17-18967189-AGT-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18967189
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 18967187
    reference: chr 17
allele count: 2
allele frequency: 2.314868399731475e-5
allele num: 86398
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000262074
  ensembl transcript: ENST00000571722
  gene symbol: SNORD3B-2
  hgvsc: ENST00000571722.2:n.259_260delAC
  variant of: http://identifiers.org/hgnc/33190
canonical: true
consequence: non coding transcript exon
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 919
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 875
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 852
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2829
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1170
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2716
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10406
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1803
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 958
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 968
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1022
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6382
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2833
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 773
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 969
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8935
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1322
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15242
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4141
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 553
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1554
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 413
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 802
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2273
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18361
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 470
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1084
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1233
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 7076
  num of homozygotes: 0
population: African
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 3004
  num of homozygotes: 0
population: East Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 46
  num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: AGT
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/17-18967189-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18967189
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 18967189
    reference: chr 17
allele count: 472
allele frequency: 5.463089423366281e-3
allele num: 86398
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000262074
  ensembl transcript: ENST00000571722
  gene symbol: SNORD3B-2
  hgvsc: ENST00000571722.2:n.261T>G
  variant of: http://identifiers.org/hgnc/33190
canonical: true
consequence: non coding transcript exon
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 958
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2716
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8935
  bin: 9.75e1
  variant carriers: 466
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2829
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1803
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6382
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2833
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 968
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 10406
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1022
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1170
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1322
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 919
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 852
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 773
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 969
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 875
  bin: 8.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2273
  bin: 7.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4141
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1084
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 413
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 2.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 470
  bin: 2.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 802
  bin: 9.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 18361
  bin: 9.75e1
  variant carriers: 462
genotype quality: GenotypeQuality
  all individuals: 553
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1554
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15242
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1233
  bin: 7.25e1
  variant carriers: 2
num of homozygotes: 0
population: Latino
  type: Population
  allele count: 10
  allele frequency: 1.413227812323347e-3
  allele num: 7076
  num of homozygotes: 0
population: East Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 46
  num of homozygotes: 0
population: European (Non-Finnish)
  type: Population
  allele count: 329
  allele frequency: 5.534993270524899e-3
  allele num: 59440
  num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: Other
reference allele: A
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD

17-18967189-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18967189
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 18967189
    reference: chr 17
allele count: 4
allele frequency: 4.629736799462951e-5
allele num: 86398
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000262074
  ensembl transcript: ENST00000571722
  gene symbol: SNORD3B-2
  hgvsc: ENST00000571722.2:n.261T>C
  variant of: http://identifiers.org/hgnc/33190
canonical: true
consequence: non coding transcript exon
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 2716
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2829
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1322
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 958
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6382
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10406
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1170
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 919
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1803
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2833
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 852
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 875
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8935
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 773
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 968
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1022
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 969
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2273
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 470
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1084
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4141
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15242
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 413
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 553
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 802
  bin: 9.25e1
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genotype quality: GenotypeQuality
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  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1554
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 5.25e1
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genotype quality: GenotypeQuality
  all individuals: 29
  bin: 2.75e1
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genotype quality: GenotypeQuality
  all individuals: 1233
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18361
  bin: 9.75e1
  variant carriers: 2
num of homozygotes: 0
population: Other
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 746
  num of homozygotes: 0
population: African
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 3004
  num of homozygotes: 0
population: Latino
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 7076
  num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: QD

17-18967190-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18967190
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 18967190
    reference: chr 17
allele count: 162
allele frequency: 1.874869800708284e-3
allele num: 86406
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000262074
  ensembl transcript: ENST00000571722
  gene symbol: SNORD3B-2
  hgvsc: ENST00000571722.2:n.260C>T
  variant of: http://identifiers.org/hgnc/33190
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10495
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1202
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 964
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2846
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 978
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  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1040
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 858
  bin: 8.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 877
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1344
  bin: 4.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 928
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2871
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2703
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1839
  bin: 4.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 6464
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 776
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8553
  bin: 9.75e1
  variant carriers: 99
genotype depth: GenotypeDepth
  all individuals: 973
  bin: 6.25e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 414
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 18114
  bin: 9.75e1
  variant carriers: 135
genotype quality: GenotypeQuality
  all individuals: 2265
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 1.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 450
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1104
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1571
  bin: 7.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1247
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 814
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 561
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4185
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15384
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 21
population: Latino
  type: Population
  allele count: 1
  allele frequency: 1.414027149321267e-4
  allele num: 7072
  num of homozygotes: 0
population: European (Non-Finnish)
  type: Population
  allele count: 105
  allele frequency: 1.76619007569386e-3
  allele num: 59450
  num of homozygotes: 4
population: African
  type: Population
  allele count: 5
  allele frequency: 1.665556295802798e-3
  allele num: 3002
  num of homozygotes: 0
population: Other
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: G
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum

17-18967190-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18967190
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 18967190
    reference: chr 17
allele count: 1
allele frequency: 1.157327037474249e-5
allele num: 86406
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000262074
  ensembl transcript: ENST00000571722
  gene symbol: SNORD3B-2
  hgvsc: ENST00000571722.2:n.260C>G
  variant of: http://identifiers.org/hgnc/33190
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2846
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1040
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2703
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1202
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 858
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10495
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1344
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 9.75e1
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genotype depth: GenotypeDepth
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  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2871
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 9.25e1
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genotype depth: GenotypeDepth
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  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 3.25e1
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genotype depth: GenotypeDepth
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  bin: 6.25e1
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genotype depth: GenotypeDepth
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  bin: 8.25e1
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genotype depth: GenotypeDepth
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  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1247
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 2.75e1
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genotype quality: GenotypeQuality
  all individuals: 450
  bin: 2.5e0
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genotype quality: GenotypeQuality
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  bin: 1.75e1
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genotype quality: GenotypeQuality
  all individuals: 414
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 3.75e1
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genotype quality: GenotypeQuality
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  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15384
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 814
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18114
  bin: 9.75e1
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genotype quality: GenotypeQuality
  all individuals: 561
  bin: 8.75e1
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genotype quality: GenotypeQuality
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  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1104
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 3002
  num of homozygotes: 0
population: East Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 48
  num of homozygotes: 0
population: European (Non-Finnish)
  type: Population
  allele count: 1
  allele frequency: 1.682085786375105e-5
  allele num: 59450
  num of homozygotes: 0
population: South Asian
population: Latino
population: European (Finnish)
population: Other
reference allele: G
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: QD

17-18967190-G-GT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18967190
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 18967191
    reference: chr 17
allele count: 3
allele frequency: 3.471981112422748e-5
allele num: 86406
alternate allele: GT
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000262074
  ensembl transcript: ENST00000571722
  gene symbol: SNORD3B-2
  hgvsc: ENST00000571722.2:n.259dupA
  variant of: http://identifiers.org/hgnc/33190
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10495
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 928
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2871
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6464
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 973
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1202
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 7.5e0
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genotype depth: GenotypeDepth
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  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1839
  bin: 4.25e1
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genotype depth: GenotypeDepth
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  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1344
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 5.75e1
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genotype depth: GenotypeDepth
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  bin: 7.75e1
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 9.25e1
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 3.25e1
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genotype quality: GenotypeQuality
  all individuals: 76
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 5.25e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 6.25e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 7.25e1
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genotype quality: GenotypeQuality
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  bin: 5.75e1
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genotype quality: GenotypeQuality
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  bin: 7.75e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 18114
  bin: 9.75e1
  variant carriers: 2
num of homozygotes: 1
population: South Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 9798
  num of homozygotes: 0
population: African
  type: Population
  allele count: 1
  allele frequency: 3.331112591605596e-4
  allele num: 3002
  num of homozygotes: 0
population: European (Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 6290
  num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: Other
population: East Asian
reference allele: G
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP

17-18967191-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18967191
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 18967191
    reference: chr 17
allele count: 22
allele frequency: 2.546414185841937e-4
allele num: 86396
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000262074
  ensembl transcript: ENST00000571722
  gene symbol: SNORD3B-2
  hgvsc: ENST00000571722.2:n.259A>G
  variant of: http://identifiers.org/hgnc/33190
canonical: true
consequence: non coding transcript exon
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 966
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2843
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 21
genotype depth: GenotypeDepth
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  bin: 5.25e1
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 9.75e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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num of homozygotes: 0
population: Other
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 746
  num of homozygotes: 0
population: African
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 2998
  num of homozygotes: 0
population: European (Non-Finnish)
  type: Population
  allele count: 11
  allele frequency: 1.850356614183824e-4
  allele num: 59448
  num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
reference allele: T
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum

17-18967191-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18967191
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 18967191
    reference: chr 17
allele count: 11
allele frequency: 1.273207092920969e-4
allele num: 86396
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000262074
  ensembl transcript: ENST00000571722
  gene symbol: SNORD3B-2
  hgvsc: ENST00000571722.2:n.259A>C
  variant of: http://identifiers.org/hgnc/33190
canonical: true
consequence: non coding transcript exon
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 879
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 931
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 776
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1839
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 10
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 8.25e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 1248
  bin: 7.25e1
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num of homozygotes: 0
population: South Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 9792
  num of homozygotes: 0
population: East Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 48
  num of homozygotes: 0
population: Latino
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 7074
  num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum

17-18967192-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18967192
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 18967192
    reference: chr 17
allele count: 1
allele frequency: 1.157514584683767e-5
allele num: 86392
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000262074
  ensembl transcript: ENST00000571722
  gene symbol: SNORD3B-2
  hgvsc: ENST00000571722.2:n.258A>G
  variant of: http://identifiers.org/hgnc/33190
canonical: true
consequence: non coding transcript exon
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 8460
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 880
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2269
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 422
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  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1572
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 418
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 816
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1103
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 563
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1250
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18024
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: Other
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 746
  num of homozygotes: 0
population: East Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 48
  num of homozygotes: 0
population: European (Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 6290
  num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: QD

17-18967193-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18967193
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 18967193
    reference: chr 17
allele count: 18
allele frequency: 2.084105224157095e-4
allele num: 86368
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000262074
  ensembl transcript: ENST00000571722
  gene symbol: SNORD3B-2
  hgvsc: ENST00000571722.2:n.257A>G
  variant of: http://identifiers.org/hgnc/33190
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 775
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2842
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1045
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6476
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2594
  bin: 2.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2876
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10497
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 974
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 968
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1341
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8458
  bin: 9.75e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 983
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 933
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1205
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1842
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4194
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 3.25e1
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genotype quality: GenotypeQuality
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  bin: 4.75e1
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genotype quality: GenotypeQuality
  all individuals: 15382
  bin: 6.25e1
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genotype quality: GenotypeQuality
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  bin: 7.5e0
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genotype quality: GenotypeQuality
  all individuals: 426
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18024
  bin: 9.75e1
  variant carriers: 17
genotype quality: GenotypeQuality
  all individuals: 1249
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1572
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 5.25e1
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genotype quality: GenotypeQuality
  all individuals: 59
  bin: 1.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 469
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 816
  bin: 9.25e1
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genotype quality: GenotypeQuality
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  bin: 4.25e1
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genotype quality: GenotypeQuality
  all individuals: 563
  bin: 8.75e1
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genotype quality: GenotypeQuality
  all individuals: 1103
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 1
population: European (Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 6288
  num of homozygotes: 0
population: East Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 48
  num of homozygotes: 0
population: African
  type: Population
  allele count: 2
  allele frequency: 6.684491978609625e-4
  allele num: 2992
  num of homozygotes: 1
population: Other
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum

17-18967193-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18967193
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 18967193
    reference: chr 17
allele count: 1
allele frequency: 1.157836235642831e-5
allele num: 86368
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000262074
  ensembl transcript: ENST00000571722
  gene symbol: SNORD3B-2
  hgvsc: ENST00000571722.2:n.257A>C
  variant of: http://identifiers.org/hgnc/33190
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 880
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1045
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2876
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 974
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genotype depth: GenotypeDepth
  all individuals: 968
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genotype depth: GenotypeDepth
  all individuals: 45
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 775
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genotype depth: GenotypeDepth
  all individuals: 10497
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genotype depth: GenotypeDepth
  all individuals: 422
  bin: 7.5e0
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genotype depth: GenotypeDepth
  all individuals: 1341
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6476
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.5e0
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1842
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 933
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2842
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4194
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1249
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genotype quality: GenotypeQuality
  all individuals: 1103
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 18024
  bin: 9.75e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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num of homozygotes: 0
population: Other
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 746
  num of homozygotes: 0
population: European (Non-Finnish)
  type: Population
  allele count: 1
  allele frequency: 1.682595234890295e-5
  allele num: 59432
  num of homozygotes: 0
population: African
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 2992
  num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
reference allele: T
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD

http://identifiers.org/exac.variant/17-18967194-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18967194
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 18967194
    reference: chr 17
allele count: 1
allele frequency: 1.157702192687953e-5
allele num: 86378
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000262074
  ensembl transcript: ENST00000571722
  gene symbol: SNORD3B-2
  hgvsc: ENST00000571722.2:n.256T>G
  variant of: http://identifiers.org/hgnc/33190
canonical: true
consequence: non coding transcript exon
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 1844
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 983
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8446
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 853
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2876
  bin: 3.75e1
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genotype depth: GenotypeDepth
  all individuals: 1342
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10500
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 933
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1206
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 434
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 8.75e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
num of homozygotes: 0
population: South Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 9792
  num of homozygotes: 0
population: European (Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 6288
  num of homozygotes: 0
population: African
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 2994
  num of homozygotes: 0
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum

17-18967194-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18967194
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 18967194
    reference: chr 17
allele count: 2
allele frequency: 2.315404385375906e-5
allele num: 86378
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000262074
  ensembl transcript: ENST00000571722
  gene symbol: SNORD3B-2
  hgvsc: ENST00000571722.2:n.256T>C
  variant of: http://identifiers.org/hgnc/33190
canonical: true
consequence: non coding transcript exon
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 983
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 968
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10500
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1844
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1206
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 775
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 880
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 8.25e1
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genotype quality: GenotypeQuality
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  bin: 7.75e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 9.75e1
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genotype quality: GenotypeQuality
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  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 434
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 1
population: European (Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 6288
  num of homozygotes: 0
population: East Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 50
  num of homozygotes: 0
population: African
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 2994
  num of homozygotes: 0
population: Latino
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD

17-18967195-C-CGAGCTAGTCTCTGTCATTGAGCCATCAAGAAGGAAAAA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18967195
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 18967233
    reference: chr 17
allele count: 1
allele frequency: 1.157970309641261e-5
allele num: 86358
alternate allele: CGAGCTAGTCTCTGTCATTGAGCCATCAAGAAGGAAAAA
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000262074
  ensembl transcript: ENST00000571722
  gene symbol: SNORD3B-2
  variant of: http://identifiers.org/hgnc/33190
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2876
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1207
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 968
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 974
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2648
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1045
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2842
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6476
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10490
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 853
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1844
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 880
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1342
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 775
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 983
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 933
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8445
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 816
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1250
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 417
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2242
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1570
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15373
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 437
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18014
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4190
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1102
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 563
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 6288
  num of homozygotes: 0
population: European (Non-Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 59424
  num of homozygotes: 0
population: Other
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 746
  num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: East Asian
reference allele: C
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff

17-18967195-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18967195
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 18967195
    reference: chr 17
allele count: 3
allele frequency: 3.473910928923782e-5
allele num: 86358
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000262074
  ensembl transcript: ENST00000571722
  gene symbol: SNORD3B-2
  hgvsc: ENST00000571722.2:n.255G>C
  variant of: http://identifiers.org/hgnc/33190
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 974
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 983
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1045
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2648
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10490
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 853
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 775
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6476
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1342
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2876
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 933
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 968
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1207
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8445
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2842
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1844
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 880
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 437
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 816
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 417
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1570
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1250
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1102
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4190
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 563
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2242
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15373
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18014
  bin: 9.75e1
  variant carriers: 3
num of homozygotes: 0
population: African
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 2992
  num of homozygotes: 0
population: East Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 50
  num of homozygotes: 0
population: Latino
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 7068
  num of homozygotes: 0
population: Other
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD

17-18967195-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18967195
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 18967195
    reference: chr 17
allele count: 7
allele frequency: 8.105792167488826e-5
allele num: 86358
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000262074
  ensembl transcript: ENST00000571722
  gene symbol: SNORD3B-2
  hgvsc: ENST00000571722.2:n.255G>A
  variant of: http://identifiers.org/hgnc/33190
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 775
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10490
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2842
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1844
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 853
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 933
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6476
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1045
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 880
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 983
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2876
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2648
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1342
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1207
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8445
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 974
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 968
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 437
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 417
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18014
  bin: 9.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 2242
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1102
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1250
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 816
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4190
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15373
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1570
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 563
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 1
population: Latino
  type: Population
  allele count: 3
  allele frequency: 4.244482173174873e-4
  allele num: 7068
  num of homozygotes: 1
population: African
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 2992
  num of homozygotes: 0
population: European (Non-Finnish)
  type: Population
  allele count: 4
  allele frequency: 6.731287022078621e-5
  allele num: 59424
  num of homozygotes: 0
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS

17-18967196-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18967196
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 18967196
    reference: chr 17
allele count: 11
allele frequency: 1.274121435355712e-4
allele num: 86334
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000262074
  ensembl transcript: ENST00000571722
  gene symbol: SNORD3B-2
  hgvsc: ENST00000571722.2:n.254C>T
  variant of: http://identifiers.org/hgnc/33190
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8438
  bin: 9.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2659
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1844
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 934
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 969
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1206
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2836
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10489
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 974
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 983
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2875
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1342
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 775
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6476
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 882
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 853
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1045
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1569
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15377
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 362
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2306
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1252
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4193
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 817
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 563
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1102
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 451
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18004
  bin: 9.75e1
  variant carriers: 11
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 46
  num of homozygotes: 0
population: South Asian
  type: Population
  allele count: 5
  allele frequency: 5.108295872496935e-4
  allele num: 9788
  num of homozygotes: 0
population: Latino
  type: Population
  allele count: 1
  allele frequency: 1.414827391058291e-4
  allele num: 7068
  num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Other
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum

17-18967196-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18967196
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 18967196
    reference: chr 17
allele count: 17
allele frequency: 1.969096763731554e-4
allele num: 86334
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000262074
  ensembl transcript: ENST00000571722
  gene symbol: SNORD3B-2
  hgvsc: ENST00000571722.2:n.254C>G
  variant of: http://identifiers.org/hgnc/33190
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1206
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2875
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1342
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 775
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10489
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 934
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1045
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 853
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2659
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2836
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 974
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 882
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8438
  bin: 9.75e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 1844
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 983
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6476
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 969
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1569
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18004
  bin: 9.75e1
  variant carriers: 17
genotype quality: GenotypeQuality
  all individuals: 1102
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15377
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2306
  bin: 7.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 362
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 563
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 451
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 817
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4193
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1252
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 6288
  num of homozygotes: 0
population: Other
  type: Population
  allele count: 1
  allele frequency: 1.340482573726542e-3
  allele num: 746
  num of homozygotes: 0
population: East Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 46
  num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
reference allele: G
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum

17-18967196-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18967196
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 18967196
    reference: chr 17
allele count: 1
allele frequency: 1.158292213959738e-5
allele num: 86334
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000262074
  ensembl transcript: ENST00000571722
  gene symbol: SNORD3B-2
  hgvsc: ENST00000571722.2:n.254C>A
  variant of: http://identifiers.org/hgnc/33190
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10489
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 853
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1206
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1342
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1045
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 983
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 974
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1844
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2875
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2659
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6476
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 969
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2836
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8438
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 882
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 934
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 775
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2306
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15377
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 563
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1102
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 817
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4193
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 451
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1569
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 362
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 5.25e1
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genotype quality: GenotypeQuality
  all individuals: 15
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1252
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18004
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: Other
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 746
  num of homozygotes: 0
population: East Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 46
  num of homozygotes: 0
population: African
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 2984
  num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: South Asian
population: European (Finnish)
reference allele: G
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: DP

22-21331126-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21331126
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 21331126
    reference: chr 22
allele count: 73
allele frequency: 6.335595632778463e-4
allele num: 115222
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000390798
  ensembl transcript: ENST00000440238
  gene symbol: AIFM3
  hgvsc: ENST00000440238.2:c.1147-30C>T
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000385800
  ensembl transcript: ENST00000405089
  gene symbol: AIFM3
  hgvsc: ENST00000405089.1:c.1165-30C>T
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000382120
  ensembl transcript: ENST00000399167
  gene symbol: AIFM3
  hgvsc: ENST00000399167.2:c.1147-30C>T
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000382116
  ensembl transcript: ENST00000399163
  gene symbol: AIFM3
  hgvsc: ENST00000399163.2:c.1147-30C>T
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000335369
  ensembl transcript: ENST00000335375
  gene symbol: AIFM3
  hgvsc: ENST00000335375.5:c.1111-30C>T
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl transcript: ENST00000465606
  gene symbol: AIFM3
  hgvsc: ENST00000465606.1:n.625-30C>T
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000327671
  ensembl transcript: ENST00000333607
  gene symbol: AIFM3
  hgvsc: ENST00000333607.6:c.1147-30C>T
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl transcript: ENST00000483107
  gene symbol: AIFM3
  hgvsc: ENST00000483107.1:n.427-30C>T
  variant of: http://identifiers.org/hgnc/26398
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 5.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 5.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 585
  bin: 1.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 1793
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2263
  bin: 1.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 2500
  bin: 7.5e0
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5874
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17645
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 4.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 26282
  bin: 2.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 857
  bin: 4.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 6.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 696
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 241
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2172
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 382
  bin: 1.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 282
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 1
population: European (Non-Finnish)
population: East Asian
population: Other
population: African
population: European (Finnish)
population: South Asian
population: Latino
reference allele: C
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP

22-21331128-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21331128
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 21331128
    reference: chr 22
allele count: 1
allele frequency: 8.675886241779598e-6
allele num: 115262
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000382120
  ensembl transcript: ENST00000399167
  gene symbol: AIFM3
  hgvsc: ENST00000399167.2:c.1147-28C>G
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl transcript: ENST00000465606
  gene symbol: AIFM3
  hgvsc: ENST00000465606.1:n.625-28C>G
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000390798
  ensembl transcript: ENST00000440238
  gene symbol: AIFM3
  hgvsc: ENST00000440238.2:c.1147-28C>G
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000327671
  ensembl transcript: ENST00000333607
  gene symbol: AIFM3
  hgvsc: ENST00000333607.6:c.1147-28C>G
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000335369
  ensembl transcript: ENST00000335375
  gene symbol: AIFM3
  hgvsc: ENST00000335375.5:c.1111-28C>G
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000382116
  ensembl transcript: ENST00000399163
  gene symbol: AIFM3
  hgvsc: ENST00000399163.2:c.1147-28C>G
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000385800
  ensembl transcript: ENST00000405089
  gene symbol: AIFM3
  hgvsc: ENST00000405089.1:c.1165-28C>G
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl transcript: ENST00000483107
  gene symbol: AIFM3
  hgvsc: ENST00000483107.1:n.427-28C>G
  variant of: http://identifiers.org/hgnc/26398
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17699
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2229
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26297
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2498
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1791
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 850
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5893
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2169
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7075
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 538
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 286
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 230
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD

22-21331129-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21331129
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 21331129
    reference: chr 22
allele count: 22
allele frequency: 1.909291305781681e-4
allele num: 115226
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl transcript: ENST00000465606
  gene symbol: AIFM3
  hgvsc: ENST00000465606.1:n.625-27C>T
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl transcript: ENST00000483107
  gene symbol: AIFM3
  hgvsc: ENST00000483107.1:n.427-27C>T
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000382120
  ensembl transcript: ENST00000399167
  gene symbol: AIFM3
  hgvsc: ENST00000399167.2:c.1147-27C>T
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000385800
  ensembl transcript: ENST00000405089
  gene symbol: AIFM3
  hgvsc: ENST00000405089.1:c.1165-27C>T
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000382116
  ensembl transcript: ENST00000399163
  gene symbol: AIFM3
  hgvsc: ENST00000399163.2:c.1147-27C>T
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000390798
  ensembl transcript: ENST00000440238
  gene symbol: AIFM3
  hgvsc: ENST00000440238.2:c.1147-27C>T
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000335369
  ensembl transcript: ENST00000335375
  gene symbol: AIFM3
  hgvsc: ENST00000335375.5:c.1111-27C>T
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000327671
  ensembl transcript: ENST00000333607
  gene symbol: AIFM3
  hgvsc: ENST00000333607.6:c.1147-27C>T
  variant of: http://identifiers.org/hgnc/26398
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1797
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 5893
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 17699
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2207
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 848
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2504
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 5.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 26302
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 597
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 522
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 691
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7072
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3116
  bin: 9.75e1
  variant carriers: 23
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum

22-21331130-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21331130
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 21331130
    reference: chr 22
allele count: 10
allele frequency: 8.681007691372814e-5
allele num: 115194
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000335369
  ensembl transcript: ENST00000335375
  gene symbol: AIFM3
  hgvsc: ENST00000335375.5:c.1111-26G>A
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000390798
  ensembl transcript: ENST00000440238
  gene symbol: AIFM3
  hgvsc: ENST00000440238.2:c.1147-26G>A
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000327671
  ensembl transcript: ENST00000333607
  gene symbol: AIFM3
  hgvsc: ENST00000333607.6:c.1147-26G>A
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000382116
  ensembl transcript: ENST00000399163
  gene symbol: AIFM3
  hgvsc: ENST00000399163.2:c.1147-26G>A
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl transcript: ENST00000465606
  gene symbol: AIFM3
  hgvsc: ENST00000465606.1:n.625-26G>A
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl transcript: ENST00000483107
  gene symbol: AIFM3
  hgvsc: ENST00000483107.1:n.427-26G>A
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000382120
  ensembl transcript: ENST00000399167
  gene symbol: AIFM3
  hgvsc: ENST00000399167.2:c.1147-26G>A
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000385800
  ensembl transcript: ENST00000405089
  gene symbol: AIFM3
  hgvsc: ENST00000405089.1:c.1165-26G>A
  variant of: http://identifiers.org/hgnc/26398
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17725
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1792
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5916
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2168
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 849
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26285
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2532
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7084
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 616
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 687
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 537
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 494
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2755
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 100
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
population: Other
population: East Asian
population: African
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQ

22-21331140-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21331140
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 21331140
    reference: chr 22
allele count: 1
allele frequency: 8.64677907479464e-6
allele num: 115650
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000327671
  ensembl transcript: ENST00000333607
  gene symbol: AIFM3
  hgvsc: ENST00000333607.6:c.1147-16C>T
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000335369
  ensembl transcript: ENST00000335375
  gene symbol: AIFM3
  hgvsc: ENST00000335375.5:c.1111-16C>T
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000382116
  ensembl transcript: ENST00000399163
  gene symbol: AIFM3
  hgvsc: ENST00000399163.2:c.1147-16C>T
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000390798
  ensembl transcript: ENST00000440238
  gene symbol: AIFM3
  hgvsc: ENST00000440238.2:c.1147-16C>T
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl transcript: ENST00000465606
  gene symbol: AIFM3
  hgvsc: ENST00000465606.1:n.625-16C>T
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000382120
  ensembl transcript: ENST00000399167
  gene symbol: AIFM3
  hgvsc: ENST00000399167.2:c.1147-16C>T
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl transcript: ENST00000483107
  gene symbol: AIFM3
  hgvsc: ENST00000483107.1:n.427-16C>T
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000385800
  ensembl transcript: ENST00000405089
  gene symbol: AIFM3
  hgvsc: ENST00000405089.1:c.1165-16C>T
  variant of: http://identifiers.org/hgnc/26398
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2115
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26455
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17838
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 848
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1794
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5930
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2398
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2182
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2887
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 263
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 250
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3104
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 618
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 219
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
population: European (Finnish)
reference allele: C
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum

22-21331147-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21331147
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 21331147
    reference: chr 22
allele count: 1
allele frequency: 8.637070305752289e-6
allele num: 115780
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000382120
  ensembl transcript: ENST00000399167
  gene symbol: AIFM3
  hgvsc: ENST00000399167.2:c.1147-9C>T
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000390798
  ensembl transcript: ENST00000440238
  gene symbol: AIFM3
  hgvsc: ENST00000440238.2:c.1147-9C>T
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000385800
  ensembl transcript: ENST00000405089
  gene symbol: AIFM3
  hgvsc: ENST00000405089.1:c.1165-9C>T
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000327671
  ensembl transcript: ENST00000333607
  gene symbol: AIFM3
  hgvsc: ENST00000333607.6:c.1147-9C>T
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000335369
  ensembl transcript: ENST00000335375
  gene symbol: AIFM3
  hgvsc: ENST00000335375.5:c.1111-9C>T
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000382116
  ensembl transcript: ENST00000399163
  gene symbol: AIFM3
  hgvsc: ENST00000399163.2:c.1147-9C>T
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl transcript: ENST00000465606
  gene symbol: AIFM3
  hgvsc: ENST00000465606.1:n.625-9C>T
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl transcript: ENST00000483107
  gene symbol: AIFM3
  hgvsc: ENST00000483107.1:n.427-9C>T
  variant of: http://identifiers.org/hgnc/26398
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 851
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5942
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26553
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17879
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1795
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2065
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2355
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 384
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2189
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2872
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 236
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7150
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: C
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum

22-21331171-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21331171
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 21331171
    reference: chr 22
allele count: 40
allele frequency: 3.430002229501449e-4
allele num: 116618
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000382120
  ensembl transcript: ENST00000399167
  gene symbol: AIFM3
  hgvsc: ENST00000399167.2:c.1162C>T
  hgvsp: ENSP00000382120.2:p.Arg388Trp
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183773
  ensembl transcript: ENST00000486003
  gene symbol: AIFM3
  hgvsc: ENST00000486003.1:n.10C>T
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000382116
  ensembl transcript: ENST00000399163
  gene symbol: AIFM3
  hgvsc: ENST00000399163.2:c.1162C>T
  hgvsp: ENSP00000382116.2:p.Arg388Trp
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000335369
  ensembl transcript: ENST00000335375
  gene symbol: AIFM3
  hgvsc: ENST00000335375.5:c.1126C>T
  hgvsp: ENSP00000335369.5:p.Arg376Trp
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183773
  ensembl transcript: ENST00000483107
  gene symbol: AIFM3
  hgvsc: ENST00000483107.1:n.442C>T
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000390798
  ensembl transcript: ENST00000440238
  gene symbol: AIFM3
  hgvsc: ENST00000440238.2:c.1162C>T
  hgvsp: ENSP00000390798.2:p.Arg388Trp
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000385800
  ensembl transcript: ENST00000405089
  gene symbol: AIFM3
  hgvsc: ENST00000405089.1:c.1180C>T
  hgvsp: ENSP00000385800.1:p.Arg394Trp
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000327671
  ensembl transcript: ENST00000333607
  gene symbol: AIFM3
  hgvsc: ENST00000333607.6:c.1162C>T
  hgvsp: ENSP00000327671.6:p.Arg388Trp
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183773
  ensembl transcript: ENST00000465606
  gene symbol: AIFM3
  hgvsc: ENST00000465606.1:n.640C>T
  variant of: http://identifiers.org/hgnc/26398
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 9.75e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 5953
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17975
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 852
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1802
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2129
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27155
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1782
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 8.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1299
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 517
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Arg388Trp
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum

22-21331172-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21331172
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 21331172
    reference: chr 22
allele count: 11
allele frequency: 9.423294383716548e-5
allele num: 116732
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000382120
  ensembl transcript: ENST00000399167
  gene symbol: AIFM3
  hgvsc: ENST00000399167.2:c.1163G>A
  hgvsp: ENSP00000382120.2:p.Arg388Gln
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000385800
  ensembl transcript: ENST00000405089
  gene symbol: AIFM3
  hgvsc: ENST00000405089.1:c.1181G>A
  hgvsp: ENSP00000385800.1:p.Arg394Gln
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000335369
  ensembl transcript: ENST00000335375
  gene symbol: AIFM3
  hgvsc: ENST00000335375.5:c.1127G>A
  hgvsp: ENSP00000335369.5:p.Arg376Gln
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000382116
  ensembl transcript: ENST00000399163
  gene symbol: AIFM3
  hgvsc: ENST00000399163.2:c.1163G>A
  hgvsp: ENSP00000382116.2:p.Arg388Gln
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000327671
  ensembl transcript: ENST00000333607
  gene symbol: AIFM3
  hgvsc: ENST00000333607.6:c.1163G>A
  hgvsp: ENSP00000327671.6:p.Arg388Gln
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000390798
  ensembl transcript: ENST00000440238
  gene symbol: AIFM3
  hgvsc: ENST00000440238.2:c.1163G>A
  hgvsp: ENSP00000390798.2:p.Arg388Gln
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183773
  ensembl transcript: ENST00000486003
  gene symbol: AIFM3
  hgvsc: ENST00000486003.1:n.11G>A
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183773
  ensembl transcript: ENST00000483107
  gene symbol: AIFM3
  hgvsc: ENST00000483107.1:n.443G>A
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183773
  ensembl transcript: ENST00000465606
  gene symbol: AIFM3
  hgvsc: ENST00000465606.1:n.641G>A
  variant of: http://identifiers.org/hgnc/26398
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27211
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2125
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1744
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1803
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17999
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 9.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5961
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 853
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 228
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Arg388Gln
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: G
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: QD

22-21331173-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21331173
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 21331173
    reference: chr 22
allele count: 6
allele frequency: 5.136898340781836e-5
allele num: 116802
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000335369
  ensembl transcript: ENST00000335375
  gene symbol: AIFM3
  hgvsc: ENST00000335375.5:c.1128G>A
  hgvsp: ENST00000335375.5:c.1128G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000390798
  ensembl transcript: ENST00000440238
  gene symbol: AIFM3
  hgvsc: ENST00000440238.2:c.1164G>A
  hgvsp: ENST00000440238.2:c.1164G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000385800
  ensembl transcript: ENST00000405089
  gene symbol: AIFM3
  hgvsc: ENST00000405089.1:c.1182G>A
  hgvsp: ENST00000405089.1:c.1182G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000382120
  ensembl transcript: ENST00000399167
  gene symbol: AIFM3
  hgvsc: ENST00000399167.2:c.1164G>A
  hgvsp: ENST00000399167.2:c.1164G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183773
  ensembl transcript: ENST00000465606
  gene symbol: AIFM3
  hgvsc: ENST00000465606.1:n.642G>A
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000382116
  ensembl transcript: ENST00000399163
  gene symbol: AIFM3
  hgvsc: ENST00000399163.2:c.1164G>A
  hgvsp: ENST00000399163.2:c.1164G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000327671
  ensembl transcript: ENST00000333607
  gene symbol: AIFM3
  hgvsc: ENST00000333607.6:c.1164G>A
  hgvsp: ENST00000333607.6:c.1164G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183773
  ensembl transcript: ENST00000483107
  gene symbol: AIFM3
  hgvsc: ENST00000483107.1:n.444G>A
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183773
  ensembl transcript: ENST00000486003
  gene symbol: AIFM3
  hgvsc: ENST00000486003.1:n.12G>A
  variant of: http://identifiers.org/hgnc/26398
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5963
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 855
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17997
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 1806
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27255
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1721
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2112
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7215
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 494
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38996
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 529
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Arg388Arg
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Other
reference allele: G
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD

22-21331174-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21331174
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 21331174
    reference: chr 22
allele count: 1
allele frequency: 8.558712769599453e-6
allele num: 116840
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000327671
  ensembl transcript: ENST00000333607
  gene symbol: AIFM3
  hgvsc: ENST00000333607.6:c.1165G>T
  hgvsp: ENSP00000327671.6:p.Val389Leu
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183773
  ensembl transcript: ENST00000465606
  gene symbol: AIFM3
  hgvsc: ENST00000465606.1:n.643G>T
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000382116
  ensembl transcript: ENST00000399163
  gene symbol: AIFM3
  hgvsc: ENST00000399163.2:c.1165G>T
  hgvsp: ENSP00000382116.2:p.Val389Leu
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183773
  ensembl transcript: ENST00000486003
  gene symbol: AIFM3
  hgvsc: ENST00000486003.1:n.13G>T
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000385800
  ensembl transcript: ENST00000405089
  gene symbol: AIFM3
  hgvsc: ENST00000405089.1:c.1183G>T
  hgvsp: ENSP00000385800.1:p.Val395Leu
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000382120
  ensembl transcript: ENST00000399167
  gene symbol: AIFM3
  hgvsc: ENST00000399167.2:c.1165G>T
  hgvsp: ENSP00000382120.2:p.Val389Leu
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000335369
  ensembl transcript: ENST00000335375
  gene symbol: AIFM3
  hgvsc: ENST00000335375.5:c.1129G>T
  hgvsp: ENSP00000335369.5:p.Val377Leu
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183773
  ensembl transcript: ENST00000483107
  gene symbol: AIFM3
  hgvsc: ENST00000483107.1:n.445G>T
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000390798
  ensembl transcript: ENST00000440238
  gene symbol: AIFM3
  hgvsc: ENST00000440238.2:c.1165G>T
  hgvsp: ENSP00000390798.2:p.Val389Leu
  variant of: http://identifiers.org/hgnc/26398
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1807
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 856
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2102
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1694
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27291
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5964
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18010
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 153
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39036
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Val389Leu
num of homozygotes: 0
population: African
population: Other
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: DP

22-21331179-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21331179
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 21331179
    reference: chr 22
allele count: 1
allele frequency: 8.539272112445135e-6
allele num: 117106
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000335369
  ensembl transcript: ENST00000335375
  gene symbol: AIFM3
  hgvsc: ENST00000335375.5:c.1134G>A
  hgvsp: ENST00000335375.5:c.1134G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000390798
  ensembl transcript: ENST00000440238
  gene symbol: AIFM3
  hgvsc: ENST00000440238.2:c.1170G>A
  hgvsp: ENST00000440238.2:c.1170G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183773
  ensembl transcript: ENST00000486003
  gene symbol: AIFM3
  hgvsc: ENST00000486003.1:n.18G>A
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000327671
  ensembl transcript: ENST00000333607
  gene symbol: AIFM3
  hgvsc: ENST00000333607.6:c.1170G>A
  hgvsp: ENST00000333607.6:c.1170G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000385800
  ensembl transcript: ENST00000405089
  gene symbol: AIFM3
  hgvsc: ENST00000405089.1:c.1188G>A
  hgvsp: ENST00000405089.1:c.1188G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183773
  ensembl transcript: ENST00000483107
  gene symbol: AIFM3
  hgvsc: ENST00000483107.1:n.450G>A
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000382116
  ensembl transcript: ENST00000399163
  gene symbol: AIFM3
  hgvsc: ENST00000399163.2:c.1170G>A
  hgvsp: ENST00000399163.2:c.1170G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000382120
  ensembl transcript: ENST00000399167
  gene symbol: AIFM3
  hgvsc: ENST00000399167.2:c.1170G>A
  hgvsp: ENST00000399167.2:c.1170G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183773
  ensembl transcript: ENST00000465606
  gene symbol: AIFM3
  hgvsc: ENST00000465606.1:n.648G>A
  variant of: http://identifiers.org/hgnc/26398
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27483
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1606
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2016
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18031
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5969
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 856
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1806
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2215
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Lys390Lys
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: South Asian
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: QD

22-21331186-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21331186
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 21331186
    reference: chr 22
allele count: 6
allele frequency: 5.109252856923889e-5
allele num: 117434
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000390798
  ensembl transcript: ENST00000440238
  gene symbol: AIFM3
  hgvsc: ENST00000440238.2:c.1177A>G
  hgvsp: ENSP00000390798.2:p.Met393Val
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000335369
  ensembl transcript: ENST00000335375
  gene symbol: AIFM3
  hgvsc: ENST00000335375.5:c.1141A>G
  hgvsp: ENSP00000335369.5:p.Met381Val
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000382116
  ensembl transcript: ENST00000399163
  gene symbol: AIFM3
  hgvsc: ENST00000399163.2:c.1177A>G
  hgvsp: ENSP00000382116.2:p.Met393Val
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183773
  ensembl transcript: ENST00000465606
  gene symbol: AIFM3
  hgvsc: ENST00000465606.1:n.655A>G
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183773
  ensembl transcript: ENST00000483107
  gene symbol: AIFM3
  hgvsc: ENST00000483107.1:n.457A>G
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000385800
  ensembl transcript: ENST00000405089
  gene symbol: AIFM3
  hgvsc: ENST00000405089.1:c.1195A>G
  hgvsp: ENSP00000385800.1:p.Met399Val
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000327671
  ensembl transcript: ENST00000333607
  gene symbol: AIFM3
  hgvsc: ENST00000333607.6:c.1177A>G
  hgvsp: ENSP00000327671.6:p.Met393Val
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000382120
  ensembl transcript: ENST00000399167
  gene symbol: AIFM3
  hgvsc: ENST00000399167.2:c.1177A>G
  hgvsp: ENSP00000382120.2:p.Met393Val
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183773
  ensembl transcript: ENST00000486003
  gene symbol: AIFM3
  hgvsc: ENST00000486003.1:n.25A>G
  variant of: http://identifiers.org/hgnc/26398
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 856
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1867
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1807
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5974
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27697
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1465
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18091
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 95
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1303
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2380
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7260
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Met393Val
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS

22-21331187-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21331187
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 21331187
    reference: chr 22
allele count: 21
allele frequency: 1.787599169192005e-4
allele num: 117476
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000327671
  ensembl transcript: ENST00000333607
  gene symbol: AIFM3
  hgvsc: ENST00000333607.6:c.1178T>G
  hgvsp: ENSP00000327671.6:p.Met393Arg
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000382116
  ensembl transcript: ENST00000399163
  gene symbol: AIFM3
  hgvsc: ENST00000399163.2:c.1178T>G
  hgvsp: ENSP00000382116.2:p.Met393Arg
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000385800
  ensembl transcript: ENST00000405089
  gene symbol: AIFM3
  hgvsc: ENST00000405089.1:c.1196T>G
  hgvsp: ENSP00000385800.1:p.Met399Arg
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000382120
  ensembl transcript: ENST00000399167
  gene symbol: AIFM3
  hgvsc: ENST00000399167.2:c.1178T>G
  hgvsp: ENSP00000382120.2:p.Met393Arg
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000390798
  ensembl transcript: ENST00000440238
  gene symbol: AIFM3
  hgvsc: ENST00000440238.2:c.1178T>G
  hgvsp: ENSP00000390798.2:p.Met393Arg
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183773
  ensembl transcript: ENST00000483107
  gene symbol: AIFM3
  hgvsc: ENST00000483107.1:n.458T>G
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000335369
  ensembl transcript: ENST00000335375
  gene symbol: AIFM3
  hgvsc: ENST00000335375.5:c.1142T>G
  hgvsp: ENSP00000335369.5:p.Met381Arg
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183773
  ensembl transcript: ENST00000465606
  gene symbol: AIFM3
  hgvsc: ENST00000465606.1:n.656T>G
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183773
  ensembl transcript: ENST00000486003
  gene symbol: AIFM3
  hgvsc: ENST00000486003.1:n.26T>G
  variant of: http://identifiers.org/hgnc/26398
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 9.75e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1449
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27727
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18092
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1807
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 856
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5977
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1844
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 8.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 210
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2160
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2364
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Met393Arg
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
reference allele: T
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: QD

22-21331194-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21331194
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 21331194
    reference: chr 22
allele count: 12
allele frequency: 1.017604558868424e-4
allele num: 117924
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000390798
  ensembl transcript: ENST00000440238
  gene symbol: AIFM3
  hgvsc: ENST00000440238.2:c.1185G>A
  hgvsp: ENST00000440238.2:c.1185G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000382120
  ensembl transcript: ENST00000399167
  gene symbol: AIFM3
  hgvsc: ENST00000399167.2:c.1185G>A
  hgvsp: ENST00000399167.2:c.1185G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183773
  ensembl transcript: ENST00000486003
  gene symbol: AIFM3
  hgvsc: ENST00000486003.1:n.33G>A
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000335369
  ensembl transcript: ENST00000335375
  gene symbol: AIFM3
  hgvsc: ENST00000335375.5:c.1149G>A
  hgvsp: ENST00000335375.5:c.1149G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000385800
  ensembl transcript: ENST00000405089
  gene symbol: AIFM3
  hgvsc: ENST00000405089.1:c.1203G>A
  hgvsp: ENST00000405089.1:c.1203G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183773
  ensembl transcript: ENST00000465606
  gene symbol: AIFM3
  hgvsc: ENST00000465606.1:n.663G>A
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183773
  ensembl transcript: ENST00000483107
  gene symbol: AIFM3
  hgvsc: ENST00000483107.1:n.465G>A
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000382116
  ensembl transcript: ENST00000399163
  gene symbol: AIFM3
  hgvsc: ENST00000399163.2:c.1185G>A
  hgvsp: ENST00000399163.2:c.1185G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000327671
  ensembl transcript: ENST00000333607
  gene symbol: AIFM3
  hgvsc: ENST00000333607.6:c.1185G>A
  hgvsp: ENST00000333607.6:c.1185G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26398
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1243
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18167
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 856
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1638
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 9.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5997
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1812
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28061
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 205
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Thr395Thr
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: G
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD

22-21331198-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21331198
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 21331198
    reference: chr 22
allele count: 1
allele frequency: 8.463530646444471e-6
allele num: 118154
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000327671
  ensembl transcript: ENST00000333607
  gene symbol: AIFM3
  hgvsc: ENST00000333607.6:c.1189G>T
  hgvsp: ENSP00000327671.6:p.Val397Leu
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183773
  ensembl transcript: ENST00000465606
  gene symbol: AIFM3
  hgvsc: ENST00000465606.1:n.667G>T
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000382120
  ensembl transcript: ENST00000399167
  gene symbol: AIFM3
  hgvsc: ENST00000399167.2:c.1189G>T
  hgvsp: ENSP00000382120.2:p.Val397Leu
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000385800
  ensembl transcript: ENST00000405089
  gene symbol: AIFM3
  hgvsc: ENST00000405089.1:c.1207G>T
  hgvsp: ENSP00000385800.1:p.Val403Leu
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000335369
  ensembl transcript: ENST00000335375
  gene symbol: AIFM3
  hgvsc: ENST00000335375.5:c.1153G>T
  hgvsp: ENSP00000335369.5:p.Val385Leu
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183773
  ensembl transcript: ENST00000483107
  gene symbol: AIFM3
  hgvsc: ENST00000483107.1:n.469G>T
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000390798
  ensembl transcript: ENST00000440238
  gene symbol: AIFM3
  hgvsc: ENST00000440238.2:c.1189G>T
  hgvsp: ENSP00000390798.2:p.Val397Leu
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183773
  ensembl transcript: ENST00000486003
  gene symbol: AIFM3
  hgvsc: ENST00000486003.1:n.37G>T
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000382116
  ensembl transcript: ENST00000399163
  gene symbol: AIFM3
  hgvsc: ENST00000399163.2:c.1189G>T
  hgvsp: ENSP00000382116.2:p.Val397Leu
  variant of: http://identifiers.org/hgnc/26398
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 28164
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1181
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1812
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6011
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1556
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18203
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 856
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39877
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1312
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Val397Leu
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Latino
reference allele: G
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum

22-21331211-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21331211
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 21331211
    reference: chr 22
allele count: 2
allele frequency: 1.684210526315789e-5
allele num: 118750
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000390798
  ensembl transcript: ENST00000440238
  gene symbol: AIFM3
  hgvsc: ENST00000440238.2:c.1202G>A
  hgvsp: ENSP00000390798.2:p.Arg401Gln
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183773
  ensembl transcript: ENST00000483107
  gene symbol: AIFM3
  hgvsc: ENST00000483107.1:n.482G>A
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000335369
  ensembl transcript: ENST00000335375
  gene symbol: AIFM3
  hgvsc: ENST00000335375.5:c.1166G>A
  hgvsp: ENSP00000335369.5:p.Arg389Gln
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000382120
  ensembl transcript: ENST00000399167
  gene symbol: AIFM3
  hgvsc: ENST00000399167.2:c.1202G>A
  hgvsp: ENSP00000382120.2:p.Arg401Gln
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183773
  ensembl transcript: ENST00000486003
  gene symbol: AIFM3
  hgvsc: ENST00000486003.1:n.50G>A
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000382116
  ensembl transcript: ENST00000399163
  gene symbol: AIFM3
  hgvsc: ENST00000399163.2:c.1202G>A
  hgvsp: ENSP00000382116.2:p.Arg401Gln
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000385800
  ensembl transcript: ENST00000405089
  gene symbol: AIFM3
  hgvsc: ENST00000405089.1:c.1220G>A
  hgvsp: ENSP00000385800.1:p.Arg407Gln
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000327671
  ensembl transcript: ENST00000333607
  gene symbol: AIFM3
  hgvsc: ENST00000333607.6:c.1202G>A
  hgvsp: ENSP00000327671.6:p.Arg401Gln
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183773
  ensembl transcript: ENST00000465606
  gene symbol: AIFM3
  hgvsc: ENST00000465606.1:n.680G>A
  variant of: http://identifiers.org/hgnc/26398
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1000
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6044
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1267
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 856
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28376
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1818
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18400
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 347
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7412
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Arg401Gln
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
population: European (Finnish)
population: Latino
population: South Asian
reference allele: G
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum

22-21331213-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21331213
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 21331213
    reference: chr 22
allele count: 6
allele frequency: 5.048040518938566e-5
allele num: 118858
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000390798
  ensembl transcript: ENST00000440238
  gene symbol: AIFM3
  hgvsc: ENST00000440238.2:c.1204G>C
  hgvsp: ENSP00000390798.2:p.Gly402Arg
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000335369
  ensembl transcript: ENST00000335375
  gene symbol: AIFM3
  hgvsc: ENST00000335375.5:c.1168G>C
  hgvsp: ENSP00000335369.5:p.Gly390Arg
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183773
  ensembl transcript: ENST00000465606
  gene symbol: AIFM3
  hgvsc: ENST00000465606.1:n.682G>C
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000382120
  ensembl transcript: ENST00000399167
  gene symbol: AIFM3
  hgvsc: ENST00000399167.2:c.1204G>C
  hgvsp: ENSP00000382120.2:p.Gly402Arg
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183773
  ensembl transcript: ENST00000486003
  gene symbol: AIFM3
  hgvsc: ENST00000486003.1:n.52G>C
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000382116
  ensembl transcript: ENST00000399163
  gene symbol: AIFM3
  hgvsc: ENST00000399163.2:c.1204G>C
  hgvsp: ENSP00000382116.2:p.Gly402Arg
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000327671
  ensembl transcript: ENST00000333607
  gene symbol: AIFM3
  hgvsc: ENST00000333607.6:c.1204G>C
  hgvsp: ENSP00000327671.6:p.Gly402Arg
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000385800
  ensembl transcript: ENST00000405089
  gene symbol: AIFM3
  hgvsc: ENST00000405089.1:c.1222G>C
  hgvsp: ENSP00000385800.1:p.Gly408Arg
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183773
  ensembl transcript: ENST00000483107
  gene symbol: AIFM3
  hgvsc: ENST00000483107.1:n.484G>C
  variant of: http://identifiers.org/hgnc/26398
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1230
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28436
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6045
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 965
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 856
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1817
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18429
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7429
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 625
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 356
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Gly402Arg
num of homozygotes: 0
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
population: East Asian
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: BaseQRankSum

22-21331214-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21331214
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 21331214
    reference: chr 22
allele count: 1
allele frequency: 8.410004541402452e-6
allele num: 118906
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000335369
  ensembl transcript: ENST00000335375
  gene symbol: AIFM3
  hgvsc: ENST00000335375.5:c.1169G>A
  hgvsp: ENSP00000335369.5:p.Gly390Asp
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183773
  ensembl transcript: ENST00000486003
  gene symbol: AIFM3
  hgvsc: ENST00000486003.1:n.53G>A
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000382116
  ensembl transcript: ENST00000399163
  gene symbol: AIFM3
  hgvsc: ENST00000399163.2:c.1205G>A
  hgvsp: ENSP00000382116.2:p.Gly402Asp
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183773
  ensembl transcript: ENST00000483107
  gene symbol: AIFM3
  hgvsc: ENST00000483107.1:n.485G>A
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000382120
  ensembl transcript: ENST00000399167
  gene symbol: AIFM3
  hgvsc: ENST00000399167.2:c.1205G>A
  hgvsp: ENSP00000382120.2:p.Gly402Asp
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000390798
  ensembl transcript: ENST00000440238
  gene symbol: AIFM3
  hgvsc: ENST00000440238.2:c.1205G>A
  hgvsp: ENSP00000390798.2:p.Gly402Asp
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000327671
  ensembl transcript: ENST00000333607
  gene symbol: AIFM3
  hgvsc: ENST00000333607.6:c.1205G>A
  hgvsp: ENSP00000327671.6:p.Gly402Asp
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183773
  ensembl transcript: ENST00000465606
  gene symbol: AIFM3
  hgvsc: ENST00000465606.1:n.683G>A
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000385800
  ensembl transcript: ENST00000405089
  gene symbol: AIFM3
  hgvsc: ENST00000405089.1:c.1223G>A
  hgvsp: ENSP00000385800.1:p.Gly408Asp
  variant of: http://identifiers.org/hgnc/26398
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 6049
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18447
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1198
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 855
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 497
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28485
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1817
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 936
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 210
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1319
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Gly402Asp
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP

22-21331217-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21331217
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 21331217
    reference: chr 22
allele count: 1
allele frequency: 8.39390937935434e-6
allele num: 119134
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000382120
  ensembl transcript: ENST00000399167
  gene symbol: AIFM3
  hgvsc: ENST00000399167.2:c.1208A>G
  hgvsp: ENSP00000382120.2:p.Gln403Arg
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000390798
  ensembl transcript: ENST00000440238
  gene symbol: AIFM3
  hgvsc: ENST00000440238.2:c.1208A>G
  hgvsp: ENSP00000390798.2:p.Gln403Arg
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183773
  ensembl transcript: ENST00000486003
  gene symbol: AIFM3
  hgvsc: ENST00000486003.1:n.56A>G
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000385800
  ensembl transcript: ENST00000405089
  gene symbol: AIFM3
  hgvsc: ENST00000405089.1:c.1226A>G
  hgvsp: ENSP00000385800.1:p.Gln409Arg
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000382116
  ensembl transcript: ENST00000399163
  gene symbol: AIFM3
  hgvsc: ENST00000399163.2:c.1208A>G
  hgvsp: ENSP00000382116.2:p.Gln403Arg
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000335369
  ensembl transcript: ENST00000335375
  gene symbol: AIFM3
  hgvsc: ENST00000335375.5:c.1172A>G
  hgvsp: ENSP00000335369.5:p.Gln391Arg
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000327671
  ensembl transcript: ENST00000333607
  gene symbol: AIFM3
  hgvsc: ENST00000333607.6:c.1208A>G
  hgvsp: ENSP00000327671.6:p.Gln403Arg
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183773
  ensembl transcript: ENST00000465606
  gene symbol: AIFM3
  hgvsc: ENST00000465606.1:n.686A>G
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183773
  ensembl transcript: ENST00000483107
  gene symbol: AIFM3
  hgvsc: ENST00000483107.1:n.488A>G
  variant of: http://identifiers.org/hgnc/26398
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 875
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 855
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1092
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28547
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18506
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1822
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6071
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2293
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 341
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 101
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Gln403Arg
num of homozygotes: 0
population: Other
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff

22-21331227-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21331227
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 21331227
    reference: chr 22
allele count: 1
allele frequency: 8.360225391676559e-6
allele num: 119614
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000183773
  ensembl transcript: ENST00000483107
  gene symbol: AIFM3
  hgvsc: ENST00000483107.1:n.498G>T
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000390798
  ensembl transcript: ENST00000440238
  gene symbol: AIFM3
  hgvsc: ENST00000440238.2:c.1218G>T
  hgvsp: ENSP00000390798.2:p.Lys406Asn
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000183773
  ensembl transcript: ENST00000465606
  gene symbol: AIFM3
  hgvsc: ENST00000465606.1:n.696G>T
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000327671
  ensembl transcript: ENST00000333607
  gene symbol: AIFM3
  hgvsc: ENST00000333607.6:c.1218G>T
  hgvsp: ENSP00000327671.6:p.Lys406Asn
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000382120
  ensembl transcript: ENST00000399167
  gene symbol: AIFM3
  hgvsc: ENST00000399167.2:c.1218G>T
  hgvsp: ENSP00000382120.2:p.Lys406Asn
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000335369
  ensembl transcript: ENST00000335375
  gene symbol: AIFM3
  hgvsc: ENST00000335375.5:c.1182G>T
  hgvsp: ENSP00000335369.5:p.Lys394Asn
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000382116
  ensembl transcript: ENST00000399163
  gene symbol: AIFM3
  hgvsc: ENST00000399163.2:c.1218G>T
  hgvsp: ENSP00000382116.2:p.Lys406Asn
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183773
  ensembl transcript: ENST00000486003
  gene symbol: AIFM3
  hgvsc: ENST00000486003.1:n.66G>T
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000385800
  ensembl transcript: ENST00000405089
  gene symbol: AIFM3
  hgvsc: ENST00000405089.1:c.1236G>T
  hgvsp: ENSP00000385800.1:p.Lys412Asn
  variant of: http://identifiers.org/hgnc/26398
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6096
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 862
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 723
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28850
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1824
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18619
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 857
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 279
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Lys406Asn
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
population: Other
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum

22-21331228-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21331228
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 21331228
    reference: chr 22
allele count: 1
allele frequency: 8.356033892073466e-6
allele num: 119674
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000390798
  ensembl transcript: ENST00000440238
  gene symbol: AIFM3
  hgvsc: ENST00000440238.2:c.1218+1G>A
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000183773
  ensembl transcript: ENST00000465606
  gene symbol: AIFM3
  hgvsc: ENST00000465606.1:n.696+1G>A
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000183773
  ensembl transcript: ENST00000483107
  gene symbol: AIFM3
  hgvsc: ENST00000483107.1:n.498+1G>A
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: true
  consequence: splice_donor_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000382120
  ensembl transcript: ENST00000399167
  gene symbol: AIFM3
  hgvsc: ENST00000399167.2:c.1218+1G>A
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000335369
  ensembl transcript: ENST00000335375
  gene symbol: AIFM3
  hgvsc: ENST00000335375.5:c.1182+1G>A
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183773
  ensembl transcript: ENST00000486003
  gene symbol: AIFM3
  hgvsc: ENST00000486003.1:n.67G>A
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000327671
  ensembl transcript: ENST00000333607
  gene symbol: AIFM3
  hgvsc: ENST00000333607.6:c.1218+1G>A
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000385800
  ensembl transcript: ENST00000405089
  gene symbol: AIFM3
  hgvsc: ENST00000405089.1:c.1236+1G>A
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000382116
  ensembl transcript: ENST00000399163
  gene symbol: AIFM3
  hgvsc: ENST00000399163.2:c.1218+1G>A
  variant of: http://identifiers.org/hgnc/26398
canonical: true
consequence: splice donor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 840
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28883
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 857
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1824
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18622
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6097
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 712
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 628
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 206
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 274
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1141
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7535
  bin: 6.75e1
  variant carriers: 0
hgvs: c.1218+1G>A
num of homozygotes: 0
population: Other
population: South Asian
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: MQ

22-21331231-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21331231
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 21331231
    reference: chr 22
allele count: 4
allele frequency: 3.339734491107957e-5
allele num: 119770
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000327671
  ensembl transcript: ENST00000333607
  gene symbol: AIFM3
  hgvsc: ENST00000333607.6:c.1218+4G>A
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183773
  ensembl transcript: ENST00000486003
  gene symbol: AIFM3
  hgvsc: ENST00000486003.1:n.70G>A
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000382120
  ensembl transcript: ENST00000399167
  gene symbol: AIFM3
  hgvsc: ENST00000399167.2:c.1218+4G>A
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl transcript: ENST00000483107
  gene symbol: AIFM3
  hgvsc: ENST00000483107.1:n.498+4G>A
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000382116
  ensembl transcript: ENST00000399163
  gene symbol: AIFM3
  hgvsc: ENST00000399163.2:c.1218+4G>A
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000390798
  ensembl transcript: ENST00000440238
  gene symbol: AIFM3
  hgvsc: ENST00000440238.2:c.1218+4G>A
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000385800
  ensembl transcript: ENST00000405089
  gene symbol: AIFM3
  hgvsc: ENST00000405089.1:c.1236+4G>A
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000335369
  ensembl transcript: ENST00000335375
  gene symbol: AIFM3
  hgvsc: ENST00000335375.5:c.1182+4G>A
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl transcript: ENST00000465606
  gene symbol: AIFM3
  hgvsc: ENST00000465606.1:n.696+4G>A
  variant of: http://identifiers.org/hgnc/26398
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18690
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 778
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6113
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28891
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 858
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1830
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 128
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2232
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 213
  bin: 3.75e1
  variant carriers: 0
hgvs: c.1218+4G>A
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: DP

22-21331232-G-GCCCTTCT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21331232
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 21331239
    reference: chr 22
allele count: 3
allele frequency: 2.504215429305999e-5
allele num: 119798
alternate allele: GCCCTTCT
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000335369
  ensembl transcript: ENST00000335375
  gene symbol: AIFM3
  hgvsc: ENST00000335375.5:c.1182+17_1182+23dupTCTCCCT
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl transcript: ENST00000465606
  gene symbol: AIFM3
  hgvsc: ENST00000465606.1:n.696+17_696+23dupTCTCCCT
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000382120
  ensembl transcript: ENST00000399167
  gene symbol: AIFM3
  hgvsc: ENST00000399167.2:c.1218+17_1218+23dupTCTCCCT
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl transcript: ENST00000483107
  gene symbol: AIFM3
  hgvsc: ENST00000483107.1:n.498+17_498+23dupTCTCCCT
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000385800
  ensembl transcript: ENST00000405089
  gene symbol: AIFM3
  hgvsc: ENST00000405089.1:c.1236+17_1236+23dupTCTCCCT
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000390798
  ensembl transcript: ENST00000440238
  gene symbol: AIFM3
  hgvsc: ENST00000440238.2:c.1218+17_1218+23dupTCTCCCT
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183773
  ensembl transcript: ENST00000486003
  gene symbol: AIFM3
  hgvsc: ENST00000486003.1:n.83_89dupTCTCCCT
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000327671
  ensembl transcript: ENST00000333607
  gene symbol: AIFM3
  hgvsc: ENST00000333607.6:c.1218+17_1218+23dupTCTCCCT
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000382116
  ensembl transcript: ENST00000399163
  gene symbol: AIFM3
  hgvsc: ENST00000399163.2:c.1218+17_1218+23dupTCTCCCT
  variant of: http://identifiers.org/hgnc/26398
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28887
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18702
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 859
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1830
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6121
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 268
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3120
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 628
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 139
  bin: 4.75e1
  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: G
site quality: QD
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ

22-21331232-GCCCTTCT-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21331232
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 21331225
    reference: chr 22
allele count: 1
allele frequency: 8.347384764353328e-6
allele num: 119798
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000382120
  ensembl transcript: ENST00000399167
  gene symbol: AIFM3
  hgvsc: ENST00000399167.2:c.1218+17_1218+23delTCTCCCT
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000385800
  ensembl transcript: ENST00000405089
  gene symbol: AIFM3
  hgvsc: ENST00000405089.1:c.1236+17_1236+23delTCTCCCT
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000382116
  ensembl transcript: ENST00000399163
  gene symbol: AIFM3
  hgvsc: ENST00000399163.2:c.1218+17_1218+23delTCTCCCT
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000327671
  ensembl transcript: ENST00000333607
  gene symbol: AIFM3
  hgvsc: ENST00000333607.6:c.1218+17_1218+23delTCTCCCT
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl transcript: ENST00000483107
  gene symbol: AIFM3
  hgvsc: ENST00000483107.1:n.498+17_498+23delTCTCCCT
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl transcript: ENST00000465606
  gene symbol: AIFM3
  hgvsc: ENST00000465606.1:n.696+17_696+23delTCTCCCT
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000390798
  ensembl transcript: ENST00000440238
  gene symbol: AIFM3
  hgvsc: ENST00000440238.2:c.1218+17_1218+23delTCTCCCT
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000335369
  ensembl transcript: ENST00000335375
  gene symbol: AIFM3
  hgvsc: ENST00000335375.5:c.1182+17_1182+23delTCTCCCT
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183773
  ensembl transcript: ENST00000486003
  gene symbol: AIFM3
  hgvsc: ENST00000486003.1:n.83_89delTCTCCCT
  variant of: http://identifiers.org/hgnc/26398
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1830
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6121
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28887
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18702
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 859
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 268
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1344
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 5.75e1
  variant carriers: 0
hgvs: c.1218+17_1218+23delTCTCCCT
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
population: European (Finnish)
reference allele: GCCCTTCT
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: FS

22-21331233-CCCTTCT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21331233
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 21331227
    reference: chr 22
allele count: 45
allele frequency: 3.758456527186169e-4
allele num: 119730
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000390798
  ensembl transcript: ENST00000440238
  gene symbol: AIFM3
  hgvsc: ENST00000440238.2:c.1218+9_1218+14delTTCTCC
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl transcript: ENST00000483107
  gene symbol: AIFM3
  hgvsc: ENST00000483107.1:n.498+9_498+14delTTCTCC
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000327671
  ensembl transcript: ENST00000333607
  gene symbol: AIFM3
  hgvsc: ENST00000333607.6:c.1218+9_1218+14delTTCTCC
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000382116
  ensembl transcript: ENST00000399163
  gene symbol: AIFM3
  hgvsc: ENST00000399163.2:c.1218+9_1218+14delTTCTCC
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183773
  ensembl transcript: ENST00000486003
  gene symbol: AIFM3
  hgvsc: ENST00000486003.1:n.75_80delTTCTCC
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000385800
  ensembl transcript: ENST00000405089
  gene symbol: AIFM3
  hgvsc: ENST00000405089.1:c.1236+9_1236+14delTTCTCC
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl transcript: ENST00000465606
  gene symbol: AIFM3
  hgvsc: ENST00000465606.1:n.696+9_696+14delTTCTCC
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000335369
  ensembl transcript: ENST00000335375
  gene symbol: AIFM3
  hgvsc: ENST00000335375.5:c.1182+9_1182+14delTTCTCC
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000382120
  ensembl transcript: ENST00000399167
  gene symbol: AIFM3
  hgvsc: ENST00000399167.2:c.1218+9_1218+14delTTCTCC
  variant of: http://identifiers.org/hgnc/26398
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 28576
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18835
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 684
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1840
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 9.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 762
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 859
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6162
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 9.75e1
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 1054
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 290
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 356
  bin: 5.75e1
  variant carriers: 0
hgvs: c.1218+9_1218+14delTTCTCC
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
reference allele: CCCTTCT
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum

22-21331257-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21331257
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 21331257
    reference: chr 22
allele count: 1
allele frequency: 8.275405494869249e-6
allele num: 120840
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000382116
  ensembl transcript: ENST00000399163
  gene symbol: AIFM3
  hgvsc: ENST00000399163.2:c.1218+30T>G
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000382120
  ensembl transcript: ENST00000399167
  gene symbol: AIFM3
  hgvsc: ENST00000399167.2:c.1218+30T>G
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl transcript: ENST00000483107
  gene symbol: AIFM3
  hgvsc: ENST00000483107.1:n.498+30T>G
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000385800
  ensembl transcript: ENST00000405089
  gene symbol: AIFM3
  hgvsc: ENST00000405089.1:c.1236+30T>G
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000390798
  ensembl transcript: ENST00000440238
  gene symbol: AIFM3
  hgvsc: ENST00000440238.2:c.1218+30T>G
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183773
  ensembl transcript: ENST00000486003
  gene symbol: AIFM3
  hgvsc: ENST00000486003.1:n.96T>G
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000335369
  ensembl transcript: ENST00000335375
  gene symbol: AIFM3
  hgvsc: ENST00000335375.5:c.1182+30T>G
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000327671
  ensembl transcript: ENST00000333607
  gene symbol: AIFM3
  hgvsc: ENST00000333607.6:c.1218+30T>G
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl transcript: ENST00000465606
  gene symbol: AIFM3
  hgvsc: ENST00000465606.1:n.696+30T>G
  variant of: http://identifiers.org/hgnc/26398
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 878
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19424
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28799
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1856
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6420
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 646
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2456
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: East Asian
population: African
population: South Asian
population: Latino
population: European (Finnish)
reference allele: T
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: QD

22-21331264-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21331264
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 21331264
    reference: chr 22
allele count: 12
allele frequency: 9.923260121725324e-5
allele num: 120928
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl transcript: ENST00000483107
  gene symbol: AIFM3
  hgvsc: ENST00000483107.1:n.498+37C>T
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000390798
  ensembl transcript: ENST00000440238
  gene symbol: AIFM3
  hgvsc: ENST00000440238.2:c.1218+37C>T
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl transcript: ENST00000465606
  gene symbol: AIFM3
  hgvsc: ENST00000465606.1:n.696+37C>T
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000382116
  ensembl transcript: ENST00000399163
  gene symbol: AIFM3
  hgvsc: ENST00000399163.2:c.1218+37C>T
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000335369
  ensembl transcript: ENST00000335375
  gene symbol: AIFM3
  hgvsc: ENST00000335375.5:c.1182+37C>T
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000327671
  ensembl transcript: ENST00000333607
  gene symbol: AIFM3
  hgvsc: ENST00000333607.6:c.1218+37C>T
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000382120
  ensembl transcript: ENST00000399167
  gene symbol: AIFM3
  hgvsc: ENST00000399167.2:c.1218+37C>T
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183773
  ensembl transcript: ENST00000486003
  gene symbol: AIFM3
  hgvsc: ENST00000486003.1:n.103C>T
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000385800
  ensembl transcript: ENST00000405089
  gene symbol: AIFM3
  hgvsc: ENST00000405089.1:c.1236+37C>T
  variant of: http://identifiers.org/hgnc/26398
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 28698
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 19524
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1875
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 888
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6480
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2406
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 144
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 141
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum

22-21331268-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21331268
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 21331268
    reference: chr 22
allele count: 1
allele frequency: 8.266239026567692e-6
allele num: 120974
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000327671
  ensembl transcript: ENST00000333607
  gene symbol: AIFM3
  hgvsc: ENST00000333607.6:c.1218+41G>A
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000382116
  ensembl transcript: ENST00000399163
  gene symbol: AIFM3
  hgvsc: ENST00000399163.2:c.1218+41G>A
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000390798
  ensembl transcript: ENST00000440238
  gene symbol: AIFM3
  hgvsc: ENST00000440238.2:c.1218+41G>A
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000385800
  ensembl transcript: ENST00000405089
  gene symbol: AIFM3
  hgvsc: ENST00000405089.1:c.1236+41G>A
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000382120
  ensembl transcript: ENST00000399167
  gene symbol: AIFM3
  hgvsc: ENST00000399167.2:c.1218+41G>A
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl transcript: ENST00000465606
  gene symbol: AIFM3
  hgvsc: ENST00000465606.1:n.696+41G>A
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl transcript: ENST00000483107
  gene symbol: AIFM3
  hgvsc: ENST00000483107.1:n.498+41G>A
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183773
  ensembl transcript: ENST00000486003
  gene symbol: AIFM3
  hgvsc: ENST00000486003.1:n.107G>A
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000335369
  ensembl transcript: ENST00000335375
  gene symbol: AIFM3
  hgvsc: ENST00000335375.5:c.1182+41G>A
  variant of: http://identifiers.org/hgnc/26398
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1880
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19558
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 887
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28701
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6495
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2487
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3137
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 7851
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 112
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1473
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
population: Other
population: East Asian
population: European (Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/22-21331270-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21331270
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 21331270
    reference: chr 22
allele count: 1
allele frequency: 8.264326209484141e-6
allele num: 121002
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000382120
  ensembl transcript: ENST00000399167
  gene symbol: AIFM3
  hgvsc: ENST00000399167.2:c.1218+43C>A
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000327671
  ensembl transcript: ENST00000333607
  gene symbol: AIFM3
  hgvsc: ENST00000333607.6:c.1218+43C>A
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000385800
  ensembl transcript: ENST00000405089
  gene symbol: AIFM3
  hgvsc: ENST00000405089.1:c.1236+43C>A
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl transcript: ENST00000465606
  gene symbol: AIFM3
  hgvsc: ENST00000465606.1:n.696+43C>A
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl transcript: ENST00000483107
  gene symbol: AIFM3
  hgvsc: ENST00000483107.1:n.498+43C>A
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000382116
  ensembl transcript: ENST00000399163
  gene symbol: AIFM3
  hgvsc: ENST00000399163.2:c.1218+43C>A
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183773
  ensembl transcript: ENST00000486003
  gene symbol: AIFM3
  hgvsc: ENST00000486003.1:n.109C>A
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000335369
  ensembl transcript: ENST00000335375
  gene symbol: AIFM3
  hgvsc: ENST00000335375.5:c.1182+43C>A
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000390798
  ensembl transcript: ENST00000440238
  gene symbol: AIFM3
  hgvsc: ENST00000440238.2:c.1218+43C>A
  variant of: http://identifiers.org/hgnc/26398
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6520
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28667
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19576
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 891
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1892
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3138
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 133
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 658
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1475
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: MQ
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum

22-21331275-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21331275
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 21331275
    reference: chr 22
allele count: 1
allele frequency: 8.261049153242462e-6
allele num: 121050
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000390798
  ensembl transcript: ENST00000440238
  gene symbol: AIFM3
  hgvsc: ENST00000440238.2:c.1219-46G>A
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000327671
  ensembl transcript: ENST00000333607
  gene symbol: AIFM3
  hgvsc: ENST00000333607.6:c.1219-46G>A
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000382116
  ensembl transcript: ENST00000399163
  gene symbol: AIFM3
  hgvsc: ENST00000399163.2:c.1219-46G>A
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl transcript: ENST00000483107
  gene symbol: AIFM3
  hgvsc: ENST00000483107.1:n.499-46G>A
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183773
  ensembl transcript: ENST00000486003
  gene symbol: AIFM3
  hgvsc: ENST00000486003.1:n.114G>A
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000385800
  ensembl transcript: ENST00000405089
  gene symbol: AIFM3
  hgvsc: ENST00000405089.1:c.1237-46G>A
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000335369
  ensembl transcript: ENST00000335375
  gene symbol: AIFM3
  hgvsc: ENST00000335375.5:c.1183-46G>A
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl transcript: ENST00000465606
  gene symbol: AIFM3
  hgvsc: ENST00000465606.1:n.697-46G>A
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000382120
  ensembl transcript: ENST00000399167
  gene symbol: AIFM3
  hgvsc: ENST00000399167.2:c.1219-46G>A
  variant of: http://identifiers.org/hgnc/26398
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1902
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 906
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19646
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6552
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28556
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 126
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1493
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 597
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 4.25e1
  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: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ

22-21331284-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21331284
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 21331284
    reference: chr 22
allele count: 1
allele frequency: 8.259138737012504e-6
allele num: 121078
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000382116
  ensembl transcript: ENST00000399163
  gene symbol: AIFM3
  hgvsc: ENST00000399163.2:c.1219-37A>T
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl transcript: ENST00000483107
  gene symbol: AIFM3
  hgvsc: ENST00000483107.1:n.499-37A>T
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl transcript: ENST00000465606
  gene symbol: AIFM3
  hgvsc: ENST00000465606.1:n.697-37A>T
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000390798
  ensembl transcript: ENST00000440238
  gene symbol: AIFM3
  hgvsc: ENST00000440238.2:c.1219-37A>T
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000327671
  ensembl transcript: ENST00000333607
  gene symbol: AIFM3
  hgvsc: ENST00000333607.6:c.1219-37A>T
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000385800
  ensembl transcript: ENST00000405089
  gene symbol: AIFM3
  hgvsc: ENST00000405089.1:c.1237-37A>T
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183773
  ensembl transcript: ENST00000486003
  gene symbol: AIFM3
  hgvsc: ENST00000486003.1:n.123A>T
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000382120
  ensembl transcript: ENST00000399167
  gene symbol: AIFM3
  hgvsc: ENST00000399167.2:c.1219-37A>T
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000335369
  ensembl transcript: ENST00000335375
  gene symbol: AIFM3
  hgvsc: ENST00000335375.5:c.1183-37A>T
  variant of: http://identifiers.org/hgnc/26398
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6594
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 908
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28452
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1916
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19743
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 273
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 101
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 665
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/22-21331286-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21331286
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 21331286
    reference: chr 22
allele count: 2
allele frequency: 1.651936896010573e-5
allele num: 121070
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000390798
  ensembl transcript: ENST00000440238
  gene symbol: AIFM3
  hgvsc: ENST00000440238.2:c.1219-35C>A
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000382120
  ensembl transcript: ENST00000399167
  gene symbol: AIFM3
  hgvsc: ENST00000399167.2:c.1219-35C>A
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183773
  ensembl transcript: ENST00000486003
  gene symbol: AIFM3
  hgvsc: ENST00000486003.1:n.125C>A
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000385800
  ensembl transcript: ENST00000405089
  gene symbol: AIFM3
  hgvsc: ENST00000405089.1:c.1237-35C>A
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl transcript: ENST00000483107
  gene symbol: AIFM3
  hgvsc: ENST00000483107.1:n.499-35C>A
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000382116
  ensembl transcript: ENST00000399163
  gene symbol: AIFM3
  hgvsc: ENST00000399163.2:c.1219-35C>A
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl transcript: ENST00000465606
  gene symbol: AIFM3
  hgvsc: ENST00000465606.1:n.697-35C>A
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000327671
  ensembl transcript: ENST00000333607
  gene symbol: AIFM3
  hgvsc: ENST00000333607.6:c.1219-35C>A
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000335369
  ensembl transcript: ENST00000335375
  gene symbol: AIFM3
  hgvsc: ENST00000335375.5:c.1183-35C>A
  variant of: http://identifiers.org/hgnc/26398
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1922
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28419
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 911
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19763
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6602
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 123
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 103
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 123
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 262
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2457
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 109
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD

22-21331287-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21331287
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 21331287
    reference: chr 22
allele count: 1
allele frequency: 8.258320257659592e-6
allele num: 121090
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000385800
  ensembl transcript: ENST00000405089
  gene symbol: AIFM3
  hgvsc: ENST00000405089.1:c.1237-34T>C
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183773
  ensembl transcript: ENST00000486003
  gene symbol: AIFM3
  hgvsc: ENST00000486003.1:n.126T>C
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000382120
  ensembl transcript: ENST00000399167
  gene symbol: AIFM3
  hgvsc: ENST00000399167.2:c.1219-34T>C
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl transcript: ENST00000465606
  gene symbol: AIFM3
  hgvsc: ENST00000465606.1:n.697-34T>C
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000382116
  ensembl transcript: ENST00000399163
  gene symbol: AIFM3
  hgvsc: ENST00000399163.2:c.1219-34T>C
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000335369
  ensembl transcript: ENST00000335375
  gene symbol: AIFM3
  hgvsc: ENST00000335375.5:c.1183-34T>C
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl transcript: ENST00000483107
  gene symbol: AIFM3
  hgvsc: ENST00000483107.1:n.499-34T>C
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000390798
  ensembl transcript: ENST00000440238
  gene symbol: AIFM3
  hgvsc: ENST00000440238.2:c.1219-34T>C
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000327671
  ensembl transcript: ENST00000333607
  gene symbol: AIFM3
  hgvsc: ENST00000333607.6:c.1219-34T>C
  variant of: http://identifiers.org/hgnc/26398
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28435
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 910
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6601
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1921
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19769
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2502
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7923
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1506
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
reference allele: T
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: DP
site quality: BaseQRankSum

22-21331288-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21331288
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 21331288
    reference: chr 22
allele count: 1
allele frequency: 8.259138737012504e-6
allele num: 121078
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000382116
  ensembl transcript: ENST00000399163
  gene symbol: AIFM3
  hgvsc: ENST00000399163.2:c.1219-33G>A
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000385800
  ensembl transcript: ENST00000405089
  gene symbol: AIFM3
  hgvsc: ENST00000405089.1:c.1237-33G>A
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183773
  ensembl transcript: ENST00000486003
  gene symbol: AIFM3
  hgvsc: ENST00000486003.1:n.127G>A
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl transcript: ENST00000483107
  gene symbol: AIFM3
  hgvsc: ENST00000483107.1:n.499-33G>A
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000382120
  ensembl transcript: ENST00000399167
  gene symbol: AIFM3
  hgvsc: ENST00000399167.2:c.1219-33G>A
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000390798
  ensembl transcript: ENST00000440238
  gene symbol: AIFM3
  hgvsc: ENST00000440238.2:c.1219-33G>A
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000335369
  ensembl transcript: ENST00000335375
  gene symbol: AIFM3
  hgvsc: ENST00000335375.5:c.1183-33G>A
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl transcript: ENST00000465606
  gene symbol: AIFM3
  hgvsc: ENST00000465606.1:n.697-33G>A
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000327671
  ensembl transcript: ENST00000333607
  gene symbol: AIFM3
  hgvsc: ENST00000333607.6:c.1219-33G>A
  variant of: http://identifiers.org/hgnc/26398
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19772
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1926
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6599
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 914
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28441
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 255
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 667
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 104
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
population: African
population: Latino
reference allele: G
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum

22-21331299-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21331299
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 21331299
    reference: chr 22
allele count: 1
allele frequency: 8.258047467256841e-6
allele num: 121094
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183773
  ensembl transcript: ENST00000486003
  gene symbol: AIFM3
  hgvsc: ENST00000486003.1:n.138T>C
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000327671
  ensembl transcript: ENST00000333607
  gene symbol: AIFM3
  hgvsc: ENST00000333607.6:c.1219-22T>C
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000390798
  ensembl transcript: ENST00000440238
  gene symbol: AIFM3
  hgvsc: ENST00000440238.2:c.1219-22T>C
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000385800
  ensembl transcript: ENST00000405089
  gene symbol: AIFM3
  hgvsc: ENST00000405089.1:c.1237-22T>C
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl transcript: ENST00000465606
  gene symbol: AIFM3
  hgvsc: ENST00000465606.1:n.697-22T>C
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl transcript: ENST00000483107
  gene symbol: AIFM3
  hgvsc: ENST00000483107.1:n.499-22T>C
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000335369
  ensembl transcript: ENST00000335375
  gene symbol: AIFM3
  hgvsc: ENST00000335375.5:c.1183-22T>C
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000382120
  ensembl transcript: ENST00000399167
  gene symbol: AIFM3
  hgvsc: ENST00000399167.2:c.1219-22T>C
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000382116
  ensembl transcript: ENST00000399163
  gene symbol: AIFM3
  hgvsc: ENST00000399163.2:c.1219-22T>C
  variant of: http://identifiers.org/hgnc/26398
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1915
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28431
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19891
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 917
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6610
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 668
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 238
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
population: Latino
reference allele: T
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum

22-21331303-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21331303
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 21331303
    reference: chr 22
allele count: 1
allele frequency: 8.259138737012504e-6
allele num: 121078
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000385800
  ensembl transcript: ENST00000405089
  gene symbol: AIFM3
  hgvsc: ENST00000405089.1:c.1237-18T>G
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl transcript: ENST00000465606
  gene symbol: AIFM3
  hgvsc: ENST00000465606.1:n.697-18T>G
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl transcript: ENST00000483107
  gene symbol: AIFM3
  hgvsc: ENST00000483107.1:n.499-18T>G
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000382116
  ensembl transcript: ENST00000399163
  gene symbol: AIFM3
  hgvsc: ENST00000399163.2:c.1219-18T>G
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000335369
  ensembl transcript: ENST00000335375
  gene symbol: AIFM3
  hgvsc: ENST00000335375.5:c.1183-18T>G
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183773
  ensembl transcript: ENST00000486003
  gene symbol: AIFM3
  hgvsc: ENST00000486003.1:n.142T>G
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000382120
  ensembl transcript: ENST00000399167
  gene symbol: AIFM3
  hgvsc: ENST00000399167.2:c.1219-18T>G
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000327671
  ensembl transcript: ENST00000333607
  gene symbol: AIFM3
  hgvsc: ENST00000333607.6:c.1219-18T>G
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000390798
  ensembl transcript: ENST00000440238
  gene symbol: AIFM3
  hgvsc: ENST00000440238.2:c.1219-18T>G
  variant of: http://identifiers.org/hgnc/26398
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6611
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 915
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19892
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28442
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1917
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 245
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7955
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 668
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2495
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: T
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ

22-21331304-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21331304
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 21331304
    reference: chr 22
allele count: 1
allele frequency: 8.259138737012504e-6
allele num: 121078
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000390798
  ensembl transcript: ENST00000440238
  gene symbol: AIFM3
  hgvsc: ENST00000440238.2:c.1219-17C>T
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000335369
  ensembl transcript: ENST00000335375
  gene symbol: AIFM3
  hgvsc: ENST00000335375.5:c.1183-17C>T
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000382120
  ensembl transcript: ENST00000399167
  gene symbol: AIFM3
  hgvsc: ENST00000399167.2:c.1219-17C>T
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183773
  ensembl transcript: ENST00000486003
  gene symbol: AIFM3
  hgvsc: ENST00000486003.1:n.143C>T
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000327671
  ensembl transcript: ENST00000333607
  gene symbol: AIFM3
  hgvsc: ENST00000333607.6:c.1219-17C>T
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl transcript: ENST00000483107
  gene symbol: AIFM3
  hgvsc: ENST00000483107.1:n.499-17C>T
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000382116
  ensembl transcript: ENST00000399163
  gene symbol: AIFM3
  hgvsc: ENST00000399163.2:c.1219-17C>T
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl transcript: ENST00000465606
  gene symbol: AIFM3
  hgvsc: ENST00000465606.1:n.697-17C>T
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000385800
  ensembl transcript: ENST00000405089
  gene symbol: AIFM3
  hgvsc: ENST00000405089.1:c.1237-17C>T
  variant of: http://identifiers.org/hgnc/26398
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1921
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19900
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6612
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28427
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 922
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 670
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7961
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
reference allele: C
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD

http://identifiers.org/exac.variant/22-21331318-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21331318
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 21331318
    reference: chr 22
allele count: 5
allele frequency: 4.130115147610316e-5
allele num: 121062
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl transcript: ENST00000483107
  gene symbol: AIFM3
  hgvsc: ENST00000483107.1:n.499-3C>A
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183773
  ensembl transcript: ENST00000486003
  gene symbol: AIFM3
  hgvsc: ENST00000486003.1:n.157C>A
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000390798
  ensembl transcript: ENST00000440238
  gene symbol: AIFM3
  hgvsc: ENST00000440238.2:c.1219-3C>A
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl transcript: ENST00000465606
  gene symbol: AIFM3
  hgvsc: ENST00000465606.1:n.697-3C>A
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000327671
  ensembl transcript: ENST00000333607
  gene symbol: AIFM3
  hgvsc: ENST00000333607.6:c.1219-3C>A
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000335369
  ensembl transcript: ENST00000335375
  gene symbol: AIFM3
  hgvsc: ENST00000335375.5:c.1183-3C>A
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000385800
  ensembl transcript: ENST00000405089
  gene symbol: AIFM3
  hgvsc: ENST00000405089.1:c.1237-3C>A
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000382120
  ensembl transcript: ENST00000399167
  gene symbol: AIFM3
  hgvsc: ENST00000399167.2:c.1219-3C>A
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000382116
  ensembl transcript: ENST00000399163
  gene symbol: AIFM3
  hgvsc: ENST00000399163.2:c.1219-3C>A
  variant of: http://identifiers.org/hgnc/26398
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6633
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 913
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28387
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19980
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1928
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 670
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2473
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
hgvs: c.1219-3C>A
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
population: Other
population: East Asian
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: QD

22-21331324-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21331324
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 21331324
    reference: chr 22
allele count: 2
allele frequency: 1.652455548945733e-5
allele num: 121032
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000390798
  ensembl transcript: ENST00000440238
  gene symbol: AIFM3
  hgvsc: ENST00000440238.2:c.1222A>G
  hgvsp: ENSP00000390798.2:p.Lys408Glu
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000385800
  ensembl transcript: ENST00000405089
  gene symbol: AIFM3
  hgvsc: ENST00000405089.1:c.1240A>G
  hgvsp: ENSP00000385800.1:p.Lys414Glu
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000382120
  ensembl transcript: ENST00000399167
  gene symbol: AIFM3
  hgvsc: ENST00000399167.2:c.1222A>G
  hgvsp: ENSP00000382120.2:p.Lys408Glu
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183773
  ensembl transcript: ENST00000486003
  gene symbol: AIFM3
  hgvsc: ENST00000486003.1:n.163A>G
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183773
  ensembl transcript: ENST00000465606
  gene symbol: AIFM3
  hgvsc: ENST00000465606.1:n.700A>G
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000382116
  ensembl transcript: ENST00000399163
  gene symbol: AIFM3
  hgvsc: ENST00000399163.2:c.1222A>G
  hgvsp: ENSP00000382116.2:p.Lys408Glu
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000327671
  ensembl transcript: ENST00000333607
  gene symbol: AIFM3
  hgvsc: ENST00000333607.6:c.1222A>G
  hgvsp: ENSP00000327671.6:p.Lys408Glu
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000335369
  ensembl transcript: ENST00000335375
  gene symbol: AIFM3
  hgvsc: ENST00000335375.5:c.1186A>G
  hgvsp: ENSP00000335369.5:p.Lys396Glu
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183773
  ensembl transcript: ENST00000483107
  gene symbol: AIFM3
  hgvsc: ENST00000483107.1:n.502A>G
  variant of: http://identifiers.org/hgnc/26398
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19994
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28378
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 914
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6631
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1926
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 279
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Lys408Glu
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: A
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum

22-21331325-AG-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21331325
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 21331324
    reference: chr 22
allele count: 1
allele frequency: 8.262141216517673e-6
allele num: 121034
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000382116
  ensembl transcript: ENST00000399163
  gene symbol: AIFM3
  hgvsc: ENST00000399163.2:c.1225delG
  hgvsp: ENSP00000382116.2:p.Glu409ArgfsTer4
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000382120
  ensembl transcript: ENST00000399167
  gene symbol: AIFM3
  hgvsc: ENST00000399167.2:c.1225delG
  hgvsp: ENSP00000382120.2:p.Glu409ArgfsTer4
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000327671
  ensembl transcript: ENST00000333607
  gene symbol: AIFM3
  hgvsc: ENST00000333607.6:c.1225delG
  hgvsp: ENSP00000327671.6:p.Glu409ArgfsTer4
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000335369
  ensembl transcript: ENST00000335375
  gene symbol: AIFM3
  hgvsc: ENST00000335375.5:c.1189delG
  hgvsp: ENSP00000335369.5:p.Glu397ArgfsTer4
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000390798
  ensembl transcript: ENST00000440238
  gene symbol: AIFM3
  hgvsc: ENST00000440238.2:c.1225delG
  hgvsp: ENSP00000390798.2:p.Glu409ArgfsTer4
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183773
  ensembl transcript: ENST00000486003
  gene symbol: AIFM3
  hgvsc: ENST00000486003.1:n.166delG
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183773
  ensembl transcript: ENST00000465606
  gene symbol: AIFM3
  hgvsc: ENST00000465606.1:n.703delG
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000385800
  ensembl transcript: ENST00000405089
  gene symbol: AIFM3
  hgvsc: ENST00000405089.1:c.1243delG
  hgvsp: ENSP00000385800.1:p.Glu415ArgfsTer4
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183773
  ensembl transcript: ENST00000483107
  gene symbol: AIFM3
  hgvsc: ENST00000483107.1:n.505delG
  variant of: http://identifiers.org/hgnc/26398
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 28378
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 914
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6629
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19999
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1923
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 41296
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Glu409ArgfsTer4
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
population: East Asian
population: European (Finnish)
population: Latino
reference allele: AG
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum

22-21331330-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21331330
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 21331330
    reference: chr 22
allele count: 8
allele frequency: 6.611351690853195e-5
allele num: 121004
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000335369
  ensembl transcript: ENST00000335375
  gene symbol: AIFM3
  hgvsc: ENST00000335375.5:c.1192G>A
  hgvsp: ENSP00000335369.5:p.Val398Ile
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183773
  ensembl transcript: ENST00000486003
  gene symbol: AIFM3
  hgvsc: ENST00000486003.1:n.169G>A
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000390798
  ensembl transcript: ENST00000440238
  gene symbol: AIFM3
  hgvsc: ENST00000440238.2:c.1228G>A
  hgvsp: ENSP00000390798.2:p.Val410Ile
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000385800
  ensembl transcript: ENST00000405089
  gene symbol: AIFM3
  hgvsc: ENST00000405089.1:c.1246G>A
  hgvsp: ENSP00000385800.1:p.Val416Ile
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000382120
  ensembl transcript: ENST00000399167
  gene symbol: AIFM3
  hgvsc: ENST00000399167.2:c.1228G>A
  hgvsp: ENSP00000382120.2:p.Val410Ile
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000327671
  ensembl transcript: ENST00000333607
  gene symbol: AIFM3
  hgvsc: ENST00000333607.6:c.1228G>A
  hgvsp: ENSP00000327671.6:p.Val410Ile
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183773
  ensembl transcript: ENST00000483107
  gene symbol: AIFM3
  hgvsc: ENST00000483107.1:n.508G>A
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000382116
  ensembl transcript: ENST00000399163
  gene symbol: AIFM3
  hgvsc: ENST00000399163.2:c.1228G>A
  hgvsp: ENSP00000382116.2:p.Val410Ile
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183773
  ensembl transcript: ENST00000465606
  gene symbol: AIFM3
  hgvsc: ENST00000465606.1:n.706G>A
  variant of: http://identifiers.org/hgnc/26398
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1921
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19997
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28375
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 6628
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 911
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 672
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Val410Ile
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: Other
population: South Asian
population: East Asian
reference allele: G
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum

22-21331330-GT-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21331330
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 21331329
    reference: chr 22
allele count: 1
allele frequency: 8.264189613566494e-6
allele num: 121004
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183773
  ensembl transcript: ENST00000465606
  gene symbol: AIFM3
  hgvsc: ENST00000465606.1:n.708delT
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183773
  ensembl transcript: ENST00000483107
  gene symbol: AIFM3
  hgvsc: ENST00000483107.1:n.510delT
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000390798
  ensembl transcript: ENST00000440238
  gene symbol: AIFM3
  hgvsc: ENST00000440238.2:c.1230delT
  hgvsp: ENSP00000390798.2:p.Val411CysfsTer2
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000327671
  ensembl transcript: ENST00000333607
  gene symbol: AIFM3
  hgvsc: ENST00000333607.6:c.1230delT
  hgvsp: ENSP00000327671.6:p.Val411CysfsTer2
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000335369
  ensembl transcript: ENST00000335375
  gene symbol: AIFM3
  hgvsc: ENST00000335375.5:c.1194delT
  hgvsp: ENSP00000335369.5:p.Val399CysfsTer2
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000382116
  ensembl transcript: ENST00000399163
  gene symbol: AIFM3
  hgvsc: ENST00000399163.2:c.1230delT
  hgvsp: ENSP00000382116.2:p.Val411CysfsTer2
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000385800
  ensembl transcript: ENST00000405089
  gene symbol: AIFM3
  hgvsc: ENST00000405089.1:c.1248delT
  hgvsp: ENSP00000385800.1:p.Val417CysfsTer2
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183773
  ensembl transcript: ENST00000486003
  gene symbol: AIFM3
  hgvsc: ENST00000486003.1:n.171delT
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000382120
  ensembl transcript: ENST00000399167
  gene symbol: AIFM3
  hgvsc: ENST00000399167.2:c.1230delT
  hgvsp: ENSP00000382120.2:p.Val411CysfsTer2
  variant of: http://identifiers.org/hgnc/26398
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1921
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6628
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28375
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 911
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19997
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1513
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Val411CysfsTer2
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: GT
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: ReadPosRankSum

22-21331331-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21331331
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 21331331
    reference: chr 22
allele count: 1
allele frequency: 8.265829062654984e-6
allele num: 120980
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000382116
  ensembl transcript: ENST00000399163
  gene symbol: AIFM3
  hgvsc: ENST00000399163.2:c.1229T>C
  hgvsp: ENSP00000382116.2:p.Val410Ala
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183773
  ensembl transcript: ENST00000486003
  gene symbol: AIFM3
  hgvsc: ENST00000486003.1:n.170T>C
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183773
  ensembl transcript: ENST00000483107
  gene symbol: AIFM3
  hgvsc: ENST00000483107.1:n.509T>C
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000390798
  ensembl transcript: ENST00000440238
  gene symbol: AIFM3
  hgvsc: ENST00000440238.2:c.1229T>C
  hgvsp: ENSP00000390798.2:p.Val410Ala
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000335369
  ensembl transcript: ENST00000335375
  gene symbol: AIFM3
  hgvsc: ENST00000335375.5:c.1193T>C
  hgvsp: ENSP00000335369.5:p.Val398Ala
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000385800
  ensembl transcript: ENST00000405089
  gene symbol: AIFM3
  hgvsc: ENST00000405089.1:c.1247T>C
  hgvsp: ENSP00000385800.1:p.Val416Ala
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183773
  ensembl transcript: ENST00000465606
  gene symbol: AIFM3
  hgvsc: ENST00000465606.1:n.707T>C
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000327671
  ensembl transcript: ENST00000333607
  gene symbol: AIFM3
  hgvsc: ENST00000333607.6:c.1229T>C
  hgvsp: ENSP00000327671.6:p.Val410Ala
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000382120
  ensembl transcript: ENST00000399167
  gene symbol: AIFM3
  hgvsc: ENST00000399167.2:c.1229T>C
  hgvsp: ENSP00000382120.2:p.Val410Ala
  variant of: http://identifiers.org/hgnc/26398
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 28362
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1924
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 911
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6631
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20000
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1515
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Val410Ala
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
reference allele: T
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ

22-21331347-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21331347
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 21331347
    reference: chr 22
allele count: 2
allele frequency: 1.654588173003739e-5
allele num: 120876
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000390798
  ensembl transcript: ENST00000440238
  gene symbol: AIFM3
  hgvsc: ENST00000440238.2:c.1245C>T
  hgvsp: ENST00000440238.2:c.1245C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000327671
  ensembl transcript: ENST00000333607
  gene symbol: AIFM3
  hgvsc: ENST00000333607.6:c.1245C>T
  hgvsp: ENST00000333607.6:c.1245C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000335369
  ensembl transcript: ENST00000335375
  gene symbol: AIFM3
  hgvsc: ENST00000335375.5:c.1209C>T
  hgvsp: ENST00000335375.5:c.1209C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000382120
  ensembl transcript: ENST00000399167
  gene symbol: AIFM3
  hgvsc: ENST00000399167.2:c.1245C>T
  hgvsp: ENST00000399167.2:c.1245C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183773
  ensembl transcript: ENST00000465606
  gene symbol: AIFM3
  hgvsc: ENST00000465606.1:n.723C>T
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000382116
  ensembl transcript: ENST00000399163
  gene symbol: AIFM3
  hgvsc: ENST00000399163.2:c.1245C>T
  hgvsp: ENST00000399163.2:c.1245C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000385800
  ensembl transcript: ENST00000405089
  gene symbol: AIFM3
  hgvsc: ENST00000405089.1:c.1263C>T
  hgvsp: ENST00000405089.1:c.1263C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183773
  ensembl transcript: ENST00000486003
  gene symbol: AIFM3
  hgvsc: ENST00000486003.1:n.186C>T
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183773
  ensembl transcript: ENST00000483107
  gene symbol: AIFM3
  hgvsc: ENST00000483107.1:n.525C>T
  variant of: http://identifiers.org/hgnc/26398
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6626
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1921
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 909
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28146
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20029
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 600
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Ser415Ser
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Non-Finnish)
population: Other
population: East Asian
population: European (Finnish)
population: African
reference allele: C
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum

22-21331353-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21331353
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 21331353
    reference: chr 22
allele count: 8
allele frequency: 6.621858755752739e-5
allele num: 120812
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183773
  ensembl transcript: ENST00000483107
  gene symbol: AIFM3
  hgvsc: ENST00000483107.1:n.531C>T
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000327671
  ensembl transcript: ENST00000333607
  gene symbol: AIFM3
  hgvsc: ENST00000333607.6:c.1251C>T
  hgvsp: ENST00000333607.6:c.1251C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000390798
  ensembl transcript: ENST00000440238
  gene symbol: AIFM3
  hgvsc: ENST00000440238.2:c.1251C>T
  hgvsp: ENST00000440238.2:c.1251C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000382120
  ensembl transcript: ENST00000399167
  gene symbol: AIFM3
  hgvsc: ENST00000399167.2:c.1251C>T
  hgvsp: ENST00000399167.2:c.1251C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000382116
  ensembl transcript: ENST00000399163
  gene symbol: AIFM3
  hgvsc: ENST00000399163.2:c.1251C>T
  hgvsp: ENST00000399163.2:c.1251C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183773
  ensembl transcript: ENST00000465606
  gene symbol: AIFM3
  hgvsc: ENST00000465606.1:n.729C>T
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183773
  ensembl transcript: ENST00000486003
  gene symbol: AIFM3
  hgvsc: ENST00000486003.1:n.192C>T
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000385800
  ensembl transcript: ENST00000405089
  gene symbol: AIFM3
  hgvsc: ENST00000405089.1:c.1269C>T
  hgvsp: ENST00000405089.1:c.1269C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000335369
  ensembl transcript: ENST00000335375
  gene symbol: AIFM3
  hgvsc: ENST00000335375.5:c.1215C>T
  hgvsp: ENST00000335375.5:c.1215C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26398
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 908
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28086
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1922
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6625
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20006
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Val417Val
num of homozygotes: 0
population: Latino
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: East Asian
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: ClippingRankSum

22-21331354-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21331354
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 21331354
    reference: chr 22
allele count: 10
allele frequency: 8.278556881964337e-5
allele num: 120794
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183773
  ensembl transcript: ENST00000465606
  gene symbol: AIFM3
  hgvsc: ENST00000465606.1:n.730G>A
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000382120
  ensembl transcript: ENST00000399167
  gene symbol: AIFM3
  hgvsc: ENST00000399167.2:c.1252G>A
  hgvsp: ENSP00000382120.2:p.Val418Met
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183773
  ensembl transcript: ENST00000486003
  gene symbol: AIFM3
  hgvsc: ENST00000486003.1:n.193G>A
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000385800
  ensembl transcript: ENST00000405089
  gene symbol: AIFM3
  hgvsc: ENST00000405089.1:c.1270G>A
  hgvsp: ENSP00000385800.1:p.Val424Met
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000327671
  ensembl transcript: ENST00000333607
  gene symbol: AIFM3
  hgvsc: ENST00000333607.6:c.1252G>A
  hgvsp: ENSP00000327671.6:p.Val418Met
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000335369
  ensembl transcript: ENST00000335375
  gene symbol: AIFM3
  hgvsc: ENST00000335375.5:c.1216G>A
  hgvsp: ENSP00000335369.5:p.Val406Met
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183773
  ensembl transcript: ENST00000483107
  gene symbol: AIFM3
  hgvsc: ENST00000483107.1:n.532G>A
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000390798
  ensembl transcript: ENST00000440238
  gene symbol: AIFM3
  hgvsc: ENST00000440238.2:c.1252G>A
  hgvsp: ENSP00000390798.2:p.Val418Met
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000382116
  ensembl transcript: ENST00000399163
  gene symbol: AIFM3
  hgvsc: ENST00000399163.2:c.1252G>A
  hgvsp: ENSP00000382116.2:p.Val418Met
  variant of: http://identifiers.org/hgnc/26398
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6629
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28064
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1923
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 909
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19991
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 7909
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Val418Met
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: G
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum

22-21331354-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21331354
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 21331354
    reference: chr 22
allele count: 1
allele frequency: 8.278556881964336e-6
allele num: 120794
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000385800
  ensembl transcript: ENST00000405089
  gene symbol: AIFM3
  hgvsc: ENST00000405089.1:c.1270G>T
  hgvsp: ENSP00000385800.1:p.Val424Leu
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000390798
  ensembl transcript: ENST00000440238
  gene symbol: AIFM3
  hgvsc: ENST00000440238.2:c.1252G>T
  hgvsp: ENSP00000390798.2:p.Val418Leu
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000335369
  ensembl transcript: ENST00000335375
  gene symbol: AIFM3
  hgvsc: ENST00000335375.5:c.1216G>T
  hgvsp: ENSP00000335369.5:p.Val406Leu
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000382116
  ensembl transcript: ENST00000399163
  gene symbol: AIFM3
  hgvsc: ENST00000399163.2:c.1252G>T
  hgvsp: ENSP00000382116.2:p.Val418Leu
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000327671
  ensembl transcript: ENST00000333607
  gene symbol: AIFM3
  hgvsc: ENST00000333607.6:c.1252G>T
  hgvsp: ENSP00000327671.6:p.Val418Leu
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000382120
  ensembl transcript: ENST00000399167
  gene symbol: AIFM3
  hgvsc: ENST00000399167.2:c.1252G>T
  hgvsp: ENSP00000382120.2:p.Val418Leu
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183773
  ensembl transcript: ENST00000486003
  gene symbol: AIFM3
  hgvsc: ENST00000486003.1:n.193G>T
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183773
  ensembl transcript: ENST00000465606
  gene symbol: AIFM3
  hgvsc: ENST00000465606.1:n.730G>T
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183773
  ensembl transcript: ENST00000483107
  gene symbol: AIFM3
  hgvsc: ENST00000483107.1:n.532G>T
  variant of: http://identifiers.org/hgnc/26398
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19991
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 909
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6629
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28064
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1923
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2465
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Val418Leu
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: Other
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD

22-21331357-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21331357
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 21331357
    reference: chr 22
allele count: 2
allele frequency: 1.656424442199069e-5
allele num: 120742
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183773
  ensembl transcript: ENST00000465606
  gene symbol: AIFM3
  hgvsc: ENST00000465606.1:n.733C>T
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000327671
  ensembl transcript: ENST00000333607
  gene symbol: AIFM3
  hgvsc: ENST00000333607.6:c.1255C>T
  hgvsp: ENSP00000327671.6:p.Arg419Trp
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000382116
  ensembl transcript: ENST00000399163
  gene symbol: AIFM3
  hgvsc: ENST00000399163.2:c.1255C>T
  hgvsp: ENSP00000382116.2:p.Arg419Trp
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000382120
  ensembl transcript: ENST00000399167
  gene symbol: AIFM3
  hgvsc: ENST00000399167.2:c.1255C>T
  hgvsp: ENSP00000382120.2:p.Arg419Trp
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000335369
  ensembl transcript: ENST00000335375
  gene symbol: AIFM3
  hgvsc: ENST00000335375.5:c.1219C>T
  hgvsp: ENSP00000335369.5:p.Arg407Trp
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000385800
  ensembl transcript: ENST00000405089
  gene symbol: AIFM3
  hgvsc: ENST00000405089.1:c.1273C>T
  hgvsp: ENSP00000385800.1:p.Arg425Trp
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183773
  ensembl transcript: ENST00000486003
  gene symbol: AIFM3
  hgvsc: ENST00000486003.1:n.196C>T
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183773
  ensembl transcript: ENST00000483107
  gene symbol: AIFM3
  hgvsc: ENST00000483107.1:n.535C>T
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000390798
  ensembl transcript: ENST00000440238
  gene symbol: AIFM3
  hgvsc: ENST00000440238.2:c.1255C>T
  hgvsp: ENSP00000390798.2:p.Arg419Trp
  variant of: http://identifiers.org/hgnc/26398
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6635
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 907
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19969
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1932
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28026
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2476
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Arg419Trp
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: Other
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum

22-21331358-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21331358
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 21331358
    reference: chr 22
allele count: 14
allele frequency: 1.159554730983302e-4
allele num: 120736
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183773
  ensembl transcript: ENST00000486003
  gene symbol: AIFM3
  hgvsc: ENST00000486003.1:n.197G>A
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000385800
  ensembl transcript: ENST00000405089
  gene symbol: AIFM3
  hgvsc: ENST00000405089.1:c.1274G>A
  hgvsp: ENSP00000385800.1:p.Arg425Gln
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000382120
  ensembl transcript: ENST00000399167
  gene symbol: AIFM3
  hgvsc: ENST00000399167.2:c.1256G>A
  hgvsp: ENSP00000382120.2:p.Arg419Gln
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000382116
  ensembl transcript: ENST00000399163
  gene symbol: AIFM3
  hgvsc: ENST00000399163.2:c.1256G>A
  hgvsp: ENSP00000382116.2:p.Arg419Gln
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000335369
  ensembl transcript: ENST00000335375
  gene symbol: AIFM3
  hgvsc: ENST00000335375.5:c.1220G>A
  hgvsp: ENSP00000335369.5:p.Arg407Gln
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000327671
  ensembl transcript: ENST00000333607
  gene symbol: AIFM3
  hgvsc: ENST00000333607.6:c.1256G>A
  hgvsp: ENSP00000327671.6:p.Arg419Gln
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183773
  ensembl transcript: ENST00000465606
  gene symbol: AIFM3
  hgvsc: ENST00000465606.1:n.734G>A
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183773
  ensembl transcript: ENST00000483107
  gene symbol: AIFM3
  hgvsc: ENST00000483107.1:n.536G>A
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000390798
  ensembl transcript: ENST00000440238
  gene symbol: AIFM3
  hgvsc: ENST00000440238.2:c.1256G>A
  hgvsp: ENSP00000390798.2:p.Arg419Gln
  variant of: http://identifiers.org/hgnc/26398
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19961
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 911
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28010
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6623
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1926
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 669
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2474
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Arg419Gln
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
population: Other
population: African
reference allele: G
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP

22-21331359-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21331359
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 21331359
    reference: chr 22
allele count: 1
allele frequency: 8.282533792737874e-6
allele num: 120736
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000382120
  ensembl transcript: ENST00000399167
  gene symbol: AIFM3
  hgvsc: ENST00000399167.2:c.1257G>A
  hgvsp: ENST00000399167.2:c.1257G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183773
  ensembl transcript: ENST00000465606
  gene symbol: AIFM3
  hgvsc: ENST00000465606.1:n.735G>A
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000382116
  ensembl transcript: ENST00000399163
  gene symbol: AIFM3
  hgvsc: ENST00000399163.2:c.1257G>A
  hgvsp: ENST00000399163.2:c.1257G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000390798
  ensembl transcript: ENST00000440238
  gene symbol: AIFM3
  hgvsc: ENST00000440238.2:c.1257G>A
  hgvsp: ENST00000440238.2:c.1257G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000327671
  ensembl transcript: ENST00000333607
  gene symbol: AIFM3
  hgvsc: ENST00000333607.6:c.1257G>A
  hgvsp: ENST00000333607.6:c.1257G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000385800
  ensembl transcript: ENST00000405089
  gene symbol: AIFM3
  hgvsc: ENST00000405089.1:c.1275G>A
  hgvsp: ENST00000405089.1:c.1275G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000335369
  ensembl transcript: ENST00000335375
  gene symbol: AIFM3
  hgvsc: ENST00000335375.5:c.1221G>A
  hgvsp: ENST00000335375.5:c.1221G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183773
  ensembl transcript: ENST00000486003
  gene symbol: AIFM3
  hgvsc: ENST00000486003.1:n.198G>A
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183773
  ensembl transcript: ENST00000483107
  gene symbol: AIFM3
  hgvsc: ENST00000483107.1:n.537G>A
  variant of: http://identifiers.org/hgnc/26398
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6622
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 907
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19986
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1922
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27985
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1493
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Arg419Arg
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum

22-21331362-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21331362
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 21331362
    reference: chr 22
allele count: 1
allele frequency: 8.286789200656313e-6
allele num: 120674
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000335369
  ensembl transcript: ENST00000335375
  gene symbol: AIFM3
  hgvsc: ENST00000335375.5:c.1224T>C
  hgvsp: ENST00000335375.5:c.1224T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000390798
  ensembl transcript: ENST00000440238
  gene symbol: AIFM3
  hgvsc: ENST00000440238.2:c.1260T>C
  hgvsp: ENST00000440238.2:c.1260T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183773
  ensembl transcript: ENST00000486003
  gene symbol: AIFM3
  hgvsc: ENST00000486003.1:n.201T>C
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000327671
  ensembl transcript: ENST00000333607
  gene symbol: AIFM3
  hgvsc: ENST00000333607.6:c.1260T>C
  hgvsp: ENST00000333607.6:c.1260T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000382116
  ensembl transcript: ENST00000399163
  gene symbol: AIFM3
  hgvsc: ENST00000399163.2:c.1260T>C
  hgvsp: ENST00000399163.2:c.1260T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183773
  ensembl transcript: ENST00000483107
  gene symbol: AIFM3
  hgvsc: ENST00000483107.1:n.540T>C
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000382120
  ensembl transcript: ENST00000399167
  gene symbol: AIFM3
  hgvsc: ENST00000399167.2:c.1260T>C
  hgvsp: ENST00000399167.2:c.1260T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000385800
  ensembl transcript: ENST00000405089
  gene symbol: AIFM3
  hgvsc: ENST00000405089.1:c.1278T>C
  hgvsp: ENST00000405089.1:c.1278T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183773
  ensembl transcript: ENST00000465606
  gene symbol: AIFM3
  hgvsc: ENST00000465606.1:n.738T>C
  variant of: http://identifiers.org/hgnc/26398
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19978
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 908
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1918
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27889
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6613
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 592
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2457
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Ala420Ala
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
population: Latino
population: Other
population: European (Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum

22-21331366-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21331366
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 21331366
    reference: chr 22
allele count: 1
allele frequency: 8.29228651508367e-6
allele num: 120594
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183773
  ensembl transcript: ENST00000483107
  gene symbol: AIFM3
  hgvsc: ENST00000483107.1:n.544G>A
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000335369
  ensembl transcript: ENST00000335375
  gene symbol: AIFM3
  hgvsc: ENST00000335375.5:c.1228G>A
  hgvsp: ENSP00000335369.5:p.Val410Ile
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000382120
  ensembl transcript: ENST00000399167
  gene symbol: AIFM3
  hgvsc: ENST00000399167.2:c.1264G>A
  hgvsp: ENSP00000382120.2:p.Val422Ile
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000385800
  ensembl transcript: ENST00000405089
  gene symbol: AIFM3
  hgvsc: ENST00000405089.1:c.1282G>A
  hgvsp: ENSP00000385800.1:p.Val428Ile
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000327671
  ensembl transcript: ENST00000333607
  gene symbol: AIFM3
  hgvsc: ENST00000333607.6:c.1264G>A
  hgvsp: ENSP00000327671.6:p.Val422Ile
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000382116
  ensembl transcript: ENST00000399163
  gene symbol: AIFM3
  hgvsc: ENST00000399163.2:c.1264G>A
  hgvsp: ENSP00000382116.2:p.Val422Ile
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000390798
  ensembl transcript: ENST00000440238
  gene symbol: AIFM3
  hgvsc: ENST00000440238.2:c.1264G>A
  hgvsp: ENSP00000390798.2:p.Val422Ile
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183773
  ensembl transcript: ENST00000465606
  gene symbol: AIFM3
  hgvsc: ENST00000465606.1:n.742G>A
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183773
  ensembl transcript: ENST00000486003
  gene symbol: AIFM3
  hgvsc: ENST00000486003.1:n.205G>A
  variant of: http://identifiers.org/hgnc/26398
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27795
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6601
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19922
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1922
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 907
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 598
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 657
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 669
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Val422Ile
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: Other
population: African
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: G
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum

22-21331371-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21331371
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 21331371
    reference: chr 22
allele count: 2
allele frequency: 1.659145208388638e-5
allele num: 120544
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000382116
  ensembl transcript: ENST00000399163
  gene symbol: AIFM3
  hgvsc: ENST00000399163.2:c.1269C>T
  hgvsp: ENST00000399163.2:c.1269C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000385800
  ensembl transcript: ENST00000405089
  gene symbol: AIFM3
  hgvsc: ENST00000405089.1:c.1287C>T
  hgvsp: ENST00000405089.1:c.1287C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000390798
  ensembl transcript: ENST00000440238
  gene symbol: AIFM3
  hgvsc: ENST00000440238.2:c.1269C>T
  hgvsp: ENST00000440238.2:c.1269C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183773
  ensembl transcript: ENST00000465606
  gene symbol: AIFM3
  hgvsc: ENST00000465606.1:n.747C>T
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000382120
  ensembl transcript: ENST00000399167
  gene symbol: AIFM3
  hgvsc: ENST00000399167.2:c.1269C>T
  hgvsp: ENST00000399167.2:c.1269C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000327671
  ensembl transcript: ENST00000333607
  gene symbol: AIFM3
  hgvsc: ENST00000333607.6:c.1269C>T
  hgvsp: ENST00000333607.6:c.1269C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183773
  ensembl protein: ENSP00000335369
  ensembl transcript: ENST00000335375
  gene symbol: AIFM3
  hgvsc: ENST00000335375.5:c.1233C>T
  hgvsp: ENST00000335375.5:c.1233C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183773
  ensembl transcript: ENST00000486003
  gene symbol: AIFM3
  hgvsc: ENST00000486003.1:n.210C>T
  variant of: http://identifiers.org/hgnc/26398
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183773
  ensembl transcript: ENST00000483107
  gene symbol: AIFM3
  hgvsc: ENST00000483107.1:n.549C>T
  variant of: http://identifiers.org/hgnc/26398
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27710
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19884
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1923
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6608
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 908
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 711
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1487
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Cys423Cys
num of homozygotes: 0
reference allele: C

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6286
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9800
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.364737550471063e-5
allele num: 59440
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 746
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 3.533e1

FS
type: SiteQuality
SIO_000300: 1.986e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.0e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.129999999999999e-1

QD
type: SiteQuality
SIO_000300: 3.29e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.36e0

VQSLOD
type: SiteQuality
SIO_000300: -4.665e-1

DP
type: SiteQuality
SIO_000300: 2.722985e6

MQRankSum
type: SiteQuality
SIO_000300: 1.32e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.05e-2

African
type: Population
allele count: 8
allele frequency: 2.663115845539281e-3
allele num: 3004
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.020408163265306e-4
allele num: 9800
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 124
allele frequency: 1.972637607381483e-2
allele num: 6286
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 746
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.05e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.32e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.129999999999999e-1

FS
type: SiteQuality
SIO_000300: 1.986e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.36e0

QD
type: SiteQuality
SIO_000300: 3.29e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.0e-1

MQ
type: SiteQuality
SIO_000300: 3.533e1

DP
type: SiteQuality
SIO_000300: 2.722985e6

VQSLOD
type: SiteQuality
SIO_000300: -4.665e-1

South Asian
type: Population
allele count: 1
allele frequency: 1.020408163265306e-4
allele num: 9800
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 46
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6286
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 5.047106325706595e-5
allele num: 59440
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.0e-1

MQ
type: SiteQuality
SIO_000300: 3.533e1

VQSLOD
type: SiteQuality
SIO_000300: -4.665e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.05e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 4.36e0

FS
type: SiteQuality
SIO_000300: 1.986e0

MQRankSum
type: SiteQuality
SIO_000300: 1.32e0

DP
type: SiteQuality
SIO_000300: 2.722985e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.129999999999999e-1

QD
type: SiteQuality
SIO_000300: 3.29e0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 746
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 48
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 5
allele frequency: 7.94912559618442e-4
allele num: 6290
num of homozygotes: 1

South Asian
type: Population
allele count: 46
allele frequency: 4.694835680751174e-3
allele num: 9798
num of homozygotes: 16

MQ
type: SiteQuality
SIO_000300: 3.545e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.7e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.79e0

VQSLOD
type: SiteQuality
SIO_000300: 1.74e0

DP
type: SiteQuality
SIO_000300: 2.622275e6

BaseQRankSum
type: SiteQuality
SIO_000300: -3.525e0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 8.02e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.38e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -7.24e-1

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9798
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7072
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 746
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 3.545e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.7e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.74e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.38e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -7.24e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.79e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.525e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.622275e6

QD
type: SiteQuality
SIO_000300: 8.02e0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.364171572750211e-5
allele num: 59450
num of homozygotes: 1

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7072
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 746
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 48
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.7e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.74e0

QD
type: SiteQuality
SIO_000300: 8.02e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.38e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -7.24e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.79e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.525e0

MQ
type: SiteQuality
SIO_000300: 3.545e1

DP
type: SiteQuality
SIO_000300: 2.622275e6

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 48
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 2
allele frequency: 3.179650238473768e-4
allele num: 6290
num of homozygotes: 0

South Asian
type: Population
allele count: 7
allele frequency: 7.148692810457516e-4
allele num: 9792
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 2.827254735651682e-4
allele num: 7074
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 3.528e1

VQSLOD
type: SiteQuality
SIO_000300: -2.763e0

QD
type: SiteQuality
SIO_000300: 4.32e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.08e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.4e-3

DP
type: SiteQuality
SIO_000300: 2.608819e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.0e-3

FS
type: SiteQuality
SIO_000300: 7.62e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.57e0

MQRankSum
type: SiteQuality
SIO_000300: 6.14e-1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2998
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 746
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 11
allele frequency: 1.850356614183824e-4
allele num: 59448
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -2.763e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.4e-3

FS
type: SiteQuality
SIO_000300: 7.62e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.0e-3

MQ
type: SiteQuality
SIO_000300: 3.528e1

DP
type: SiteQuality
SIO_000300: 2.608819e6

ClippingRankSum
type: SiteQuality
SIO_000300: -7.08e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.14e-1

QD
type: SiteQuality
SIO_000300: 4.32e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.57e0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7070
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3000
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.02124183006536e-4
allele num: 9792
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 59446
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.25e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 3.525e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.24e0

MQRankSum
type: SiteQuality
SIO_000300: 1.09e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -4.009e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.094e0

DP
type: SiteQuality
SIO_000300: 2.603959e6

QD
type: SiteQuality
SIO_000300: 9.93e0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 746
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.414427157001414e-4
allele num: 7070
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 15
allele frequency: 2.523892852335442e-4
allele num: 59432
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9792
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.41e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.3e-2

QD
type: SiteQuality
SIO_000300: 6.68e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.7e-1

MQ
type: SiteQuality
SIO_000300: 3.507e1

MQRankSum
type: SiteQuality
SIO_000300: 1.33e0

DP
type: SiteQuality
SIO_000300: 2.602995e6

VQSLOD
type: SiteQuality
SIO_000300: -2.073e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.22e0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7070
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6288
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9792
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 48
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.22e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.3e-2

DP
type: SiteQuality
SIO_000300: 2.602995e6

MQRankSum
type: SiteQuality
SIO_000300: 1.33e0

MQ
type: SiteQuality
SIO_000300: 3.507e1

VQSLOD
type: SiteQuality
SIO_000300: -2.073e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.7e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.41e-2

QD
type: SiteQuality
SIO_000300: 6.68e0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 50
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7070
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 746
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.6824253844342e-5
allele num: 59438
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.779e0

MQRankSum
type: SiteQuality
SIO_000300: 1.63e0

MQ
type: SiteQuality
SIO_000300: 3.645e1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.48e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.27e-2

VQSLOD
type: SiteQuality
SIO_000300: -3.443e0

QD
type: SiteQuality
SIO_000300: 4.29e0

DP
type: SiteQuality
SIO_000300: 2.600325e6

ClippingRankSum
type: SiteQuality
SIO_000300: -2.208e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.53e0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7070
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 2.042483660130719e-4
allele num: 9792
num of homozygotes: 1

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 746
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 59438
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.63e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.53e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.27e-2

QD
type: SiteQuality
SIO_000300: 4.29e0

MQ
type: SiteQuality
SIO_000300: 3.645e1

FS
type: SiteQuality
SIO_000300: 1.779e0

DP
type: SiteQuality
SIO_000300: 2.600325e6

BaseQRankSum
type: SiteQuality
SIO_000300: 5.48e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.208e0

VQSLOD
type: SiteQuality
SIO_000300: -3.443e0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2992
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.021450459652707e-4
allele num: 9790
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7068
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 50
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 3.538e1

VQSLOD
type: SiteQuality
SIO_000300: 3.52e0

DP
type: SiteQuality
SIO_000300: 2.599753e6

QD
type: SiteQuality
SIO_000300: 4.0e0

MQRankSum
type: SiteQuality
SIO_000300: 6.37e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.72e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.342e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.6e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.9e-2

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 746
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9790
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6288
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 5.048465266558966e-5
allele num: 59424
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.599753e6

VQSLOD
type: SiteQuality
SIO_000300: 3.52e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.6e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.9e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.342e0

MQ
type: SiteQuality
SIO_000300: 3.538e1

MQRankSum
type: SiteQuality
SIO_000300: 6.37e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.72e-1

QD
type: SiteQuality
SIO_000300: 4.0e0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 50
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 746
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6288
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9790
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.72e-1

DP
type: SiteQuality
SIO_000300: 2.599753e6

QD
type: SiteQuality
SIO_000300: 4.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.9e-2

MQ
type: SiteQuality
SIO_000300: 3.538e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.6e-2

VQSLOD
type: SiteQuality
SIO_000300: 3.52e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.342e0

MQRankSum
type: SiteQuality
SIO_000300: 6.37e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 8.415524960447032e-5
allele num: 59414
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2984
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 746
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6288
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.55e-2

FS
type: SiteQuality
SIO_000300: 1.689e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.55e-1

MQ
type: SiteQuality
SIO_000300: 3.501e1

QD
type: SiteQuality
SIO_000300: 3.26e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.58e0

MQRankSum
type: SiteQuality
SIO_000300: 1.28e0

VQSLOD
type: SiteQuality
SIO_000300: -2.606e0

DP
type: SiteQuality
SIO_000300: 2.59839e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.57e-1

South Asian
type: Population
allele count: 1
allele frequency: 1.021659174499387e-4
allele num: 9788
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 2.829654782116582e-4
allele num: 7068
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2984
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 13
allele frequency: 2.188036489716229e-4
allele num: 59414
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 3.26e0

MQ
type: SiteQuality
SIO_000300: 3.501e1

VQSLOD
type: SiteQuality
SIO_000300: -2.606e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.58e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.55e-2

FS
type: SiteQuality
SIO_000300: 1.689e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.55e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.28e0

DP
type: SiteQuality
SIO_000300: 2.59839e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.57e-1

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.683104992089406e-5
allele num: 59414
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7068
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9788
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6288
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 3.501e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.55e-2

VQSLOD
type: SiteQuality
SIO_000300: -2.606e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.55e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.28e0

FS
type: SiteQuality
SIO_000300: 1.689e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.58e0

QD
type: SiteQuality
SIO_000300: 3.26e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.57e-1

DP
type: SiteQuality
SIO_000300: 2.59839e6

GenotypeQuality
all individuals: 7057
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1295
bin: 8.25e1
variant carriers: 3

GenotypeQuality
all individuals: 522
bin: 8.75e1
variant carriers: 2

GenotypeQuality
all individuals: 2923
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 531
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3167
bin: 9.75e1
variant carriers: 71

GenotypeQuality
all individuals: 2118
bin: 7.75e1
variant carriers: 2

GenotypeQuality
all individuals: 596
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 37731
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 618
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64822
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8616
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 9.798157946306095e-5
allele num: 10206
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6576
num of homozygotes: 0

South Asian
type: Population
allele count: 72
allele frequency: 5.689900426742532e-3
allele num: 12654
num of homozygotes: 1

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

ClippingRankSum
type: SiteQuality
SIO_000300: 1.6e-2

MQRankSum
type: SiteQuality
SIO_000300: 8.0e-2

FS
type: SiteQuality
SIO_000300: 6.77e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.86e-1

QD
type: SiteQuality
SIO_000300: 1.478e1

VQSLOD
type: SiteQuality
SIO_000300: 3.99e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.9e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.200000000000001e-3

DP
type: SiteQuality
SIO_000300: 1.569006e6

GenotypeQuality
all individuals: 372
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 74
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 522
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 699
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2918
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 596
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3099
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1293
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2130
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37835
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 617
bin: 9.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12650
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64850
num of homozygotes: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.160092807424594e-4
allele num: 8620
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6578
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.07e0

MQRankSum
type: SiteQuality
SIO_000300: -7.29e-1

QD
type: SiteQuality
SIO_000300: 9.199999999999999e0

DP
type: SiteQuality
SIO_000300: 1.568166e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.3e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.93e-1

FS
type: SiteQuality
SIO_000300: 1.3024e1

MQ
type: SiteQuality
SIO_000300: 5.973e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -2.154e0

GenotypeQuality
all individuals: 236
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 402
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2862
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 544
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 290
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2167
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1288
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2124
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 614
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37832
bin: 6.25e1
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: 11508
num of homozygotes: 0

African
type: Population
allele count: 20
allele frequency: 1.958096729978461e-3
allele num: 10214
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.083184312758217e-5
allele num: 64868
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6574
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12604
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 5.55e0

QD
type: SiteQuality
SIO_000300: 1.436e1

MQRankSum
type: SiteQuality
SIO_000300: 3.17e-1

MQ
type: SiteQuality
SIO_000300: 5.97e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.41e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.56931e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.48e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.870000000000001e-1

GenotypeQuality
all individuals: 588
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 242
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1291
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 100
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37773
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2177
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 292
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 523
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3109
bin: 9.75e1
variant carriers: 10

GenotypeQuality
all individuals: 66
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2124
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 4.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.084420591591869e-5
allele num: 64842
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6578
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12582
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8616
num of homozygotes: 0

African
type: Population
allele count: 8
allele frequency: 7.820136852394917e-4
allele num: 10230
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 3.04e0

FS
type: SiteQuality
SIO_000300: 6.81e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.6e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 8.1e-2

DP
type: SiteQuality
SIO_000300: 1.569224e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

MQRankSum
type: SiteQuality
SIO_000300: 1.27e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.63e0

QD
type: SiteQuality
SIO_000300: 1.325e1

MQ
type: SiteQuality
SIO_000300: 5.968e1

GenotypeQuality
all individuals: 666
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 459
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2134
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1301
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 574
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38187
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7120
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 521
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 4.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11524
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8622
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12706
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.537373551025428e-5
allele num: 65046
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10300
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 854
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6598
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 9.039999999999999e0

VQSLOD
type: SiteQuality
SIO_000300: -2.148e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

FS
type: SiteQuality
SIO_000300: 8.457000000000001e0

MQRankSum
type: SiteQuality
SIO_000300: 2.7e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.573891e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.96e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.575e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.538e0

GenotypeQuality
all individuals: 523
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 234
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 561
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38295
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 179
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 650
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 617
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2141
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1301
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3105
bin: 9.75e1
variant carriers: 1

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10324
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11522
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.536003932170066e-5
allele num: 65104
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12752
num of homozygotes: 0

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

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

QD
type: SiteQuality
SIO_000300: 1.207e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.491e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -1.579e0

VQSLOD
type: SiteQuality
SIO_000300: -3.25e-2

FS
type: SiteQuality
SIO_000300: 2.48e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.2e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

DP
type: SiteQuality
SIO_000300: 1.576696e6

ClippingRankSum
type: SiteQuality
SIO_000300: -9.14e-1

GenotypeQuality
all individuals: 38850
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 137
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 527
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7196
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 229
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3144
bin: 9.75e1
variant carriers: 40

GenotypeQuality
all individuals: 573
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2675
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2206
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 621
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2149
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 5.75e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.539203860072376e-5
allele num: 13264
num of homozygotes: 0

African
type: Population
allele count: 23
allele frequency: 2.220505889167793e-3
allele num: 10358
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.158211721102618e-4
allele num: 8634
num of homozygotes: 0

Latino
type: Population
allele count: 4
allele frequency: 3.468007629616785e-4
allele num: 11534
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 7
allele frequency: 1.070925891928279e-4
allele num: 65364
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 4
allele frequency: 6.055101422948834e-4
allele num: 6606
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.67e-1

MQ
type: SiteQuality
SIO_000300: 5.956e1

FS
type: SiteQuality
SIO_000300: 1.154e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 2.83e0

BaseQRankSum
type: SiteQuality
SIO_000300: 8.51e-1

DP
type: SiteQuality
SIO_000300: 1.590305e6

QD
type: SiteQuality
SIO_000300: 1.222e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.21e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.31e-1

GenotypeQuality
all individuals: 111
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 506
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2154
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 38944
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 2.5e0
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GenotypeQuality
all individuals: 7208
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 568
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variant carriers: 0

GenotypeQuality
all individuals: 2674
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 5.25e1
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GenotypeQuality
all individuals: 3121
bin: 9.75e1
variant carriers: 11

GenotypeQuality
all individuals: 165
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variant carriers: 0

GenotypeQuality
all individuals: 2208
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1301
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 528
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 621
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 4.75e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 9.652509652509652e-5
allele num: 10360
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13340
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.667013347200555e-5
allele num: 11538
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 9
allele frequency: 1.376357241168374e-4
allele num: 65390
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8636
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.952e1

VQSLOD
type: SiteQuality
SIO_000300: 4.22e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 4.08e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.199999999999999e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.01e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 8.23e-1

DP
type: SiteQuality
SIO_000300: 1.589732e6

QD
type: SiteQuality
SIO_000300: 1.189e1

GenotypeQuality
all individuals: 2208
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 158
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 622
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2665
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2155
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 78
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 102
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 232
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1301
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3118
bin: 9.75e1
variant carriers: 6

GenotypeQuality
all individuals: 561
bin: 2.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10360
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8636
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 9.172348426942244e-5
allele num: 65414
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6608
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13386
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.953e1

MQRankSum
type: SiteQuality
SIO_000300: 4.65e-1

DP
type: SiteQuality
SIO_000300: 1.589842e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.084e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.0e-1

FS
type: SiteQuality
SIO_000300: 4.347e0

QD
type: SiteQuality
SIO_000300: 9.039999999999999e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.919999999999999e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.13e0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 7.25e1
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GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 7220
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2154
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10360
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6608
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13404
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.528210770829513e-5
allele num: 65436
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.962e1

MQRankSum
type: SiteQuality
SIO_000300: -2.56e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.79e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.82e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.017e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.77e-1

QD
type: SiteQuality
SIO_000300: 1.054e1

FS
type: SiteQuality
SIO_000300: 4.167e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

DP
type: SiteQuality
SIO_000300: 1.589911e6

GenotypeQuality
all individuals: 2543
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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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 9.652509652509652e-5
allele num: 10360
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6608
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11534
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13584
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8636
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65520
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.36e-1

FS
type: SiteQuality
SIO_000300: 2.148e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.462e0

VQSLOD
type: SiteQuality
SIO_000300: 1.74e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

DP
type: SiteQuality
SIO_000300: 1.592816e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.11e0

MQRankSum
type: SiteQuality
SIO_000300: 3.82e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.499e1

GenotypeQuality
all individuals: 622
bin: 9.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 6

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

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8638
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10360
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 1
allele frequency: 7.236937328122738e-5
allele num: 13818
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.621951219512195e-5
allele num: 65600
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.966e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.95e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.71e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.06e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.08e0

QD
type: SiteQuality
SIO_000300: 1.282e1

BaseQRankSum
type: SiteQuality
SIO_000300: -8.01e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

DP
type: SiteQuality
SIO_000300: 1.597593e6

FS
type: SiteQuality
SIO_000300: 1.746e0

GenotypeQuality
all individuals: 110
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 89
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 425
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variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13844
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.650646593321752e-5
allele num: 10362
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8638
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 20
allele frequency: 3.048222886057429e-4
allele num: 65612
num of homozygotes: 0

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

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: 2.31e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.31e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.6e-3

MQRankSum
type: SiteQuality
SIO_000300: 8.500000000000001e-2

DP
type: SiteQuality
SIO_000300: 1.599802e6

MQ
type: SiteQuality
SIO_000300: 5.954e1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.3e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 3.01e0

QD
type: SiteQuality
SIO_000300: 1.178e1

GenotypeQuality
all individuals: 39789
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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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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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variant carriers: 12

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 2167
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GenotypeQuality
all individuals: 98
bin: 4.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10370
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.157407407407407e-4
allele num: 8640
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.057163020465773e-5
allele num: 14170
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 7
allele frequency: 1.059001512859304e-3
allele num: 6610
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.565654106044926e-5
allele num: 65708
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11552
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.605079e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.93e0

MQRankSum
type: SiteQuality
SIO_000300: -5.0e-3

MQ
type: SiteQuality
SIO_000300: 5.942e1

FS
type: SiteQuality
SIO_000300: 5.22e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.84e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.36e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.5e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.52e-1

QD
type: SiteQuality
SIO_000300: 1.215e1

GenotypeQuality
all individuals: 115
bin: 5.25e1
variant carriers: 0

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
all individuals: 623
bin: 9.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 876
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10372
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.157139551029854e-4
allele num: 8642
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6608
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14346
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65758
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11552
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 9.82e0

FS
type: SiteQuality
SIO_000300: 6.459e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.819e0

DP
type: SiteQuality
SIO_000300: 1.606093e6

MQRankSum
type: SiteQuality
SIO_000300: 5.610000000000001e-1

MQ
type: SiteQuality
SIO_000300: 5.941e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.56e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.16e-2

VQSLOD
type: SiteQuality
SIO_000300: 2.0e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.36e-1

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.517680983457277e-5
allele num: 65890
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.632055480639569e-5
allele num: 10382
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8642
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6604
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11562
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14790
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.614267e6

VQSLOD
type: SiteQuality
SIO_000300: 1.56e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.034e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.062e0

QD
type: SiteQuality
SIO_000300: 1.129e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.99e-1

MQ
type: SiteQuality
SIO_000300: 5.98e1

FS
type: SiteQuality
SIO_000300: 6.16e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.19e0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 3118
bin: 9.75e1
variant carriers: 6

GenotypeQuality
all individuals: 1628
bin: 2.25e1
variant carriers: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 882
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65922
num of homozygotes: 0

South Asian
type: Population
allele count: 6
allele frequency: 4.038228563736707e-4
allele num: 14858
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11562
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10384
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 6.392e0

VQSLOD
type: SiteQuality
SIO_000300: 8.39e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.012e0

MQRankSum
type: SiteQuality
SIO_000300: 2.09e-1

DP
type: SiteQuality
SIO_000300: 1.615337e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.74e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.199e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.38e0

GenotypeQuality
all individuals: 2276
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1591
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variant carriers: 0

GenotypeQuality
all individuals: 3113
bin: 9.75e1
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GenotypeQuality
all individuals: 27
bin: 1.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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European (Finnish)
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African
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Other
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South Asian
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European (Non-Finnish)
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MQ
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BaseQRankSum
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FS
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VQSLOD
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MQRankSum
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ClippingRankSum
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InbreedingCoeff
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ReadPosRankSum
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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African
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South Asian
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European (Finnish)
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East Asian
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European (Non-Finnish)
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ClippingRankSum
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MQRankSum
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QD
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MQ
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BaseQRankSum
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FS
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ReadPosRankSum
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DP
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InbreedingCoeff
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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European (Non-Finnish)
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African
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Latino
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Other
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South Asian
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InbreedingCoeff
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VQSLOD
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BaseQRankSum
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FS
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MQ
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DP
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ClippingRankSum
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MQRankSum
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QD
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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African
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European (Finnish)
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East Asian
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Latino
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European (Non-Finnish)
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DP
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FS
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ClippingRankSum
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BaseQRankSum
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InbreedingCoeff
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VQSLOD
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ReadPosRankSum
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QD
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MQRankSum
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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Latino
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African
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East Asian
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European (Non-Finnish)
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Other
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FS
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VQSLOD
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InbreedingCoeff
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QD
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BaseQRankSum
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MQRankSum
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ClippingRankSum
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MQ
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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East Asian
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European (Non-Finnish)
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South Asian
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Latino
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QD
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FS
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DP
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VQSLOD
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InbreedingCoeff
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MQRankSum
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ClippingRankSum
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ReadPosRankSum
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BaseQRankSum
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MQ
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GenotypeQuality
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African
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European (Non-Finnish)
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European (Finnish)
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MQ
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DP
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MQRankSum
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VQSLOD
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InbreedingCoeff
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QD
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FS
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African
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European (Non-Finnish)
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QD
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FS
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DP
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MQ
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VQSLOD
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MQRankSum
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ReadPosRankSum
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European (Non-Finnish)
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allele frequency: 1.505479947007106e-5
allele num: 66424
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

MQRankSum
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InbreedingCoeff
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ReadPosRankSum
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BaseQRankSum
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FS
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ClippingRankSum
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DP
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VQSLOD
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MQ
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QD
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SIO_000300: 9.109999999999999e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 12

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10394
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66436
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 11564
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South Asian
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allele frequency: 7.320644216691069e-4
allele num: 16392
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6586
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 5.55e-1

MQRankSum
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BaseQRankSum
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MQ
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FS
type: SiteQuality
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DP
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ReadPosRankSum
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InbreedingCoeff
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QD
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ClippingRankSum
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SIO_000300: -2.74e-1

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66454
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10394
num of homozygotes: 0

Latino
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allele count: 1
allele frequency: 8.647526807333103e-5
allele num: 11564
num of homozygotes: 0

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

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6582
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.214e0

FS
type: SiteQuality
SIO_000300: 4.543e0

VQSLOD
type: SiteQuality
SIO_000300: -7.776999999999999e-1

DP
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ReadPosRankSum
type: SiteQuality
SIO_000300: -1.061e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.05e-1

MQRankSum
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SIO_000300: 1.81e0

QD
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InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16438
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11560
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6582
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10396
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.504438092372499e-5
allele num: 66470
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.536e1

DP
type: SiteQuality
SIO_000300: 1.652179e6

MQRankSum
type: SiteQuality
SIO_000300: -9.56e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.19e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

FS
type: SiteQuality
SIO_000300: 4.24e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.6e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.06e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.982e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11560
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10390
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European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66486
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.15606936416185e-4
allele num: 8650
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16478
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MQRankSum
type: SiteQuality
SIO_000300: 1.75e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.93e-1

DP
type: SiteQuality
SIO_000300: 1.653728e6

ReadPosRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

FS
type: SiteQuality
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BaseQRankSum
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QD
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: 2.35e-1

MQ
type: SiteQuality
SIO_000300: 5.97e1

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

Latino
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allele count: 1
allele frequency: 8.652015919709292e-5
allele num: 11558
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10396
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6582
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66488
num of homozygotes: 0

Other
type: Population
allele count: 0
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allele num: 904
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 9.360000000000001e-1

InbreedingCoeff
type: SiteQuality
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VQSLOD
type: SiteQuality
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ClippingRankSum
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DP
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MQRankSum
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QD
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BaseQRankSum
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SIO_000300: -3.517e0

MQ
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11558
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.312138728323699e-4
allele num: 8650
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
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European (Finnish)
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 66484
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South Asian
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InbreedingCoeff
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BaseQRankSum
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DP
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ClippingRankSum
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FS
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ReadPosRankSum
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MQRankSum
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QD
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MQ
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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num of homozygotes: 0

European (Finnish)
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African
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South Asian
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Latino
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European (Non-Finnish)
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allele num: 66498
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East Asian
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ReadPosRankSum
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FS
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ClippingRankSum
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InbreedingCoeff
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VQSLOD
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MQRankSum
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MQ
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QD
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DP
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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num of homozygotes: 0

European (Non-Finnish)
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allele num: 66488
num of homozygotes: 0

East Asian
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European (Finnish)
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allele count: 0
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Other
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African
type: Population
allele count: 0
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Latino
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ReadPosRankSum
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QD
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BaseQRankSum
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MQRankSum
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InbreedingCoeff
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FS
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MQ
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DP
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VQSLOD
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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East Asian
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Other
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African
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European (Non-Finnish)
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Latino
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ClippingRankSum
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MQ
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FS
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MQRankSum
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BaseQRankSum
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InbreedingCoeff
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DP
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VQSLOD
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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Latino
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South Asian
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African
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European (Non-Finnish)
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European (Finnish)
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Other
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QD
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ReadPosRankSum
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ClippingRankSum
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DP
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InbreedingCoeff
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BaseQRankSum
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MQRankSum
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VQSLOD
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FS
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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South Asian
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European (Non-Finnish)
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African
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European (Finnish)
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Other
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MQRankSum
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DP
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BaseQRankSum
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VQSLOD
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InbreedingCoeff
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MQ
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ClippingRankSum
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FS
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ReadPosRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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European (Non-Finnish)
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African
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Latino
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South Asian
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Other
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East Asian
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BaseQRankSum
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FS
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ReadPosRankSum
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VQSLOD
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MQRankSum
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DP
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InbreedingCoeff
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MQ
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ClippingRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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African
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Other
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East Asian
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Latino
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European (Non-Finnish)
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FS
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MQ
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BaseQRankSum
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VQSLOD
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InbreedingCoeff
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QD
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MQRankSum
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ReadPosRankSum
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DP
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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European (Non-Finnish)
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Other
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South Asian
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East Asian
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European (Finnish)
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Latino
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FS
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DP
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VQSLOD
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MQ
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BaseQRankSum
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QD
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InbreedingCoeff
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ReadPosRankSum
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MQRankSum
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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African
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Latino
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South Asian
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East Asian
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QD
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DP
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ClippingRankSum
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MQRankSum
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VQSLOD
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MQ
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FS
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InbreedingCoeff
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BaseQRankSum
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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Latino
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African
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European (Finnish)
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East Asian
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MQRankSum
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ClippingRankSum
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FS
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DP
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VQSLOD
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MQ
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QD
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ReadPosRankSum
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GenotypeQuality
all individuals: 600
bin: 8.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6508
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.633911368015414e-5
allele num: 10380
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66482
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8648
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11552
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
num of homozygotes: 0

InbreedingCoeff
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SIO_000300: -1.0e-4

VQSLOD
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SIO_000300: -2.646e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.31e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.31e0

QD
type: SiteQuality
SIO_000300: 9.630000000000001e0

DP
type: SiteQuality
SIO_000300: 1.65872e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.07e0

FS
type: SiteQuality
SIO_000300: 4.372e0

MQRankSum
type: SiteQuality
SIO_000300: -1.84e-1

MQ
type: SiteQuality
SIO_000300: 5.96e1

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 2

Latino
type: Population
allele count: 2
allele frequency: 1.731301939058172e-4
allele num: 11552
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66454
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 898
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8646
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6444
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10378
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.656921e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.6e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.94e-1

FS
type: SiteQuality
SIO_000300: 3.108e0

QD
type: SiteQuality
SIO_000300: 1.201e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.43e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.633e0

MQRankSum
type: SiteQuality
SIO_000300: 4.0e-2

GenotypeQuality
all individuals: 20
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 8.659508139937652e-5
allele num: 11548
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 896
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10378
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6420
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.011050555538827e-5
allele num: 66422
num of homozygotes: 0

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

East Asian
type: Population
allele count: 4
allele frequency: 4.627487274409995e-4
allele num: 8644
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 1.67e0

MQRankSum
type: SiteQuality
SIO_000300: 4.7e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.6e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.27e-1

QD
type: SiteQuality
SIO_000300: 1.11e1

DP
type: SiteQuality
SIO_000300: 1.65618e6

ClippingRankSum
type: SiteQuality
SIO_000300: 3.99e-1

GenotypeQuality
all individuals: 110
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variant carriers: 0

GenotypeQuality
all individuals: 7
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 10

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: 72
bin: 3.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6410
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 896
num of homozygotes: 0

African
type: Population
allele count: 3
allele frequency: 2.891287586738628e-4
allele num: 10376
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 7
allele frequency: 1.053931163238881e-4
allele num: 66418
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11546
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -3.8e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 4.6e-2

QD
type: SiteQuality
SIO_000300: 1.001e1

FS
type: SiteQuality
SIO_000300: 1.756e0

VQSLOD
type: SiteQuality
SIO_000300: 1.51e0

MQ
type: SiteQuality
SIO_000300: 5.976e1

DP
type: SiteQuality
SIO_000300: 1.65604e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 7.32e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.76e-1

GenotypeQuality
all individuals: 7
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 7909
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variant carriers: 0

GenotypeQuality
all individuals: 670
bin: 9.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6410
num of homozygotes: 0

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

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

African
type: Population
allele count: 1
allele frequency: 9.637625289128758e-5
allele num: 10376
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11546
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 896
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -3.8e-2

FS
type: SiteQuality
SIO_000300: 1.756e0

VQSLOD
type: SiteQuality
SIO_000300: 1.51e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.76e-1

DP
type: SiteQuality
SIO_000300: 1.65604e6

MQRankSum
type: SiteQuality
SIO_000300: 7.32e-1

MQ
type: SiteQuality
SIO_000300: 5.976e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 4.6e-2

QD
type: SiteQuality
SIO_000300: 1.001e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 12
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GenotypeQuality
all individuals: 22
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 10372
num of homozygotes: 0

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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 896
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6388
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.06060606060606e-5
allele num: 16500
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.506069459923492e-5
allele num: 66398
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
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QD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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DP
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.927e1

MQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 1.021e0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.15e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.19e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 14

European (Non-Finnish)
type: Population
allele count: 10
allele frequency: 1.506160195198361e-4
allele num: 66394
num of homozygotes: 0

South Asian
type: Population
allele count: 4
allele frequency: 2.424242424242424e-4
allele num: 16500
num of homozygotes: 0

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

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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 896
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10374
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 9.98e0

FS
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -4.28e-1

MQ
type: SiteQuality
SIO_000300: 5.946e1

VQSLOD
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MQRankSum
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BaseQRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.37e-1

DP
type: SiteQuality
SIO_000300: 1.655561e6

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele frequency: 0.0e0
allele num: 16500
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.506160195198361e-5
allele num: 66394
num of homozygotes: 0

Other
type: Population
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VQSLOD
type: SiteQuality
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QD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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MQRankSum
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InbreedingCoeff
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MQ
type: SiteQuality
SIO_000300: 5.932e1

FS
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DP
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: -8.24e-1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 101
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GenotypeQuality
all individuals: 7892
bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66372
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.643201542912247e-5
allele num: 10370
num of homozygotes: 0

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

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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 896
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6358
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.47e0

MQRankSum
type: SiteQuality
SIO_000300: 2.4e-2

QD
type: SiteQuality
SIO_000300: 1.204e1

FS
type: SiteQuality
SIO_000300: 5.54e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.370000000000001e-1

DP
type: SiteQuality
SIO_000300: 1.653136e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -1.839e0

MQ
type: SiteQuality
SIO_000300: 5.987e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.453e0

GenotypeQuality
all individuals: 170
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40683
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 7873
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2469
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 136
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1492
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3165
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2453
bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66344
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11528
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10368
num of homozygotes: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.156871818602499e-4
allele num: 8644
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6318
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.651202e6

MQRankSum
type: SiteQuality
SIO_000300: -4.41e-1

QD
type: SiteQuality
SIO_000300: 1.142e1

VQSLOD
type: SiteQuality
SIO_000300: 6.78e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.18e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.65e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.18e-1

GenotypeQuality
all individuals: 8
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 40554
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2447
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3165
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 192
bin: 2.75e1
variant carriers: 0

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