1-204501983-CCT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 204501983
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 204501981
    reference: chr 1
allele count: 1
allele frequency: 8.703523186185769e-6
allele num: 114896
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356150
  ensembl transcript: ENST00000367182
  gene symbol: MDM4
  hgvsc: ENST00000367182.3:c.343+614_343+615delCT
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000443816
  ensembl transcript: ENST00000507825
  gene symbol: MDM4
  hgvsc: ENST00000507825.2:c.343+614_343+615delCT
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000471783
  gene symbol: MDM4
  hgvsc: ENST00000471783.1:n.227-5349_227-5348delCT
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356148
  ensembl transcript: ENST00000367180
  gene symbol: MDM4
  hgvsc: ENST00000367180.1:c.394+41_394+42delCT
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000396840
  ensembl transcript: ENST00000454264
  gene symbol: MDM4
  hgvsc: ENST00000454264.2:c.343+614_343+615delCT
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000470908
  gene symbol: MDM4
  hgvsc: ENST00000470908.1:n.437+614_437+615delCT
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356151
  ensembl transcript: ENST00000367183
  gene symbol: MDM4
  hgvsc: ENST00000367183.3:c.78+7264_78+7265delCT
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000375811
  ensembl transcript: ENST00000391947
  gene symbol: MDM4
  hgvsc: ENST00000391947.2:c.343+614_343+615delCT
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000463049
  gene symbol: MDM4
  hgvsc: ENST00000463049.1:n.482+614_482+615delCT
  variant of: http://identifiers.org/hgnc/6974
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3713
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3915
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5293
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6008
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 885
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1719
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8224
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2950
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6990
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8116
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 968
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1415
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2028
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2455
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1145
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 702
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 363
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3151
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 353
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 155
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 263
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
population: Other
population: European (Finnish)
population: South Asian
reference allele: CCT
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: DP

1-204501985-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 204501985
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 204501985
    reference: chr 1
allele count: 2
allele frequency: 1.740674337238246e-5
allele num: 114898
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000470908
  gene symbol: MDM4
  hgvsc: ENST00000470908.1:n.437+611T>A
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000463049
  gene symbol: MDM4
  hgvsc: ENST00000463049.1:n.482+611T>A
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356151
  ensembl transcript: ENST00000367183
  gene symbol: MDM4
  hgvsc: ENST00000367183.3:c.78+7261T>A
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356150
  ensembl transcript: ENST00000367182
  gene symbol: MDM4
  hgvsc: ENST00000367182.3:c.343+611T>A
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000471783
  gene symbol: MDM4
  hgvsc: ENST00000471783.1:n.227-5352T>A
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000443816
  ensembl transcript: ENST00000507825
  gene symbol: MDM4
  hgvsc: ENST00000507825.2:c.343+611T>A
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000375811
  ensembl transcript: ENST00000391947
  gene symbol: MDM4
  hgvsc: ENST00000391947.2:c.343+611T>A
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000396840
  ensembl transcript: ENST00000454264
  gene symbol: MDM4
  hgvsc: ENST00000454264.2:c.343+611T>A
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356148
  ensembl transcript: ENST00000367180
  gene symbol: MDM4
  hgvsc: ENST00000367180.1:c.394+38T>A
  variant of: http://identifiers.org/hgnc/6974
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2029
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1204
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1415
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5290
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5830
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8081
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3915
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1145
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2950
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 702
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8195
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6991
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3713
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 885
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1719
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2455
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 112
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 448
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 261
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 173
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3587
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: African
population: Other
population: East Asian
reference allele: T
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: MQ

1-204501988-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 204501988
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 204501988
    reference: chr 1
allele count: 2
allele frequency: 1.741098633237573e-5
allele num: 114870
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000470908
  gene symbol: MDM4
  hgvsc: ENST00000470908.1:n.437+614C>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000375811
  ensembl transcript: ENST00000391947
  gene symbol: MDM4
  hgvsc: ENST00000391947.2:c.343+614C>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000471783
  gene symbol: MDM4
  hgvsc: ENST00000471783.1:n.227-5349C>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000463049
  gene symbol: MDM4
  hgvsc: ENST00000463049.1:n.482+614C>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000443816
  ensembl transcript: ENST00000507825
  gene symbol: MDM4
  hgvsc: ENST00000507825.2:c.343+614C>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000396840
  ensembl transcript: ENST00000454264
  gene symbol: MDM4
  hgvsc: ENST00000454264.2:c.343+614C>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356150
  ensembl transcript: ENST00000367182
  gene symbol: MDM4
  hgvsc: ENST00000367182.3:c.343+614C>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356151
  ensembl transcript: ENST00000367183
  gene symbol: MDM4
  hgvsc: ENST00000367183.3:c.78+7264C>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356148
  ensembl transcript: ENST00000367180
  gene symbol: MDM4
  hgvsc: ENST00000367180.1:c.394+41C>G
  variant of: http://identifiers.org/hgnc/6974
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5903
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2455
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1249
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 884
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 702
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6992
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1416
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8171
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1719
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7981
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2027
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3713
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 575
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1145
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5290
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3914
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2950
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 186
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 247
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 255
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 498
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
reference allele: C
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: DP

1-204501990-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 204501990
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 204501990
    reference: chr 1
allele count: 2
allele frequency: 1.741098633237573e-5
allele num: 114870
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356151
  ensembl transcript: ENST00000367183
  gene symbol: MDM4
  hgvsc: ENST00000367183.3:c.78+7266A>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000375811
  ensembl transcript: ENST00000391947
  gene symbol: MDM4
  hgvsc: ENST00000391947.2:c.343+616A>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000463049
  gene symbol: MDM4
  hgvsc: ENST00000463049.1:n.482+616A>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000396840
  ensembl transcript: ENST00000454264
  gene symbol: MDM4
  hgvsc: ENST00000454264.2:c.343+616A>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000470908
  gene symbol: MDM4
  hgvsc: ENST00000470908.1:n.437+616A>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000471783
  gene symbol: MDM4
  hgvsc: ENST00000471783.1:n.227-5347A>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356148
  ensembl transcript: ENST00000367180
  gene symbol: MDM4
  hgvsc: ENST00000367180.1:c.394+43A>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356150
  ensembl transcript: ENST00000367182
  gene symbol: MDM4
  hgvsc: ENST00000367182.3:c.343+616A>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000443816
  ensembl transcript: ENST00000507825
  gene symbol: MDM4
  hgvsc: ENST00000507825.2:c.343+616A>G
  variant of: http://identifiers.org/hgnc/6974
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7854
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6984
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2028
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8108
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3714
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6096
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 885
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1145
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1248
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3912
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1414
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5292
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1719
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 702
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2950
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2455
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 252
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 424
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 575
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 679
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2155
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 225
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/1-204506020-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 204506020
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 204506020
    reference: chr 1
allele count: 0
allele frequency: 0.0e0
allele num: 19394
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356151
  ensembl transcript: ENST00000367183
  gene symbol: MDM4
  hgvsc: ENST00000367183.3:c.78+11296A>C
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000471783
  gene symbol: MDM4
  hgvsc: ENST00000471783.1:n.227-1317A>C
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000396840
  ensembl transcript: ENST00000454264
  gene symbol: MDM4
  hgvsc: ENST00000454264.2:c.344-538A>C
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000470908
  gene symbol: MDM4
  hgvsc: ENST00000470908.1:n.438-1317A>C
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356150
  ensembl transcript: ENST00000367182
  gene symbol: MDM4
  hgvsc: ENST00000367182.3:c.344-538A>C
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000375811
  ensembl transcript: ENST00000391947
  gene symbol: MDM4
  hgvsc: ENST00000391947.2:c.344-1317A>C
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000463049
  gene symbol: MDM4
  hgvsc: ENST00000463049.1:n.483-567A>C
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000443816
  ensembl transcript: ENST00000507825
  gene symbol: MDM4
  hgvsc: ENST00000507825.2:c.343+4646A>C
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356148
  ensembl transcript: ENST00000367180
  gene symbol: MDM4
  hgvsc: ENST00000367180.1:c.395-26A>C
  variant of: http://identifiers.org/hgnc/6974
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 3537
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22843
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 721
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3168
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22975
  bin: 2.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 667
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19045
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3531
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 127
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 975
  bin: 3.25e1
  variant carriers: 2
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
population: Latino
reference allele: A
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff

1-204506031-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 204506031
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 204506031
    reference: chr 1
allele count: 1
allele frequency: 5.054589567327133e-5
allele num: 19784
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356148
  ensembl transcript: ENST00000367180
  gene symbol: MDM4
  hgvsc: ENST00000367180.1:c.395-15A>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000396840
  ensembl transcript: ENST00000454264
  gene symbol: MDM4
  hgvsc: ENST00000454264.2:c.344-527A>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356151
  ensembl transcript: ENST00000367183
  gene symbol: MDM4
  hgvsc: ENST00000367183.3:c.78+11307A>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000443816
  ensembl transcript: ENST00000507825
  gene symbol: MDM4
  hgvsc: ENST00000507825.2:c.343+4657A>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000375811
  ensembl transcript: ENST00000391947
  gene symbol: MDM4
  hgvsc: ENST00000391947.2:c.344-1306A>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356150
  ensembl transcript: ENST00000367182
  gene symbol: MDM4
  hgvsc: ENST00000367182.3:c.344-527A>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000463049
  gene symbol: MDM4
  hgvsc: ENST00000463049.1:n.483-556A>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000471783
  gene symbol: MDM4
  hgvsc: ENST00000471783.1:n.227-1306A>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000470908
  gene symbol: MDM4
  hgvsc: ENST00000470908.1:n.438-1306A>G
  variant of: http://identifiers.org/hgnc/6974
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21356
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2894
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 668
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24433
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4041
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 100
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2481
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 290
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4253
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 828
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff

1-204506037-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 204506037
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 204506037
    reference: chr 1
allele count: 0
allele frequency: 0.0e0
allele num: 19962
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356150
  ensembl transcript: ENST00000367182
  gene symbol: MDM4
  hgvsc: ENST00000367182.3:c.344-521G>T
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000463049
  gene symbol: MDM4
  hgvsc: ENST00000463049.1:n.483-550G>T
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000471783
  gene symbol: MDM4
  hgvsc: ENST00000471783.1:n.227-1300G>T
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000375811
  ensembl transcript: ENST00000391947
  gene symbol: MDM4
  hgvsc: ENST00000391947.2:c.344-1300G>T
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356151
  ensembl transcript: ENST00000367183
  gene symbol: MDM4
  hgvsc: ENST00000367183.3:c.78+11313G>T
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000396840
  ensembl transcript: ENST00000454264
  gene symbol: MDM4
  hgvsc: ENST00000454264.2:c.344-521G>T
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356148
  ensembl transcript: ENST00000367180
  gene symbol: MDM4
  hgvsc: ENST00000367180.1:c.395-9G>T
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000470908
  gene symbol: MDM4
  hgvsc: ENST00000470908.1:n.438-1300G>T
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000443816
  ensembl transcript: ENST00000507825
  gene symbol: MDM4
  hgvsc: ENST00000507825.2:c.343+4663G>T
  variant of: http://identifiers.org/hgnc/6974
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20434
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 667
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4187
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25265
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2850
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 884
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2191
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1002
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 749
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19082
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
reference allele: G
site quality: QD
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum

1-204506051-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 204506051
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 204506051
    reference: chr 1
allele count: 6
allele frequency: 2.936282666144661e-4
allele num: 20434
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000471783
  gene symbol: MDM4
  hgvsc: ENST00000471783.1:n.227-1286C>T
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000396840
  ensembl transcript: ENST00000454264
  gene symbol: MDM4
  hgvsc: ENST00000454264.2:c.344-507C>T
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000375811
  ensembl transcript: ENST00000391947
  gene symbol: MDM4
  hgvsc: ENST00000391947.2:c.344-1286C>T
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356148
  ensembl transcript: ENST00000367180
  gene symbol: MDM4
  hgvsc: ENST00000367180.1:c.*4C>T
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000463049
  gene symbol: MDM4
  hgvsc: ENST00000463049.1:n.483-536C>T
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000443816
  ensembl transcript: ENST00000507825
  gene symbol: MDM4
  hgvsc: ENST00000507825.2:c.343+4677C>T
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356150
  ensembl transcript: ENST00000367182
  gene symbol: MDM4
  hgvsc: ENST00000367182.3:c.344-507C>T
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000470908
  gene symbol: MDM4
  hgvsc: ENST00000470908.1:n.438-1286C>T
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356151
  ensembl transcript: ENST00000367183
  gene symbol: MDM4
  hgvsc: ENST00000367183.3:c.78+11327C>T
  variant of: http://identifiers.org/hgnc/6974
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4124
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 25768
  bin: 7.5e0
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 667
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3020
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 990
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19663
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 914
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 104
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1756
  bin: 9.75e1
  variant carriers: 5
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: African
population: South Asian
population: Latino
reference allele: C
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: MQRankSum

1-204506052-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 204506052
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 204506052
    reference: chr 1
allele count: 1
allele frequency: 4.88615264340858e-5
allele num: 20466
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356148
  ensembl transcript: ENST00000367180
  gene symbol: MDM4
  hgvsc: ENST00000367180.1:c.*5G>A
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000375811
  ensembl transcript: ENST00000391947
  gene symbol: MDM4
  hgvsc: ENST00000391947.2:c.344-1285G>A
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000443816
  ensembl transcript: ENST00000507825
  gene symbol: MDM4
  hgvsc: ENST00000507825.2:c.343+4678G>A
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000470908
  gene symbol: MDM4
  hgvsc: ENST00000470908.1:n.438-1285G>A
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000463049
  gene symbol: MDM4
  hgvsc: ENST00000463049.1:n.483-535G>A
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000396840
  ensembl transcript: ENST00000454264
  gene symbol: MDM4
  hgvsc: ENST00000454264.2:c.344-506G>A
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356150
  ensembl transcript: ENST00000367182
  gene symbol: MDM4
  hgvsc: ENST00000367182.3:c.344-506G>A
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356151
  ensembl transcript: ENST00000367183
  gene symbol: MDM4
  hgvsc: ENST00000367183.3:c.78+11328G>A
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000471783
  gene symbol: MDM4
  hgvsc: ENST00000471783.1:n.227-1285G>A
  variant of: http://identifiers.org/hgnc/6974
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4094
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3033
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1004
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25798
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19620
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 667
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 386
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 760
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22930
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: Other
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: QD

1-204506070-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 204506070
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 204506070
    reference: chr 1
allele count: 0
allele frequency: 0.0e0
allele num: 20488
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000463049
  gene symbol: MDM4
  hgvsc: ENST00000463049.1:n.483-517A>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356150
  ensembl transcript: ENST00000367182
  gene symbol: MDM4
  hgvsc: ENST00000367182.3:c.344-488A>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000471783
  gene symbol: MDM4
  hgvsc: ENST00000471783.1:n.227-1267A>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356151
  ensembl transcript: ENST00000367183
  gene symbol: MDM4
  hgvsc: ENST00000367183.3:c.78+11346A>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000470908
  gene symbol: MDM4
  hgvsc: ENST00000470908.1:n.438-1267A>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000375811
  ensembl transcript: ENST00000391947
  gene symbol: MDM4
  hgvsc: ENST00000391947.2:c.344-1267A>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000396840
  ensembl transcript: ENST00000454264
  gene symbol: MDM4
  hgvsc: ENST00000454264.2:c.344-488A>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356148
  ensembl transcript: ENST00000367180
  gene symbol: MDM4
  hgvsc: ENST00000367180.1:c.*23A>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000443816
  ensembl transcript: ENST00000507825
  gene symbol: MDM4
  hgvsc: ENST00000507825.2:c.343+4696A>G
  variant of: http://identifiers.org/hgnc/6974
canonical: false
consequence: 3' UTR
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1033
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20765
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3381
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 848
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3164
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24576
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 667
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19795
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1751
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3087
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1104
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3212
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: Other
reference allele: A
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP

1-204506076-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 204506076
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 204506076
    reference: chr 1
allele count: 0
allele frequency: 0.0e0
allele num: 20458
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000463049
  gene symbol: MDM4
  hgvsc: ENST00000463049.1:n.483-511T>C
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356151
  ensembl transcript: ENST00000367183
  gene symbol: MDM4
  hgvsc: ENST00000367183.3:c.78+11352T>C
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000396840
  ensembl transcript: ENST00000454264
  gene symbol: MDM4
  hgvsc: ENST00000454264.2:c.344-482T>C
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000471783
  gene symbol: MDM4
  hgvsc: ENST00000471783.1:n.227-1261T>C
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356148
  ensembl transcript: ENST00000367180
  gene symbol: MDM4
  hgvsc: ENST00000367180.1:c.*29T>C
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356150
  ensembl transcript: ENST00000367182
  gene symbol: MDM4
  hgvsc: ENST00000367182.3:c.344-482T>C
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000443816
  ensembl transcript: ENST00000507825
  gene symbol: MDM4
  hgvsc: ENST00000507825.2:c.343+4702T>C
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000375811
  ensembl transcript: ENST00000391947
  gene symbol: MDM4
  hgvsc: ENST00000391947.2:c.344-1261T>C
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000470908
  gene symbol: MDM4
  hgvsc: ENST00000470908.1:n.438-1261T>C
  variant of: http://identifiers.org/hgnc/6974
canonical: false
consequence: 3' UTR
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 978
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24373
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3470
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2692
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1247
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20923
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 667
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1240
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3289
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3058
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19953
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1227
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: MQ

1-204506077-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 204506077
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 204506077
    reference: chr 1
allele count: 88
allele frequency: 4.280988519167153e-3
allele num: 20556
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356148
  ensembl transcript: ENST00000367180
  gene symbol: MDM4
  hgvsc: ENST00000367180.1:c.*30T>C
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000375811
  ensembl transcript: ENST00000391947
  gene symbol: MDM4
  hgvsc: ENST00000391947.2:c.344-1260T>C
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000396840
  ensembl transcript: ENST00000454264
  gene symbol: MDM4
  hgvsc: ENST00000454264.2:c.344-481T>C
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000443816
  ensembl transcript: ENST00000507825
  gene symbol: MDM4
  hgvsc: ENST00000507825.2:c.343+4703T>C
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356150
  ensembl transcript: ENST00000367182
  gene symbol: MDM4
  hgvsc: ENST00000367182.3:c.344-481T>C
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356151
  ensembl transcript: ENST00000367183
  gene symbol: MDM4
  hgvsc: ENST00000367183.3:c.78+11353T>C
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000470908
  gene symbol: MDM4
  hgvsc: ENST00000470908.1:n.438-1260T>C
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000463049
  gene symbol: MDM4
  hgvsc: ENST00000463049.1:n.483-510T>C
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000471783
  gene symbol: MDM4
  hgvsc: ENST00000471783.1:n.227-1260T>C
  variant of: http://identifiers.org/hgnc/6974
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 955
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2606
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20877
  bin: 2.5e0
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24331
  bin: 7.5e0
  variant carriers: 113
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3519
  bin: 1.25e1
  variant carriers: 55
genotype depth: GenotypeDepth
  all individuals: 1364
  bin: 1.75e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 668
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3799
  bin: 1.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 2952
  bin: 6.25e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 18125
  bin: 2.25e1
  variant carriers: 15
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 5.75e1
  variant carriers: 12
genotype quality: GenotypeQuality
  all individuals: 19849
  bin: 7.5e0
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 676
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Other
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum

1-204506088-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 204506088
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 204506088
    reference: chr 1
allele count: 18
allele frequency: 8.847817538340543e-4
allele num: 20344
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000470908
  gene symbol: MDM4
  hgvsc: ENST00000470908.1:n.438-1249C>T
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000396840
  ensembl transcript: ENST00000454264
  gene symbol: MDM4
  hgvsc: ENST00000454264.2:c.344-470C>T
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356148
  ensembl transcript: ENST00000367180
  gene symbol: MDM4
  hgvsc: ENST00000367180.1:c.*41C>T
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000375811
  ensembl transcript: ENST00000391947
  gene symbol: MDM4
  hgvsc: ENST00000391947.2:c.344-1249C>T
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000463049
  gene symbol: MDM4
  hgvsc: ENST00000463049.1:n.483-499C>T
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356150
  ensembl transcript: ENST00000367182
  gene symbol: MDM4
  hgvsc: ENST00000367182.3:c.344-470C>T
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000443816
  ensembl transcript: ENST00000507825
  gene symbol: MDM4
  hgvsc: ENST00000507825.2:c.343+4714C>T
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356151
  ensembl transcript: ENST00000367183
  gene symbol: MDM4
  hgvsc: ENST00000367183.3:c.78+11364C>T
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000471783
  gene symbol: MDM4
  hgvsc: ENST00000471783.1:n.227-1249C>T
  variant of: http://identifiers.org/hgnc/6974
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24368
  bin: 7.5e0
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 666
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2155
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1964
  bin: 2.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 740
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20706
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3601
  bin: 1.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 553
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 367
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15127
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4910
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 987
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19600
  bin: 7.5e0
  variant carriers: 1
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: African
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
reference allele: C
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum

1-204506089-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 204506089
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 204506089
    reference: chr 1
allele count: 8
allele frequency: 3.913894324853229e-4
allele num: 20440
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000443816
  ensembl transcript: ENST00000507825
  gene symbol: MDM4
  hgvsc: ENST00000507825.2:c.343+4715G>A
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356148
  ensembl transcript: ENST00000367180
  gene symbol: MDM4
  hgvsc: ENST00000367180.1:c.*42G>A
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000375811
  ensembl transcript: ENST00000391947
  gene symbol: MDM4
  hgvsc: ENST00000391947.2:c.344-1248G>A
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000396840
  ensembl transcript: ENST00000454264
  gene symbol: MDM4
  hgvsc: ENST00000454264.2:c.344-469G>A
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000470908
  gene symbol: MDM4
  hgvsc: ENST00000470908.1:n.438-1248G>A
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000463049
  gene symbol: MDM4
  hgvsc: ENST00000463049.1:n.483-498G>A
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356150
  ensembl transcript: ENST00000367182
  gene symbol: MDM4
  hgvsc: ENST00000367182.3:c.344-469G>A
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000471783
  gene symbol: MDM4
  hgvsc: ENST00000471783.1:n.227-1248G>A
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356151
  ensembl transcript: ENST00000367183
  gene symbol: MDM4
  hgvsc: ENST00000367183.3:c.78+11365G>A
  variant of: http://identifiers.org/hgnc/6974
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 665
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20691
  bin: 2.5e0
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 733
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3663
  bin: 1.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2142
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24364
  bin: 7.5e0
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1985
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1008
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14912
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5053
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1761
  bin: 9.75e1
  variant carriers: 9
genotype quality: GenotypeQuality
  all individuals: 200
  bin: 5.25e1
  variant carriers: 1
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD

1-204506513-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 204506513
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 204506513
    reference: chr 1
allele count: 1
allele frequency: 8.253276550790664e-6
allele num: 121164
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000443816
  ensembl transcript: ENST00000507825
  gene symbol: MDM4
  hgvsc: ENST00000507825.2:c.343+5139G>A
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356151
  ensembl transcript: ENST00000367183
  gene symbol: MDM4
  hgvsc: ENST00000367183.3:c.78+11789G>A
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000396840
  ensembl transcript: ENST00000454264
  gene symbol: MDM4
  hgvsc: ENST00000454264.2:c.344-45G>A
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356150
  ensembl transcript: ENST00000367182
  gene symbol: MDM4
  hgvsc: ENST00000367182.3:c.344-45G>A
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000471783
  gene symbol: MDM4
  hgvsc: ENST00000471783.1:n.227-824G>A
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000463049
  gene symbol: MDM4
  hgvsc: ENST00000463049.1:n.483-74G>A
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000375811
  ensembl transcript: ENST00000391947
  gene symbol: MDM4
  hgvsc: ENST00000391947.2:c.344-824G>A
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000470908
  gene symbol: MDM4
  hgvsc: ENST00000470908.1:n.438-824G>A
  variant of: http://identifiers.org/hgnc/6974
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2407
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4223
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1203
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5124
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 736
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6698
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7455
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8264
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7946
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1076
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6655
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1746
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3530
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1588
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2041
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 386
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3402
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 259
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3638
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 167
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 540
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP

1-204506513-GTTA-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 204506513
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 204506510
    reference: chr 1
allele count: 1
allele frequency: 8.253276550790664e-6
allele num: 121164
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000463049
  gene symbol: MDM4
  hgvsc: ENST00000463049.1:n.483-70_483-68delTTA
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000471783
  gene symbol: MDM4
  hgvsc: ENST00000471783.1:n.227-820_227-818delTTA
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356150
  ensembl transcript: ENST00000367182
  gene symbol: MDM4
  hgvsc: ENST00000367182.3:c.344-41_344-39delTTA
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000443816
  ensembl transcript: ENST00000507825
  gene symbol: MDM4
  hgvsc: ENST00000507825.2:c.343+5143_343+5145delTTA
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000375811
  ensembl transcript: ENST00000391947
  gene symbol: MDM4
  hgvsc: ENST00000391947.2:c.344-820_344-818delTTA
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000396840
  ensembl transcript: ENST00000454264
  gene symbol: MDM4
  hgvsc: ENST00000454264.2:c.344-41_344-39delTTA
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356151
  ensembl transcript: ENST00000367183
  gene symbol: MDM4
  hgvsc: ENST00000367183.3:c.78+11793_78+11795delTTA
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000470908
  gene symbol: MDM4
  hgvsc: ENST00000470908.1:n.438-820_438-818delTTA
  variant of: http://identifiers.org/hgnc/6974
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5124
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1746
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4223
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3530
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7946
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6698
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8264
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1588
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7455
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2407
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1076
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1203
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6655
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 736
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 259
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7028
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 251
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33507
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 167
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 144
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
reference allele: GTTA
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum

1-204506514-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 204506514
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 204506514
    reference: chr 1
allele count: 1
allele frequency: 8.252731654177533e-6
allele num: 121172
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000463049
  gene symbol: MDM4
  hgvsc: ENST00000463049.1:n.483-73T>C
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356151
  ensembl transcript: ENST00000367183
  gene symbol: MDM4
  hgvsc: ENST00000367183.3:c.78+11790T>C
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000471783
  gene symbol: MDM4
  hgvsc: ENST00000471783.1:n.227-823T>C
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356150
  ensembl transcript: ENST00000367182
  gene symbol: MDM4
  hgvsc: ENST00000367182.3:c.344-44T>C
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000443816
  ensembl transcript: ENST00000507825
  gene symbol: MDM4
  hgvsc: ENST00000507825.2:c.343+5140T>C
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000375811
  ensembl transcript: ENST00000391947
  gene symbol: MDM4
  hgvsc: ENST00000391947.2:c.344-823T>C
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000396840
  ensembl transcript: ENST00000454264
  gene symbol: MDM4
  hgvsc: ENST00000454264.2:c.344-44T>C
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000470908
  gene symbol: MDM4
  hgvsc: ENST00000470908.1:n.438-823T>C
  variant of: http://identifiers.org/hgnc/6974
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1746
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8270
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1076
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2406
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6713
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1098
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7946
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4306
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7464
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1588
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3529
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 736
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5123
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 556
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6655
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2039
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 142
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 170
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7186
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 338
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3642
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3451
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
population: South Asian
population: European (Finnish)
reference allele: T
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: QD

1-204506527-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 204506527
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 204506527
    reference: chr 1
allele count: 1
allele frequency: 8.247422680412371e-6
allele num: 121250
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000463049
  gene symbol: MDM4
  hgvsc: ENST00000463049.1:n.483-60A>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356150
  ensembl transcript: ENST00000367182
  gene symbol: MDM4
  hgvsc: ENST00000367182.3:c.344-31A>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000443816
  ensembl transcript: ENST00000507825
  gene symbol: MDM4
  hgvsc: ENST00000507825.2:c.343+5153A>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356151
  ensembl transcript: ENST00000367183
  gene symbol: MDM4
  hgvsc: ENST00000367183.3:c.78+11803A>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000396840
  ensembl transcript: ENST00000454264
  gene symbol: MDM4
  hgvsc: ENST00000454264.2:c.344-31A>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000375811
  ensembl transcript: ENST00000391947
  gene symbol: MDM4
  hgvsc: ENST00000391947.2:c.344-810A>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000470908
  gene symbol: MDM4
  hgvsc: ENST00000470908.1:n.438-810A>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000471783
  gene symbol: MDM4
  hgvsc: ENST00000471783.1:n.227-810A>G
  variant of: http://identifiers.org/hgnc/6974
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 7954
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5080
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5125
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7131
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6660
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7581
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8287
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1077
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1589
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 736
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2404
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3528
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1747
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 99
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2078
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3237
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: A
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD

1-204506527-AG-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 204506527
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 204506526
    reference: chr 1
allele count: 1
allele frequency: 8.247422680412371e-6
allele num: 121250
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356150
  ensembl transcript: ENST00000367182
  gene symbol: MDM4
  hgvsc: ENST00000367182.3:c.344-29delG
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356151
  ensembl transcript: ENST00000367183
  gene symbol: MDM4
  hgvsc: ENST00000367183.3:c.78+11805delG
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000396840
  ensembl transcript: ENST00000454264
  gene symbol: MDM4
  hgvsc: ENST00000454264.2:c.344-29delG
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000463049
  gene symbol: MDM4
  hgvsc: ENST00000463049.1:n.483-58delG
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000470908
  gene symbol: MDM4
  hgvsc: ENST00000470908.1:n.438-808delG
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000471783
  gene symbol: MDM4
  hgvsc: ENST00000471783.1:n.227-808delG
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000443816
  ensembl transcript: ENST00000507825
  gene symbol: MDM4
  hgvsc: ENST00000507825.2:c.343+5155delG
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000375811
  ensembl transcript: ENST00000391947
  gene symbol: MDM4
  hgvsc: ENST00000391947.2:c.344-808delG
  variant of: http://identifiers.org/hgnc/6974
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1077
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1747
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1589
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7581
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 736
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3528
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5125
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8287
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6660
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2404
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5080
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7131
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7954
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33512
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2078
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3450
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
population: Latino
population: South Asian
population: European (Finnish)
reference allele: AG
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum

1-204506534-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 204506534
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 204506534
    reference: chr 1
allele count: 28
allele frequency: 2.309964195554969e-4
allele num: 121214
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356150
  ensembl transcript: ENST00000367182
  gene symbol: MDM4
  hgvsc: ENST00000367182.3:c.344-24C>T
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000375811
  ensembl transcript: ENST00000391947
  gene symbol: MDM4
  hgvsc: ENST00000391947.2:c.344-803C>T
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000471783
  gene symbol: MDM4
  hgvsc: ENST00000471783.1:n.227-803C>T
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000463049
  gene symbol: MDM4
  hgvsc: ENST00000463049.1:n.483-53C>T
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000470908
  gene symbol: MDM4
  hgvsc: ENST00000470908.1:n.438-803C>T
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000443816
  ensembl transcript: ENST00000507825
  gene symbol: MDM4
  hgvsc: ENST00000507825.2:c.343+5160C>T
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356151
  ensembl transcript: ENST00000367183
  gene symbol: MDM4
  hgvsc: ENST00000367183.3:c.78+11810C>T
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000396840
  ensembl transcript: ENST00000454264
  gene symbol: MDM4
  hgvsc: ENST00000454264.2:c.344-24C>T
  variant of: http://identifiers.org/hgnc/6974
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 6665
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 741
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1077
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 7229
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3528
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1591
  bin: 6.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7606
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5133
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8290
  bin: 3.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 2406
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5127
  bin: 5.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1750
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 7955
  bin: 4.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 5.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 2.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2080
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
population: Other
reference allele: C
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD

1-204506535-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 204506535
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 204506535
    reference: chr 1
allele count: 1
allele frequency: 8.24347940778844e-6
allele num: 121308
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000470908
  gene symbol: MDM4
  hgvsc: ENST00000470908.1:n.438-802C>T
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000375811
  ensembl transcript: ENST00000391947
  gene symbol: MDM4
  hgvsc: ENST00000391947.2:c.344-802C>T
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000396840
  ensembl transcript: ENST00000454264
  gene symbol: MDM4
  hgvsc: ENST00000454264.2:c.344-23C>T
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000463049
  gene symbol: MDM4
  hgvsc: ENST00000463049.1:n.483-52C>T
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356151
  ensembl transcript: ENST00000367183
  gene symbol: MDM4
  hgvsc: ENST00000367183.3:c.78+11811C>T
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000443816
  ensembl transcript: ENST00000507825
  gene symbol: MDM4
  hgvsc: ENST00000507825.2:c.343+5161C>T
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000471783
  gene symbol: MDM4
  hgvsc: ENST00000471783.1:n.227-802C>T
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356150
  ensembl transcript: ENST00000367182
  gene symbol: MDM4
  hgvsc: ENST00000367182.3:c.344-23C>T
  variant of: http://identifiers.org/hgnc/6974
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5146
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7950
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7606
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7247
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 742
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5124
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1746
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2413
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1591
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8287
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6665
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1073
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3532
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3778
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: QD

1-204506540-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 204506540
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 204506540
    reference: chr 1
allele count: 27
allele frequency: 2.227061268930021e-4
allele num: 121236
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000443816
  ensembl transcript: ENST00000507825
  gene symbol: MDM4
  hgvsc: ENST00000507825.2:c.343+5166G>T
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000396840
  ensembl transcript: ENST00000454264
  gene symbol: MDM4
  hgvsc: ENST00000454264.2:c.344-18G>T
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000471783
  gene symbol: MDM4
  hgvsc: ENST00000471783.1:n.227-797G>T
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356151
  ensembl transcript: ENST00000367183
  gene symbol: MDM4
  hgvsc: ENST00000367183.3:c.78+11816G>T
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000463049
  gene symbol: MDM4
  hgvsc: ENST00000463049.1:n.483-47G>T
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000375811
  ensembl transcript: ENST00000391947
  gene symbol: MDM4
  hgvsc: ENST00000391947.2:c.344-797G>T
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356150
  ensembl transcript: ENST00000367182
  gene symbol: MDM4
  hgvsc: ENST00000367182.3:c.344-18G>T
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000470908
  gene symbol: MDM4
  hgvsc: ENST00000470908.1:n.438-797G>T
  variant of: http://identifiers.org/hgnc/6974
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 1590
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5165
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 750
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1749
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 8280
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1074
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7945
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7282
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2417
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 596
  bin: 8.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 7606
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3533
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5121
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 6663
  bin: 4.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 33465
  bin: 9.75e1
  variant carriers: 14
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2078
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3422
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 2
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum

1-204506545-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 204506545
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 204506545
    reference: chr 1
allele count: 1
allele frequency: 8.24551856066228e-6
allele num: 121278
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356151
  ensembl transcript: ENST00000367183
  gene symbol: MDM4
  hgvsc: ENST00000367183.3:c.78+11821A>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000375811
  ensembl transcript: ENST00000391947
  gene symbol: MDM4
  hgvsc: ENST00000391947.2:c.344-792A>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000470908
  gene symbol: MDM4
  hgvsc: ENST00000470908.1:n.438-792A>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000471783
  gene symbol: MDM4
  hgvsc: ENST00000471783.1:n.227-792A>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000463049
  gene symbol: MDM4
  hgvsc: ENST00000463049.1:n.483-42A>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356150
  ensembl transcript: ENST00000367182
  gene symbol: MDM4
  hgvsc: ENST00000367182.3:c.344-13A>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000396840
  ensembl transcript: ENST00000454264
  gene symbol: MDM4
  hgvsc: ENST00000454264.2:c.344-13A>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000443816
  ensembl transcript: ENST00000507825
  gene symbol: MDM4
  hgvsc: ENST00000507825.2:c.343+5171A>G
  variant of: http://identifiers.org/hgnc/6974
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 7949
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1766
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8288
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7305
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5184
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1585
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 744
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7600
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3525
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1080
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6659
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2416
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5120
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2078
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3235
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
reference allele: A
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: QD

1-204506545-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 204506545
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 204506545
    reference: chr 1
allele count: 6
allele frequency: 4.947311136397368e-5
allele num: 121278
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000375811
  ensembl transcript: ENST00000391947
  gene symbol: MDM4
  hgvsc: ENST00000391947.2:c.344-792A>T
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356150
  ensembl transcript: ENST00000367182
  gene symbol: MDM4
  hgvsc: ENST00000367182.3:c.344-13A>T
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000443816
  ensembl transcript: ENST00000507825
  gene symbol: MDM4
  hgvsc: ENST00000507825.2:c.343+5171A>T
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000463049
  gene symbol: MDM4
  hgvsc: ENST00000463049.1:n.483-42A>T
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000396840
  ensembl transcript: ENST00000454264
  gene symbol: MDM4
  hgvsc: ENST00000454264.2:c.344-13A>T
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000471783
  gene symbol: MDM4
  hgvsc: ENST00000471783.1:n.227-792A>T
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356151
  ensembl transcript: ENST00000367183
  gene symbol: MDM4
  hgvsc: ENST00000367183.3:c.78+11821A>T
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000470908
  gene symbol: MDM4
  hgvsc: ENST00000470908.1:n.438-792A>T
  variant of: http://identifiers.org/hgnc/6974
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7305
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1766
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 5120
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1585
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7949
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6659
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3525
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 744
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5184
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1080
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8288
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7600
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2416
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3426
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2078
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
population: South Asian
population: African
reference allele: A
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: QD

1-204506546-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 204506546
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 204506546
    reference: chr 1
allele count: 2
allele frequency: 1.648505629646725e-5
allele num: 121322
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356151
  ensembl transcript: ENST00000367183
  gene symbol: MDM4
  hgvsc: ENST00000367183.3:c.78+11822C>T
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000471783
  gene symbol: MDM4
  hgvsc: ENST00000471783.1:n.227-791C>T
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000470908
  gene symbol: MDM4
  hgvsc: ENST00000470908.1:n.438-791C>T
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356150
  ensembl transcript: ENST00000367182
  gene symbol: MDM4
  hgvsc: ENST00000367182.3:c.344-12C>T
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000396840
  ensembl transcript: ENST00000454264
  gene symbol: MDM4
  hgvsc: ENST00000454264.2:c.344-12C>T
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000463049
  gene symbol: MDM4
  hgvsc: ENST00000463049.1:n.483-41C>T
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000375811
  ensembl transcript: ENST00000391947
  gene symbol: MDM4
  hgvsc: ENST00000391947.2:c.344-791C>T
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000443816
  ensembl transcript: ENST00000507825
  gene symbol: MDM4
  hgvsc: ENST00000507825.2:c.343+5172C>T
  variant of: http://identifiers.org/hgnc/6974
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 7949
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7311
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3529
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7606
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6658
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1747
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5126
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5185
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2410
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 745
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8291
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1078
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1588
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2085
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2080
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: C
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: ReadPosRankSum

1-204506552-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 204506552
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 204506552
    reference: chr 1
allele count: 1
allele frequency: 8.238996819747227e-6
allele num: 121374
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000375811
  ensembl transcript: ENST00000391947
  gene symbol: MDM4
  hgvsc: ENST00000391947.2:c.344-785A>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000471783
  gene symbol: MDM4
  hgvsc: ENST00000471783.1:n.227-785A>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000443816
  ensembl transcript: ENST00000507825
  gene symbol: MDM4
  hgvsc: ENST00000507825.2:c.343+5178A>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000396840
  ensembl transcript: ENST00000454264
  gene symbol: MDM4
  hgvsc: ENST00000454264.2:c.344-6A>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356150
  ensembl transcript: ENST00000367182
  gene symbol: MDM4
  hgvsc: ENST00000367182.3:c.344-6A>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356151
  ensembl transcript: ENST00000367183
  gene symbol: MDM4
  hgvsc: ENST00000367183.3:c.78+11828A>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000470908
  gene symbol: MDM4
  hgvsc: ENST00000470908.1:n.438-785A>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000463049
  gene symbol: MDM4
  hgvsc: ENST00000463049.1:n.483-35A>G
  variant of: http://identifiers.org/hgnc/6974
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8291
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7949
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5196
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1590
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1076
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5128
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3529
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2411
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6658
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7329
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7612
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1746
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 746
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2085
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3240
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33516
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.75e1
  variant carriers: 0
hgvs: c.344-6A>G
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
population: South Asian
population: East Asian
reference allele: A
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum

1-204506558-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 204506558
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 204506558
    reference: chr 1
allele count: 1
allele frequency: 8.237639422047218e-6
allele num: 121394
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000463049
  gene symbol: MDM4
  hgvsc: ENST00000463049.1:n.483-29A>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000471783
  gene symbol: MDM4
  hgvsc: ENST00000471783.1:n.227-779A>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356151
  ensembl transcript: ENST00000367183
  gene symbol: MDM4
  hgvsc: ENST00000367183.3:c.78+11834A>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356150
  ensembl transcript: ENST00000367182
  gene symbol: MDM4
  hgvsc: ENST00000367182.3:c.344A>G
  hgvsp: ENSP00000356150.3:p.Asp115Gly
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000443816
  ensembl transcript: ENST00000507825
  gene symbol: MDM4
  hgvsc: ENST00000507825.2:c.343+5184A>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000470908
  gene symbol: MDM4
  hgvsc: ENST00000470908.1:n.438-779A>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000375811
  ensembl transcript: ENST00000391947
  gene symbol: MDM4
  hgvsc: ENST00000391947.2:c.344-779A>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000396840
  ensembl transcript: ENST00000454264
  gene symbol: MDM4
  hgvsc: ENST00000454264.2:c.344A>G
  hgvsp: ENSP00000396840.2:p.Asp115Gly
  variant of: http://identifiers.org/hgnc/6974
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 8290
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5128
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3530
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5191
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7345
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 746
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1076
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7951
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7616
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2411
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1589
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6658
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1747
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 9075
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33516
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Asp115Gly
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
population: European (Finnish)
population: Other
reference allele: A
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum

http://identifiers.org/exac.variant/1-204506574-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 204506574
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 204506574
    reference: chr 1
allele count: 1
allele frequency: 8.237503706876667e-6
allele num: 121396
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000463049
  gene symbol: MDM4
  hgvsc: ENST00000463049.1:n.483-13C>A
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356150
  ensembl transcript: ENST00000367182
  gene symbol: MDM4
  hgvsc: ENST00000367182.3:c.360C>A
  hgvsp: ENST00000367182.3:c.360C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000470908
  gene symbol: MDM4
  hgvsc: ENST00000470908.1:n.438-763C>A
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000375811
  ensembl transcript: ENST00000391947
  gene symbol: MDM4
  hgvsc: ENST00000391947.2:c.344-763C>A
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000396840
  ensembl transcript: ENST00000454264
  gene symbol: MDM4
  hgvsc: ENST00000454264.2:c.360C>A
  hgvsp: ENST00000454264.2:c.360C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000471783
  gene symbol: MDM4
  hgvsc: ENST00000471783.1:n.227-763C>A
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356151
  ensembl transcript: ENST00000367183
  gene symbol: MDM4
  hgvsc: ENST00000367183.3:c.79-11820C>A
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000443816
  ensembl transcript: ENST00000507825
  gene symbol: MDM4
  hgvsc: ENST00000507825.2:c.343+5200C>A
  variant of: http://identifiers.org/hgnc/6974
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7360
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1077
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1589
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6658
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7621
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7949
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5128
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 746
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5183
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8290
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2411
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3530
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1747
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3793
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9087
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Leu120Leu
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
reference allele: C
site quality: DP
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum

1-204506577-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 204506577
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 204506577
    reference: chr 1
allele count: 1
allele frequency: 8.237367996177861e-6
allele num: 121398
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356151
  ensembl transcript: ENST00000367183
  gene symbol: MDM4
  hgvsc: ENST00000367183.3:c.79-11817T>C
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000443816
  ensembl transcript: ENST00000507825
  gene symbol: MDM4
  hgvsc: ENST00000507825.2:c.343+5203T>C
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000375811
  ensembl transcript: ENST00000391947
  gene symbol: MDM4
  hgvsc: ENST00000391947.2:c.344-760T>C
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000463049
  gene symbol: MDM4
  hgvsc: ENST00000463049.1:n.483-10T>C
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000471783
  gene symbol: MDM4
  hgvsc: ENST00000471783.1:n.227-760T>C
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356150
  ensembl transcript: ENST00000367182
  gene symbol: MDM4
  hgvsc: ENST00000367182.3:c.363T>C
  hgvsp: ENST00000367182.3:c.363T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000470908
  gene symbol: MDM4
  hgvsc: ENST00000470908.1:n.438-760T>C
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000396840
  ensembl transcript: ENST00000454264
  gene symbol: MDM4
  hgvsc: ENST00000454264.2:c.363T>C
  hgvsp: ENST00000454264.2:c.363T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6974
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7623
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2411
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5182
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5128
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 746
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1589
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6659
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7949
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3529
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7360
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1747
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1077
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8291
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3793
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Ala121Ala
num of homozygotes: 0
population: East Asian
population: Other
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
reference allele: T
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum

1-204506581-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 204506581
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 204506581
    reference: chr 1
allele count: 2
allele frequency: 1.647419317638919e-5
allele num: 121402
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000463049
  gene symbol: MDM4
  hgvsc: ENST00000463049.1:n.483-6G>A
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000443816
  ensembl transcript: ENST00000507825
  gene symbol: MDM4
  hgvsc: ENST00000507825.2:c.343+5207G>A
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000375811
  ensembl transcript: ENST00000391947
  gene symbol: MDM4
  hgvsc: ENST00000391947.2:c.344-756G>A
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356150
  ensembl transcript: ENST00000367182
  gene symbol: MDM4
  hgvsc: ENST00000367182.3:c.367G>A
  hgvsp: ENSP00000356150.3:p.Ala123Thr
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000396840
  ensembl transcript: ENST00000454264
  gene symbol: MDM4
  hgvsc: ENST00000454264.2:c.367G>A
  hgvsp: ENSP00000396840.2:p.Ala123Thr
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000471783
  gene symbol: MDM4
  hgvsc: ENST00000471783.1:n.227-756G>A
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356151
  ensembl transcript: ENST00000367183
  gene symbol: MDM4
  hgvsc: ENST00000367183.3:c.79-11813G>A
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000470908
  gene symbol: MDM4
  hgvsc: ENST00000470908.1:n.438-756G>A
  variant of: http://identifiers.org/hgnc/6974
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2412
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7361
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7624
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5184
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7948
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8291
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6657
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5128
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1589
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 746
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1747
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3530
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1077
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3430
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3453
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Ala123Thr
num of homozygotes: 0
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
reference allele: G
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ

1-204506583-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 204506583
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 204506583
    reference: chr 1
allele count: 1
allele frequency: 8.237096588194593e-6
allele num: 121402
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000443816
  ensembl transcript: ENST00000507825
  gene symbol: MDM4
  hgvsc: ENST00000507825.2:c.343+5209A>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356150
  ensembl transcript: ENST00000367182
  gene symbol: MDM4
  hgvsc: ENST00000367182.3:c.369A>G
  hgvsp: ENST00000367182.3:c.369A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000463049
  gene symbol: MDM4
  hgvsc: ENST00000463049.1:n.483-4A>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000470908
  gene symbol: MDM4
  hgvsc: ENST00000470908.1:n.438-754A>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000375811
  ensembl transcript: ENST00000391947
  gene symbol: MDM4
  hgvsc: ENST00000391947.2:c.344-754A>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000396840
  ensembl transcript: ENST00000454264
  gene symbol: MDM4
  hgvsc: ENST00000454264.2:c.369A>G
  hgvsp: ENST00000454264.2:c.369A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000471783
  gene symbol: MDM4
  hgvsc: ENST00000471783.1:n.227-754A>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356151
  ensembl transcript: ENST00000367183
  gene symbol: MDM4
  hgvsc: ENST00000367183.3:c.79-11811A>G
  variant of: http://identifiers.org/hgnc/6974
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1589
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8292
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1077
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 746
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7363
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7624
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1747
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5181
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5128
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7949
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2411
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6657
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3530
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3430
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9089
  bin: 6.25e1
  variant carriers: 0
hgvs: n.483-4A>G
num of homozygotes: 0
population: Other
population: European (Finnish)
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
reference allele: A
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: DP

1-204506593-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 204506593
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 204506593
    reference: chr 1
allele count: 1
allele frequency: 8.237096588194593e-6
allele num: 121402
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000471783
  gene symbol: MDM4
  hgvsc: ENST00000471783.1:n.227-744A>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000375811
  ensembl transcript: ENST00000391947
  gene symbol: MDM4
  hgvsc: ENST00000391947.2:c.344-744A>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356150
  ensembl transcript: ENST00000367182
  gene symbol: MDM4
  hgvsc: ENST00000367182.3:c.379A>G
  hgvsp: ENSP00000356150.3:p.Ser127Gly
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000396840
  ensembl transcript: ENST00000454264
  gene symbol: MDM4
  hgvsc: ENST00000454264.2:c.379A>G
  hgvsp: ENSP00000396840.2:p.Ser127Gly
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000443816
  ensembl transcript: ENST00000507825
  gene symbol: MDM4
  hgvsc: ENST00000507825.2:c.343+5219A>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356151
  ensembl transcript: ENST00000367183
  gene symbol: MDM4
  hgvsc: ENST00000367183.3:c.79-11801A>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000463049
  gene symbol: MDM4
  hgvsc: ENST00000463049.1:n.489A>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000470908
  gene symbol: MDM4
  hgvsc: ENST00000470908.1:n.438-744A>G
  variant of: http://identifiers.org/hgnc/6974
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3530
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 746
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6657
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1077
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5128
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7369
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7626
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5172
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7949
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1747
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2410
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1589
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8293
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33513
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2089
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3245
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Ser127Gly
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: African
population: Latino
population: East Asian
population: Other
reference allele: A
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum

1-204506607-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 204506607
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 204506607
    reference: chr 1
allele count: 1
allele frequency: 8.237503706876667e-6
allele num: 121396
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000470908
  gene symbol: MDM4
  hgvsc: ENST00000470908.1:n.438-730A>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000443816
  ensembl transcript: ENST00000507825
  gene symbol: MDM4
  hgvsc: ENST00000507825.2:c.343+5233A>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356150
  ensembl transcript: ENST00000367182
  gene symbol: MDM4
  hgvsc: ENST00000367182.3:c.393A>G
  hgvsp: ENST00000367182.3:c.393A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000463049
  gene symbol: MDM4
  hgvsc: ENST00000463049.1:n.503A>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000375811
  ensembl transcript: ENST00000391947
  gene symbol: MDM4
  hgvsc: ENST00000391947.2:c.344-730A>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356151
  ensembl transcript: ENST00000367183
  gene symbol: MDM4
  hgvsc: ENST00000367183.3:c.79-11787A>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000471783
  gene symbol: MDM4
  hgvsc: ENST00000471783.1:n.227-730A>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000396840
  ensembl transcript: ENST00000454264
  gene symbol: MDM4
  hgvsc: ENST00000454264.2:c.393A>G
  hgvsp: ENST00000454264.2:c.393A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6974
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5128
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8293
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6657
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1747
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2409
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7950
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1589
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7622
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7370
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 746
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5165
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3530
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1077
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3242
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2087
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9082
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Pro131Pro
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: East Asian
reference allele: A
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum

1-204506640-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 204506640
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 204506640
    reference: chr 1
allele count: 2
allele frequency: 1.648315421639085e-5
allele num: 121336
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000443816
  ensembl transcript: ENST00000507825
  gene symbol: MDM4
  hgvsc: ENST00000507825.2:c.343+5266C>T
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000463049
  gene symbol: MDM4
  hgvsc: ENST00000463049.1:n.521+15C>T
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000470908
  gene symbol: MDM4
  hgvsc: ENST00000470908.1:n.438-697C>T
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000375811
  ensembl transcript: ENST00000391947
  gene symbol: MDM4
  hgvsc: ENST00000391947.2:c.344-697C>T
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000471783
  gene symbol: MDM4
  hgvsc: ENST00000471783.1:n.227-697C>T
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356151
  ensembl transcript: ENST00000367183
  gene symbol: MDM4
  hgvsc: ENST00000367183.3:c.79-11754C>T
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000396840
  ensembl transcript: ENST00000454264
  gene symbol: MDM4
  hgvsc: ENST00000454264.2:c.411+15C>T
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356150
  ensembl transcript: ENST00000367182
  gene symbol: MDM4
  hgvsc: ENST00000367182.3:c.411+15C>T
  variant of: http://identifiers.org/hgnc/6974
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7354
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2410
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7957
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 746
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7636
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4836
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6658
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8296
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5128
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1589
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1078
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1746
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3530
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3454
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 105
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33512
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 8701
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: East Asian
population: Latino
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: QD

1-204506641-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 204506641
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 204506641
    reference: chr 1
allele count: 6
allele frequency: 4.944783253667381e-5
allele num: 121340
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356150
  ensembl transcript: ENST00000367182
  gene symbol: MDM4
  hgvsc: ENST00000367182.3:c.411+16G>A
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000375811
  ensembl transcript: ENST00000391947
  gene symbol: MDM4
  hgvsc: ENST00000391947.2:c.344-696G>A
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000471783
  gene symbol: MDM4
  hgvsc: ENST00000471783.1:n.227-696G>A
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000443816
  ensembl transcript: ENST00000507825
  gene symbol: MDM4
  hgvsc: ENST00000507825.2:c.343+5267G>A
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000470908
  gene symbol: MDM4
  hgvsc: ENST00000470908.1:n.438-696G>A
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000396840
  ensembl transcript: ENST00000454264
  gene symbol: MDM4
  hgvsc: ENST00000454264.2:c.411+16G>A
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356151
  ensembl transcript: ENST00000367183
  gene symbol: MDM4
  hgvsc: ENST00000367183.3:c.79-11753G>A
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000463049
  gene symbol: MDM4
  hgvsc: ENST00000463049.1:n.521+16G>A
  variant of: http://identifiers.org/hgnc/6974
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1591
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1078
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7957
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 746
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5130
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2409
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7352
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8291
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1748
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 4800
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7636
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3531
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6655
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8651
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3425
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3756
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: African
population: East Asian
population: Latino
population: South Asian
reference allele: G
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum

1-204506654-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 204506654
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 204506654
    reference: chr 1
allele count: 2
allele frequency: 1.648532805802836e-5
allele num: 121320
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000470908
  gene symbol: MDM4
  hgvsc: ENST00000470908.1:n.438-683G>A
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000375811
  ensembl transcript: ENST00000391947
  gene symbol: MDM4
  hgvsc: ENST00000391947.2:c.344-683G>A
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000396840
  ensembl transcript: ENST00000454264
  gene symbol: MDM4
  hgvsc: ENST00000454264.2:c.411+29G>A
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000463049
  gene symbol: MDM4
  hgvsc: ENST00000463049.1:n.521+29G>A
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000471783
  gene symbol: MDM4
  hgvsc: ENST00000471783.1:n.227-683G>A
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000443816
  ensembl transcript: ENST00000507825
  gene symbol: MDM4
  hgvsc: ENST00000507825.2:c.343+5280G>A
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356151
  ensembl transcript: ENST00000367183
  gene symbol: MDM4
  hgvsc: ENST00000367183.3:c.79-11740G>A
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356150
  ensembl transcript: ENST00000367182
  gene symbol: MDM4
  hgvsc: ENST00000367182.3:c.411+29G>A
  variant of: http://identifiers.org/hgnc/6974
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8297
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1747
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7010
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5129
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1077
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2407
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7584
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 746
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4185
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3530
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7952
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1589
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 881
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6656
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3218
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 188
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3616
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 318
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 165
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: South Asian
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
reference allele: G
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD

1-204506659-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 204506659
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 204506659
    reference: chr 1
allele count: 2
allele frequency: 1.648777431534517e-5
allele num: 121302
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000463049
  gene symbol: MDM4
  hgvsc: ENST00000463049.1:n.521+34A>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000396840
  ensembl transcript: ENST00000454264
  gene symbol: MDM4
  hgvsc: ENST00000454264.2:c.411+34A>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000443816
  ensembl transcript: ENST00000507825
  gene symbol: MDM4
  hgvsc: ENST00000507825.2:c.343+5285A>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000471783
  gene symbol: MDM4
  hgvsc: ENST00000471783.1:n.227-678A>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356151
  ensembl transcript: ENST00000367183
  gene symbol: MDM4
  hgvsc: ENST00000367183.3:c.79-11735A>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356150
  ensembl transcript: ENST00000367182
  gene symbol: MDM4
  hgvsc: ENST00000367182.3:c.411+34A>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000375811
  ensembl transcript: ENST00000391947
  gene symbol: MDM4
  hgvsc: ENST00000391947.2:c.344-678A>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000470908
  gene symbol: MDM4
  hgvsc: ENST00000470908.1:n.438-678A>G
  variant of: http://identifiers.org/hgnc/6974
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1109
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1077
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1589
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6898
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1746
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7507
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5129
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8289
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4112
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6656
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3533
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 746
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7952
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2407
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 87
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 258
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 211
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 414
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 196
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
population: East Asian
reference allele: A
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD

1-204506665-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 204506665
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 204506665
    reference: chr 1
allele count: 1
allele frequency: 8.246606521416436e-6
allele num: 121262
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000396840
  ensembl transcript: ENST00000454264
  gene symbol: MDM4
  hgvsc: ENST00000454264.2:c.411+40T>A
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000375811
  ensembl transcript: ENST00000391947
  gene symbol: MDM4
  hgvsc: ENST00000391947.2:c.344-672T>A
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000463049
  gene symbol: MDM4
  hgvsc: ENST00000463049.1:n.521+40T>A
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000470908
  gene symbol: MDM4
  hgvsc: ENST00000470908.1:n.438-672T>A
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356151
  ensembl transcript: ENST00000367183
  gene symbol: MDM4
  hgvsc: ENST00000367183.3:c.79-11729T>A
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356150
  ensembl transcript: ENST00000367182
  gene symbol: MDM4
  hgvsc: ENST00000367182.3:c.411+40T>A
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000471783
  gene symbol: MDM4
  hgvsc: ENST00000471783.1:n.227-672T>A
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000443816
  ensembl transcript: ENST00000507825
  gene symbol: MDM4
  hgvsc: ENST00000507825.2:c.343+5291T>A
  variant of: http://identifiers.org/hgnc/6974
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1746
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4065
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6478
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6655
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1589
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7392
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5129
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1077
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2407
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1675
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8283
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7944
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 746
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3532
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3408
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 265
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 261
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3215
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3451
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 619
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
population: South Asian
population: Other
reference allele: T
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum

1-204506668-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 204506668
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 204506668
    reference: chr 1
allele count: 103
allele frequency: 8.497648708852405e-4
allele num: 121210
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000396840
  ensembl transcript: ENST00000454264
  gene symbol: MDM4
  hgvsc: ENST00000454264.2:c.411+43C>T
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000463049
  gene symbol: MDM4
  hgvsc: ENST00000463049.1:n.521+43C>T
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356150
  ensembl transcript: ENST00000367182
  gene symbol: MDM4
  hgvsc: ENST00000367182.3:c.411+43C>T
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000375811
  ensembl transcript: ENST00000391947
  gene symbol: MDM4
  hgvsc: ENST00000391947.2:c.344-669C>T
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356151
  ensembl transcript: ENST00000367183
  gene symbol: MDM4
  hgvsc: ENST00000367183.3:c.79-11726C>T
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000470908
  gene symbol: MDM4
  hgvsc: ENST00000470908.1:n.438-669C>T
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000471783
  gene symbol: MDM4
  hgvsc: ENST00000471783.1:n.227-669C>T
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000443816
  ensembl transcript: ENST00000507825
  gene symbol: MDM4
  hgvsc: ENST00000507825.2:c.343+5294C>T
  variant of: http://identifiers.org/hgnc/6974
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8274
  bin: 3.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2416
  bin: 6.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 7933
  bin: 4.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 4260
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1723
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 6292
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3540
  bin: 5.75e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 7336
  bin: 3.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6647
  bin: 4.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 1080
  bin: 7.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 1591
  bin: 6.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 5124
  bin: 5.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 1747
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 748
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 8.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 695
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2070
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3414
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 270
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 263
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 520
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 2
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
population: Other
population: East Asian
reference allele: C
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP

http://identifiers.org/exac.variant/1-204506670-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 204506670
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 204506670
    reference: chr 1
allele count: 1
allele frequency: 8.250961236984109e-6
allele num: 121198
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000470908
  gene symbol: MDM4
  hgvsc: ENST00000470908.1:n.438-667C>A
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356150
  ensembl transcript: ENST00000367182
  gene symbol: MDM4
  hgvsc: ENST00000367182.3:c.411+45C>A
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000471783
  gene symbol: MDM4
  hgvsc: ENST00000471783.1:n.227-667C>A
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000375811
  ensembl transcript: ENST00000391947
  gene symbol: MDM4
  hgvsc: ENST00000391947.2:c.344-667C>A
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000443816
  ensembl transcript: ENST00000507825
  gene symbol: MDM4
  hgvsc: ENST00000507825.2:c.343+5296C>A
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356151
  ensembl transcript: ENST00000367183
  gene symbol: MDM4
  hgvsc: ENST00000367183.3:c.79-11724C>A
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000463049
  gene symbol: MDM4
  hgvsc: ENST00000463049.1:n.521+45C>A
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000396840
  ensembl transcript: ENST00000454264
  gene symbol: MDM4
  hgvsc: ENST00000454264.2:c.411+45C>A
  variant of: http://identifiers.org/hgnc/6974
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 747
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1714
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7264
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2408
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4443
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6653
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1588
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5130
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6194
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8275
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1747
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7932
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3537
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1077
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3399
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 274
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2072
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 530
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5707
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 1.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 840
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: Latino
reference allele: C
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum

1-204506671-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 204506671
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 204506671
    reference: chr 1
allele count: 2
allele frequency: 1.649974425396406e-5
allele num: 121214
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000471783
  gene symbol: MDM4
  hgvsc: ENST00000471783.1:n.227-666C>T
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000443816
  ensembl transcript: ENST00000507825
  gene symbol: MDM4
  hgvsc: ENST00000507825.2:c.343+5297C>T
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000470908
  gene symbol: MDM4
  hgvsc: ENST00000470908.1:n.438-666C>T
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000396840
  ensembl transcript: ENST00000454264
  gene symbol: MDM4
  hgvsc: ENST00000454264.2:c.411+46C>T
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356150
  ensembl transcript: ENST00000367182
  gene symbol: MDM4
  hgvsc: ENST00000367182.3:c.411+46C>T
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000463049
  gene symbol: MDM4
  hgvsc: ENST00000463049.1:n.521+46C>T
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356151
  ensembl transcript: ENST00000367183
  gene symbol: MDM4
  hgvsc: ENST00000367183.3:c.79-11723C>T
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000375811
  ensembl transcript: ENST00000391947
  gene symbol: MDM4
  hgvsc: ENST00000391947.2:c.344-666C>T
  variant of: http://identifiers.org/hgnc/6974
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8266
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1747
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 747
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2408
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4543
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6134
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6652
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7929
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1708
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3537
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1588
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7240
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5130
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1077
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3443
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3400
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 291
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 748
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 529
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 274
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: Latino
reference allele: C
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum

1-204506675-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 204506675
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 204506675
    reference: chr 1
allele count: 1
allele frequency: 8.250961236984109e-6
allele num: 121198
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356151
  ensembl transcript: ENST00000367183
  gene symbol: MDM4
  hgvsc: ENST00000367183.3:c.79-11719T>C
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000375811
  ensembl transcript: ENST00000391947
  gene symbol: MDM4
  hgvsc: ENST00000391947.2:c.344-662T>C
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000463049
  gene symbol: MDM4
  hgvsc: ENST00000463049.1:n.521+50T>C
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000396840
  ensembl transcript: ENST00000454264
  gene symbol: MDM4
  hgvsc: ENST00000454264.2:c.411+50T>C
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000471783
  gene symbol: MDM4
  hgvsc: ENST00000471783.1:n.227-662T>C
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356150
  ensembl transcript: ENST00000367182
  gene symbol: MDM4
  hgvsc: ENST00000367182.3:c.411+50T>C
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000470908
  gene symbol: MDM4
  hgvsc: ENST00000470908.1:n.438-662T>C
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000443816
  ensembl transcript: ENST00000507825
  gene symbol: MDM4
  hgvsc: ENST00000507825.2:c.343+5301T>C
  variant of: http://identifiers.org/hgnc/6974
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3536
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2408
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1694
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4694
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 748
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7123
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1747
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5131
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6651
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6132
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1076
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1588
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7929
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8243
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3295
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 544
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4462
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 279
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 761
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
reference allele: T
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD

1-204506675-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 204506675
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 204506675
    reference: chr 1
allele count: 1
allele frequency: 8.250961236984109e-6
allele num: 121198
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356151
  ensembl transcript: ENST00000367183
  gene symbol: MDM4
  hgvsc: ENST00000367183.3:c.79-11719T>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000470908
  gene symbol: MDM4
  hgvsc: ENST00000470908.1:n.438-662T>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356150
  ensembl transcript: ENST00000367182
  gene symbol: MDM4
  hgvsc: ENST00000367182.3:c.411+50T>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000443816
  ensembl transcript: ENST00000507825
  gene symbol: MDM4
  hgvsc: ENST00000507825.2:c.343+5301T>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000375811
  ensembl transcript: ENST00000391947
  gene symbol: MDM4
  hgvsc: ENST00000391947.2:c.344-662T>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000463049
  gene symbol: MDM4
  hgvsc: ENST00000463049.1:n.521+50T>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000396840
  ensembl transcript: ENST00000454264
  gene symbol: MDM4
  hgvsc: ENST00000454264.2:c.411+50T>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000471783
  gene symbol: MDM4
  hgvsc: ENST00000471783.1:n.227-662T>G
  variant of: http://identifiers.org/hgnc/6974
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4694
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1747
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1694
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3536
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6651
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2408
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7123
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1076
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5131
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7929
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6132
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8243
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1588
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 748
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3217
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 761
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 253
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 525
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 279
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3448
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3411
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: DP

1-204506996-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 204506996
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 204506996
    reference: chr 1
allele count: 3
allele frequency: 2.636574562328623e-5
allele num: 113784
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356147
  ensembl transcript: ENST00000367179
  gene symbol: MDM4
  hgvsc: ENST00000367179.3:c.-46A>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000470908
  gene symbol: MDM4
  hgvsc: ENST00000470908.1:n.438-341A>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000375811
  ensembl transcript: ENST00000391947
  gene symbol: MDM4
  hgvsc: ENST00000391947.2:c.344-341A>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356150
  ensembl transcript: ENST00000367182
  gene symbol: MDM4
  hgvsc: ENST00000367182.3:c.412-341A>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000443816
  ensembl transcript: ENST00000507825
  gene symbol: MDM4
  hgvsc: ENST00000507825.2:c.343+5622A>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000471783
  gene symbol: MDM4
  hgvsc: ENST00000471783.1:n.227-341A>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356151
  ensembl transcript: ENST00000367183
  gene symbol: MDM4
  hgvsc: ENST00000367183.3:c.79-11398A>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000463049
  gene symbol: MDM4
  hgvsc: ENST00000463049.1:n.522-341A>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000396840
  ensembl transcript: ENST00000454264
  gene symbol: MDM4
  hgvsc: ENST00000454264.2:c.412-341A>G
  variant of: http://identifiers.org/hgnc/6974
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 951
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2018
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2660
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11067
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9620
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4223
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 690
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1087
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9113
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 718
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6160
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1406
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1305
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1875
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4076
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9066
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2837
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17788
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 894
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 143
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 914
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
population: African
population: Latino
population: European (Non-Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP

1-204507001-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 204507001
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 204507001
    reference: chr 1
allele count: 1
allele frequency: 8.786574114752658e-6
allele num: 113810
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000470908
  gene symbol: MDM4
  hgvsc: ENST00000470908.1:n.438-336C>T
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356147
  ensembl transcript: ENST00000367179
  gene symbol: MDM4
  hgvsc: ENST00000367179.3:c.-41C>T
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000471783
  gene symbol: MDM4
  hgvsc: ENST00000471783.1:n.227-336C>T
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000375811
  ensembl transcript: ENST00000391947
  gene symbol: MDM4
  hgvsc: ENST00000391947.2:c.344-336C>T
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000463049
  gene symbol: MDM4
  hgvsc: ENST00000463049.1:n.522-336C>T
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356151
  ensembl transcript: ENST00000367183
  gene symbol: MDM4
  hgvsc: ENST00000367183.3:c.79-11393C>T
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000443816
  ensembl transcript: ENST00000507825
  gene symbol: MDM4
  hgvsc: ENST00000507825.2:c.343+5627C>T
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000396840
  ensembl transcript: ENST00000454264
  gene symbol: MDM4
  hgvsc: ENST00000454264.2:c.412-336C>T
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356150
  ensembl transcript: ENST00000367182
  gene symbol: MDM4
  hgvsc: ENST00000367182.3:c.412-336C>T
  variant of: http://identifiers.org/hgnc/6974
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1046
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1894
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1406
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2662
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9332
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1306
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4085
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10513
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 718
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 686
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2893
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11382
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1876
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 951
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6185
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2177
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 451
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1204
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 998
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3964
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 838
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: DP

1-204507003-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 204507003
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 204507003
    reference: chr 1
allele count: 1
allele frequency: 8.779168788299123e-6
allele num: 113906
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356151
  ensembl transcript: ENST00000367183
  gene symbol: MDM4
  hgvsc: ENST00000367183.3:c.79-11391T>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000396840
  ensembl transcript: ENST00000454264
  gene symbol: MDM4
  hgvsc: ENST00000454264.2:c.412-334T>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356150
  ensembl transcript: ENST00000367182
  gene symbol: MDM4
  hgvsc: ENST00000367182.3:c.412-334T>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000463049
  gene symbol: MDM4
  hgvsc: ENST00000463049.1:n.522-334T>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000462012
  gene symbol: MDM4
  hgvsc: ENST00000462012.1:n.1T>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000375811
  ensembl transcript: ENST00000391947
  gene symbol: MDM4
  hgvsc: ENST00000391947.2:c.344-334T>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000443816
  ensembl transcript: ENST00000507825
  gene symbol: MDM4
  hgvsc: ENST00000507825.2:c.343+5629T>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000471783
  gene symbol: MDM4
  hgvsc: ENST00000471783.1:n.227-334T>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356147
  ensembl transcript: ENST00000367179
  gene symbol: MDM4
  hgvsc: ENST00000367179.3:c.-39T>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000470908
  gene symbol: MDM4
  hgvsc: ENST00000470908.1:n.438-334T>G
  variant of: http://identifiers.org/hgnc/6974
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11025
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11561
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1751
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1037
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1875
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9393
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 693
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 718
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 951
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4089
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2662
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1406
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1305
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6192
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2276
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 390
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3167
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 800
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum

1-204507004-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 204507004
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 204507004
    reference: chr 1
allele count: 5
allele frequency: 4.390201071209061e-5
allele num: 113890
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356150
  ensembl transcript: ENST00000367182
  gene symbol: MDM4
  hgvsc: ENST00000367182.3:c.412-333C>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000375811
  ensembl transcript: ENST00000391947
  gene symbol: MDM4
  hgvsc: ENST00000391947.2:c.344-333C>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000396840
  ensembl transcript: ENST00000454264
  gene symbol: MDM4
  hgvsc: ENST00000454264.2:c.412-333C>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356147
  ensembl transcript: ENST00000367179
  gene symbol: MDM4
  hgvsc: ENST00000367179.3:c.-38C>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000463049
  gene symbol: MDM4
  hgvsc: ENST00000463049.1:n.522-333C>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000443816
  ensembl transcript: ENST00000507825
  gene symbol: MDM4
  hgvsc: ENST00000507825.2:c.343+5630C>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356151
  ensembl transcript: ENST00000367183
  gene symbol: MDM4
  hgvsc: ENST00000367183.3:c.79-11390C>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000471783
  gene symbol: MDM4
  hgvsc: ENST00000471783.1:n.227-333C>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000470908
  gene symbol: MDM4
  hgvsc: ENST00000470908.1:n.438-333C>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000462012
  gene symbol: MDM4
  hgvsc: ENST00000462012.1:n.2C>G
  variant of: http://identifiers.org/hgnc/6974
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1875
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 691
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11671
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1968
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11262
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9438
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1034
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4095
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 951
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1305
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1406
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6196
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 718
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2662
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1662
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17808
  bin: 9.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 501
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 974
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: East Asian
reference allele: C
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP

1-204507007-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 204507007
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 204507007
    reference: chr 1
allele count: 1
allele frequency: 8.775162779269556e-6
allele num: 113958
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000463049
  gene symbol: MDM4
  hgvsc: ENST00000463049.1:n.522-330G>A
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356147
  ensembl transcript: ENST00000367179
  gene symbol: MDM4
  hgvsc: ENST00000367179.3:c.-35G>A
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000396840
  ensembl transcript: ENST00000454264
  gene symbol: MDM4
  hgvsc: ENST00000454264.2:c.412-330G>A
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000443816
  ensembl transcript: ENST00000507825
  gene symbol: MDM4
  hgvsc: ENST00000507825.2:c.343+5633G>A
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000375811
  ensembl transcript: ENST00000391947
  gene symbol: MDM4
  hgvsc: ENST00000391947.2:c.344-330G>A
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356151
  ensembl transcript: ENST00000367183
  gene symbol: MDM4
  hgvsc: ENST00000367183.3:c.79-11387G>A
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000471783
  gene symbol: MDM4
  hgvsc: ENST00000471783.1:n.227-330G>A
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000462012
  gene symbol: MDM4
  hgvsc: ENST00000462012.1:n.5G>A
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356150
  ensembl transcript: ENST00000367182
  gene symbol: MDM4
  hgvsc: ENST00000367182.3:c.412-330G>A
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000470908
  gene symbol: MDM4
  hgvsc: ENST00000470908.1:n.438-330G>A
  variant of: http://identifiers.org/hgnc/6974
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1340
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1406
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11864
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6211
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2662
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9602
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1000
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11939
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1262
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1306
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1875
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4100
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 951
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 718
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 357
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2882
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4063
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4684
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
population: Latino
population: African
population: European (Finnish)
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP

http://identifiers.org/exac.variant/1-204507011-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 204507011
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 204507011
    reference: chr 1
allele count: 1
allele frequency: 8.764088271897075e-6
allele num: 114102
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356147
  ensembl transcript: ENST00000367179
  gene symbol: MDM4
  hgvsc: ENST00000367179.3:c.-31C>A
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000463049
  gene symbol: MDM4
  hgvsc: ENST00000463049.1:n.522-326C>A
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000470908
  gene symbol: MDM4
  hgvsc: ENST00000470908.1:n.438-326C>A
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000471783
  gene symbol: MDM4
  hgvsc: ENST00000471783.1:n.227-326C>A
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356150
  ensembl transcript: ENST00000367182
  gene symbol: MDM4
  hgvsc: ENST00000367182.3:c.412-326C>A
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000443816
  ensembl transcript: ENST00000507825
  gene symbol: MDM4
  hgvsc: ENST00000507825.2:c.343+5637C>A
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000462012
  gene symbol: MDM4
  hgvsc: ENST00000462012.1:n.9C>A
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000375811
  ensembl transcript: ENST00000391947
  gene symbol: MDM4
  hgvsc: ENST00000391947.2:c.344-326C>A
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356151
  ensembl transcript: ENST00000367183
  gene symbol: MDM4
  hgvsc: ENST00000367183.3:c.79-11383C>A
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000396840
  ensembl transcript: ENST00000454264
  gene symbol: MDM4
  hgvsc: ENST00000454264.2:c.412-326C>A
  variant of: http://identifiers.org/hgnc/6974
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1307
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6226
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1876
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 615
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 637
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12142
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2669
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4113
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 966
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 951
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12553
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 870
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 719
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9843
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1406
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 431
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 644
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4749
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: BaseQRankSum

1-204507011-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 204507011
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 204507011
    reference: chr 1
allele count: 2
allele frequency: 1.752817654379415e-5
allele num: 114102
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000463049
  gene symbol: MDM4
  hgvsc: ENST00000463049.1:n.522-326C>T
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356150
  ensembl transcript: ENST00000367182
  gene symbol: MDM4
  hgvsc: ENST00000367182.3:c.412-326C>T
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000396840
  ensembl transcript: ENST00000454264
  gene symbol: MDM4
  hgvsc: ENST00000454264.2:c.412-326C>T
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000462012
  gene symbol: MDM4
  hgvsc: ENST00000462012.1:n.9C>T
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356147
  ensembl transcript: ENST00000367179
  gene symbol: MDM4
  hgvsc: ENST00000367179.3:c.-31C>T
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000375811
  ensembl transcript: ENST00000391947
  gene symbol: MDM4
  hgvsc: ENST00000391947.2:c.344-326C>T
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000471783
  gene symbol: MDM4
  hgvsc: ENST00000471783.1:n.227-326C>T
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356151
  ensembl transcript: ENST00000367183
  gene symbol: MDM4
  hgvsc: ENST00000367183.3:c.79-11383C>T
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000443816
  ensembl transcript: ENST00000507825
  gene symbol: MDM4
  hgvsc: ENST00000507825.2:c.343+5637C>T
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000470908
  gene symbol: MDM4
  hgvsc: ENST00000470908.1:n.438-326C>T
  variant of: http://identifiers.org/hgnc/6974
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 719
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 637
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 966
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12553
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 951
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4113
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1876
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9843
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12142
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 615
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 870
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6226
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2669
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1406
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1307
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13880
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 175
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3235
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2225
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
reference allele: C
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP

1-204507012-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 204507012
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 204507012
    reference: chr 1
allele count: 3
allele frequency: 2.62614237193179e-5
allele num: 114236
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000375811
  ensembl transcript: ENST00000391947
  gene symbol: MDM4
  hgvsc: ENST00000391947.2:c.344-325G>A
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356147
  ensembl transcript: ENST00000367179
  gene symbol: MDM4
  hgvsc: ENST00000367179.3:c.-30G>A
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000471783
  gene symbol: MDM4
  hgvsc: ENST00000471783.1:n.227-325G>A
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000470908
  gene symbol: MDM4
  hgvsc: ENST00000470908.1:n.438-325G>A
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000463049
  gene symbol: MDM4
  hgvsc: ENST00000463049.1:n.522-325G>A
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000443816
  ensembl transcript: ENST00000507825
  gene symbol: MDM4
  hgvsc: ENST00000507825.2:c.343+5638G>A
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356150
  ensembl transcript: ENST00000367182
  gene symbol: MDM4
  hgvsc: ENST00000367182.3:c.412-325G>A
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000462012
  gene symbol: MDM4
  hgvsc: ENST00000462012.1:n.10G>A
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000396840
  ensembl transcript: ENST00000454264
  gene symbol: MDM4
  hgvsc: ENST00000454264.2:c.412-325G>A
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356151
  ensembl transcript: ENST00000367183
  gene symbol: MDM4
  hgvsc: ENST00000367183.3:c.79-11382G>A
  variant of: http://identifiers.org/hgnc/6974
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 436
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 959
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12239
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12810
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9901
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6247
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4117
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2667
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1406
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1306
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 685
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1874
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 718
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 952
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 181
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 334
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 122
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum

1-204507014-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 204507014
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 204507014
    reference: chr 1
allele count: 7
allele frequency: 6.122199093914534e-5
allele num: 114338
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356150
  ensembl transcript: ENST00000367182
  gene symbol: MDM4
  hgvsc: ENST00000367182.3:c.412-323G>T
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356147
  ensembl transcript: ENST00000367179
  gene symbol: MDM4
  hgvsc: ENST00000367179.3:c.-28G>T
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000396840
  ensembl transcript: ENST00000454264
  gene symbol: MDM4
  hgvsc: ENST00000454264.2:c.412-323G>T
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000443816
  ensembl transcript: ENST00000507825
  gene symbol: MDM4
  hgvsc: ENST00000507825.2:c.343+5640G>T
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000375811
  ensembl transcript: ENST00000391947
  gene symbol: MDM4
  hgvsc: ENST00000391947.2:c.344-323G>T
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356151
  ensembl transcript: ENST00000367183
  gene symbol: MDM4
  hgvsc: ENST00000367183.3:c.79-11380G>T
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000470908
  gene symbol: MDM4
  hgvsc: ENST00000470908.1:n.438-323G>T
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000462012
  gene symbol: MDM4
  hgvsc: ENST00000462012.1:n.12G>T
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000471783
  gene symbol: MDM4
  hgvsc: ENST00000471783.1:n.227-323G>T
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000463049
  gene symbol: MDM4
  hgvsc: ENST00000463049.1:n.522-323G>T
  variant of: http://identifiers.org/hgnc/6974
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4117
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2671
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9949
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1874
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12330
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1406
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 958
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6268
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12990
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 950
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 718
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1310
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 244
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4174
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
population: African
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ

1-204507017-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 204507017
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 204507017
    reference: chr 1
allele count: 1
allele frequency: 8.731489242805253e-6
allele num: 114528
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000462012
  gene symbol: MDM4
  hgvsc: ENST00000462012.1:n.15G>A
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000375811
  ensembl transcript: ENST00000391947
  gene symbol: MDM4
  hgvsc: ENST00000391947.2:c.344-320G>A
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000463049
  gene symbol: MDM4
  hgvsc: ENST00000463049.1:n.522-320G>A
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000396840
  ensembl transcript: ENST00000454264
  gene symbol: MDM4
  hgvsc: ENST00000454264.2:c.412-320G>A
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356147
  ensembl transcript: ENST00000367179
  gene symbol: MDM4
  hgvsc: ENST00000367179.3:c.-25G>A
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356151
  ensembl transcript: ENST00000367183
  gene symbol: MDM4
  hgvsc: ENST00000367183.3:c.79-11377G>A
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000470908
  gene symbol: MDM4
  hgvsc: ENST00000470908.1:n.438-320G>A
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356150
  ensembl transcript: ENST00000367182
  gene symbol: MDM4
  hgvsc: ENST00000367182.3:c.412-320G>A
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000471783
  gene symbol: MDM4
  hgvsc: ENST00000471783.1:n.227-320G>A
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000443816
  ensembl transcript: ENST00000507825
  gene symbol: MDM4
  hgvsc: ENST00000507825.2:c.343+5643G>A
  variant of: http://identifiers.org/hgnc/6974
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 949
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4136
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 960
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1406
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13086
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10088
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6302
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2676
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1873
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1310
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 718
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12480
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2952
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: MQ
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

1-204507020-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 204507020
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 204507020
    reference: chr 1
allele count: 3
allele frequency: 2.616431187859759e-5
allele num: 114660
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356147
  ensembl transcript: ENST00000367179
  gene symbol: MDM4
  hgvsc: ENST00000367179.3:c.-22G>C
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000463049
  gene symbol: MDM4
  hgvsc: ENST00000463049.1:n.522-317G>C
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000375811
  ensembl transcript: ENST00000391947
  gene symbol: MDM4
  hgvsc: ENST00000391947.2:c.344-317G>C
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000396840
  ensembl transcript: ENST00000454264
  gene symbol: MDM4
  hgvsc: ENST00000454264.2:c.412-317G>C
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000471783
  gene symbol: MDM4
  hgvsc: ENST00000471783.1:n.227-317G>C
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000470908
  gene symbol: MDM4
  hgvsc: ENST00000470908.1:n.438-317G>C
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356150
  ensembl transcript: ENST00000367182
  gene symbol: MDM4
  hgvsc: ENST00000367182.3:c.412-317G>C
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356151
  ensembl transcript: ENST00000367183
  gene symbol: MDM4
  hgvsc: ENST00000367183.3:c.79-11374G>C
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000462012
  gene symbol: MDM4
  hgvsc: ENST00000462012.1:n.18G>C
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000443816
  ensembl transcript: ENST00000507825
  gene symbol: MDM4
  hgvsc: ENST00000507825.2:c.343+5646G>C
  variant of: http://identifiers.org/hgnc/6974
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10134
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2675
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6314
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4128
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1310
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13159
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 719
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1874
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 966
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12588
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 950
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1406
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4906
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4217
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15120
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: Other
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD

1-204507032-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 204507032
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 204507032
    reference: chr 1
allele count: 3
allele frequency: 2.610148256420965e-5
allele num: 114936
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000463049
  gene symbol: MDM4
  hgvsc: ENST00000463049.1:n.522-305T>C
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356150
  ensembl transcript: ENST00000367182
  gene symbol: MDM4
  hgvsc: ENST00000367182.3:c.412-305T>C
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356147
  ensembl transcript: ENST00000367179
  gene symbol: MDM4
  hgvsc: ENST00000367179.3:c.-10T>C
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000443816
  ensembl transcript: ENST00000507825
  gene symbol: MDM4
  hgvsc: ENST00000507825.2:c.343+5658T>C
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000470908
  gene symbol: MDM4
  hgvsc: ENST00000470908.1:n.438-305T>C
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356151
  ensembl transcript: ENST00000367183
  gene symbol: MDM4
  hgvsc: ENST00000367183.3:c.79-11362T>C
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000462012
  gene symbol: MDM4
  hgvsc: ENST00000462012.1:n.30T>C
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000375811
  ensembl transcript: ENST00000391947
  gene symbol: MDM4
  hgvsc: ENST00000391947.2:c.344-305T>C
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000471783
  gene symbol: MDM4
  hgvsc: ENST00000471783.1:n.227-305T>C
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000396840
  ensembl transcript: ENST00000454264
  gene symbol: MDM4
  hgvsc: ENST00000454264.2:c.412-305T>C
  variant of: http://identifiers.org/hgnc/6974
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4132
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13348
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 718
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1875
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6320
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1406
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 970
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 949
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1310
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2678
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10156
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12708
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17872
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4929
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: South Asian
reference allele: T
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum

1-204507032-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 204507032
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 204507032
    reference: chr 1
allele count: 1
allele frequency: 8.700494188069882e-6
allele num: 114936
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000443816
  ensembl transcript: ENST00000507825
  gene symbol: MDM4
  hgvsc: ENST00000507825.2:c.343+5658T>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000463049
  gene symbol: MDM4
  hgvsc: ENST00000463049.1:n.522-305T>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356147
  ensembl transcript: ENST00000367179
  gene symbol: MDM4
  hgvsc: ENST00000367179.3:c.-10T>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000462012
  gene symbol: MDM4
  hgvsc: ENST00000462012.1:n.30T>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000471783
  gene symbol: MDM4
  hgvsc: ENST00000471783.1:n.227-305T>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000470908
  gene symbol: MDM4
  hgvsc: ENST00000470908.1:n.438-305T>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000396840
  ensembl transcript: ENST00000454264
  gene symbol: MDM4
  hgvsc: ENST00000454264.2:c.412-305T>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000375811
  ensembl transcript: ENST00000391947
  gene symbol: MDM4
  hgvsc: ENST00000391947.2:c.344-305T>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356151
  ensembl transcript: ENST00000367183
  gene symbol: MDM4
  hgvsc: ENST00000367183.3:c.79-11362T>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356150
  ensembl transcript: ENST00000367182
  gene symbol: MDM4
  hgvsc: ENST00000367182.3:c.412-305T>G
  variant of: http://identifiers.org/hgnc/6974
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1875
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 949
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13348
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6320
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12708
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1406
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1310
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 718
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 970
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4132
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10156
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2678
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2281
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Other
population: East Asian
population: European (Finnish)
population: African
population: Latino
reference allele: T
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: DP

1-204507044-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 204507044
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 204507044
    reference: chr 1
allele count: 12
allele frequency: 1.043206120142571e-4
allele num: 115030
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000470908
  gene symbol: MDM4
  hgvsc: ENST00000470908.1:n.438-293G>A
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356151
  ensembl transcript: ENST00000367183
  gene symbol: MDM4
  hgvsc: ENST00000367183.3:c.79-11350G>A
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356147
  ensembl transcript: ENST00000367179
  gene symbol: MDM4
  hgvsc: ENST00000367179.3:c.3G>A
  hgvsp: ENSP00000356147.3:p.Met1?
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000471783
  gene symbol: MDM4
  hgvsc: ENST00000471783.1:n.227-293G>A
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000443816
  ensembl transcript: ENST00000507825
  gene symbol: MDM4
  hgvsc: ENST00000507825.2:c.343+5670G>A
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000463049
  gene symbol: MDM4
  hgvsc: ENST00000463049.1:n.522-293G>A
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000396840
  ensembl transcript: ENST00000454264
  gene symbol: MDM4
  hgvsc: ENST00000454264.2:c.412-293G>A
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356150
  ensembl transcript: ENST00000367182
  gene symbol: MDM4
  hgvsc: ENST00000367182.3:c.412-293G>A
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000462012
  gene symbol: MDM4
  hgvsc: ENST00000462012.1:n.42G>A
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000375811
  ensembl transcript: ENST00000391947
  gene symbol: MDM4
  hgvsc: ENST00000391947.2:c.344-293G>A
  variant of: http://identifiers.org/hgnc/6974
canonical: false
consequence: start lost
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2676
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10160
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 721
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1313
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1004
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4136
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13377
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6323
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1875
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1406
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 950
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12740
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 175
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17880
  bin: 9.75e1
  variant carriers: 12
genotype quality: GenotypeQuality
  all individuals: 2282
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Met1?
num of homozygotes: 0
population: European (Finnish)
population: Other
population: East Asian
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: DP

1-204507048-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 204507048
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 204507048
    reference: chr 1
allele count: 5
allele frequency: 4.345785457263546e-5
allele num: 115054
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000463049
  gene symbol: MDM4
  hgvsc: ENST00000463049.1:n.522-289A>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000396840
  ensembl transcript: ENST00000454264
  gene symbol: MDM4
  hgvsc: ENST00000454264.2:c.412-289A>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000470908
  gene symbol: MDM4
  hgvsc: ENST00000470908.1:n.438-289A>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356147
  ensembl transcript: ENST00000367179
  gene symbol: MDM4
  hgvsc: ENST00000367179.3:c.7A>G
  hgvsp: ENSP00000356147.3:p.Asn3Asp
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000443816
  ensembl transcript: ENST00000507825
  gene symbol: MDM4
  hgvsc: ENST00000507825.2:c.343+5674A>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356150
  ensembl transcript: ENST00000367182
  gene symbol: MDM4
  hgvsc: ENST00000367182.3:c.412-289A>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000462012
  gene symbol: MDM4
  hgvsc: ENST00000462012.1:n.46A>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000375811
  ensembl transcript: ENST00000391947
  gene symbol: MDM4
  hgvsc: ENST00000391947.2:c.344-289A>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356151
  ensembl transcript: ENST00000367183
  gene symbol: MDM4
  hgvsc: ENST00000367183.3:c.79-11346A>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000471783
  gene symbol: MDM4
  hgvsc: ENST00000471783.1:n.227-289A>G
  variant of: http://identifiers.org/hgnc/6974
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 718
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1310
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 949
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1407
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10165
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4132
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1009
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2676
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12750
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6326
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1877
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13386
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2282
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15557
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Asn3Asp
num of homozygotes: 0
population: Latino
population: African
population: Other
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP

1-204507071-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 204507071
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 204507071
    reference: chr 1
allele count: 1
allele frequency: 8.685682520932494e-6
allele num: 115132
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000470908
  gene symbol: MDM4
  hgvsc: ENST00000470908.1:n.438-266T>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000396840
  ensembl transcript: ENST00000454264
  gene symbol: MDM4
  hgvsc: ENST00000454264.2:c.412-266T>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356147
  ensembl transcript: ENST00000367179
  gene symbol: MDM4
  hgvsc: ENST00000367179.3:c.30T>G
  hgvsp: ENST00000367179.3:c.30T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000375811
  ensembl transcript: ENST00000391947
  gene symbol: MDM4
  hgvsc: ENST00000391947.2:c.344-266T>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356150
  ensembl transcript: ENST00000367182
  gene symbol: MDM4
  hgvsc: ENST00000367182.3:c.412-266T>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000463049
  gene symbol: MDM4
  hgvsc: ENST00000463049.1:n.522-266T>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000462012
  gene symbol: MDM4
  hgvsc: ENST00000462012.1:n.69T>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000443816
  ensembl transcript: ENST00000507825
  gene symbol: MDM4
  hgvsc: ENST00000507825.2:c.343+5697T>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356151
  ensembl transcript: ENST00000367183
  gene symbol: MDM4
  hgvsc: ENST00000367183.3:c.79-11323T>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000471783
  gene symbol: MDM4
  hgvsc: ENST00000471783.1:n.227-266T>G
  variant of: http://identifiers.org/hgnc/6974
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2676
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 949
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1311
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1405
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6331
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4132
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12765
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 719
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1034
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1875
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10175
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13402
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 936
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Val10Val
num of homozygotes: 0
population: Other
population: South Asian
population: African
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: DP
site quality: ReadPosRankSum

1-204507075-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 204507075
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 204507075
    reference: chr 1
allele count: 1
allele frequency: 8.685682520932494e-6
allele num: 115132
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000462012
  gene symbol: MDM4
  hgvsc: ENST00000462012.1:n.73A>T
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356150
  ensembl transcript: ENST00000367182
  gene symbol: MDM4
  hgvsc: ENST00000367182.3:c.412-262A>T
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356147
  ensembl transcript: ENST00000367179
  gene symbol: MDM4
  hgvsc: ENST00000367179.3:c.34A>T
  hgvsp: ENSP00000356147.3:p.Thr12Ser
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000375811
  ensembl transcript: ENST00000391947
  gene symbol: MDM4
  hgvsc: ENST00000391947.2:c.344-262A>T
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356151
  ensembl transcript: ENST00000367183
  gene symbol: MDM4
  hgvsc: ENST00000367183.3:c.79-11319A>T
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000463049
  gene symbol: MDM4
  hgvsc: ENST00000463049.1:n.522-262A>T
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000443816
  ensembl transcript: ENST00000507825
  gene symbol: MDM4
  hgvsc: ENST00000507825.2:c.343+5701A>T
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000470908
  gene symbol: MDM4
  hgvsc: ENST00000470908.1:n.438-262A>T
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000471783
  gene symbol: MDM4
  hgvsc: ENST00000471783.1:n.227-262A>T
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000396840
  ensembl transcript: ENST00000454264
  gene symbol: MDM4
  hgvsc: ENST00000454264.2:c.412-262A>T
  variant of: http://identifiers.org/hgnc/6974
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1076
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 719
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12765
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10174
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4133
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13403
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 949
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2676
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1875
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1311
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6331
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1405
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 253
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15591
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17870
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Thr12Ser
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
population: African
population: Latino
reference allele: A
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff

1-204507079-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 204507079
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 204507079
    reference: chr 1
allele count: 1
allele frequency: 8.685380767092829e-6
allele num: 115136
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356147
  ensembl transcript: ENST00000367179
  gene symbol: MDM4
  hgvsc: ENST00000367179.3:c.38A>G
  hgvsp: ENSP00000356147.3:p.Asp13Gly
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000396840
  ensembl transcript: ENST00000454264
  gene symbol: MDM4
  hgvsc: ENST00000454264.2:c.412-258A>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000463049
  gene symbol: MDM4
  hgvsc: ENST00000463049.1:n.522-258A>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000375811
  ensembl transcript: ENST00000391947
  gene symbol: MDM4
  hgvsc: ENST00000391947.2:c.344-258A>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000462012
  gene symbol: MDM4
  hgvsc: ENST00000462012.1:n.77A>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000471783
  gene symbol: MDM4
  hgvsc: ENST00000471783.1:n.227-258A>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356151
  ensembl transcript: ENST00000367183
  gene symbol: MDM4
  hgvsc: ENST00000367183.3:c.79-11315A>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000470908
  gene symbol: MDM4
  hgvsc: ENST00000470908.1:n.438-258A>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000443816
  ensembl transcript: ENST00000507825
  gene symbol: MDM4
  hgvsc: ENST00000507825.2:c.343+5705A>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356150
  ensembl transcript: ENST00000367182
  gene symbol: MDM4
  hgvsc: ENST00000367182.3:c.412-258A>G
  variant of: http://identifiers.org/hgnc/6974
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13399
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2676
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10175
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6331
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 719
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1099
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1405
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4132
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1875
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1311
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 949
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12768
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 275
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Asp13Gly
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: African
population: Latino
population: East Asian
reference allele: A
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum

1-204507083-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 204507083
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 204507083
    reference: chr 1
allele count: 245
allele frequency: 2.127881325018673e-3
allele num: 115138
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000471783
  gene symbol: MDM4
  hgvsc: ENST00000471783.1:n.227-254C>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000443816
  ensembl transcript: ENST00000507825
  gene symbol: MDM4
  hgvsc: ENST00000507825.2:c.343+5709C>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356150
  ensembl transcript: ENST00000367182
  gene symbol: MDM4
  hgvsc: ENST00000367182.3:c.412-254C>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000463049
  gene symbol: MDM4
  hgvsc: ENST00000463049.1:n.522-254C>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000462012
  gene symbol: MDM4
  hgvsc: ENST00000462012.1:n.81C>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000396840
  ensembl transcript: ENST00000454264
  gene symbol: MDM4
  hgvsc: ENST00000454264.2:c.412-254C>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000375811
  ensembl transcript: ENST00000391947
  gene symbol: MDM4
  hgvsc: ENST00000391947.2:c.344-254C>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356147
  ensembl transcript: ENST00000367179
  gene symbol: MDM4
  hgvsc: ENST00000367179.3:c.42C>G
  hgvsp: ENSP00000356147.3:p.Ser14Arg
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356151
  ensembl transcript: ENST00000367183
  gene symbol: MDM4
  hgvsc: ENST00000367183.3:c.79-11311C>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000470908
  gene symbol: MDM4
  hgvsc: ENST00000470908.1:n.438-254C>G
  variant of: http://identifiers.org/hgnc/6974
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13310
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1869
  bin: 5.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1144
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12722
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4128
  bin: 4.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1316
  bin: 5.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 8.25e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 6313
  bin: 3.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 9.25e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 2672
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10136
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1496
  bin: 9.75e1
  variant carriers: 98
genotype depth: GenotypeDepth
  all individuals: 731
  bin: 6.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 960
  bin: 6.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 8.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 436
  bin: 7.75e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 556
  bin: 7.25e1
  variant carriers: 19
genotype quality: GenotypeQuality
  all individuals: 293
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15511
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4915
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Ser14Arg
num of homozygotes: 1
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum

1-204507087-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 204507087
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 204507087
    reference: chr 1
allele count: 3
allele frequency: 2.605206940271289e-5
allele num: 115154
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356147
  ensembl transcript: ENST00000367179
  gene symbol: MDM4
  hgvsc: ENST00000367179.3:c.46T>A
  hgvsp: ENSP00000356147.3:p.Phe16Ile
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356150
  ensembl transcript: ENST00000367182
  gene symbol: MDM4
  hgvsc: ENST00000367182.3:c.412-250T>A
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000470908
  gene symbol: MDM4
  hgvsc: ENST00000470908.1:n.438-250T>A
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000462012
  gene symbol: MDM4
  hgvsc: ENST00000462012.1:n.85T>A
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000471783
  gene symbol: MDM4
  hgvsc: ENST00000471783.1:n.227-250T>A
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000396840
  ensembl transcript: ENST00000454264
  gene symbol: MDM4
  hgvsc: ENST00000454264.2:c.412-250T>A
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000375811
  ensembl transcript: ENST00000391947
  gene symbol: MDM4
  hgvsc: ENST00000391947.2:c.344-250T>A
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000443816
  ensembl transcript: ENST00000507825
  gene symbol: MDM4
  hgvsc: ENST00000507825.2:c.343+5713T>A
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356151
  ensembl transcript: ENST00000367183
  gene symbol: MDM4
  hgvsc: ENST00000367183.3:c.79-11307T>A
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000463049
  gene symbol: MDM4
  hgvsc: ENST00000463049.1:n.522-250T>A
  variant of: http://identifiers.org/hgnc/6974
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12760
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1874
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1159
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6335
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2693
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 728
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 958
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13317
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10172
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1408
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4159
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1315
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3405
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Phe16Ile
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
population: South Asian
reference allele: T
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum

1-204507089-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 204507089
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 204507089
    reference: chr 1
allele count: 8
allele frequency: 6.946735902467828e-5
allele num: 115162
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356147
  ensembl transcript: ENST00000367179
  gene symbol: MDM4
  hgvsc: ENST00000367179.3:c.48T>C
  hgvsp: ENST00000367179.3:c.48T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356151
  ensembl transcript: ENST00000367183
  gene symbol: MDM4
  hgvsc: ENST00000367183.3:c.79-11305T>C
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000470908
  gene symbol: MDM4
  hgvsc: ENST00000470908.1:n.438-248T>C
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000443816
  ensembl transcript: ENST00000507825
  gene symbol: MDM4
  hgvsc: ENST00000507825.2:c.343+5715T>C
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000463049
  gene symbol: MDM4
  hgvsc: ENST00000463049.1:n.522-248T>C
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000462012
  gene symbol: MDM4
  hgvsc: ENST00000462012.1:n.87T>C
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000396840
  ensembl transcript: ENST00000454264
  gene symbol: MDM4
  hgvsc: ENST00000454264.2:c.412-248T>C
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000375811
  ensembl transcript: ENST00000391947
  gene symbol: MDM4
  hgvsc: ENST00000391947.2:c.344-248T>C
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356150
  ensembl transcript: ENST00000367182
  gene symbol: MDM4
  hgvsc: ENST00000367182.3:c.412-248T>C
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000471783
  gene symbol: MDM4
  hgvsc: ENST00000471783.1:n.227-248T>C
  variant of: http://identifiers.org/hgnc/6974
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2694
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1316
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10171
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 959
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13313
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1874
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4159
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1149
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1410
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 6335
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 729
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12758
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 325
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Phe16Phe
num of homozygotes: 0
population: African
population: Latino
population: Other
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: QD

1-204507106-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 204507106
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 204507106
    reference: chr 1
allele count: 1
allele frequency: 8.678596844462188e-6
allele num: 115226
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000463049
  gene symbol: MDM4
  hgvsc: ENST00000463049.1:n.522-231G>T
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356151
  ensembl transcript: ENST00000367183
  gene symbol: MDM4
  hgvsc: ENST00000367183.3:c.79-11288G>T
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000462012
  gene symbol: MDM4
  hgvsc: ENST00000462012.1:n.104G>T
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000375811
  ensembl transcript: ENST00000391947
  gene symbol: MDM4
  hgvsc: ENST00000391947.2:c.344-231G>T
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000396840
  ensembl transcript: ENST00000454264
  gene symbol: MDM4
  hgvsc: ENST00000454264.2:c.412-231G>T
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356150
  ensembl transcript: ENST00000367182
  gene symbol: MDM4
  hgvsc: ENST00000367182.3:c.412-231G>T
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000471783
  gene symbol: MDM4
  hgvsc: ENST00000471783.1:n.227-231G>T
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000443816
  ensembl transcript: ENST00000507825
  gene symbol: MDM4
  hgvsc: ENST00000507825.2:c.343+5732G>T
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356147
  ensembl transcript: ENST00000367179
  gene symbol: MDM4
  hgvsc: ENST00000367179.3:c.65G>T
  hgvsp: ENSP00000356147.3:p.Gly22Val
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000470908
  gene symbol: MDM4
  hgvsc: ENST00000470908.1:n.438-231G>T
  variant of: http://identifiers.org/hgnc/6974
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6336
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1265
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1317
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12764
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13281
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 959
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1875
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2695
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 728
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4160
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10174
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1408
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 466
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Gly22Val
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
population: African
reference allele: G
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: QD

1-204507120-G-GT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 204507120
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 204507121
    reference: chr 1
allele count: 5
allele frequency: 4.339599715322259e-5
allele num: 115218
alternate allele: GT
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356150
  ensembl transcript: ENST00000367182
  gene symbol: MDM4
  hgvsc: ENST00000367182.3:c.412-209dupT
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000375811
  ensembl transcript: ENST00000391947
  gene symbol: MDM4
  hgvsc: ENST00000391947.2:c.344-209dupT
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000470908
  gene symbol: MDM4
  hgvsc: ENST00000470908.1:n.438-209dupT
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000396840
  ensembl transcript: ENST00000454264
  gene symbol: MDM4
  hgvsc: ENST00000454264.2:c.412-209dupT
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356147
  ensembl transcript: ENST00000367179
  gene symbol: MDM4
  hgvsc: ENST00000367179.3:c.78+9dupT
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000443816
  ensembl transcript: ENST00000507825
  gene symbol: MDM4
  hgvsc: ENST00000507825.2:c.343+5754dupT
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000471783
  gene symbol: MDM4
  hgvsc: ENST00000471783.1:n.227-209dupT
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000462012
  gene symbol: MDM4
  hgvsc: ENST00000462012.1:n.126dupT
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356151
  ensembl transcript: ENST00000367183
  gene symbol: MDM4
  hgvsc: ENST00000367183.3:c.79-11266dupT
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000463049
  gene symbol: MDM4
  hgvsc: ENST00000463049.1:n.522-209dupT
  variant of: http://identifiers.org/hgnc/6974
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 666
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1296
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2726
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4237
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1412
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1912
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12702
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13023
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6399
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10186
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 972
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 548
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 737
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1352
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1204
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3382
  bin: 7.25e1
  variant carriers: 0
hgvs: c.78+9dupT
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
reference allele: G
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD

1-204507120-GT-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 204507120
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 204507119
    reference: chr 1
allele count: 11
allele frequency: 9.547119373708969e-5
allele num: 115218
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356147
  ensembl transcript: ENST00000367179
  gene symbol: MDM4
  hgvsc: ENST00000367179.3:c.78+9delT
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000375811
  ensembl transcript: ENST00000391947
  gene symbol: MDM4
  hgvsc: ENST00000391947.2:c.344-209delT
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000471783
  gene symbol: MDM4
  hgvsc: ENST00000471783.1:n.227-209delT
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000470908
  gene symbol: MDM4
  hgvsc: ENST00000470908.1:n.438-209delT
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356150
  ensembl transcript: ENST00000367182
  gene symbol: MDM4
  hgvsc: ENST00000367182.3:c.412-209delT
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356151
  ensembl transcript: ENST00000367183
  gene symbol: MDM4
  hgvsc: ENST00000367183.3:c.79-11266delT
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000463049
  gene symbol: MDM4
  hgvsc: ENST00000463049.1:n.522-209delT
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000443816
  ensembl transcript: ENST00000507825
  gene symbol: MDM4
  hgvsc: ENST00000507825.2:c.343+5754delT
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000462012
  gene symbol: MDM4
  hgvsc: ENST00000462012.1:n.126delT
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000396840
  ensembl transcript: ENST00000454264
  gene symbol: MDM4
  hgvsc: ENST00000454264.2:c.412-209delT
  variant of: http://identifiers.org/hgnc/6974
canonical: false
consequence: splice donor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 548
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 972
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10186
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1912
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1412
  bin: 9.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1296
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12702
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6399
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2726
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1352
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13023
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 666
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4237
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 737
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2949
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4904
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 1.75e1
  variant carriers: 0
hgvs: c.78+9delT
num of homozygotes: 0
population: European (Finnish)
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: GT
site quality: MQ
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum

1-204507122-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 204507122
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 204507122
    reference: chr 1
allele count: 2
allele frequency: 1.734485031394179e-5
allele num: 115308
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356150
  ensembl transcript: ENST00000367182
  gene symbol: MDM4
  hgvsc: ENST00000367182.3:c.412-215T>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000462012
  gene symbol: MDM4
  hgvsc: ENST00000462012.1:n.120T>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000463049
  gene symbol: MDM4
  hgvsc: ENST00000463049.1:n.522-215T>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000443816
  ensembl transcript: ENST00000507825
  gene symbol: MDM4
  hgvsc: ENST00000507825.2:c.343+5748T>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000471783
  gene symbol: MDM4
  hgvsc: ENST00000471783.1:n.227-215T>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356147
  ensembl transcript: ENST00000367179
  gene symbol: MDM4
  hgvsc: ENST00000367179.3:c.78+3T>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000375811
  ensembl transcript: ENST00000391947
  gene symbol: MDM4
  hgvsc: ENST00000391947.2:c.344-215T>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000470908
  gene symbol: MDM4
  hgvsc: ENST00000470908.1:n.438-215T>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000396840
  ensembl transcript: ENST00000454264
  gene symbol: MDM4
  hgvsc: ENST00000454264.2:c.412-215T>G
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356151
  ensembl transcript: ENST00000367183
  gene symbol: MDM4
  hgvsc: ENST00000367183.3:c.79-11272T>G
  variant of: http://identifiers.org/hgnc/6974
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 732
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 965
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1302
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4231
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1414
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10206
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1898
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 668
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12983
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1340
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6392
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2739
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12758
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 180
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17988
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 2963
  bin: 9.25e1
  variant carriers: 0
hgvs: c.78+3T>G
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Latino
population: Other
population: African
population: European (Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD

1-204507126-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 204507126
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 204507126
    reference: chr 1
allele count: 0
allele frequency: 0.0e0
allele num: 115414
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356147
  ensembl transcript: ENST00000367179
  gene symbol: MDM4
  hgvsc: ENST00000367179.3:c.78+7T>C
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000470908
  gene symbol: MDM4
  hgvsc: ENST00000470908.1:n.438-211T>C
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356151
  ensembl transcript: ENST00000367183
  gene symbol: MDM4
  hgvsc: ENST00000367183.3:c.79-11268T>C
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000375811
  ensembl transcript: ENST00000391947
  gene symbol: MDM4
  hgvsc: ENST00000391947.2:c.344-211T>C
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000396840
  ensembl transcript: ENST00000454264
  gene symbol: MDM4
  hgvsc: ENST00000454264.2:c.412-211T>C
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000471783
  gene symbol: MDM4
  hgvsc: ENST00000471783.1:n.227-211T>C
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000443816
  ensembl transcript: ENST00000507825
  gene symbol: MDM4
  hgvsc: ENST00000507825.2:c.343+5752T>C
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000463049
  gene symbol: MDM4
  hgvsc: ENST00000463049.1:n.522-211T>C
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000462012
  gene symbol: MDM4
  hgvsc: ENST00000462012.1:n.124T>C
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356150
  ensembl transcript: ENST00000367182
  gene symbol: MDM4
  hgvsc: ENST00000367182.3:c.412-211T>C
  variant of: http://identifiers.org/hgnc/6974
canonical: false
consequence: splice region
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 6388
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10228
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 962
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12781
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1313
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 732
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12969
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1329
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4210
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1889
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2732
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1410
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15322
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2971
  bin: 9.25e1
  variant carriers: 0
hgvs: c.78+7T>C
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: T
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP

1-204507127-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 204507127
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 204507127
    reference: chr 1
allele count: 1
allele frequency: 8.663859576163989e-6
allele num: 115422
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356151
  ensembl transcript: ENST00000367183
  gene symbol: MDM4
  hgvsc: ENST00000367183.3:c.79-11267T>A
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356150
  ensembl transcript: ENST00000367182
  gene symbol: MDM4
  hgvsc: ENST00000367182.3:c.412-210T>A
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000375811
  ensembl transcript: ENST00000391947
  gene symbol: MDM4
  hgvsc: ENST00000391947.2:c.344-210T>A
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000462012
  gene symbol: MDM4
  hgvsc: ENST00000462012.1:n.125T>A
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000443816
  ensembl transcript: ENST00000507825
  gene symbol: MDM4
  hgvsc: ENST00000507825.2:c.343+5753T>A
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000356147
  ensembl transcript: ENST00000367179
  gene symbol: MDM4
  hgvsc: ENST00000367179.3:c.78+8T>A
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000463049
  gene symbol: MDM4
  hgvsc: ENST00000463049.1:n.522-210T>A
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000471783
  gene symbol: MDM4
  hgvsc: ENST00000471783.1:n.227-210T>A
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl transcript: ENST00000470908
  gene symbol: MDM4
  hgvsc: ENST00000470908.1:n.438-210T>A
  variant of: http://identifiers.org/hgnc/6974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198625
  ensembl protein: ENSP00000396840
  ensembl transcript: ENST00000454264
  gene symbol: MDM4
  hgvsc: ENST00000454264.2:c.412-210T>A
  variant of: http://identifiers.org/hgnc/6974
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4211
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10229
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1306
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2732
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1890
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 732
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1329
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12951
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6390
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12778
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 709
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 962
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1410
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2286
  bin: 8.75e1
  variant carriers: 0
hgvs: c.78+8T>A
num of homozygotes: 0
reference allele: T

GenotypeQuality
all individuals: 12
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3552
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2183
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 101
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3590
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 213
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8690
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4180
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 204
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1900
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28475
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 165
bin: 2.75e1
variant carriers: 0

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

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

Latino
type: Population
allele count: 1
allele frequency: 8.739730816290858e-5
allele num: 11442
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62794
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8488
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: 6610
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16214
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.046e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.01e0

MQRankSum
type: SiteQuality
SIO_000300: 6.51e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-3

VQSLOD
type: SiteQuality
SIO_000300: 2.05e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.87e-1

FS
type: SiteQuality
SIO_000300: 7.78e-1

QD
type: SiteQuality
SIO_000300: 1.805e1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.9e-1

DP
type: SiteQuality
SIO_000300: 2.759825e6

GenotypeQuality
all individuals: 251
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4164
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2181
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1899
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 250
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 211
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8241
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3547
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 403
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3150
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 335
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 176
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28472
bin: 9.75e1
variant carriers: 2

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11438
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: 2
allele frequency: 3.184713375796178e-5
allele num: 62800
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16214
num of homozygotes: 0

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: 2.01e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.091e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-3

FS
type: SiteQuality
SIO_000300: 4.463e0

MQRankSum
type: SiteQuality
SIO_000300: 2.57e0

BaseQRankSum
type: SiteQuality
SIO_000300: -8.04e-1

DP
type: SiteQuality
SIO_000300: 2.758159e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.36e0

QD
type: SiteQuality
SIO_000300: 9.69e0

MQ
type: SiteQuality
SIO_000300: 5.941e1

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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bin: 9.75e1
variant carriers: 2

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16200
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11438
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.185322036057845e-5
allele num: 62788
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 8490
num of homozygotes: 0

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: -1.968e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.7e-1

FS
type: SiteQuality
SIO_000300: 8.56e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.2e-3

MQ
type: SiteQuality
SIO_000300: 5.978e1

MQRankSum
type: SiteQuality
SIO_000300: -4.0e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.49e-1

QD
type: SiteQuality
SIO_000300: 1.38e1

VQSLOD
type: SiteQuality
SIO_000300: 2.32e0

DP
type: SiteQuality
SIO_000300: 2.756932e6

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 8.741258741258741e-5
allele num: 11440
num of homozygotes: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 8490
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16202
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.592661018028923e-5
allele num: 62788
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.6e-3

VQSLOD
type: SiteQuality
SIO_000300: 9.3e-2

MQRankSum
type: SiteQuality
SIO_000300: -1.31e-1

FS
type: SiteQuality
SIO_000300: 7.65e0

BaseQRankSum
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SIO_000300: 7.18e0

QD
type: SiteQuality
SIO_000300: 1.802e1

DP
type: SiteQuality
SIO_000300: 2.75545e6

ClippingRankSum
type: SiteQuality
SIO_000300: 4.29e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.66e0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 1906
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 752
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7030
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1306
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7620
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 220
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 560
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -7.737000000000001e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.27e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.58e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 1.23e0

DP
type: SiteQuality
SIO_000300: 5.29029e5

BaseQRankSum
type: SiteQuality
SIO_000300: 3.58e-1

QD
type: SiteQuality
SIO_000300: 1.229e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.01e-2

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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variant carriers: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 574
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 5.230125523012552e-4
allele num: 1912
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7126
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 226
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1334
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 782
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7830
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.24e-1

VQSLOD
type: SiteQuality
SIO_000300: -9.77e-1

MQ
type: SiteQuality
SIO_000300: 5.992e1

FS
type: SiteQuality
SIO_000300: 1.636e0

MQRankSum
type: SiteQuality
SIO_000300: -8.6e-1

DP
type: SiteQuality
SIO_000300: 5.45027e5

QD
type: SiteQuality
SIO_000300: 1.459e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.93e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.116e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.82e-2

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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variant carriers: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 794
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1370
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1904
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7916
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7162
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 588
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 228
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.183e1

FS
type: SiteQuality
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MQ
type: SiteQuality
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VQSLOD
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: 1.98e-1

BaseQRankSum
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SIO_000300: -9.22e-1

DP
type: SiteQuality
SIO_000300: 5.53239e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.76e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.98e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.98e-1

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 844
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 1932
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 226
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 8182
num of homozygotes: 0

African
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allele count: 5
allele frequency: 3.472222222222222e-3
allele num: 1440
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7184
num of homozygotes: 0

Latino
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allele count: 1
allele frequency: 1.597444089456869e-3
allele num: 626
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.49e-1

InbreedingCoeff
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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QD
type: SiteQuality
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FS
type: SiteQuality
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BaseQRankSum
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MQ
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VQSLOD
type: SiteQuality
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DP
type: SiteQuality
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MQRankSum
type: SiteQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 1944
num of homozygotes: 0

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

East Asian
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allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
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Other
type: Population
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allele num: 228
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South Asian
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allele num: 7202
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BaseQRankSum
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MQ
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VQSLOD
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InbreedingCoeff
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ClippingRankSum
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FS
type: SiteQuality
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MQRankSum
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DP
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ReadPosRankSum
type: SiteQuality
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QD
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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variant carriers: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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Latino
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East Asian
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African
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Other
type: Population
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InbreedingCoeff
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FS
type: SiteQuality
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MQ
type: SiteQuality
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MQRankSum
type: SiteQuality
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QD
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BaseQRankSum
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VQSLOD
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ClippingRankSum
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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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GenotypeQuality
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GenotypeQuality
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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: 23
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 602
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7180
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1426
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1932
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8216
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 228
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.38e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.2e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.2e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.2e-1

DP
type: SiteQuality
SIO_000300: 5.39401e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.99e-2

QD
type: SiteQuality
SIO_000300: 1.415e1

VQSLOD
type: SiteQuality
SIO_000300: -7.494e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 100
bin: 5.25e1
variant carriers: 13

GenotypeQuality
all individuals: 222
bin: 4.75e1
variant carriers: 9

GenotypeQuality
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bin: 7.25e1
variant carriers: 7

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 3.25e1
variant carriers: 1

GenotypeQuality
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bin: 2.75e1
variant carriers: 6

GenotypeQuality
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bin: 8.25e1
variant carriers: 4

GenotypeQuality
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bin: 4.25e1
variant carriers: 3

GenotypeQuality
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bin: 9.75e1
variant carriers: 91

GenotypeQuality
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bin: 6.75e1
variant carriers: 14

GenotypeQuality
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bin: 7.75e1
variant carriers: 7

GenotypeQuality
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bin: 8.75e1
variant carriers: 9

GenotypeQuality
all individuals: 3354
bin: 1.75e1
variant carriers: 6

GenotypeQuality
all individuals: 30
bin: 9.25e1
variant carriers: 9

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 228
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 4.901960784313725e-3
allele num: 612
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 3
allele frequency: 1.556016597510373e-3
allele num: 1928
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 1.392757660167131e-3
allele num: 1436
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 79
allele frequency: 9.520366353338154e-3
allele num: 8298
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.39314572304263e-4
allele num: 7178
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.8e-2

DP
type: SiteQuality
SIO_000300: 5.38754e5

MQRankSum
type: SiteQuality
SIO_000300: 4.06e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.26e0

VQSLOD
type: SiteQuality
SIO_000300: 5.54e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.412e1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.81e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.33e-1

GenotypeQuality
all individuals: 2003
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1492
bin: 3.25e1
variant carriers: 1

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 19

GenotypeQuality
all individuals: 66
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1745
bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 15
allele frequency: 1.827040194884287e-3
allele num: 8210
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 230
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1428
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 4.257734885041158e-4
allele num: 7046
num of homozygotes: 0

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1930
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.899e0

VQSLOD
type: SiteQuality
SIO_000300: 2.99e0

DP
type: SiteQuality
SIO_000300: 5.29382e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.24e-2

MQRankSum
type: SiteQuality
SIO_000300: 3.58e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 8.96e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.25e-1

QD
type: SiteQuality
SIO_000300: 1.23e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.06e-1

GenotypeQuality
all individuals: 1737
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 251
bin: 6.75e1
variant carriers: 5

GenotypeQuality
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variant carriers: 3

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 3

GenotypeQuality
all individuals: 4880
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 588
bin: 4.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7100
num of homozygotes: 0

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

African
type: Population
allele count: 7
allele frequency: 4.888268156424581e-3
allele num: 1432
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 224
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1942
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 616
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.213886865744113e-4
allele num: 8238
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 3.49e0

MQRankSum
type: SiteQuality
SIO_000300: 2.96e-1

FS
type: SiteQuality
SIO_000300: 1.491e0

DP
type: SiteQuality
SIO_000300: 5.29191e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.58e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.19e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 1.98e-1

QD
type: SiteQuality
SIO_000300: 1.226e1

GenotypeQuality
all individuals: 3227
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2080
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 401
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variant carriers: 0

GenotypeQuality
all individuals: 8
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GenotypeQuality
all individuals: 18
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 3449
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7028
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33507
bin: 9.75e1
variant carriers: 1

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10398
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16428
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11566
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501411326647048e-5
allele num: 66604
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.03e-1

MQ
type: SiteQuality
SIO_000300: 5.907e1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 7.91e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.15e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.28e0

QD
type: SiteQuality
SIO_000300: 1.55e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.6e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.7e-3

DP
type: SiteQuality
SIO_000300: 2.688096e6

GenotypeQuality
all individuals: 8
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 401
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 386
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variant carriers: 0

GenotypeQuality
all individuals: 540
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3638
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 3449
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2041
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3402
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2080
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3227
bin: 7.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
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: 10398
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16428
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501411326647048e-5
allele num: 66604
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11566
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.03e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.7e-3

VQSLOD
type: SiteQuality
SIO_000300: 4.28e0

MQ
type: SiteQuality
SIO_000300: 5.907e1

DP
type: SiteQuality
SIO_000300: 2.688096e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.6e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 2.15e-1

QD
type: SiteQuality
SIO_000300: 1.55e1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.91e-1

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

GenotypeQuality
all individuals: 115
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GenotypeQuality
all individuals: 235
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 379
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variant carriers: 0

GenotypeQuality
all individuals: 243
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
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GenotypeQuality
all individuals: 498
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 1.25e1
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GenotypeQuality
all individuals: 3412
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33507
bin: 9.75e1
variant carriers: 1

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: 1.501411326647048e-5
allele num: 66604
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11568
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16434
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 4.05e-1

DP
type: SiteQuality
SIO_000300: 2.688787e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.89e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.14e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -7.199999999999999e-2

FS
type: SiteQuality
SIO_000300: 8.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.419e0

MQ
type: SiteQuality
SIO_000300: 5.983e1

QD
type: SiteQuality
SIO_000300: 1.187e1

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 102
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
all individuals: 45
bin: 5.25e1
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GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3450
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2084
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 90
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3430
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33512
bin: 9.75e1
variant carriers: 1

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11574
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10398
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66632
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8652
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.070908207867897e-5
allele num: 16472
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.99e1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.9e-1

DP
type: SiteQuality
SIO_000300: 2.701036e6

FS
type: SiteQuality
SIO_000300: 1.7071e1

MQRankSum
type: SiteQuality
SIO_000300: 1.14e0

VQSLOD
type: SiteQuality
SIO_000300: -1.154e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.49e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.52e-1

QD
type: SiteQuality
SIO_000300: 1.562e1

GenotypeQuality
all individuals: 4
bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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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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bin: 7.25e1
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 99
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 90
bin: 3.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8652
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10398
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500780405811022e-5
allele num: 66632
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11574
num of homozygotes: 0

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

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

MQRankSum
type: SiteQuality
SIO_000300: 1.14e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.52e-1

MQ
type: SiteQuality
SIO_000300: 5.99e1

DP
type: SiteQuality
SIO_000300: 2.701036e6

FS
type: SiteQuality
SIO_000300: 1.7071e1

QD
type: SiteQuality
SIO_000300: 1.562e1

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

BaseQRankSum
type: SiteQuality
SIO_000300: 7.9e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.49e0

GenotypeQuality
all individuals: 3444
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3775
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3423
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 70
bin: 2.25e1
variant carriers: 1

GenotypeQuality
all individuals: 65
bin: 3.25e1
variant carriers: 1

GenotypeQuality
all individuals: 25
bin: 4.25e1
variant carriers: 1

GenotypeQuality
all individuals: 30
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 4.75e1
variant carriers: 3

GenotypeQuality
all individuals: 8825
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 2080
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33456
bin: 9.75e1
variant carriers: 14

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

East Asian
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allele frequency: 0.0e0
allele num: 8652
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 20
allele frequency: 3.002642325246217e-4
allele num: 66608
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16482
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

African
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allele count: 7
allele frequency: 6.747638326585695e-4
allele num: 10374
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Other
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allele frequency: 1.101321585903084e-3
allele num: 908
num of homozygotes: 0

DP
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SIO_000300: 2.704189e6

MQRankSum
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SIO_000300: -6.830000000000001e-1

BaseQRankSum
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ReadPosRankSum
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SIO_000300: -1.72e-1

InbreedingCoeff
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MQ
type: SiteQuality
SIO_000300: 5.73e1

QD
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SIO_000300: 1.54e0

FS
type: SiteQuality
SIO_000300: 7.0123e1

ClippingRankSum
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SIO_000300: 3.06e0

VQSLOD
type: SiteQuality
SIO_000300: -2.396e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

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

Latino
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allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
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Other
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allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
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East Asian
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allele frequency: 1.155802126675913e-4
allele num: 8652
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66670
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.971e1

VQSLOD
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SIO_000300: 9.5e-1

InbreedingCoeff
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ClippingRankSum
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FS
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BaseQRankSum
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MQRankSum
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DP
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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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East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8652
num of homozygotes: 0

African
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allele frequency: 6.755452615325227e-4
allele num: 10362
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Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 20
allele frequency: 3.001831116981359e-4
allele num: 66626
num of homozygotes: 0

QD
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VQSLOD
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MQRankSum
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ReadPosRankSum
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MQ
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ClippingRankSum
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SIO_000300: 1.72e0

DP
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FS
type: SiteQuality
SIO_000300: 5.0963e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

BaseQRankSum
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SIO_000300: -3.452e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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allele frequency: 0.0e0
allele num: 8652
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

South Asian
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allele frequency: 6.059871530723549e-5
allele num: 16502
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66636
num of homozygotes: 0

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

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

MQ
type: SiteQuality
SIO_000300: 5.945e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.466e0

MQRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 1.7136e1

InbreedingCoeff
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SIO_000300: 1.0e-4

ClippingRankSum
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SIO_000300: 2.26e0

VQSLOD
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BaseQRankSum
type: SiteQuality
SIO_000300: -1.914e0

DP
type: SiteQuality
SIO_000300: 2.708024e6

QD
type: SiteQuality
SIO_000300: 1.01e0

GenotypeQuality
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variant carriers: 0

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

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

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

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

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

European (Non-Finnish)
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allele count: 6
allele frequency: 9.004141905276428e-5
allele num: 66636
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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10388
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.7136e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

ReadPosRankSum
type: SiteQuality
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VQSLOD
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SIO_000300: -5.513e0

ClippingRankSum
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MQ
type: SiteQuality
SIO_000300: 5.945e1

MQRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 2.708024e6

BaseQRankSum
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QD
type: SiteQuality
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GenotypeQuality
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variant carriers: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

Other
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African
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 2
allele frequency: 2.999940001199976e-5
allele num: 66668
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South Asian
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East Asian
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 2.6943e1

MQRankSum
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ClippingRankSum
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MQ
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InbreedingCoeff
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VQSLOD
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BaseQRankSum
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DP
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QD
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele num: 11578
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European (Non-Finnish)
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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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East Asian
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MQ
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FS
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InbreedingCoeff
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BaseQRankSum
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QD
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DP
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VQSLOD
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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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GenotypeQuality
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East Asian
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num of homozygotes: 0

African
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allele frequency: 0.0e0
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European (Non-Finnish)
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Latino
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South Asian
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European (Finnish)
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allele num: 6614
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Other
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VQSLOD
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MQ
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ClippingRankSum
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FS
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MQRankSum
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InbreedingCoeff
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QD
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DP
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ReadPosRankSum
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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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East Asian
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European (Finnish)
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African
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European (Non-Finnish)
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South Asian
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Latino
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Other
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DP
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FS
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MQ
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ReadPosRankSum
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InbreedingCoeff
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VQSLOD
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QD
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ClippingRankSum
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MQRankSum
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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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East Asian
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allele num: 8652
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Other
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South Asian
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European (Finnish)
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European (Non-Finnish)
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Latino
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InbreedingCoeff
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QD
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MQRankSum
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MQ
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ClippingRankSum
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ReadPosRankSum
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FS
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VQSLOD
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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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European (Finnish)
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African
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European (Non-Finnish)
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East Asian
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Latino
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South Asian
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FS
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MQRankSum
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ClippingRankSum
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QD
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InbreedingCoeff
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VQSLOD
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DP
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BaseQRankSum
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ReadPosRankSum
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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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European (Finnish)
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South Asian
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East Asian
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European (Non-Finnish)
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Latino
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African
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VQSLOD
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ClippingRankSum
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ReadPosRankSum
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MQRankSum
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InbreedingCoeff
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FS
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MQ
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BaseQRankSum
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QD
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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South Asian
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African
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Latino
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East Asian
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Other
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ClippingRankSum
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VQSLOD
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FS
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InbreedingCoeff
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QD
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DP
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BaseQRankSum
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MQRankSum
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MQ
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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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African
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South Asian
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European (Finnish)
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Other
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European (Non-Finnish)
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East Asian
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QD
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MQRankSum
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InbreedingCoeff
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ReadPosRankSum
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FS
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VQSLOD
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MQ
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DP
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BaseQRankSum
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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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African
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European (Non-Finnish)
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European (Finnish)
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Other
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East Asian
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Latino
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South Asian
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InbreedingCoeff
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ClippingRankSum
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MQRankSum
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VQSLOD
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MQ
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ReadPosRankSum
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FS
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DP
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BaseQRankSum
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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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European (Finnish)
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African
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East Asian
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Latino
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South Asian
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MQ
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InbreedingCoeff
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MQRankSum
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BaseQRankSum
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ClippingRankSum
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QD
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FS
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VQSLOD
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DP
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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South Asian
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European (Non-Finnish)
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African
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Latino
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East Asian
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DP
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MQ
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VQSLOD
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ReadPosRankSum
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MQRankSum
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FS
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ClippingRankSum
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BaseQRankSum
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QD
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GenotypeQuality
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African
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European (Non-Finnish)
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FS
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MQRankSum
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MQ
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DP
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InbreedingCoeff
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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African
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.073858114674441e-5
allele num: 16464
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

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.5e-3

QD
type: SiteQuality
SIO_000300: 1.274e1

MQRankSum
type: SiteQuality
SIO_000300: 3.32e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.35e0

DP
type: SiteQuality
SIO_000300: 2.68646e6

ClippingRankSum
type: SiteQuality
SIO_000300: -9.02e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 6.8e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.01e-1

GenotypeQuality
all individuals: 12
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 505
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3396
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3194
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1994
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33515
bin: 9.75e1
variant carriers: 101

GenotypeQuality
all individuals: 6005
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 713
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 184
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3442
bin: 9.25e1
variant carriers: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.216397031991242e-4
allele num: 16442
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.504127269998499e-5
allele num: 66630
num of homozygotes: 0

Latino
type: Population
allele count: 83
allele frequency: 7.171245895973734e-3
allele num: 11574
num of homozygotes: 2

African
type: Population
allele count: 2
allele frequency: 1.923446816695518e-4
allele num: 10398
num of homozygotes: 0

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

East Asian
type: Population
allele count: 11
allele frequency: 1.271970397779833e-3
allele num: 8648
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 1.88e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.44e0

QD
type: SiteQuality
SIO_000300: 1.441e1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.02e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.35e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.07e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.25e0

DP
type: SiteQuality
SIO_000300: 2.685023e6

GenotypeQuality
all individuals: 178
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 727
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 258
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2002
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3443
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3207
bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 486
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 7.5e0
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10402
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8640
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16442
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500870504892838e-5
allele num: 66628
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11568
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 5.61e0

FS
type: SiteQuality
SIO_000300: 2.545e0

MQRankSum
type: SiteQuality
SIO_000300: 1.16e0

DP
type: SiteQuality
SIO_000300: 2.682964e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.79e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.712e0

VQSLOD
type: SiteQuality
SIO_000300: -1.351e0

MQ
type: SiteQuality
SIO_000300: 5.959e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.22e0

GenotypeQuality
all individuals: 262
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 529
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3394
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
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variant carriers: 0

GenotypeQuality
all individuals: 3
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variant carriers: 0

GenotypeQuality
all individuals: 928
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 766
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3205
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33483
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 5325
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2075
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1995
bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

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

East Asian
type: Population
allele count: 2
allele frequency: 2.316423442205235e-4
allele num: 8634
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66638
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11570
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 3.188e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.52e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.8e-3

MQRankSum
type: SiteQuality
SIO_000300: 1.16e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 6.81e-1

QD
type: SiteQuality
SIO_000300: 1.327e1

DP
type: SiteQuality
SIO_000300: 2.682254e6

BaseQRankSum
type: SiteQuality
SIO_000300: -3.772e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.94e-1

GenotypeQuality
all individuals: 253
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1303
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1044
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3411
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
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variant carriers: 0

GenotypeQuality
all individuals: 3217
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2010
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 525
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variant carriers: 0

GenotypeQuality
all individuals: 528
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3448
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33481
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2076
bin: 8.75e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11572
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501005673801447e-5
allele num: 66622
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10400
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16446
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.9e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 1.85e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.47e0

MQRankSum
type: SiteQuality
SIO_000300: 2.99e-1

DP
type: SiteQuality
SIO_000300: 2.680959e6

FS
type: SiteQuality
SIO_000300: 4.105e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.64e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.48e-1

QD
type: SiteQuality
SIO_000300: 1.55e1

GenotypeQuality
all individuals: 9
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 33481
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2076
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1044
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41
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variant carriers: 0

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

GenotypeQuality
all individuals: 3295
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 544
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2010
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4462
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1303
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 528
bin: 3.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8638
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: 10400
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501005673801447e-5
allele num: 66622
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16446
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11572
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: 1.85e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.64e-1

QD
type: SiteQuality
SIO_000300: 1.55e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.47e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 2.99e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.48e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.9e-3

FS
type: SiteQuality
SIO_000300: 4.105e0

DP
type: SiteQuality
SIO_000300: 2.680959e6

GenotypeQuality
all individuals: 750
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 256
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 96
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 391
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5572
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3106
bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
all individuals: 471
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1281
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1997
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2157
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3939
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1681
bin: 5.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8298
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16180
num of homozygotes: 0

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

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

African
type: Population
allele count: 1
allele frequency: 1.182312603452353e-4
allele num: 8458
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11370
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.224038430538092e-5
allele num: 62034
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.89e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.89e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.617e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.15e-1

MQ
type: SiteQuality
SIO_000300: 5.96e1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.04e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.8e-3

VQSLOD
type: SiteQuality
SIO_000300: 2.86e0

DP
type: SiteQuality
SIO_000300: 2.084117e6

GenotypeQuality
all individuals: 2854
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 110
bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 777
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variant carriers: 0

GenotypeQuality
all individuals: 84
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variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 858
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4563
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3110
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 575
bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 5609
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 810
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10207
bin: 6.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8452
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11364
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8298
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16176
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.610928539210001e-5
allele num: 62076
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.866e0

QD
type: SiteQuality
SIO_000300: 1.288e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.4e-3

VQSLOD
type: SiteQuality
SIO_000300: 2.25e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.61e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.165e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.89e-1

MQ
type: SiteQuality
SIO_000300: 5.965e1

DP
type: SiteQuality
SIO_000300: 2.096528e6

GenotypeQuality
all individuals: 11283
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4014
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 774
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17805
bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1128
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 639
bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1046
bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2190
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5745
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2870
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8452
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11384
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8304
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.609839338034064e-5
allele num: 62118
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16202
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.3e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -1.391e0

DP
type: SiteQuality
SIO_000300: 2.102568e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.65e0

QD
type: SiteQuality
SIO_000300: 1.702e1

MQRankSum
type: SiteQuality
SIO_000300: -7.03e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.67e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.494e0

GenotypeQuality
all individuals: 63
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 772
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
all individuals: 11888
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 776
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 226
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2190
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2871
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 978
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 201
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5747
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variant carriers: 0

GenotypeQuality
all individuals: 4018
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4637
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3153
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 600
bin: 4.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11378
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8450
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16204
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 8.050751940231217e-5
allele num: 62106
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8306
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.54e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.3e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.5e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.09e-1

QD
type: SiteQuality
SIO_000300: 1.455e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 4.73e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.5e-3

DP
type: SiteQuality
SIO_000300: 2.106242e6

GenotypeQuality
all individuals: 340
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.608855138683313e-5
allele num: 62156
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16204
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11386
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8450
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 3.23e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.21e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.8e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.39e0

QD
type: SiteQuality
SIO_000300: 1.634e1

MQRankSum
type: SiteQuality
SIO_000300: 2.09e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.254e0

DP
type: SiteQuality
SIO_000300: 2.116042e6

GenotypeQuality
all individuals: 175
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 257
bin: 4.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.606012912343815e-5
allele num: 62266
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8454
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6588
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16208
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11398
num of homozygotes: 0

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: -4.91e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.06e-1

QD
type: SiteQuality
SIO_000300: 1.079e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.06e-2

VQSLOD
type: SiteQuality
SIO_000300: 3.87e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.73e-1

DP
type: SiteQuality
SIO_000300: 2.129421e6

MQ
type: SiteQuality
SIO_000300: 5.95e1

FS
type: SiteQuality
SIO_000300: 6.944e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.329e0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 200
bin: 5.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16208
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6588
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11398
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.606012912343815e-5
allele num: 62266
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 1.182872013248167e-4
allele num: 8454
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.079e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.329e0

MQRankSum
type: SiteQuality
SIO_000300: -1.73e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.87e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.06e-1

MQ
type: SiteQuality
SIO_000300: 5.95e1

FS
type: SiteQuality
SIO_000300: 6.944e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.91e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.06e-2

DP
type: SiteQuality
SIO_000300: 2.129421e6

GenotypeQuality
all individuals: 2238
bin: 8.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 329
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GenotypeQuality
all individuals: 4800
bin: 7.75e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11404
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.603694913079736e-5
allele num: 62356
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8460
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.197891710589363e-4
allele num: 8348
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6588
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.165228113440197e-5
allele num: 16220
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -5.37e-1

DP
type: SiteQuality
SIO_000300: 2.134324e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.4e-3

QD
type: SiteQuality
SIO_000300: 1.408e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.23e0

MQ
type: SiteQuality
SIO_000300: 5.975e1

FS
type: SiteQuality
SIO_000300: 3.04e0

VQSLOD
type: SiteQuality
SIO_000300: 8.35e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.26e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.589e0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 17849
bin: 9.75e1
variant carriers: 7

Latino
type: Population
allele count: 7
allele frequency: 6.138197123816205e-4
allele num: 11404
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62428
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8362
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16226
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8464
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6594
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.7e-1

FS
type: SiteQuality
SIO_000300: 6.58e-1

QD
type: SiteQuality
SIO_000300: 1.287e1

DP
type: SiteQuality
SIO_000300: 2.138818e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.099999999999999e-2

VQSLOD
type: SiteQuality
SIO_000300: 2.7e0

MQRankSum
type: SiteQuality
SIO_000300: 9.5e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -3.012e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.9e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 3360
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 800
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 114
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variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11418
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16234
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8398
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6594
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.598823266076168e-5
allele num: 62546
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.969e1

DP
type: SiteQuality
SIO_000300: 2.146144e6

QD
type: SiteQuality
SIO_000300: 1.215e1

VQSLOD
type: SiteQuality
SIO_000300: 1.34e0

MQRankSum
type: SiteQuality
SIO_000300: 3.35e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 9.360000000000001e-1

FS
type: SiteQuality
SIO_000300: 2.801e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.41e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.2e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -5.11e-1

GenotypeQuality
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bin: 9.75e1
variant carriers: 3

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16240
num of homozygotes: 0

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

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11426
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8430
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.790801660811242e-5
allele num: 62620
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.926e0

ClippingRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.964e1

ReadPosRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
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QD
type: SiteQuality
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DP
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 3.5e-3

BaseQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: 1.09e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 127
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 16
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variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 4.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11440
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8506
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8484
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62778
num of homozygotes: 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: 862
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 1.845018450184502e-4
allele num: 16260
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.75e0

VQSLOD
type: SiteQuality
SIO_000300: 2.42e0

MQRankSum
type: SiteQuality
SIO_000300: 4.57e-1

DP
type: SiteQuality
SIO_000300: 2.154157e6

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.3e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.12e0

QD
type: SiteQuality
SIO_000300: 1.316e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.13e0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
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GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.59291471534614e-5
allele num: 62778
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8484
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8506
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11440
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.12e0

VQSLOD
type: SiteQuality
SIO_000300: 2.42e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.13e0

MQRankSum
type: SiteQuality
SIO_000300: 4.57e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.75e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.3e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.316e1

DP
type: SiteQuality
SIO_000300: 2.154157e6

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8496
num of homozygotes: 0

Latino
type: Population
allele count: 12
allele frequency: 1.048218029350105e-3
allele num: 11448
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16262
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62844
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.9e-3

VQSLOD
type: SiteQuality
SIO_000300: 6.53e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.23e-1

MQ
type: SiteQuality
SIO_000300: 5.946e1

FS
type: SiteQuality
SIO_000300: 6.205e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.21e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.06e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.045e0

QD
type: SiteQuality
SIO_000300: 1.107e1

DP
type: SiteQuality
SIO_000300: 2.156009e6

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 5

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11448
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8510
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: 8496
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.953424744695065e-5
allele num: 62866
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16264
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.57e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.830000000000001e-1

QD
type: SiteQuality
SIO_000300: 1.326e1

MQ
type: SiteQuality
SIO_000300: 5.962e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.2e-3

FS
type: SiteQuality
SIO_000300: 7.358e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.19e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.2e0

VQSLOD
type: SiteQuality
SIO_000300: 4.22e-1

DP
type: SiteQuality
SIO_000300: 2.156309e6

GenotypeQuality
all individuals: 2
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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
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GenotypeQuality
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16266
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.174812030075188e-4
allele num: 8512
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11454
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8502
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: 0
allele frequency: 0.0e0
allele num: 62920
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.09e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.17e0

MQRankSum
type: SiteQuality
SIO_000300: 5.580000000000001e-1

FS
type: SiteQuality
SIO_000300: 8.031000000000001e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.68e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.1e-3

QD
type: SiteQuality
SIO_000300: 1.259e1

MQ
type: SiteQuality
SIO_000300: 5.945e1

DP
type: SiteQuality
SIO_000300: 2.157828e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.23e-1

GenotypeQuality
all individuals: 10
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2284
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 7.75e1
variant carriers: 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: 1
allele frequency: 1.589319771137953e-5
allele num: 62920
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8502
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16266
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8512
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11454
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.148e0

MQRankSum
type: SiteQuality
SIO_000300: -3.88e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.28e-1

MQ
type: SiteQuality
SIO_000300: 5.961e1

DP
type: SiteQuality
SIO_000300: 2.157919e6

VQSLOD
type: SiteQuality
SIO_000300: 1.4e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.39e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.05e-1

QD
type: SiteQuality
SIO_000300: 9.199999999999999e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.6e-3

GenotypeQuality
all individuals: 4
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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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GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.589319771137953e-5
allele num: 62920
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16266
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11458
num of homozygotes: 0

East Asian
type: Population
allele count: 0
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allele num: 8504
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VQSLOD
type: SiteQuality
SIO_000300: 5.7e-1

InbreedingCoeff
type: SiteQuality
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QD
type: SiteQuality
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DP
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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FS
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.978e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.42e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.18e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.45e-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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GenotypeQuality
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African
type: Population
allele count: 40
allele frequency: 4.699248120300752e-3
allele num: 8512
num of homozygotes: 1

East Asian
type: Population
allele count: 0
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num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.147792942333702e-5
allele num: 16266
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 172
allele frequency: 2.73371690136368e-3
allele num: 62918
num of homozygotes: 0

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

Latino
type: Population
allele count: 29
allele frequency: 2.530982719497294e-3
allele num: 11458
num of homozygotes: 0

Other
type: Population
allele count: 3
allele frequency: 3.456221198156682e-3
allele num: 868
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
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DP
type: SiteQuality
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FS
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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VQSLOD
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MQ
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SIO_000300: 5.967e1

MQRankSum
type: SiteQuality
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ClippingRankSum
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QD
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ReadPosRankSum
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GenotypeQuality
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variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8520
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62924
num of homozygotes: 0

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

East Asian
type: Population
allele count: 3
allele frequency: 3.526093088857546e-4
allele num: 8508
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16266
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.94e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.51e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.01e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.5e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 4.22e-1

FS
type: SiteQuality
SIO_000300: 3.213e0

DP
type: SiteQuality
SIO_000300: 2.161741e6

QD
type: SiteQuality
SIO_000300: 1.245e1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.1e-2

MQRankSum
type: SiteQuality
SIO_000300: 4.33e-1

GenotypeQuality
all individuals: 4933
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4213
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 118
bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1028
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2277
bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2952
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15542
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17935
bin: 9.75e1
variant carriers: 8

GenotypeQuality
all individuals: 2
bin: 4.75e1
variant carriers: 0

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

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16268
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 8
allele frequency: 1.271253774034642e-4
allele num: 62930
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -7.099999999999999e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.162237e6

ClippingRankSum
type: SiteQuality
SIO_000300: -4.28e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.09e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.71e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.71e0

MQ
type: SiteQuality
SIO_000300: 5.955e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.8e-3

QD
type: SiteQuality
SIO_000300: 1.379e1

GenotypeQuality
all individuals: 7
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 94
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2277
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3405
bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2952
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4216
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15519
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4929
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17933
bin: 9.75e1
variant carriers: 1

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11462
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.588259585146596e-5
allele num: 62962
num of homozygotes: 0

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16280
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8536
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.38e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.378e0

MQRankSum
type: SiteQuality
SIO_000300: 9.31e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.9e-1

DP
type: SiteQuality
SIO_000300: 2.163486e6

VQSLOD
type: SiteQuality
SIO_000300: -8.3e-3

MQ
type: SiteQuality
SIO_000300: 5.958e1

FS
type: SiteQuality
SIO_000300: 3.951e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.1e-3

QD
type: SiteQuality
SIO_000300: 6.56e0

GenotypeQuality
all individuals: 15242
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 40
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6180
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 74
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2949
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4202
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 80
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 208
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 575
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2277
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4904
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18005
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 59
bin: 5.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.588461416272199e-5
allele num: 62954
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8502
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: 1
allele frequency: 6.140997297961189e-5
allele num: 16284
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 2.620545073375262e-4
allele num: 11448
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.83e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.4e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.95e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.58e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.58e-1

DP
type: SiteQuality
SIO_000300: 2.172888e6

QD
type: SiteQuality
SIO_000300: 9.640000000000001e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.77e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.14e0

GenotypeQuality
all individuals: 50
bin: 1.25e1
variant carriers: 1

GenotypeQuality
all individuals: 59
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15242
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18005
bin: 9.75e1
variant carriers: 10

GenotypeQuality
all individuals: 2277
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1204
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 575
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 208
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 6180
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 80
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 3.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3382
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4202
bin: 8.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 2
allele frequency: 3.026634382566586e-4
allele num: 6608
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 3
allele frequency: 3.528581510232887e-4
allele num: 8502
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.942307081360994e-5
allele num: 62954
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11448
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.140997297961189e-5
allele num: 16284
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 5.83e-1

DP
type: SiteQuality
SIO_000300: 2.172888e6

MQRankSum
type: SiteQuality
SIO_000300: 3.58e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.4e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -3.58e-1

QD
type: SiteQuality
SIO_000300: 9.640000000000001e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.95e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.14e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.77e-1

GenotypeQuality
all individuals: 6207
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4924
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4213
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 592
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15296
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35
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variant carriers: 0

GenotypeQuality
all individuals: 2283
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1195
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3392
bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62994
num of homozygotes: 0

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

East Asian
type: Population
allele count: 2
allele frequency: 2.351281448389372e-4
allele num: 8506
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8578
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: 1.59e-1

FS
type: SiteQuality
SIO_000300: 1.197e0

QD
type: SiteQuality
SIO_000300: 1.265e1

DP
type: SiteQuality
SIO_000300: 2.171683e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.3e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.9e-3

MQRankSum
type: SiteQuality
SIO_000300: -5.76e-1

MQ
type: SiteQuality
SIO_000300: 5.981e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.38e0

VQSLOD
type: SiteQuality
SIO_000300: 9.0e-1

GenotypeQuality
all individuals: 25
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 138
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 649
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4933
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6232
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4221
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3403
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1176
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 18008
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2287
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 88
bin: 1.75e1
variant carriers: 1

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16298
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11478
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8590
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: 0
allele frequency: 0.0e0
allele num: 63054
num of homozygotes: 0

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.36e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.36e-1

MQRankSum
type: SiteQuality
SIO_000300: -7.36e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.762e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.36e-1

VQSLOD
type: SiteQuality
SIO_000300: -8.552999999999999e-1

DP
type: SiteQuality
SIO_000300: 2.170231e6