e-5
allele num: 10870
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9470
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.395602e6

VQSLOD
type: SiteQuality
SIO_000300: 3.37e0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.91e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.12e-1

FS
type: SiteQuality
SIO_000300: 1.336e0

MQRankSum
type: SiteQuality
SIO_000300: 2.66e-1

MQ
type: SiteQuality
SIO_000300: 5.981e1

QD
type: SiteQuality
SIO_000300: 1.477e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.4e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.2e-2

GenotypeQuality
all individuals: 212
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12306
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 469
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1455
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GenotypeQuality
all individuals: 202
bin: 4.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 778
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9260
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12292
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5996
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.216841080554879e-4
allele num: 8218
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10618
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.650382888830209e-5
allele num: 60592
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-3

VQSLOD
type: SiteQuality
SIO_000300: -1.38e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.33e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.11e-1

DP
type: SiteQuality
SIO_000300: 1.33517e6

QD
type: SiteQuality
SIO_000300: 7.62e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.4e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.37e-1

GenotypeQuality
all individuals: 170
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 76
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variant carriers: 1

GenotypeQuality
all individuals: 2376
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 52
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 715
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 357
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GenotypeQuality
all individuals: 415
bin: 5.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7770
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5584
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9868
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10672
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 56934
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 724
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.148633126579371e-4
allele num: 8706
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.147e1

FS
type: SiteQuality
SIO_000300: 5.31e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.6e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -9.379999999999999e-1

QD
type: SiteQuality
SIO_000300: 1.78e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.51e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.679999999999999e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.843e0

DP
type: SiteQuality
SIO_000300: 1.169242e6

VQSLOD
type: SiteQuality
SIO_000300: -7.181999999999999e-1

GenotypeQuality
all individuals: 76
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 150
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2660
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GenotypeQuality
all individuals: 836
bin: 5.25e1
variant carriers: 0

African
type: Population
allele count: 2
allele frequency: 2.358490566037736e-4
allele num: 8480
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7616
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.602565026298725e-5
allele num: 55516
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9598
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 9.968102073365231e-5
allele num: 10032
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 704
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5410
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.1e0

QD
type: SiteQuality
SIO_000300: 2.223e1

MQRankSum
type: SiteQuality
SIO_000300: -3.59e-1

DP
type: SiteQuality
SIO_000300: 1.116016e6

ClippingRankSum
type: SiteQuality
SIO_000300: -6.0e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 2.694e0

VQSLOD
type: SiteQuality
SIO_000300: -1.4e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.6e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 1.45e0

GenotypeQuality
all individuals: 32
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variant carriers: 0

GenotypeQuality
all individuals: 375
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 75
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 855
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GenotypeQuality
all individuals: 24198
bin: 6.25e1
variant carriers: 0

Latino
type: Population
allele count: 2
allele frequency: 2.107037505267594e-4
allele num: 9492
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5380
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.022076860179886e-4
allele num: 9784
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.189060642092747e-4
allele num: 8410
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 690
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 55134
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7566
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -3.6e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 2.532e0

QD
type: SiteQuality
SIO_000300: 1.243e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-3

VQSLOD
type: SiteQuality
SIO_000300: 1.7e0

DP
type: SiteQuality
SIO_000300: 1.100705e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.23e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.36e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.485e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1359
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variant carriers: 0

GenotypeQuality
all individuals: 3359
bin: 3.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 4.073651621313345e-5
allele num: 49096
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8018
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 614
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7628
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6868
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4840
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 2.403268445085316e-4
allele num: 8322
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 9.68e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 8.88628e5

VQSLOD
type: SiteQuality
SIO_000300: 4.01e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.06e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.06e-1

QD
type: SiteQuality
SIO_000300: 1.479e1

MQRankSum
type: SiteQuality
SIO_000300: -4.06e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.7e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.06e-1

GenotypeQuality
all individuals: 876
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 154
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GenotypeQuality
all individuals: 61
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GenotypeQuality
all individuals: 18
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GenotypeQuality
all individuals: 277
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GenotypeQuality
all individuals: 149
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GenotypeQuality
all individuals: 369
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GenotypeQuality
all individuals: 69
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variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6782
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6394
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4414
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: 7002
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.216017373576209e-5
allele num: 45126
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7624
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.331e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.82e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.31e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.31e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.31e-1

MQ
type: SiteQuality
SIO_000300: 5.829e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.09e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 7.78868e5

QD
type: SiteQuality
SIO_000300: 4.42e0

GenotypeQuality
all individuals: 273
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1501
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5887
bin: 7.5e0
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GenotypeQuality
all individuals: 62
bin: 8.25e1
variant carriers: 3

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 121
bin: 9.75e1
variant carriers: 54

GenotypeQuality
all individuals: 17
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 8.75e1
variant carriers: 2

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4232
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 528
num of homozygotes: 0

African
type: Population
allele count: 58
allele frequency: 8.745476477683957e-3
allele num: 6632
num of homozygotes: 1

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 43126
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6114
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 2.75330396475771e-4
allele num: 7264
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6270
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 7.27696e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.56e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 5.52e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.18e-2

MQRankSum
type: SiteQuality
SIO_000300: 9.2e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.041e0

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.345e1

GenotypeQuality
all individuals: 605
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 29

GenotypeQuality
all individuals: 90
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6901
bin: 7.5e0
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 24
allele frequency: 6.007810153199159e-4
allele num: 39948
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 476
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6620
num of homozygotes: 0

African
type: Population
allele count: 4
allele frequency: 6.613756613756613e-4
allele num: 6048
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5724
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 3.549875754348598e-4
allele num: 5634
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3806
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 3.59e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.49e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.61e0

FS
type: SiteQuality
SIO_000300: 8.43e-1

DP
type: SiteQuality
SIO_000300: 6.82032e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.37e-1

QD
type: SiteQuality
SIO_000300: 1.244e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.94e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.3e-2

GenotypeQuality
all individuals: 77
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7018
bin: 7.5e0
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 16
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variant carriers: 0

GenotypeQuality
all individuals: 4622
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variant carriers: 0

GenotypeQuality
all individuals: 4028
bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 5.047445992327882e-5
allele num: 39624
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6538
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.656177542232527e-4
allele num: 6038
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 478
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5680
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5516
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 1.773e0

MQRankSum
type: SiteQuality
SIO_000300: 2.59e-1

QD
type: SiteQuality
SIO_000300: 1.296e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.28e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.56e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 7.62e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.63e-1

DP
type: SiteQuality
SIO_000300: 6.78719e5

BaseQRankSum
type: SiteQuality
SIO_000300: -6.830000000000001e-1

GenotypeQuality
all individuals: 2375
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 421
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variant carriers: 0

GenotypeQuality
all individuals: 120
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variant carriers: 0

GenotypeQuality
all individuals: 3472
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4234
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 428
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variant carriers: 0

GenotypeQuality
all individuals: 32070
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 9.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5634
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 466
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 5.111690436027194e-5
allele num: 39126
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5432
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5914
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3732
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6478
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.896e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.256e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.56e-2

MQRankSum
type: SiteQuality
SIO_000300: -4.52e-1

FS
type: SiteQuality
SIO_000300: 1.404e0

VQSLOD
type: SiteQuality
SIO_000300: -9.173e-1

QD
type: SiteQuality
SIO_000300: 1.204e1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.97e-1

DP
type: SiteQuality
SIO_000300: 6.64388e5

BaseQRankSum
type: SiteQuality
SIO_000300: 1.15e0

GenotypeQuality
all individuals: 287
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 430
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30042
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variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2420
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variant carriers: 0

GenotypeQuality
all individuals: 47
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variant carriers: 0

GenotypeQuality
all individuals: 4607
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2233
bin: 1.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3346
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.82882223847842e-4
allele num: 5468
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5244
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 438
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 36128
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4730
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5858
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.216e1

FS
type: SiteQuality
SIO_000300: 1.078e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -3.34e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.67e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.5e-1

VQSLOD
type: SiteQuality
SIO_000300: -5.177e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.39e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.48e-1

DP
type: SiteQuality
SIO_000300: 6.38017e5

GenotypeQuality
all individuals: 1046
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 430
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 454
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variant carriers: 0

GenotypeQuality
all individuals: 287
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
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variant carriers: 0

GenotypeQuality
all individuals: 4191
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variant carriers: 0

GenotypeQuality
all individuals: 61
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variant carriers: 0

GenotypeQuality
all individuals: 340
bin: 5.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 438
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5468
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.906941266209001e-4
allele num: 5244
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4730
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.707067258449983e-4
allele num: 5858
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3346
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 36128
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 1.078e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.48e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.67e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.39e-2

VQSLOD
type: SiteQuality
SIO_000300: -5.177e-1

DP
type: SiteQuality
SIO_000300: 6.38017e5

MQRankSum
type: SiteQuality
SIO_000300: -3.34e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.5e-1

QD
type: SiteQuality
SIO_000300: 1.216e1

GenotypeQuality
all individuals: 430
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 81
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variant carriers: 0

GenotypeQuality
all individuals: 16
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GenotypeQuality
all individuals: 1691
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GenotypeQuality
all individuals: 8248
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GenotypeQuality
all individuals: 2233
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variant carriers: 0

GenotypeQuality
all individuals: 47
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GenotypeQuality
all individuals: 4607
bin: 2.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3346
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5468
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4730
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 438
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.767936226749336e-5
allele num: 36128
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5244
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5858
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.39e-2

MQRankSum
type: SiteQuality
SIO_000300: -3.34e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.5e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.67e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.48e-1

VQSLOD
type: SiteQuality
SIO_000300: -5.177e-1

FS
type: SiteQuality
SIO_000300: 1.078e0

DP
type: SiteQuality
SIO_000300: 6.38017e5

QD
type: SiteQuality
SIO_000300: 1.216e1

GenotypeQuality
all individuals: 4318
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1977
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variant carriers: 0

GenotypeQuality
all individuals: 29791
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 129
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GenotypeQuality
all individuals: 17
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GenotypeQuality
all individuals: 70
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variant carriers: 4

GenotypeQuality
all individuals: 52
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variant carriers: 0

GenotypeQuality
all individuals: 247
bin: 4.75e1
variant carriers: 0

Latino
type: Population
allele count: 2
allele frequency: 3.825554705432288e-4
allele num: 5228
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 400
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.910584638899503e-4
allele num: 5234
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 32912
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4790
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3278
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4062
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.25e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.12e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.43e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.12e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.09e-2

FS
type: SiteQuality
SIO_000300: 1.556e0

DP
type: SiteQuality
SIO_000300: 5.85306e5

QD
type: SiteQuality
SIO_000300: 9.82e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.701e0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 221
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GenotypeQuality
all individuals: 2920
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GenotypeQuality
all individuals: 90
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GenotypeQuality
all individuals: 267
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GenotypeQuality
all individuals: 67
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variant carriers: 1

GenotypeQuality
all individuals: 16
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GenotypeQuality
all individuals: 4372
bin: 3.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5050
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3922
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 31908
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 2.130379207498935e-4
allele num: 4694
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 392
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5074
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3218
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.518e0

VQSLOD
type: SiteQuality
SIO_000300: -1.112e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.15e0

DP
type: SiteQuality
SIO_000300: 5.71674e5

FS
type: SiteQuality
SIO_000300: 4.26e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.14e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -5.37e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.266e0

QD
type: SiteQuality
SIO_000300: 7.71e0

GenotypeQuality
all individuals: 4659
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variant carriers: 0

GenotypeQuality
all individuals: 4422
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25513
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variant carriers: 0

GenotypeQuality
all individuals: 69
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variant carriers: 3

GenotypeQuality
all individuals: 4012
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GenotypeQuality
all individuals: 64
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GenotypeQuality
all individuals: 43
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GenotypeQuality
all individuals: 60
bin: 5.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4436
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 374
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4850
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4598
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3624
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2982
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.345600535296086e-5
allele num: 29890
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 9.22e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.5e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.21e-1

FS
type: SiteQuality
SIO_000300: 1.854e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.31e-2

MQ
type: SiteQuality
SIO_000300: 6.119e1

BaseQRankSum
type: SiteQuality
SIO_000300: 9.22e-1

DP
type: SiteQuality
SIO_000300: 5.52584e5

VQSLOD
type: SiteQuality
SIO_000300: 8.25e-1

QD
type: SiteQuality
SIO_000300: 2.068e1

GenotypeQuality
all individuals: 63
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1029
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4406
bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 419
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 37
bin: 5.75e1
variant carriers: 0

East Asian
type: Population
allele count: 1
allele frequency: 2.331002331002331e-4
allele num: 4290
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2866
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3466
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 352
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4358
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 28642
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4694
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -2.661e0

FS
type: SiteQuality
SIO_000300: 2.233e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.87e0

DP
type: SiteQuality
SIO_000300: 5.41899e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.39e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 3.9e-1

QD
type: SiteQuality
SIO_000300: 2.174e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.85e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.383e0

GenotypeQuality
all individuals: 441
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1903
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 142
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.616636528028933e-5
allele num: 27650
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2784
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4128
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4182
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 340
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4552
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3316
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 4.06e-1

DP
type: SiteQuality
SIO_000300: 5.38385e5

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.33e-2

QD
type: SiteQuality
SIO_000300: 1.295e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.889999999999999e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.47e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.54e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.21e-1

GenotypeQuality
all individuals: 1903
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4290
bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 1

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 74
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 181
bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 27650
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3316
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 340
num of homozygotes: 0

East Asian
type: Population
allele count: 4
allele frequency: 9.689922480620155e-4
allele num: 4128
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4182
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2784
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4552
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.54e0

DP
type: SiteQuality
SIO_000300: 5.38385e5

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 4.06e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.33e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -4.21e-1

QD
type: SiteQuality
SIO_000300: 1.295e1

VQSLOD
type: SiteQuality
SIO_000300: 5.47e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.889999999999999e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 459
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 8.25e1
variant carriers: 1

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 66
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variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 490
bin: 4.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3270
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4104
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.659250585480094e-5
allele num: 27328
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 328
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4090
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2756
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4540
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.05e0

QD
type: SiteQuality
SIO_000300: 1.219e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.25e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -2.547e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.6e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.2e0

DP
type: SiteQuality
SIO_000300: 5.34891e5

BaseQRankSum
type: SiteQuality
SIO_000300: -5.55e-1

GenotypeQuality
all individuals: 11734
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 8523
bin: 1.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 613
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variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 144
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4297
bin: 2.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 24934
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 316
num of homozygotes: 0

East Asian
type: Population
allele count: 3
allele frequency: 7.982969664715274e-4
allele num: 3758
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2512
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3622
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2954
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4234
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.48e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.44e-1

QD
type: SiteQuality
SIO_000300: 7.79e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 5.25212e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.71e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -2.037e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.35e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.06e0

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

GenotypeQuality
all individuals: 11822
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 143
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 564
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 613
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 19345
bin: 2.25e1
variant carriers: 2

Other
type: Population
allele count: 1
allele frequency: 3.164556962025316e-3
allele num: 316
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4316
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 7.913896802785692e-5
allele num: 25272
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3694
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2544
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3808
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2980
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 6.5e-2

FS
type: SiteQuality
SIO_000300: 3.68e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.25e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.22e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.39e-1

DP
type: SiteQuality
SIO_000300: 5.26263e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.63e-2

QD
type: SiteQuality
SIO_000300: 1.289e1

VQSLOD
type: SiteQuality
SIO_000300: 6.03e-1

GenotypeQuality
all individuals: 8218
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 498
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2270
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1022
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5869
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 654
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 534
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1385
bin: 9.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6606
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8524
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.715356458079135e-5
allele num: 11474
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.107174490699734e-4
allele num: 9032
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10180
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 788
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63870
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.44e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.2e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 6.81e-1

DP
type: SiteQuality
SIO_000300: 1.755726e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.67e-1

FS
type: SiteQuality
SIO_000300: 8.765000000000001e0

QD
type: SiteQuality
SIO_000300: 1.553e1

VQSLOD
type: SiteQuality
SIO_000300: -1.37e-2

MQRankSum
type: SiteQuality
SIO_000300: 4.09e-1

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 537
bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 2

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 8378
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3340
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1023
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28264
bin: 6.25e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.106439477760567e-4
allele num: 9038
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 788
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63894
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10186
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.712319219376198e-5
allele num: 11478
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6606
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8526
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.44e-1

DP
type: SiteQuality
SIO_000300: 1.758709e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.14e0

VQSLOD
type: SiteQuality
SIO_000300: 2.8e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.24e-1

FS
type: SiteQuality
SIO_000300: 7.111e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 3.89e0

QD
type: SiteQuality
SIO_000300: 1.593e1

GenotypeQuality
all individuals: 1518
bin: 2.5e0
variant carriers: 2

GenotypeQuality
all individuals: 3122
bin: 7.75e1
variant carriers: 18

GenotypeQuality
all individuals: 7976
bin: 6.75e1
variant carriers: 10

GenotypeQuality
all individuals: 402
bin: 3.25e1
variant carriers: 10

GenotypeQuality
all individuals: 1252
bin: 9.25e1
variant carriers: 10

GenotypeQuality
all individuals: 928
bin: 8.75e1
variant carriers: 5

GenotypeQuality
all individuals: 334
bin: 5.25e1
variant carriers: 6

GenotypeQuality
all individuals: 2045
bin: 8.25e1
variant carriers: 6

East Asian
type: Population
allele count: 9
allele frequency: 1.06508875739645e-3
allele num: 8450
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9038
num of homozygotes: 0

African
type: Population
allele count: 34
allele frequency: 3.54388159266208e-3
allele num: 9594
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 36
allele frequency: 5.926901547579849e-3
allele num: 6074
num of homozygotes: 0

Latino
type: Population
allele count: 8
allele frequency: 7.027406886858749e-4
allele num: 11384
num of homozygotes: 0

Other
type: Population
allele count: 5
allele frequency: 6.793478260869565e-3
allele num: 736
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 131
allele frequency: 2.109025340502946e-3
allele num: 62114
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.744014e6

BaseQRankSum
type: SiteQuality
SIO_000300: -3.583e0

VQSLOD
type: SiteQuality
SIO_000300: -8.930999999999999e0

MQ
type: SiteQuality
SIO_000300: 5.923e1

FS
type: SiteQuality
SIO_000300: 4.1475e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.08e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.09e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.77e-1

QD
type: SiteQuality
SIO_000300: 1.17e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.82e-1

GenotypeQuality
all individuals: 347
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 108
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 952
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1291
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variant carriers: 0

GenotypeQuality
all individuals: 112
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variant carriers: 0

GenotypeQuality
all individuals: 2139
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8569
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5351
bin: 9.75e1
variant carriers: 1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8528
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.103509159126021e-4
allele num: 9062
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 788
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10192
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63960
num of homozygotes: 0

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.719e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.33e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.196e0

FS
type: SiteQuality
SIO_000300: 7.068e0

QD
type: SiteQuality
SIO_000300: 1.511e1

VQSLOD
type: SiteQuality
SIO_000300: 1.02e0

MQRankSum
type: SiteQuality
SIO_000300: 1.14e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-4

DP
type: SiteQuality
SIO_000300: 1.732299e6

MQ
type: SiteQuality
SIO_000300: 6.061e1

GenotypeQuality
all individuals: 75
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 149
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2722
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 151
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8564
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3245
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 948
bin: 8.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 788
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9104
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.809691975671964e-5
allele num: 10194
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.345765892563922e-4
allele num: 8526
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.688672168042011e-5
allele num: 63984
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: 2.3e-2

MQ
type: SiteQuality
SIO_000300: 5.959e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.2e-3

VQSLOD
type: SiteQuality
SIO_000300: 2.15e0

DP
type: SiteQuality
SIO_000300: 1.736769e6

MQRankSum
type: SiteQuality
SIO_000300: -2.78e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.52e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.05e-1

QD
type: SiteQuality
SIO_000300: 1.395e1

GenotypeQuality
all individuals: 76
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 5.25e1
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2737
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 296
bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2131
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 949
bin: 8.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8534
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9120
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 9.800078400627205e-5
allele num: 10204
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 788
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.562548829650927e-5
allele num: 63998
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.93e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.38e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.46e0

FS
type: SiteQuality
SIO_000300: 6.59e-1

QD
type: SiteQuality
SIO_000300: 1.17e1

MQRankSum
type: SiteQuality
SIO_000300: 4.11e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -2.125e0

DP
type: SiteQuality
SIO_000300: 1.737069e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 1280
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 163
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variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30811
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
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variant carriers: 0

GenotypeQuality
all individuals: 5333
bin: 9.75e1
variant carriers: 2

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9310
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.56011107990889e-5
allele num: 64098
num of homozygotes: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.169864295741694e-4
allele num: 8548
num of homozygotes: 0

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: 2.3e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.77e-1

QD
type: SiteQuality
SIO_000300: 1.123e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.162e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.978e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.7e-3

VQSLOD
type: SiteQuality
SIO_000300: 6.860000000000001e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.04e0

DP
type: SiteQuality
SIO_000300: 1.745932e6

GenotypeQuality
all individuals: 132
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5336
bin: 9.75e1
variant carriers: 6

GenotypeQuality
all individuals: 1279
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 941
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 3
allele frequency: 2.611420612813371e-4
allele num: 11488
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 1
allele frequency: 1.067463706233988e-4
allele num: 9368
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.120124804992199e-5
allele num: 64100
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8550
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.5e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 1.85e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 1.57e0

FS
type: SiteQuality
SIO_000300: 6.6e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.62e-1

QD
type: SiteQuality
SIO_000300: 1.327e1

DP
type: SiteQuality
SIO_000300: 1.747142e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.32e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.009e0

GenotypeQuality
all individuals: 2863
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2128
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 206
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1279
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8613
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 201
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variant carriers: 0

GenotypeQuality
all individuals: 160
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 942
bin: 8.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9476
num of homozygotes: 0

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

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.233831000841567e-5
allele num: 64166
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 5.22e-1

DP
type: SiteQuality
SIO_000300: 1.749999e6

FS
type: SiteQuality
SIO_000300: 1.43e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.1e-3

QD
type: SiteQuality
SIO_000300: 1.236e1

VQSLOD
type: SiteQuality
SIO_000300: 1.95e0

MQ
type: SiteQuality
SIO_000300: 5.975e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.97e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.16e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.109e0

GenotypeQuality
all individuals: 30932
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3268
bin: 7.75e1
variant carriers: 5

GenotypeQuality
all individuals: 196
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 5.75e1
variant carriers: 3

GenotypeQuality
all individuals: 5405
bin: 9.75e1
variant carriers: 109

GenotypeQuality
all individuals: 1275
bin: 9.25e1
variant carriers: 3

GenotypeQuality
all individuals: 65
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 5.25e1
variant carriers: 3

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64216
num of homozygotes: 0

South Asian
type: Population
allele count: 105
allele frequency: 1.088308457711443e-2
allele num: 9648
num of homozygotes: 1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8566
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 796
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: 10228
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.700191404210893e-5
allele num: 11494
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.107e0

DP
type: SiteQuality
SIO_000300: 1.756239e6

VQSLOD
type: SiteQuality
SIO_000300: 4.0e0

MQRankSum
type: SiteQuality
SIO_000300: 2.07e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.76e-2

FS
type: SiteQuality
SIO_000300: 6.36e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.66e-1

QD
type: SiteQuality
SIO_000300: 1.253e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.87e-1

GenotypeQuality
all individuals: 209
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 89
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variant carriers: 0

GenotypeQuality
all individuals: 76
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variant carriers: 0

GenotypeQuality
all individuals: 1018
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variant carriers: 0

GenotypeQuality
all individuals: 939
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31023
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1275
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2127
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 4.25e1
variant carriers: 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: 8580
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 804
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11496
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9838
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.111774956435151e-5
allele num: 64272
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -8.688e-1

FS
type: SiteQuality
SIO_000300: 3.937e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.228e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.1e-3

QD
type: SiteQuality
SIO_000300: 1.728e1

MQ
type: SiteQuality
SIO_000300: 5.853e1

MQRankSum
type: SiteQuality
SIO_000300: 6.22e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.23e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.0e-2

DP
type: SiteQuality
SIO_000300: 1.755708e6

GenotypeQuality
all individuals: 8634
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 216
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
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variant carriers: 0

GenotypeQuality
all individuals: 3417
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variant carriers: 0

GenotypeQuality
all individuals: 1274
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variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5322
bin: 9.75e1
variant carriers: 29

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.555597038143239e-5
allele num: 64284
num of homozygotes: 0

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

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8588
num of homozygotes: 0

Other
type: Population
allele count: 2
allele frequency: 2.487562189054726e-3
allele num: 804
num of homozygotes: 0

South Asian
type: Population
allele count: 23
allele frequency: 2.316680096696213e-3
allele num: 9928
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.78e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.48e-1

DP
type: SiteQuality
SIO_000300: 1.757156e6

VQSLOD
type: SiteQuality
SIO_000300: 3.82e0

FS
type: SiteQuality
SIO_000300: 6.24e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 8.1e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 3.61e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.245e1

GenotypeQuality
all individuals: 252
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 906
bin: 7.5e0
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5293
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1274
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variant carriers: 0

GenotypeQuality
all individuals: 31046
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GenotypeQuality
all individuals: 13
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GenotypeQuality
all individuals: 940
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GenotypeQuality
all individuals: 2754
bin: 7.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8586
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.555306706482518e-5
allele num: 64296
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10248
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11498
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: 804
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.478e1

VQSLOD
type: SiteQuality
SIO_000300: -8.28e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

FS
type: SiteQuality
SIO_000300: 4.752e0

MQRankSum
type: SiteQuality
SIO_000300: -1.587e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.459e0

DP
type: SiteQuality
SIO_000300: 1.756859e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.35e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.257e0

GenotypeQuality
all individuals: 1274
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
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GenotypeQuality
all individuals: 3408
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GenotypeQuality
all individuals: 3272
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GenotypeQuality
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GenotypeQuality
all individuals: 255
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 5292
bin: 9.75e1
variant carriers: 2

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10250
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.110129692408174e-5
allele num: 64306
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11498
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: 804
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8586
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.757846e6

MQRankSum
type: SiteQuality
SIO_000300: 1.07e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.54e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.06e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.1e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.95e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.44e-1

MQ
type: SiteQuality
SIO_000300: 5.904e1

QD
type: SiteQuality
SIO_000300: 1.182e1

GenotypeQuality
all individuals: 31074
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3271
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 940
bin: 8.75e1
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GenotypeQuality
all individuals: 2754
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variant carriers: 0

GenotypeQuality
all individuals: 26
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GenotypeQuality
all individuals: 5290
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GenotypeQuality
all individuals: 44
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GenotypeQuality
all individuals: 1273
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11500
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: 1.553663538624075e-5
allele num: 64364
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 804
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10250
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10138
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: 1.35e0

MQ
type: SiteQuality
SIO_000300: 5.971e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

QD
type: SiteQuality
SIO_000300: 1.256e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.71e-1

DP
type: SiteQuality
SIO_000300: 1.758564e6

MQRankSum
type: SiteQuality
SIO_000300: 3.8e-2

FS
type: SiteQuality
SIO_000300: 6.401e0

VQSLOD
type: SiteQuality
SIO_000300: 8.85e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -8.080000000000001e-1

GenotypeQuality
all individuals: 305
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1272
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3274
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2752
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 939
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2131
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 103
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 5.75e1
variant carriers: 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: 10254
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 2.87411381490707e-4
allele num: 10438
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8606
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.551879325863621e-5
allele num: 64438
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11504
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 1.27e0

QD
type: SiteQuality
SIO_000300: 1.218e1

VQSLOD
type: SiteQuality
SIO_000300: 1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.09e0

MQRankSum
type: SiteQuality
SIO_000300: 1.26e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

FS
type: SiteQuality
SIO_000300: 9.367000000000001e0

DP
type: SiteQuality
SIO_000300: 1.761875e6

ClippingRankSum
type: SiteQuality
SIO_000300: -6.42e-1

MQ
type: SiteQuality
SIO_000300: 5.984e1

GenotypeQuality
all individuals: 395
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 939
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 148
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31371
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5289
bin: 9.75e1
variant carriers: 2

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: 820
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.738994935722633e-5
allele num: 10268
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.548562933597621e-5
allele num: 64576
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11516
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8614
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10848
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 3.51e0

MQRankSum
type: SiteQuality
SIO_000300: -6.7e-1

MQ
type: SiteQuality
SIO_000300: 5.66e1

QD
type: SiteQuality
SIO_000300: 1.605e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.14e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -6.34e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.59e-1

DP
type: SiteQuality
SIO_000300: 1.766539e6

FS
type: SiteQuality
SIO_000300: 1.8e0

GenotypeQuality
all individuals: 3529
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8665
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5287
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1273
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 145
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 306
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31426
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 94
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2129
bin: 8.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 820
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10270
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8614
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: 1.548227279764669e-5
allele num: 64590
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11516
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10882
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.951e1

FS
type: SiteQuality
SIO_000300: 4.838e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 5.16e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.95e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.44e0

MQRankSum
type: SiteQuality
SIO_000300: -4.76e-1

QD
type: SiteQuality
SIO_000300: 1.251e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.2e-1

DP
type: SiteQuality
SIO_000300: 1.767142e6

GenotypeQuality
all individuals: 2129
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3550
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8664
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1273
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 941
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2756
bin: 7.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8618
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11516
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 820
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: 10984
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10276
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.547891771407343e-5
allele num: 64604
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.1e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.32e-1

MQ
type: SiteQuality
SIO_000300: 5.919e1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -6.08e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.016e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.65e0

QD
type: SiteQuality
SIO_000300: 1.059e1

DP
type: SiteQuality
SIO_000300: 1.768039e6

GenotypeQuality
all individuals: 50
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3274
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 940
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8673
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5287
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2129
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1273
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 5.25e1
variant carriers: 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: 824
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10288
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11526
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11372
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8626
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.54435384235236e-5
allele num: 64752
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -1.324e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.35e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 7.3e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.773127e6

MQRankSum
type: SiteQuality
SIO_000300: 2.79e-1

QD
type: SiteQuality
SIO_000300: 6.86e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.535e0

GenotypeQuality
all individuals: 277
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3207
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8694
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2758
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3272
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5286
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 940
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 80
bin: 4.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64852
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10292
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 836
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: 8630
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11526
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 8.582217645039479e-5
allele num: 11652
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.435e0

FS
type: SiteQuality
SIO_000300: 2.028e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.5e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.07e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.274e1

VQSLOD
type: SiteQuality
SIO_000300: 1.82e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

MQRankSum
type: SiteQuality
SIO_000300: 4.89e-1

DP
type: SiteQuality
SIO_000300: 1.775593e6

GenotypeQuality
all individuals: 162
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8723
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2128
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3275
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 80
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2763
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 940
bin: 8.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12268
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: 1.537988311288834e-5
allele num: 65020
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11536
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8632
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10306
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: 8.76e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.562e0

MQRankSum
type: SiteQuality
SIO_000300: 3.42e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-3

FS
type: SiteQuality
SIO_000300: 7.14e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.139999999999999e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 3.84e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.462e0

DP
type: SiteQuality
SIO_000300: 1.782159e6

GenotypeQuality
all individuals: 163
bin: 7.5e0
variant carriers: 1

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

GenotypeQuality
all individuals: 1168
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2695
bin: 7.25e1
variant carriers: 1

GenotypeQuality
all individuals: 2743
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2023
bin: 8.25e1
variant carriers: 2

GenotypeQuality
all individuals: 8622
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 32116
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 4.75e1
variant carriers: 1

Latino
type: Population
allele count: 74
allele frequency: 6.412478336221837e-3
allele num: 11540
num of homozygotes: 1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8630
num of homozygotes: 0

Other
type: Population
allele count: 18
allele frequency: 2.132701421800948e-2
allele num: 844
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 281
allele frequency: 4.248563652857575e-2
allele num: 6614
num of homozygotes: 5

European (Non-Finnish)
type: Population
allele count: 1430
allele frequency: 2.196823055888408e-2
allele num: 65094
num of homozygotes: 16

African
type: Population
allele count: 39
allele frequency: 3.78200155159038e-3
allele num: 10312
num of homozygotes: 0

South Asian
type: Population
allele count: 46
allele frequency: 3.715070263285414e-3
allele num: 12382
num of homozygotes: 1

DP
type: SiteQuality
SIO_000300: 1.902192e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.394e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.679999999999999e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.97e0

MQRankSum
type: SiteQuality
SIO_000300: 1.76e-1

QD
type: SiteQuality
SIO_000300: 1.212e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.0e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.7e-3

MQ
type: SiteQuality
SIO_000300: 5.956e1

GenotypeQuality
all individuals: 44
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 8968
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2082
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2784
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 914
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 87
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1213
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65328
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13012
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8636
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 856
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: 1
allele frequency: 9.680542110358181e-5
allele num: 10330
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

FS
type: SiteQuality
SIO_000300: 9.25e-1

QD
type: SiteQuality
SIO_000300: 1.08e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.93e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.41e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.367e0

MQRankSum
type: SiteQuality
SIO_000300: -6.900000000000001e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.81e-1

MQ
type: SiteQuality
SIO_000300: 5.844e1

DP
type: SiteQuality
SIO_000300: 1.767559e6

GenotypeQuality
all individuals: 3275
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2082
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 63
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33651
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2783
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8962
bin: 6.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10332
num of homozygotes: 0

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

South Asian
type: Population
allele count: 2
allele frequency: 1.527883880825057e-4
allele num: 13090
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8636
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65336
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 856
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.769522e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.775e0

MQRankSum
type: SiteQuality
SIO_000300: 1.3e0

QD
type: SiteQuality
SIO_000300: 1.054e1

VQSLOD
type: SiteQuality
SIO_000300: 2.95e-1

FS
type: SiteQuality
SIO_000300: 7.38e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.81e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.76e-1

GenotypeQuality
all individuals: 9008
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 234
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1826
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 187
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 914
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 102
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2082
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65638
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 1
allele frequency: 8.653513326410523e-5
allele num: 11556
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10350
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: 13930
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.283e0

QD
type: SiteQuality
SIO_000300: 1.11e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.69e-1

FS
type: SiteQuality
SIO_000300: 2.439e0

VQSLOD
type: SiteQuality
SIO_000300: -7.299e-1

MQ
type: SiteQuality
SIO_000300: 5.877e1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.49e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.24e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

DP
type: SiteQuality
SIO_000300: 1.77879e6

GenotypeQuality
all individuals: 2083
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1212
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 139
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4266
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 9100
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 914
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3288
bin: 7.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.678242286630158e-5
allele num: 14974
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8648
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11560
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10378
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66074
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.13e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 7.4e-2

FS
type: SiteQuality
SIO_000300: 6.67e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.33e0

QD
type: SiteQuality
SIO_000300: 1.461e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.399999999999999e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.78e-1

DP
type: SiteQuality
SIO_000300: 1.795142e6

GenotypeQuality
all individuals: 2805
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4265
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 914
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35314
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9106
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2083
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11560
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8648
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10380
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15086
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.512081531436175e-5
allele num: 66134
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.868e0

MQRankSum
type: SiteQuality
SIO_000300: 1.37e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.86e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.9e-2

DP
type: SiteQuality
SIO_000300: 1.796442e6

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 5.95e0

MQ
type: SiteQuality
SIO_000300: 5.922e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.2e0