8-106813887-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 106813887
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 106813887
    reference: chr 8
allele count: 1
allele frequency: 8.3301401129567e-6
allele num: 120046
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000521622
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000521622.1:n.279-3217C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520078
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520078.1:n.149-3217C>T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000367733
  ensembl transcript: ENST00000378472
  gene symbol: ZFPM2
  hgvsc: ENST00000378472.4:c.770G>A
  hgvsp: ENSP00000367733.4:p.Arg257Gln
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000524045
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000524045.2:n.154-3217C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000518932
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000518932.1:n.66-3217C>T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000428720
  ensembl transcript: ENST00000517361
  gene symbol: ZFPM2
  hgvsc: ENST00000517361.1:c.1181G>A
  hgvsp: ENSP00000428720.1:p.Arg394Gln
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520594
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520594.1:n.155-3217C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169946
  ensembl transcript: ENST00000522296
  gene symbol: ZFPM2
  hgvsc: ENST00000522296.1:n.1371G>A
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520433
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520433.1:n.212-3217C>T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000384179
  ensembl transcript: ENST00000407775
  gene symbol: ZFPM2
  hgvsc: ENST00000407775.2:c.1577G>A
  hgvsp: ENSP00000384179.2:p.Arg526Gln
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000430757
  ensembl transcript: ENST00000520492
  gene symbol: ZFPM2
  hgvsc: ENST00000520492.1:c.1181G>A
  hgvsp: ENSP00000430757.1:p.Arg394Gln
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000509144
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000509144.2:n.140-3217C>T
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1327
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 905
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8130
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16608
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26541
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2224
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 585
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 784
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg526Gln
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: DP

8-106813888-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 106813888
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 106813888
    reference: chr 8
allele count: 85
allele frequency: 7.080265218405358e-4
allele num: 120052
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000384179
  ensembl transcript: ENST00000407775
  gene symbol: ZFPM2
  hgvsc: ENST00000407775.2:c.1578G>T
  hgvsp: ENST00000407775.2:c.1578G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000428720
  ensembl transcript: ENST00000517361
  gene symbol: ZFPM2
  hgvsc: ENST00000517361.1:c.1182G>T
  hgvsp: ENST00000517361.1:c.1182G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000521622
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000521622.1:n.279-3218C>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169946
  ensembl transcript: ENST00000522296
  gene symbol: ZFPM2
  hgvsc: ENST00000522296.1:n.1372G>T
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000518932
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000518932.1:n.66-3218C>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520433
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520433.1:n.212-3218C>A
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000524045
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000524045.2:n.154-3218C>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520594
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520594.1:n.155-3218C>A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000367733
  ensembl transcript: ENST00000378472
  gene symbol: ZFPM2
  hgvsc: ENST00000378472.4:c.771G>T
  hgvsp: ENST00000378472.4:c.771G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000430757
  ensembl transcript: ENST00000520492
  gene symbol: ZFPM2
  hgvsc: ENST00000520492.1:c.1182G>T
  hgvsp: ENST00000520492.1:c.1182G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520078
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520078.1:n.149-3218C>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000509144
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000509144.2:n.140-3218C>A
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8116
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26530
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 849
  bin: 9.75e1
  variant carriers: 67
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 9.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2217
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1322
  bin: 4.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16592
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 665
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 585
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 905
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg526Arg
num of homozygotes: 1
population: Other
population: East Asian
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum

8-106813893-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 106813893
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 106813893
    reference: chr 8
allele count: 1
allele frequency: 8.328058896032513e-6
allele num: 120076
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000518932
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000518932.1:n.66-3223A>C
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000524045
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000524045.2:n.154-3223A>C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000384179
  ensembl transcript: ENST00000407775
  gene symbol: ZFPM2
  hgvsc: ENST00000407775.2:c.1583T>G
  hgvsp: ENSP00000384179.2:p.Leu528Arg
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169946
  ensembl transcript: ENST00000522296
  gene symbol: ZFPM2
  hgvsc: ENST00000522296.1:n.1377T>G
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000367733
  ensembl transcript: ENST00000378472
  gene symbol: ZFPM2
  hgvsc: ENST00000378472.4:c.776T>G
  hgvsp: ENSP00000367733.4:p.Leu259Arg
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520078
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520078.1:n.149-3223A>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520433
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520433.1:n.212-3223A>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000521622
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000521622.1:n.279-3223A>C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000430757
  ensembl transcript: ENST00000520492
  gene symbol: ZFPM2
  hgvsc: ENST00000520492.1:c.1187T>G
  hgvsp: ENSP00000430757.1:p.Leu396Arg
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000428720
  ensembl transcript: ENST00000517361
  gene symbol: ZFPM2
  hgvsc: ENST00000517361.1:c.1187T>G
  hgvsp: ENSP00000428720.1:p.Leu396Arg
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520594
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520594.1:n.155-3223A>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000509144
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000509144.2:n.140-3223A>C
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16633
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8131
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26574
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 788
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1318
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2220
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 901
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 585
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu528Arg
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
population: Latino
population: Other
reference allele: T
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD

8-106813896-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 106813896
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 106813896
    reference: chr 8
allele count: 1
allele frequency: 8.329030001166064e-6
allele num: 120062
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520078
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520078.1:n.149-3226C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000518932
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000518932.1:n.66-3226C>T
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000524045
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000524045.2:n.154-3226C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169946
  ensembl transcript: ENST00000522296
  gene symbol: ZFPM2
  hgvsc: ENST00000522296.1:n.1380G>A
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000384179
  ensembl transcript: ENST00000407775
  gene symbol: ZFPM2
  hgvsc: ENST00000407775.2:c.1586G>A
  hgvsp: ENSP00000384179.2:p.Arg529Lys
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520594
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520594.1:n.155-3226C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000521622
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000521622.1:n.279-3226C>T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000367733
  ensembl transcript: ENST00000378472
  gene symbol: ZFPM2
  hgvsc: ENST00000378472.4:c.779G>A
  hgvsp: ENSP00000367733.4:p.Arg260Lys
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000430757
  ensembl transcript: ENST00000520492
  gene symbol: ZFPM2
  hgvsc: ENST00000520492.1:c.1190G>A
  hgvsp: ENSP00000430757.1:p.Arg397Lys
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000428720
  ensembl transcript: ENST00000517361
  gene symbol: ZFPM2
  hgvsc: ENST00000517361.1:c.1190G>A
  hgvsp: ENSP00000428720.1:p.Arg397Lys
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000509144
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000509144.2:n.140-3226C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520433
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520433.1:n.212-3226C>T
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 584
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2220
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26582
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16620
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8133
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1317
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 901
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 788
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Arg529Lys
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff

8-106813897-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 106813897
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 106813897
    reference: chr 8
allele count: 4
allele frequency: 3.331723000549734e-5
allele num: 120058
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000367733
  ensembl transcript: ENST00000378472
  gene symbol: ZFPM2
  hgvsc: ENST00000378472.4:c.780G>A
  hgvsp: ENST00000378472.4:c.780G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520433
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520433.1:n.212-3227C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520594
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520594.1:n.155-3227C>T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000384179
  ensembl transcript: ENST00000407775
  gene symbol: ZFPM2
  hgvsc: ENST00000407775.2:c.1587G>A
  hgvsp: ENST00000407775.2:c.1587G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000524045
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000524045.2:n.154-3227C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520078
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520078.1:n.149-3227C>T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000428720
  ensembl transcript: ENST00000517361
  gene symbol: ZFPM2
  hgvsc: ENST00000517361.1:c.1191G>A
  hgvsp: ENST00000517361.1:c.1191G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000430757
  ensembl transcript: ENST00000520492
  gene symbol: ZFPM2
  hgvsc: ENST00000520492.1:c.1191G>A
  hgvsp: ENST00000520492.1:c.1191G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000518932
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000518932.1:n.66-3227C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169946
  ensembl transcript: ENST00000522296
  gene symbol: ZFPM2
  hgvsc: ENST00000522296.1:n.1381G>A
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000509144
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000509144.2:n.140-3227C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000521622
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000521622.1:n.279-3227C>T
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 584
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8138
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 902
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26582
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16602
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1313
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2218
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 791
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg529Arg
num of homozygotes: 0
population: Latino
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: G
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum

8-106813902-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 106813902
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 106813902
    reference: chr 8
allele count: 2
allele frequency: 1.666194578202842e-5
allele num: 120034
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520433
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520433.1:n.212-3232C>T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000428720
  ensembl transcript: ENST00000517361
  gene symbol: ZFPM2
  hgvsc: ENST00000517361.1:c.1196G>A
  hgvsp: ENSP00000428720.1:p.Gly399Asp
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000367733
  ensembl transcript: ENST00000378472
  gene symbol: ZFPM2
  hgvsc: ENST00000378472.4:c.785G>A
  hgvsp: ENSP00000367733.4:p.Gly262Asp
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000384179
  ensembl transcript: ENST00000407775
  gene symbol: ZFPM2
  hgvsc: ENST00000407775.2:c.1592G>A
  hgvsp: ENSP00000384179.2:p.Gly531Asp
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169946
  ensembl transcript: ENST00000522296
  gene symbol: ZFPM2
  hgvsc: ENST00000522296.1:n.1386G>A
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000521622
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000521622.1:n.279-3232C>T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000430757
  ensembl transcript: ENST00000520492
  gene symbol: ZFPM2
  hgvsc: ENST00000520492.1:c.1196G>A
  hgvsp: ENSP00000430757.1:p.Gly399Asp
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520594
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520594.1:n.155-3232C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520078
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520078.1:n.149-3232C>T
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000524045
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000524045.2:n.154-3232C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000509144
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000509144.2:n.140-3232C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000518932
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000518932.1:n.66-3232C>T
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 901
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 684
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16602
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2217
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8130
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1313
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 584
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26554
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 789
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
hgvs: p.Gly531Asp
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
population: Other
population: European (Finnish)
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: DP

8-106813913-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 106813913
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 106813913
    reference: chr 8
allele count: 1
allele frequency: 8.332083520805212e-6
allele num: 120018
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000367733
  ensembl transcript: ENST00000378472
  gene symbol: ZFPM2
  hgvsc: ENST00000378472.4:c.796T>C
  hgvsp: ENSP00000367733.4:p.Tyr266His
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000524045
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000524045.2:n.154-3243A>G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000428720
  ensembl transcript: ENST00000517361
  gene symbol: ZFPM2
  hgvsc: ENST00000517361.1:c.1207T>C
  hgvsp: ENSP00000428720.1:p.Tyr403His
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000384179
  ensembl transcript: ENST00000407775
  gene symbol: ZFPM2
  hgvsc: ENST00000407775.2:c.1603T>C
  hgvsp: ENSP00000384179.2:p.Tyr535His
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000430757
  ensembl transcript: ENST00000520492
  gene symbol: ZFPM2
  hgvsc: ENST00000520492.1:c.1207T>C
  hgvsp: ENSP00000430757.1:p.Tyr403His
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520594
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520594.1:n.155-3243A>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000509144
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000509144.2:n.140-3243A>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000518932
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000518932.1:n.66-3243A>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169946
  ensembl transcript: ENST00000522296
  gene symbol: ZFPM2
  hgvsc: ENST00000522296.1:n.1397T>C
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520078
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520078.1:n.149-3243A>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000521622
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000521622.1:n.279-3243A>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520433
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520433.1:n.212-3243A>G
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 699
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26512
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1315
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2221
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16550
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8121
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 900
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 584
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 788
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Tyr535His
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
population: African
population: East Asian
population: European (Finnish)
reference allele: T
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD

8-106813915-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 106813915
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 106813915
    reference: chr 8
allele count: 1
allele frequency: 8.333611120370679e-6
allele num: 119996
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000428720
  ensembl transcript: ENST00000517361
  gene symbol: ZFPM2
  hgvsc: ENST00000517361.1:c.1209C>T
  hgvsp: ENST00000517361.1:c.1209C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520594
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520594.1:n.155-3245G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169946
  ensembl transcript: ENST00000522296
  gene symbol: ZFPM2
  hgvsc: ENST00000522296.1:n.1399C>T
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520078
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520078.1:n.149-3245G>A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000430757
  ensembl transcript: ENST00000520492
  gene symbol: ZFPM2
  hgvsc: ENST00000520492.1:c.1209C>T
  hgvsp: ENST00000520492.1:c.1209C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000367733
  ensembl transcript: ENST00000378472
  gene symbol: ZFPM2
  hgvsc: ENST00000378472.4:c.798C>T
  hgvsp: ENST00000378472.4:c.798C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000384179
  ensembl transcript: ENST00000407775
  gene symbol: ZFPM2
  hgvsc: ENST00000407775.2:c.1605C>T
  hgvsp: ENST00000407775.2:c.1605C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000521622
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000521622.1:n.279-3245G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520433
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520433.1:n.212-3245G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000518932
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000518932.1:n.66-3245G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000509144
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000509144.2:n.140-3245G>A
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000524045
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000524045.2:n.154-3245G>A
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26513
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 585
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8115
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1317
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16556
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 691
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2225
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 787
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 900
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Tyr535Tyr
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD

8-106813917-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 106813917
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 106813917
    reference: chr 8
allele count: 1
allele frequency: 8.33152816889674e-6
allele num: 120026
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000430757
  ensembl transcript: ENST00000520492
  gene symbol: ZFPM2
  hgvsc: ENST00000520492.1:c.1211C>T
  hgvsp: ENSP00000430757.1:p.Pro404Leu
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000367733
  ensembl transcript: ENST00000378472
  gene symbol: ZFPM2
  hgvsc: ENST00000378472.4:c.800C>T
  hgvsp: ENSP00000367733.4:p.Pro267Leu
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000521622
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000521622.1:n.279-3247G>A
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000524045
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000524045.2:n.154-3247G>A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000428720
  ensembl transcript: ENST00000517361
  gene symbol: ZFPM2
  hgvsc: ENST00000517361.1:c.1211C>T
  hgvsp: ENSP00000428720.1:p.Pro404Leu
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000509144
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000509144.2:n.140-3247G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520078
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520078.1:n.149-3247G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000518932
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000518932.1:n.66-3247G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169946
  ensembl transcript: ENST00000522296
  gene symbol: ZFPM2
  hgvsc: ENST00000522296.1:n.1401C>T
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000384179
  ensembl transcript: ENST00000407775
  gene symbol: ZFPM2
  hgvsc: ENST00000407775.2:c.1607C>T
  hgvsp: ENSP00000384179.2:p.Pro536Leu
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520594
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520594.1:n.155-3247G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520433
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520433.1:n.212-3247G>A
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2223
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8122
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 585
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1312
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 901
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 685
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26505
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16563
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 788
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 702
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro536Leu
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
population: European (Finnish)
reference allele: C
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum

8-106813922-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 106813922
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 106813922
    reference: chr 8
allele count: 29
allele frequency: 2.417069511585264e-4
allele num: 119980
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000430757
  ensembl transcript: ENST00000520492
  gene symbol: ZFPM2
  hgvsc: ENST00000520492.1:c.1216G>A
  hgvsp: ENSP00000430757.1:p.Val406Ile
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000367733
  ensembl transcript: ENST00000378472
  gene symbol: ZFPM2
  hgvsc: ENST00000378472.4:c.805G>A
  hgvsp: ENSP00000367733.4:p.Val269Ile
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000521622
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000521622.1:n.279-3252C>T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000384179
  ensembl transcript: ENST00000407775
  gene symbol: ZFPM2
  hgvsc: ENST00000407775.2:c.1612G>A
  hgvsp: ENSP00000384179.2:p.Val538Ile
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520433
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520433.1:n.212-3252C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520594
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520594.1:n.155-3252C>T
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000524045
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000524045.2:n.154-3252C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520078
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520078.1:n.149-3252C>T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000428720
  ensembl transcript: ENST00000517361
  gene symbol: ZFPM2
  hgvsc: ENST00000517361.1:c.1216G>A
  hgvsp: ENSP00000428720.1:p.Val406Ile
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000509144
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000509144.2:n.140-3252C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000518932
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000518932.1:n.66-3252C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169946
  ensembl transcript: ENST00000522296
  gene symbol: ZFPM2
  hgvsc: ENST00000522296.1:n.1406G>A
  variant of: http://identifiers.org/hgnc/16700
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16583
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8113
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26486
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2212
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 899
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 676
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 815
  bin: 9.75e1
  variant carriers: 29
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 584
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1308
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 699
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val538Ile
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
population: Other
reference allele: G
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: MQ

8-106813936-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 106813936
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 106813936
    reference: chr 8
allele count: 1
allele frequency: 8.332500083325001e-6
allele num: 120012
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000428720
  ensembl transcript: ENST00000517361
  gene symbol: ZFPM2
  hgvsc: ENST00000517361.1:c.1230T>C
  hgvsp: ENST00000517361.1:c.1230T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000384179
  ensembl transcript: ENST00000407775
  gene symbol: ZFPM2
  hgvsc: ENST00000407775.2:c.1626T>C
  hgvsp: ENST00000407775.2:c.1626T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169946
  ensembl transcript: ENST00000522296
  gene symbol: ZFPM2
  hgvsc: ENST00000522296.1:n.1420T>C
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520433
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520433.1:n.212-3266A>G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000430757
  ensembl transcript: ENST00000520492
  gene symbol: ZFPM2
  hgvsc: ENST00000520492.1:c.1230T>C
  hgvsp: ENST00000520492.1:c.1230T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520594
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520594.1:n.155-3266A>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520078
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520078.1:n.149-3266A>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000509144
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000509144.2:n.140-3266A>G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000367733
  ensembl transcript: ENST00000378472
  gene symbol: ZFPM2
  hgvsc: ENST00000378472.4:c.819T>C
  hgvsp: ENST00000378472.4:c.819T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000521622
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000521622.1:n.279-3266A>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000518932
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000518932.1:n.66-3266A>G
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000524045
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000524045.2:n.154-3266A>G
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 699
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 899
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 654
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8127
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16593
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 584
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1309
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 786
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26534
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2206
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro542Pro
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
population: East Asian
reference allele: T
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP

8-106813939-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 106813939
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 106813939
    reference: chr 8
allele count: 1
allele frequency: 8.334305668994715e-6
allele num: 119986
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000521622
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000521622.1:n.279-3269C>G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000367733
  ensembl transcript: ENST00000378472
  gene symbol: ZFPM2
  hgvsc: ENST00000378472.4:c.822G>C
  hgvsp: ENSP00000367733.4:p.Leu274Phe
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000428720
  ensembl transcript: ENST00000517361
  gene symbol: ZFPM2
  hgvsc: ENST00000517361.1:c.1233G>C
  hgvsp: ENSP00000428720.1:p.Leu411Phe
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000518932
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000518932.1:n.66-3269C>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520594
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520594.1:n.155-3269C>G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000384179
  ensembl transcript: ENST00000407775
  gene symbol: ZFPM2
  hgvsc: ENST00000407775.2:c.1629G>C
  hgvsp: ENSP00000384179.2:p.Leu543Phe
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520078
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520078.1:n.149-3269C>G
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000524045
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000524045.2:n.154-3269C>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169946
  ensembl transcript: ENST00000522296
  gene symbol: ZFPM2
  hgvsc: ENST00000522296.1:n.1423G>C
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000509144
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000509144.2:n.140-3269C>G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000430757
  ensembl transcript: ENST00000520492
  gene symbol: ZFPM2
  hgvsc: ENST00000520492.1:c.1233G>C
  hgvsp: ENSP00000430757.1:p.Leu411Phe
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520433
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520433.1:n.212-3269C>G
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26521
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 651
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16611
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 585
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8130
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 699
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1308
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2205
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 899
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 787
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Leu543Phe
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
reference allele: G
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ

8-106813942-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 106813942
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 106813942
    reference: chr 8
allele count: 414
allele frequency: 3.45028752396033e-3
allele num: 119990
alternate allele: A
annotation: Annotation
  canonical: false
  clinical significance: pathogenic
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000521622
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000521622.1:n.279-3272C>T
annotation: Annotation
  canonical: false
  clinical significance: pathogenic
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000367733
  ensembl transcript: ENST00000378472
  gene symbol: ZFPM2
  hgvsc: ENST00000378472.4:c.825G>A
  hgvsp: ENSP00000367733.4:p.Met275Ile
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  clinical significance: pathogenic
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000518932
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000518932.1:n.66-3272C>T
annotation: Annotation
  canonical: false
  clinical significance: pathogenic
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000509144
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000509144.2:n.140-3272C>T
annotation: Annotation
  canonical: false
  clinical significance: pathogenic
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000428720
  ensembl transcript: ENST00000517361
  gene symbol: ZFPM2
  hgvsc: ENST00000517361.1:c.1236G>A
  hgvsp: ENSP00000428720.1:p.Met412Ile
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: true
  clinical significance: pathogenic
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000384179
  ensembl transcript: ENST00000407775
  gene symbol: ZFPM2
  hgvsc: ENST00000407775.2:c.1632G>A
  hgvsp: ENSP00000384179.2:p.Met544Ile
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: true
  clinical significance: pathogenic
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000524045
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000524045.2:n.154-3272C>T
annotation: Annotation
  canonical: false
  clinical significance: pathogenic
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000430757
  ensembl transcript: ENST00000520492
  gene symbol: ZFPM2
  hgvsc: ENST00000520492.1:c.1236G>A
  hgvsp: ENSP00000430757.1:p.Met412Ile
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  clinical significance: pathogenic
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520594
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520594.1:n.155-3272C>T
annotation: Annotation
  canonical: false
  clinical significance: pathogenic
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520433
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520433.1:n.212-3272C>T
annotation: Annotation
  canonical: false
  clinical significance: pathogenic
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169946
  ensembl transcript: ENST00000522296
  gene symbol: ZFPM2
  hgvsc: ENST00000522296.1:n.1426G>A
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  clinical significance: pathogenic
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520078
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520078.1:n.149-3272C>T
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 685
  bin: 5.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 9.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1115
  bin: 9.75e1
  variant carriers: 341
genotype depth: GenotypeDepth
  all individuals: 26451
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 7.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 7.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 1.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 2140
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 8.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8084
  bin: 3.25e1
  variant carriers: 5
genotype quality: GenotypeQuality
hgvs: p.Met544Ile
num of homozygotes: 2
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: African
population: Latino
population: Other
reference allele: G
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: MQ

8-106813942-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 106813942
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 106813942
    reference: chr 8
allele count: 1
allele frequency: 8.334027835652971e-6
allele num: 119990
alternate allele: T
annotation: Annotation
  canonical: false
  clinical significance: pathogenic
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000428720
  ensembl transcript: ENST00000517361
  gene symbol: ZFPM2
  hgvsc: ENST00000517361.1:c.1236G>T
  hgvsp: ENSP00000428720.1:p.Met412Ile
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  clinical significance: pathogenic
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000509144
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000509144.2:n.140-3272C>A
annotation: Annotation
  canonical: false
  clinical significance: pathogenic
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000518932
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000518932.1:n.66-3272C>A
annotation: Annotation
  canonical: false
  clinical significance: pathogenic
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520433
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520433.1:n.212-3272C>A
annotation: Annotation
  canonical: false
  clinical significance: pathogenic
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000521622
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000521622.1:n.279-3272C>A
annotation: Annotation
  canonical: false
  clinical significance: pathogenic
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000430757
  ensembl transcript: ENST00000520492
  gene symbol: ZFPM2
  hgvsc: ENST00000520492.1:c.1236G>T
  hgvsp: ENSP00000430757.1:p.Met412Ile
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: true
  clinical significance: pathogenic
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000524045
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000524045.2:n.154-3272C>A
annotation: Annotation
  canonical: false
  clinical significance: pathogenic
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520594
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520594.1:n.155-3272C>A
annotation: Annotation
  canonical: false
  clinical significance: pathogenic
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520078
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520078.1:n.149-3272C>A
annotation: Annotation
  canonical: true
  clinical significance: pathogenic
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000384179
  ensembl transcript: ENST00000407775
  gene symbol: ZFPM2
  hgvsc: ENST00000407775.2:c.1632G>T
  hgvsp: ENSP00000384179.2:p.Met544Ile
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  clinical significance: pathogenic
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169946
  ensembl transcript: ENST00000522296
  gene symbol: ZFPM2
  hgvsc: ENST00000522296.1:n.1426G>T
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  clinical significance: pathogenic
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000367733
  ensembl transcript: ENST00000378472
  gene symbol: ZFPM2
  hgvsc: ENST00000378472.4:c.825G>T
  hgvsp: ENSP00000367733.4:p.Met275Ile
  variant of: http://identifiers.org/hgnc/16700
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26451
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8084
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16592
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2140
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1115
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Met544Ile
num of homozygotes: 0
population: Other
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
reference allele: G
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: QD

8-106813945-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 106813945
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 106813945
    reference: chr 8
allele count: 3
allele frequency: 2.500041667361123e-5
allele num: 119998
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520433
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520433.1:n.212-3275G>A
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000524045
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000524045.2:n.154-3275G>A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000384179
  ensembl transcript: ENST00000407775
  gene symbol: ZFPM2
  hgvsc: ENST00000407775.2:c.1635C>T
  hgvsp: ENST00000407775.2:c.1635C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000430757
  ensembl transcript: ENST00000520492
  gene symbol: ZFPM2
  hgvsc: ENST00000520492.1:c.1239C>T
  hgvsp: ENST00000520492.1:c.1239C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169946
  ensembl transcript: ENST00000522296
  gene symbol: ZFPM2
  hgvsc: ENST00000522296.1:n.1429C>T
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520078
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520078.1:n.149-3275G>A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000367733
  ensembl transcript: ENST00000378472
  gene symbol: ZFPM2
  hgvsc: ENST00000378472.4:c.828C>T
  hgvsp: ENST00000378472.4:c.828C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520594
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520594.1:n.155-3275G>A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000428720
  ensembl transcript: ENST00000517361
  gene symbol: ZFPM2
  hgvsc: ENST00000517361.1:c.1239C>T
  hgvsp: ENST00000517361.1:c.1239C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000509144
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000509144.2:n.140-3275G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000521622
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000521622.1:n.279-3275G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000518932
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000518932.1:n.66-3275G>A
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 684
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16650
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8173
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2176
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 802
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26604
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 555
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 869
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1281
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro545Pro
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD

8-106813948-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 106813948
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 106813948
    reference: chr 8
allele count: 1
allele frequency: 8.332083520805212e-6
allele num: 120018
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520433
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520433.1:n.212-3278C>T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000384179
  ensembl transcript: ENST00000407775
  gene symbol: ZFPM2
  hgvsc: ENST00000407775.2:c.1638G>A
  hgvsp: ENST00000407775.2:c.1638G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000521622
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000521622.1:n.279-3278C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000518932
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000518932.1:n.66-3278C>T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000428720
  ensembl transcript: ENST00000517361
  gene symbol: ZFPM2
  hgvsc: ENST00000517361.1:c.1242G>A
  hgvsp: ENST00000517361.1:c.1242G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169946
  ensembl transcript: ENST00000522296
  gene symbol: ZFPM2
  hgvsc: ENST00000522296.1:n.1432G>A
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000367733
  ensembl transcript: ENST00000378472
  gene symbol: ZFPM2
  hgvsc: ENST00000378472.4:c.831G>A
  hgvsp: ENST00000378472.4:c.831G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000430757
  ensembl transcript: ENST00000520492
  gene symbol: ZFPM2
  hgvsc: ENST00000520492.1:c.1242G>A
  hgvsp: ENST00000520492.1:c.1242G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520594
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520594.1:n.155-3278C>T
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000524045
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000524045.2:n.154-3278C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520078
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520078.1:n.149-3278C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000509144
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000509144.2:n.140-3278C>T
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8177
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26615
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1283
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 684
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16677
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 618
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2173
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 800
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 870
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys546Lys
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: MQ

8-106813952-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 106813952
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 106813952
    reference: chr 8
allele count: 1
allele frequency: 8.328613785521537e-6
allele num: 120068
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000384179
  ensembl transcript: ENST00000407775
  gene symbol: ZFPM2
  hgvsc: ENST00000407775.2:c.1642G>A
  hgvsp: ENSP00000384179.2:p.Ala548Thr
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000524045
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000524045.2:n.154-3282C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000521622
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000521622.1:n.279-3282C>T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000430757
  ensembl transcript: ENST00000520492
  gene symbol: ZFPM2
  hgvsc: ENST00000520492.1:c.1246G>A
  hgvsp: ENSP00000430757.1:p.Ala416Thr
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000428720
  ensembl transcript: ENST00000517361
  gene symbol: ZFPM2
  hgvsc: ENST00000517361.1:c.1246G>A
  hgvsp: ENSP00000428720.1:p.Ala416Thr
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000518932
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000518932.1:n.66-3282C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520433
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520433.1:n.212-3282C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000509144
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000509144.2:n.140-3282C>T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000367733
  ensembl transcript: ENST00000378472
  gene symbol: ZFPM2
  hgvsc: ENST00000378472.4:c.835G>A
  hgvsp: ENSP00000367733.4:p.Ala279Thr
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169946
  ensembl transcript: ENST00000522296
  gene symbol: ZFPM2
  hgvsc: ENST00000522296.1:n.1436G>A
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520594
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520594.1:n.155-3282C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520078
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520078.1:n.149-3282C>T
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8185
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16705
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 683
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26675
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 869
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 800
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1283
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2172
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala548Thr
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: African
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum

8-106813973-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 106813973
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 106813973
    reference: chr 8
allele count: 1
allele frequency: 8.31849867735871e-6
allele num: 120214
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000384179
  ensembl transcript: ENST00000407775
  gene symbol: ZFPM2
  hgvsc: ENST00000407775.2:c.1663A>G
  hgvsp: ENSP00000384179.2:p.Ile555Val
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000521622
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000521622.1:n.279-3303T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520433
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520433.1:n.212-3303T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000518932
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000518932.1:n.66-3303T>C
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000524045
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000524045.2:n.154-3303T>C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000428720
  ensembl transcript: ENST00000517361
  gene symbol: ZFPM2
  hgvsc: ENST00000517361.1:c.1267A>G
  hgvsp: ENSP00000428720.1:p.Ile423Val
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520594
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520594.1:n.155-3303T>C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000367733
  ensembl transcript: ENST00000378472
  gene symbol: ZFPM2
  hgvsc: ENST00000378472.4:c.856A>G
  hgvsp: ENSP00000367733.4:p.Ile286Val
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000430757
  ensembl transcript: ENST00000520492
  gene symbol: ZFPM2
  hgvsc: ENST00000520492.1:c.1267A>G
  hgvsp: ENSP00000430757.1:p.Ile423Val
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000509144
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000509144.2:n.140-3303T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169946
  ensembl transcript: ENST00000522296
  gene symbol: ZFPM2
  hgvsc: ENST00000522296.1:n.1457A>G
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520078
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520078.1:n.149-3303T>C
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26814
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 870
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 683
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16956
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8198
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1280
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2175
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 801
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile555Val
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: A
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD

8-106813976-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 106813976
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 106813976
    reference: chr 8
allele count: 3
allele frequency: 2.494761001896018e-5
allele num: 120252
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000384179
  ensembl transcript: ENST00000407775
  gene symbol: ZFPM2
  hgvsc: ENST00000407775.2:c.1666A>G
  hgvsp: ENSP00000384179.2:p.Thr556Ala
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000509144
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000509144.2:n.140-3306T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520078
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520078.1:n.149-3306T>C
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000524045
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000524045.2:n.154-3306T>C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000430757
  ensembl transcript: ENST00000520492
  gene symbol: ZFPM2
  hgvsc: ENST00000520492.1:c.1270A>G
  hgvsp: ENSP00000430757.1:p.Thr424Ala
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169946
  ensembl transcript: ENST00000522296
  gene symbol: ZFPM2
  hgvsc: ENST00000522296.1:n.1460A>G
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000428720
  ensembl transcript: ENST00000517361
  gene symbol: ZFPM2
  hgvsc: ENST00000517361.1:c.1270A>G
  hgvsp: ENSP00000428720.1:p.Thr424Ala
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520594
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520594.1:n.155-3306T>C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000367733
  ensembl transcript: ENST00000378472
  gene symbol: ZFPM2
  hgvsc: ENST00000378472.4:c.859A>G
  hgvsp: ENSP00000367733.4:p.Thr287Ala
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000521622
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000521622.1:n.279-3306T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000518932
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000518932.1:n.66-3306T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520433
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520433.1:n.212-3306T>C
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 682
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 869
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 803
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 26835
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8198
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16994
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1283
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2175
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr556Ala
num of homozygotes: 0
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: South Asian
reference allele: A
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ

8-106813977-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 106813977
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 106813977
    reference: chr 8
allele count: 3
allele frequency: 2.494595044071179e-5
allele num: 120260
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000518932
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000518932.1:n.66-3307G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169946
  ensembl transcript: ENST00000522296
  gene symbol: ZFPM2
  hgvsc: ENST00000522296.1:n.1461C>T
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520594
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520594.1:n.155-3307G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520078
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520078.1:n.149-3307G>A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000367733
  ensembl transcript: ENST00000378472
  gene symbol: ZFPM2
  hgvsc: ENST00000378472.4:c.860C>T
  hgvsp: ENSP00000367733.4:p.Thr287Ile
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000430757
  ensembl transcript: ENST00000520492
  gene symbol: ZFPM2
  hgvsc: ENST00000520492.1:c.1271C>T
  hgvsp: ENSP00000430757.1:p.Thr424Ile
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000509144
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000509144.2:n.140-3307G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520433
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520433.1:n.212-3307G>A
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000524045
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000524045.2:n.154-3307G>A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000428720
  ensembl transcript: ENST00000517361
  gene symbol: ZFPM2
  hgvsc: ENST00000517361.1:c.1271C>T
  hgvsp: ENSP00000428720.1:p.Thr424Ile
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000384179
  ensembl transcript: ENST00000407775
  gene symbol: ZFPM2
  hgvsc: ENST00000407775.2:c.1667C>T
  hgvsp: ENSP00000384179.2:p.Thr556Ile
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000521622
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000521622.1:n.279-3307G>A
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26846
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8201
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 803
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17027
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 682
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2176
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1282
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 869
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr556Ile
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: South Asian
population: African
population: Latino
population: European (Finnish)
population: East Asian
reference allele: C
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: VQSLOD

http://identifiers.org/exac.variant/8-106813985-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 106813985
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 106813985
    reference: chr 8
allele count: 1
allele frequency: 8.310479514667997e-6
allele num: 120330
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520078
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520078.1:n.149-3315T>G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000384179
  ensembl transcript: ENST00000407775
  gene symbol: ZFPM2
  hgvsc: ENST00000407775.2:c.1675A>C
  hgvsp: ENSP00000384179.2:p.Asn559His
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520594
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520594.1:n.155-3315T>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000518932
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000518932.1:n.66-3315T>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000521622
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000521622.1:n.279-3315T>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169946
  ensembl transcript: ENST00000522296
  gene symbol: ZFPM2
  hgvsc: ENST00000522296.1:n.1469A>C
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000367733
  ensembl transcript: ENST00000378472
  gene symbol: ZFPM2
  hgvsc: ENST00000378472.4:c.868A>C
  hgvsp: ENSP00000367733.4:p.Asn290His
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000509144
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000509144.2:n.140-3315T>G
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000524045
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000524045.2:n.154-3315T>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520433
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520433.1:n.212-3315T>G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000428720
  ensembl transcript: ENST00000517361
  gene symbol: ZFPM2
  hgvsc: ENST00000517361.1:c.1279A>C
  hgvsp: ENSP00000428720.1:p.Asn427His
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000430757
  ensembl transcript: ENST00000520492
  gene symbol: ZFPM2
  hgvsc: ENST00000520492.1:c.1279A>C
  hgvsp: ENSP00000430757.1:p.Asn427His
  variant of: http://identifiers.org/hgnc/16700
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1282
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 869
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 681
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2180
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8198
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17089
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26862
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 801
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Asn559His
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: A
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ

8-106813987-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 106813987
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 106813987
    reference: chr 8
allele count: 1
allele frequency: 8.30937463646486e-6
allele num: 120346
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000524045
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000524045.2:n.154-3317A>C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000384179
  ensembl transcript: ENST00000407775
  gene symbol: ZFPM2
  hgvsc: ENST00000407775.2:c.1677T>G
  hgvsp: ENSP00000384179.2:p.Asn559Lys
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520594
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520594.1:n.155-3317A>C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000428720
  ensembl transcript: ENST00000517361
  gene symbol: ZFPM2
  hgvsc: ENST00000517361.1:c.1281T>G
  hgvsp: ENSP00000428720.1:p.Asn427Lys
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000367733
  ensembl transcript: ENST00000378472
  gene symbol: ZFPM2
  hgvsc: ENST00000378472.4:c.870T>G
  hgvsp: ENSP00000367733.4:p.Asn290Lys
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520433
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520433.1:n.212-3317A>C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000430757
  ensembl transcript: ENST00000520492
  gene symbol: ZFPM2
  hgvsc: ENST00000520492.1:c.1281T>G
  hgvsp: ENSP00000430757.1:p.Asn427Lys
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169946
  ensembl transcript: ENST00000522296
  gene symbol: ZFPM2
  hgvsc: ENST00000522296.1:n.1471T>G
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520078
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520078.1:n.149-3317A>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000509144
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000509144.2:n.140-3317A>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000518932
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000518932.1:n.66-3317A>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000521622
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000521622.1:n.279-3317A>C
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 869
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1281
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 681
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26867
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8201
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2180
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 801
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17108
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn559Lys
num of homozygotes: 0
population: Latino
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: T
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: QD

8-106814003-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 106814003
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 106814003
    reference: chr 8
allele count: 1
allele frequency: 8.304958059961797e-6
allele num: 120410
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000518932
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000518932.1:n.66-3333C>A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000367733
  ensembl transcript: ENST00000378472
  gene symbol: ZFPM2
  hgvsc: ENST00000378472.4:c.886G>T
  hgvsp: ENSP00000367733.4:p.Val296Leu
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520078
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520078.1:n.149-3333C>A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000430757
  ensembl transcript: ENST00000520492
  gene symbol: ZFPM2
  hgvsc: ENST00000520492.1:c.1297G>T
  hgvsp: ENSP00000430757.1:p.Val433Leu
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169946
  ensembl transcript: ENST00000522296
  gene symbol: ZFPM2
  hgvsc: ENST00000522296.1:n.1487G>T
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000521622
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000521622.1:n.279-3333C>A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000428720
  ensembl transcript: ENST00000517361
  gene symbol: ZFPM2
  hgvsc: ENST00000517361.1:c.1297G>T
  hgvsp: ENSP00000428720.1:p.Val433Leu
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520594
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520594.1:n.155-3333C>A
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000524045
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000524045.2:n.154-3333C>A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000384179
  ensembl transcript: ENST00000407775
  gene symbol: ZFPM2
  hgvsc: ENST00000407775.2:c.1693G>T
  hgvsp: ENSP00000384179.2:p.Val565Leu
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000509144
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000509144.2:n.140-3333C>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520433
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520433.1:n.212-3333C>A
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 681
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26928
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1281
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 869
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8209
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2182
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 801
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17136
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val565Leu
num of homozygotes: 0
population: European (Finnish)
population: Other
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
reference allele: G
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum

8-106814014-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 106814014
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 106814014
    reference: chr 8
allele count: 1
allele frequency: 8.303440945927993e-6
allele num: 120432
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520433
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520433.1:n.212-3344C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000518932
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000518932.1:n.66-3344C>T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000430757
  ensembl transcript: ENST00000520492
  gene symbol: ZFPM2
  hgvsc: ENST00000520492.1:c.1308G>A
  hgvsp: ENST00000520492.1:c.1308G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000509144
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000509144.2:n.140-3344C>T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000384179
  ensembl transcript: ENST00000407775
  gene symbol: ZFPM2
  hgvsc: ENST00000407775.2:c.1704G>A
  hgvsp: ENST00000407775.2:c.1704G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520594
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520594.1:n.155-3344C>T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000428720
  ensembl transcript: ENST00000517361
  gene symbol: ZFPM2
  hgvsc: ENST00000517361.1:c.1308G>A
  hgvsp: ENST00000517361.1:c.1308G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000367733
  ensembl transcript: ENST00000378472
  gene symbol: ZFPM2
  hgvsc: ENST00000378472.4:c.897G>A
  hgvsp: ENST00000378472.4:c.897G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000524045
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000524045.2:n.154-3344C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520078
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520078.1:n.149-3344C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169946
  ensembl transcript: ENST00000522296
  gene symbol: ZFPM2
  hgvsc: ENST00000522296.1:n.1498G>A
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000521622
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000521622.1:n.279-3344C>T
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2188
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26937
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17112
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1285
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 681
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 870
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 555
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8231
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 802
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Lys568Lys
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
population: African
population: Latino
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: MQ

8-106814017-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 106814017
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 106814017
    reference: chr 8
allele count: 1
allele frequency: 8.302475798283047e-6
allele num: 120446
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000524045
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000524045.2:n.154-3347A>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520433
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520433.1:n.212-3347A>C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000430757
  ensembl transcript: ENST00000520492
  gene symbol: ZFPM2
  hgvsc: ENST00000520492.1:c.1311T>G
  hgvsp: ENSP00000430757.1:p.His437Gln
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169946
  ensembl transcript: ENST00000522296
  gene symbol: ZFPM2
  hgvsc: ENST00000522296.1:n.1501T>G
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520594
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520594.1:n.155-3347A>C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000384179
  ensembl transcript: ENST00000407775
  gene symbol: ZFPM2
  hgvsc: ENST00000407775.2:c.1707T>G
  hgvsp: ENSP00000384179.2:p.His569Gln
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520078
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520078.1:n.149-3347A>C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000367733
  ensembl transcript: ENST00000378472
  gene symbol: ZFPM2
  hgvsc: ENST00000378472.4:c.900T>G
  hgvsp: ENSP00000367733.4:p.His300Gln
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000521622
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000521622.1:n.279-3347A>C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000428720
  ensembl transcript: ENST00000517361
  gene symbol: ZFPM2
  hgvsc: ENST00000517361.1:c.1311T>G
  hgvsp: ENSP00000428720.1:p.His437Gln
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000509144
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000509144.2:n.140-3347A>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000518932
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000518932.1:n.66-3347A>C
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8229
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17142
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1285
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2189
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 681
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26924
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 869
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 801
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His569Gln
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: Other
population: East Asian
population: European (Finnish)
population: African
population: South Asian
reference allele: T
site quality: FS
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum

8-106814025-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 106814025
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 106814025
    reference: chr 8
allele count: 13
allele frequency: 1.094534065267908e-4
allele num: 118772
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520433
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520433.1:n.212-3355C>G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000430757
  ensembl transcript: ENST00000520492
  gene symbol: ZFPM2
  hgvsc: ENST00000520492.1:c.1319G>C
  hgvsp: ENSP00000430757.1:p.Ser440Thr
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169946
  ensembl transcript: ENST00000522296
  gene symbol: ZFPM2
  hgvsc: ENST00000522296.1:n.1509G>C
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000384179
  ensembl transcript: ENST00000407775
  gene symbol: ZFPM2
  hgvsc: ENST00000407775.2:c.1715G>C
  hgvsp: ENSP00000384179.2:p.Ser572Thr
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000521622
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000521622.1:n.279-3355C>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520078
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520078.1:n.149-3355C>G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000428720
  ensembl transcript: ENST00000517361
  gene symbol: ZFPM2
  hgvsc: ENST00000517361.1:c.1319G>C
  hgvsp: ENSP00000428720.1:p.Ser440Thr
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000367733
  ensembl transcript: ENST00000378472
  gene symbol: ZFPM2
  hgvsc: ENST00000378472.4:c.908G>C
  hgvsp: ENSP00000367733.4:p.Ser303Thr
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520594
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520594.1:n.155-3355C>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000518932
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000518932.1:n.66-3355C>G
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000524045
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000524045.2:n.154-3355C>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000509144
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000509144.2:n.140-3355C>G
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.95to100.00
genotype depth: GenotypeDepth
  all individuals: 1298
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 652
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2215
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26778
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 839
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16900
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1254
  bin: 9.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8242
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser572Thr
num of homozygotes: 0
population: East Asian
population: Other
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: DP

8-106814031-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 106814031
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 106814031
    reference: chr 8
allele count: 6
allele frequency: 4.975701988622228e-5
allele num: 120586
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520594
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520594.1:n.155-3361C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520433
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520433.1:n.212-3361C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520078
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520078.1:n.149-3361C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000509144
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000509144.2:n.140-3361C>T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000384179
  ensembl transcript: ENST00000407775
  gene symbol: ZFPM2
  hgvsc: ENST00000407775.2:c.1721G>A
  hgvsp: ENSP00000384179.2:p.Arg574Gln
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169946
  ensembl transcript: ENST00000522296
  gene symbol: ZFPM2
  hgvsc: ENST00000522296.1:n.1515G>A
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000428720
  ensembl transcript: ENST00000517361
  gene symbol: ZFPM2
  hgvsc: ENST00000517361.1:c.1325G>A
  hgvsp: ENSP00000428720.1:p.Arg442Gln
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000518932
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000518932.1:n.66-3361C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000521622
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000521622.1:n.279-3361C>T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000367733
  ensembl transcript: ENST00000378472
  gene symbol: ZFPM2
  hgvsc: ENST00000378472.4:c.914G>A
  hgvsp: ENSP00000367733.4:p.Arg305Gln
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000430757
  ensembl transcript: ENST00000520492
  gene symbol: ZFPM2
  hgvsc: ENST00000520492.1:c.1325G>A
  hgvsp: ENSP00000430757.1:p.Arg442Gln
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000524045
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000524045.2:n.154-3361C>T
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2207
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16985
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8405
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 834
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 775
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 27169
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1272
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg574Gln
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum

8-106814037-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 106814037
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 106814037
    reference: chr 8
allele count: 1
allele frequency: 8.291186468783682e-6
allele num: 120610
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000518932
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000518932.1:n.66-3367T>C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000384179
  ensembl transcript: ENST00000407775
  gene symbol: ZFPM2
  hgvsc: ENST00000407775.2:c.1727A>G
  hgvsp: ENSP00000384179.2:p.Gln576Arg
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000428720
  ensembl transcript: ENST00000517361
  gene symbol: ZFPM2
  hgvsc: ENST00000517361.1:c.1331A>G
  hgvsp: ENSP00000428720.1:p.Gln444Arg
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520078
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520078.1:n.149-3367T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520433
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520433.1:n.212-3367T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169946
  ensembl transcript: ENST00000522296
  gene symbol: ZFPM2
  hgvsc: ENST00000522296.1:n.1521A>G
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000524045
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000524045.2:n.154-3367T>C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000430757
  ensembl transcript: ENST00000520492
  gene symbol: ZFPM2
  hgvsc: ENST00000520492.1:c.1331A>G
  hgvsp: ENSP00000430757.1:p.Gln444Arg
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000509144
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000509144.2:n.140-3367T>C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000367733
  ensembl transcript: ENST00000378472
  gene symbol: ZFPM2
  hgvsc: ENST00000378472.4:c.920A>G
  hgvsp: ENSP00000367733.4:p.Gln307Arg
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000521622
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000521622.1:n.279-3367T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520594
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520594.1:n.155-3367T>C
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2210
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 834
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17005
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1271
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27200
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 770
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8400
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln576Arg
num of homozygotes: 0
population: African
population: Other
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
reference allele: A
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: DP

8-106814041-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 106814041
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 106814041
    reference: chr 8
allele count: 1
allele frequency: 8.290499088045101e-6
allele num: 120620
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000509144
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000509144.2:n.140-3371C>T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000430757
  ensembl transcript: ENST00000520492
  gene symbol: ZFPM2
  hgvsc: ENST00000520492.1:c.1335G>A
  hgvsp: ENST00000520492.1:c.1335G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000518932
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000518932.1:n.66-3371C>T
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000524045
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000524045.2:n.154-3371C>T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000367733
  ensembl transcript: ENST00000378472
  gene symbol: ZFPM2
  hgvsc: ENST00000378472.4:c.924G>A
  hgvsp: ENST00000378472.4:c.924G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000428720
  ensembl transcript: ENST00000517361
  gene symbol: ZFPM2
  hgvsc: ENST00000517361.1:c.1335G>A
  hgvsp: ENST00000517361.1:c.1335G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520594
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520594.1:n.155-3371C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520078
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520078.1:n.149-3371C>T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000384179
  ensembl transcript: ENST00000407775
  gene symbol: ZFPM2
  hgvsc: ENST00000407775.2:c.1731G>A
  hgvsp: ENST00000407775.2:c.1731G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169946
  ensembl transcript: ENST00000522296
  gene symbol: ZFPM2
  hgvsc: ENST00000522296.1:n.1525G>A
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520433
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520433.1:n.212-3371C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000521622
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000521622.1:n.279-3371C>T
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8401
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2209
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1273
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 834
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 770
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27207
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17020
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln577Gln
num of homozygotes: 0
population: Latino
population: South Asian
population: Other
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum

8-106814044-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 106814044
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 106814044
    reference: chr 8
allele count: 1
allele frequency: 8.290911502810618e-6
allele num: 120614
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000384179
  ensembl transcript: ENST00000407775
  gene symbol: ZFPM2
  hgvsc: ENST00000407775.2:c.1734G>T
  hgvsp: ENSP00000384179.2:p.Met578Ile
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000509144
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000509144.2:n.140-3374C>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520594
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520594.1:n.155-3374C>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000521622
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000521622.1:n.279-3374C>A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000428720
  ensembl transcript: ENST00000517361
  gene symbol: ZFPM2
  hgvsc: ENST00000517361.1:c.1338G>T
  hgvsp: ENSP00000428720.1:p.Met446Ile
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000524045
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000524045.2:n.154-3374C>A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000367733
  ensembl transcript: ENST00000378472
  gene symbol: ZFPM2
  hgvsc: ENST00000378472.4:c.927G>T
  hgvsp: ENSP00000367733.4:p.Met309Ile
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520433
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520433.1:n.212-3374C>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169946
  ensembl transcript: ENST00000522296
  gene symbol: ZFPM2
  hgvsc: ENST00000522296.1:n.1528G>T
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520078
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520078.1:n.149-3374C>A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000430757
  ensembl transcript: ENST00000520492
  gene symbol: ZFPM2
  hgvsc: ENST00000520492.1:c.1338G>T
  hgvsp: ENSP00000430757.1:p.Met446Ile
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000518932
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000518932.1:n.66-3374C>A
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 835
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2211
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1273
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8403
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17019
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 770
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27202
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Met578Ile
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: East Asian
reference allele: G
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum

8-106814054-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 106814054
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 106814054
    reference: chr 8
allele count: 2
allele frequency: 1.658044833532299e-5
allele num: 120624
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520433
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520433.1:n.212-3384G>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000509144
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000509144.2:n.140-3384G>C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000428720
  ensembl transcript: ENST00000517361
  gene symbol: ZFPM2
  hgvsc: ENST00000517361.1:c.1348C>G
  hgvsp: ENSP00000428720.1:p.Pro450Ala
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000521622
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000521622.1:n.279-3384G>C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000384179
  ensembl transcript: ENST00000407775
  gene symbol: ZFPM2
  hgvsc: ENST00000407775.2:c.1744C>G
  hgvsp: ENSP00000384179.2:p.Pro582Ala
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000430757
  ensembl transcript: ENST00000520492
  gene symbol: ZFPM2
  hgvsc: ENST00000520492.1:c.1348C>G
  hgvsp: ENSP00000430757.1:p.Pro450Ala
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169946
  ensembl transcript: ENST00000522296
  gene symbol: ZFPM2
  hgvsc: ENST00000522296.1:n.1538C>G
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000518932
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000518932.1:n.66-3384G>C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000367733
  ensembl transcript: ENST00000378472
  gene symbol: ZFPM2
  hgvsc: ENST00000378472.4:c.937C>G
  hgvsp: ENSP00000367733.4:p.Pro313Ala
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520078
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520078.1:n.149-3384G>C
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000524045
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000524045.2:n.154-3384G>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520594
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520594.1:n.155-3384G>C
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 834
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8406
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2211
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 771
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27213
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17031
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1274
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro582Ala
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum

8-106814061-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 106814061
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 106814061
    reference: chr 8
allele count: 1
allele frequency: 8.28953694646617e-6
allele num: 120634
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000428720
  ensembl transcript: ENST00000517361
  gene symbol: ZFPM2
  hgvsc: ENST00000517361.1:c.1355T>G
  hgvsp: ENSP00000428720.1:p.Phe452Cys
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520594
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520594.1:n.155-3391A>C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000430757
  ensembl transcript: ENST00000520492
  gene symbol: ZFPM2
  hgvsc: ENST00000520492.1:c.1355T>G
  hgvsp: ENSP00000430757.1:p.Phe452Cys
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000524045
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000524045.2:n.154-3391A>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000518932
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000518932.1:n.66-3391A>C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000384179
  ensembl transcript: ENST00000407775
  gene symbol: ZFPM2
  hgvsc: ENST00000407775.2:c.1751T>G
  hgvsp: ENSP00000384179.2:p.Phe584Cys
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000521622
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000521622.1:n.279-3391A>C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000367733
  ensembl transcript: ENST00000378472
  gene symbol: ZFPM2
  hgvsc: ENST00000378472.4:c.944T>G
  hgvsp: ENSP00000367733.4:p.Phe315Cys
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520078
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520078.1:n.149-3391A>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169946
  ensembl transcript: ENST00000522296
  gene symbol: ZFPM2
  hgvsc: ENST00000522296.1:n.1545T>G
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520433
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520433.1:n.212-3391A>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000509144
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000509144.2:n.140-3391A>C
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1274
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27224
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17044
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8408
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 833
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2210
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Phe584Cys
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: South Asian
population: East Asian
population: African
population: European (Finnish)
population: Latino
reference allele: T
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

8-106814066-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 106814066
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 106814066
    reference: chr 8
allele count: 7
allele frequency: 5.80286827489016e-5
allele num: 120630
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000518932
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000518932.1:n.66-3396T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520433
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520433.1:n.212-3396T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000521622
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000521622.1:n.279-3396T>C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000428720
  ensembl transcript: ENST00000517361
  gene symbol: ZFPM2
  hgvsc: ENST00000517361.1:c.1360A>G
  hgvsp: ENSP00000428720.1:p.Ser454Gly
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169946
  ensembl transcript: ENST00000522296
  gene symbol: ZFPM2
  hgvsc: ENST00000522296.1:n.1550A>G
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000367733
  ensembl transcript: ENST00000378472
  gene symbol: ZFPM2
  hgvsc: ENST00000378472.4:c.949A>G
  hgvsp: ENSP00000367733.4:p.Ser317Gly
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520078
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520078.1:n.149-3396T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520594
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520594.1:n.155-3396T>C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000430757
  ensembl transcript: ENST00000520492
  gene symbol: ZFPM2
  hgvsc: ENST00000520492.1:c.1360A>G
  hgvsp: ENSP00000430757.1:p.Ser454Gly
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000509144
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000509144.2:n.140-3396T>C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000384179
  ensembl transcript: ENST00000407775
  gene symbol: ZFPM2
  hgvsc: ENST00000407775.2:c.1756A>G
  hgvsp: ENSP00000384179.2:p.Ser586Gly
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000524045
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000524045.2:n.154-3396T>C
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 776
  bin: 9.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27219
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8408
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1273
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17050
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 833
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2211
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser586Gly
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
reference allele: A
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff

8-106814080-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 106814080
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 106814080
    reference: chr 8
allele count: 1
allele frequency: 8.290224167661493e-6
allele num: 120624
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000521622
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000521622.1:n.279-3410C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169946
  ensembl transcript: ENST00000522296
  gene symbol: ZFPM2
  hgvsc: ENST00000522296.1:n.1564G>A
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000384179
  ensembl transcript: ENST00000407775
  gene symbol: ZFPM2
  hgvsc: ENST00000407775.2:c.1770G>A
  hgvsp: ENST00000407775.2:c.1770G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000509144
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000509144.2:n.140-3410C>T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000430757
  ensembl transcript: ENST00000520492
  gene symbol: ZFPM2
  hgvsc: ENST00000520492.1:c.1374G>A
  hgvsp: ENST00000520492.1:c.1374G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000428720
  ensembl transcript: ENST00000517361
  gene symbol: ZFPM2
  hgvsc: ENST00000517361.1:c.1374G>A
  hgvsp: ENST00000517361.1:c.1374G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520433
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520433.1:n.212-3410C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520078
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520078.1:n.149-3410C>T
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000524045
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000524045.2:n.154-3410C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520594
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520594.1:n.155-3410C>T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000367733
  ensembl transcript: ENST00000378472
  gene symbol: ZFPM2
  hgvsc: ENST00000378472.4:c.963G>A
  hgvsp: ENST00000378472.4:c.963G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000518932
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000518932.1:n.66-3410C>T
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 772
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8409
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17032
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2207
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27243
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 833
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1276
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys590Lys
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum

8-106814080-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 106814080
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 106814080
    reference: chr 8
allele count: 1
allele frequency: 8.290224167661493e-6
allele num: 120624
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520594
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520594.1:n.155-3410C>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000509144
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000509144.2:n.140-3410C>G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000367733
  ensembl transcript: ENST00000378472
  gene symbol: ZFPM2
  hgvsc: ENST00000378472.4:c.963G>C
  hgvsp: ENSP00000367733.4:p.Lys321Asn
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169946
  ensembl transcript: ENST00000522296
  gene symbol: ZFPM2
  hgvsc: ENST00000522296.1:n.1564G>C
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000384179
  ensembl transcript: ENST00000407775
  gene symbol: ZFPM2
  hgvsc: ENST00000407775.2:c.1770G>C
  hgvsp: ENSP00000384179.2:p.Lys590Asn
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000428720
  ensembl transcript: ENST00000517361
  gene symbol: ZFPM2
  hgvsc: ENST00000517361.1:c.1374G>C
  hgvsp: ENSP00000428720.1:p.Lys458Asn
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000430757
  ensembl transcript: ENST00000520492
  gene symbol: ZFPM2
  hgvsc: ENST00000520492.1:c.1374G>C
  hgvsp: ENSP00000430757.1:p.Lys458Asn
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520078
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520078.1:n.149-3410C>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000518932
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000518932.1:n.66-3410C>G
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000524045
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000524045.2:n.154-3410C>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520433
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520433.1:n.212-3410C>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000521622
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000521622.1:n.279-3410C>G
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17032
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27243
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8409
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 833
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1276
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 772
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2207
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys590Asn
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Finnish)
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum

8-106814085-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 106814085
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 106814085
    reference: chr 8
allele count: 2
allele frequency: 1.658072325114821e-5
allele num: 120622
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000518932
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000518932.1:n.66-3415G>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520433
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520433.1:n.212-3415G>C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000428720
  ensembl transcript: ENST00000517361
  gene symbol: ZFPM2
  hgvsc: ENST00000517361.1:c.1379C>G
  hgvsp: ENSP00000428720.1:p.Pro460Arg
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520078
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520078.1:n.149-3415G>C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000430757
  ensembl transcript: ENST00000520492
  gene symbol: ZFPM2
  hgvsc: ENST00000520492.1:c.1379C>G
  hgvsp: ENSP00000430757.1:p.Pro460Arg
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000384179
  ensembl transcript: ENST00000407775
  gene symbol: ZFPM2
  hgvsc: ENST00000407775.2:c.1775C>G
  hgvsp: ENSP00000384179.2:p.Pro592Arg
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000367733
  ensembl transcript: ENST00000378472
  gene symbol: ZFPM2
  hgvsc: ENST00000378472.4:c.968C>G
  hgvsp: ENSP00000367733.4:p.Pro323Arg
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169946
  ensembl transcript: ENST00000522296
  gene symbol: ZFPM2
  hgvsc: ENST00000522296.1:n.1569C>G
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000524045
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000524045.2:n.154-3415G>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520594
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520594.1:n.155-3415G>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000521622
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000521622.1:n.279-3415G>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000509144
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000509144.2:n.140-3415G>C
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8407
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17037
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1275
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 834
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 772
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2209
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27245
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro592Arg
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: QD

8-106814086-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 106814086
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 106814086
    reference: chr 8
allele count: 3896
allele frequency: 3.229924889323672e-2
allele num: 120622
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520433
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520433.1:n.212-3416A>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520594
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520594.1:n.155-3416A>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000518932
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000518932.1:n.66-3416A>G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000367733
  ensembl transcript: ENST00000378472
  gene symbol: ZFPM2
  hgvsc: ENST00000378472.4:c.969T>C
  hgvsp: ENST00000378472.4:c.969T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000509144
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000509144.2:n.140-3416A>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520078
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520078.1:n.149-3416A>G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000428720
  ensembl transcript: ENST00000517361
  gene symbol: ZFPM2
  hgvsc: ENST00000517361.1:c.1380T>C
  hgvsp: ENST00000517361.1:c.1380T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000524045
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000524045.2:n.154-3416A>G
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000384179
  ensembl transcript: ENST00000407775
  gene symbol: ZFPM2
  hgvsc: ENST00000407775.2:c.1776T>C
  hgvsp: ENST00000407775.2:c.1776T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169946
  ensembl transcript: ENST00000522296
  gene symbol: ZFPM2
  hgvsc: ENST00000522296.1:n.1570T>C
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000430757
  ensembl transcript: ENST00000520492
  gene symbol: ZFPM2
  hgvsc: ENST00000520492.1:c.1380T>C
  hgvsp: ENST00000520492.1:c.1380T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000521622
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000521622.1:n.279-3416A>G
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 1.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.75e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 8.25e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 26977
  bin: 2.75e1
  variant carriers: 33
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 6.75e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 4.75e1
  variant carriers: 32
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 903
  bin: 4.25e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 9.25e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 8111
  bin: 3.25e1
  variant carriers: 33
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 5.25e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 8.75e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 1.75e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16800
  bin: 2.25e1
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 1843
  bin: 3.75e1
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 7.25e1
  variant carriers: 29
genotype depth: GenotypeDepth
  all individuals: 3590
  bin: 9.75e1
  variant carriers: 3348
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 6.25e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 5.75e1
  variant carriers: 29
genotype quality: GenotypeQuality
hgvs: p.Pro592Pro
num of homozygotes: 152
population: East Asian
population: European (Finnish)
population: African
population: Other
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: T
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD

8-106814087-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 106814087
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 106814087
    reference: chr 8
allele count: 2
allele frequency: 1.658319790388379e-5
allele num: 120604
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000518932
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000518932.1:n.66-3417C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520078
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520078.1:n.149-3417C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000509144
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000509144.2:n.140-3417C>T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000384179
  ensembl transcript: ENST00000407775
  gene symbol: ZFPM2
  hgvsc: ENST00000407775.2:c.1777G>A
  hgvsp: ENSP00000384179.2:p.Glu593Lys
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169946
  ensembl transcript: ENST00000522296
  gene symbol: ZFPM2
  hgvsc: ENST00000522296.1:n.1571G>A
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520594
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520594.1:n.155-3417C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520433
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520433.1:n.212-3417C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000521622
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000521622.1:n.279-3417C>T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000367733
  ensembl transcript: ENST00000378472
  gene symbol: ZFPM2
  hgvsc: ENST00000378472.4:c.970G>A
  hgvsp: ENSP00000367733.4:p.Glu324Lys
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000430757
  ensembl transcript: ENST00000520492
  gene symbol: ZFPM2
  hgvsc: ENST00000520492.1:c.1381G>A
  hgvsp: ENSP00000430757.1:p.Glu461Lys
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000428720
  ensembl transcript: ENST00000517361
  gene symbol: ZFPM2
  hgvsc: ENST00000517361.1:c.1381G>A
  hgvsp: ENSP00000428720.1:p.Glu461Lys
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000524045
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000524045.2:n.154-3417C>T
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2082
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1043
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8794
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17196
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28335
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 606
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 531
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu593Lys
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: G
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum

8-106814096-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 106814096
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 106814096
    reference: chr 8
allele count: 1
allele frequency: 8.291461452995706e-6
allele num: 120606
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520433
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520433.1:n.212-3426T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000518932
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000518932.1:n.66-3426T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169946
  ensembl transcript: ENST00000522296
  gene symbol: ZFPM2
  hgvsc: ENST00000522296.1:n.1580A>G
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000384179
  ensembl transcript: ENST00000407775
  gene symbol: ZFPM2
  hgvsc: ENST00000407775.2:c.1786A>G
  hgvsp: ENSP00000384179.2:p.Ser596Gly
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000428720
  ensembl transcript: ENST00000517361
  gene symbol: ZFPM2
  hgvsc: ENST00000517361.1:c.1390A>G
  hgvsp: ENSP00000428720.1:p.Ser464Gly
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000367733
  ensembl transcript: ENST00000378472
  gene symbol: ZFPM2
  hgvsc: ENST00000378472.4:c.979A>G
  hgvsp: ENSP00000367733.4:p.Ser327Gly
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520594
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520594.1:n.155-3426T>C
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000524045
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000524045.2:n.154-3426T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520078
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520078.1:n.149-3426T>C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000430757
  ensembl transcript: ENST00000520492
  gene symbol: ZFPM2
  hgvsc: ENST00000520492.1:c.1390A>G
  hgvsp: ENSP00000430757.1:p.Ser464Gly
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000521622
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000521622.1:n.279-3426T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000509144
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000509144.2:n.140-3426T>C
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17205
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1042
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28335
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2079
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 531
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8795
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser596Gly
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: Other
population: South Asian
population: East Asian
reference allele: A
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: ClippingRankSum

8-106814108-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 106814108
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 106814108
    reference: chr 8
allele count: 1
allele frequency: 8.293799555452344e-6
allele num: 120572
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000384179
  ensembl transcript: ENST00000407775
  gene symbol: ZFPM2
  hgvsc: ENST00000407775.2:c.1798G>A
  hgvsp: ENSP00000384179.2:p.Gly600Ser
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520594
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520594.1:n.155-3438C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520078
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520078.1:n.149-3438C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000521622
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000521622.1:n.279-3438C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000518932
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000518932.1:n.66-3438C>T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000367733
  ensembl transcript: ENST00000378472
  gene symbol: ZFPM2
  hgvsc: ENST00000378472.4:c.991G>A
  hgvsp: ENSP00000367733.4:p.Gly331Ser
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000428720
  ensembl transcript: ENST00000517361
  gene symbol: ZFPM2
  hgvsc: ENST00000517361.1:c.1402G>A
  hgvsp: ENSP00000428720.1:p.Gly468Ser
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520433
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520433.1:n.212-3438C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169946
  ensembl transcript: ENST00000522296
  gene symbol: ZFPM2
  hgvsc: ENST00000522296.1:n.1592G>A
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000509144
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000509144.2:n.140-3438C>T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000430757
  ensembl transcript: ENST00000520492
  gene symbol: ZFPM2
  hgvsc: ENST00000520492.1:c.1402G>A
  hgvsp: ENSP00000430757.1:p.Gly468Ser
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000524045
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000524045.2:n.154-3438C>T
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2076
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1041
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17164
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28314
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8801
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly600Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
population: European (Finnish)
population: Other
population: Latino
reference allele: G
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: QD

8-106814115-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 106814115
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 106814115
    reference: chr 8
allele count: 1
allele frequency: 8.296827293243064e-6
allele num: 120528
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520433
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520433.1:n.212-3445G>C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000430757
  ensembl transcript: ENST00000520492
  gene symbol: ZFPM2
  hgvsc: ENST00000520492.1:c.1409C>G
  hgvsp: ENSP00000430757.1:p.Thr470Ser
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520078
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520078.1:n.149-3445G>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000518932
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000518932.1:n.66-3445G>C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000367733
  ensembl transcript: ENST00000378472
  gene symbol: ZFPM2
  hgvsc: ENST00000378472.4:c.998C>G
  hgvsp: ENSP00000367733.4:p.Thr333Ser
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520594
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520594.1:n.155-3445G>C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000428720
  ensembl transcript: ENST00000517361
  gene symbol: ZFPM2
  hgvsc: ENST00000517361.1:c.1409C>G
  hgvsp: ENSP00000428720.1:p.Thr470Ser
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000384179
  ensembl transcript: ENST00000407775
  gene symbol: ZFPM2
  hgvsc: ENST00000407775.2:c.1805C>G
  hgvsp: ENSP00000384179.2:p.Thr602Ser
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000521622
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000521622.1:n.279-3445G>C
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000524045
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000524045.2:n.154-3445G>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169946
  ensembl transcript: ENST00000522296
  gene symbol: ZFPM2
  hgvsc: ENST00000522296.1:n.1599C>G
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000509144
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000509144.2:n.140-3445G>C
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8794
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2079
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17133
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 531
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28294
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1041
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr602Ser
num of homozygotes: 0
population: South Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
reference allele: C
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: VQSLOD

8-106814120-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 106814120
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 106814120
    reference: chr 8
allele count: 2
allele frequency: 1.659448067572725e-5
allele num: 120522
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169946
  ensembl transcript: ENST00000522296
  gene symbol: ZFPM2
  hgvsc: ENST00000522296.1:n.1604A>G
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520078
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520078.1:n.149-3450T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000509144
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000509144.2:n.140-3450T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520433
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520433.1:n.212-3450T>C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000384179
  ensembl transcript: ENST00000407775
  gene symbol: ZFPM2
  hgvsc: ENST00000407775.2:c.1810A>G
  hgvsp: ENSP00000384179.2:p.Ile604Val
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000428720
  ensembl transcript: ENST00000517361
  gene symbol: ZFPM2
  hgvsc: ENST00000517361.1:c.1414A>G
  hgvsp: ENSP00000428720.1:p.Ile472Val
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000430757
  ensembl transcript: ENST00000520492
  gene symbol: ZFPM2
  hgvsc: ENST00000520492.1:c.1414A>G
  hgvsp: ENSP00000430757.1:p.Ile472Val
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000521622
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000521622.1:n.279-3450T>C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000367733
  ensembl transcript: ENST00000378472
  gene symbol: ZFPM2
  hgvsc: ENST00000378472.4:c.1003A>G
  hgvsp: ENSP00000367733.4:p.Ile335Val
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000518932
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000518932.1:n.66-3450T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520594
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520594.1:n.155-3450T>C
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000524045
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000524045.2:n.154-3450T>C
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2076
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8788
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17133
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1043
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28303
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile604Val
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: Other
reference allele: A
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: QD

8-106814121-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 106814121
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 106814121
    reference: chr 8
allele count: 1
allele frequency: 8.298204268596276e-6
allele num: 120508
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000384179
  ensembl transcript: ENST00000407775
  gene symbol: ZFPM2
  hgvsc: ENST00000407775.2:c.1811T>C
  hgvsp: ENSP00000384179.2:p.Ile604Thr
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000521622
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000521622.1:n.279-3451A>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520078
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520078.1:n.149-3451A>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520433
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520433.1:n.212-3451A>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520594
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520594.1:n.155-3451A>G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000367733
  ensembl transcript: ENST00000378472
  gene symbol: ZFPM2
  hgvsc: ENST00000378472.4:c.1004T>C
  hgvsp: ENSP00000367733.4:p.Ile335Thr
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000430757
  ensembl transcript: ENST00000520492
  gene symbol: ZFPM2
  hgvsc: ENST00000520492.1:c.1415T>C
  hgvsp: ENSP00000430757.1:p.Ile472Thr
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000518932
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000518932.1:n.66-3451A>G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000428720
  ensembl transcript: ENST00000517361
  gene symbol: ZFPM2
  hgvsc: ENST00000517361.1:c.1415T>C
  hgvsp: ENSP00000428720.1:p.Ile472Thr
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169946
  ensembl transcript: ENST00000522296
  gene symbol: ZFPM2
  hgvsc: ENST00000522296.1:n.1605T>C
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000524045
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000524045.2:n.154-3451A>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000509144
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000509144.2:n.140-3451A>G
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8787
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28299
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17128
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2078
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1042
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Ile604Thr
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: QD

8-106814125-CCTT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 106814125
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 106814122
    reference: chr 8
allele count: 1
allele frequency: 8.298755186721992e-6
allele num: 120500
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520433
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520433.1:n.212-3458_212-3456delAAG
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520078
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520078.1:n.149-3458_149-3456delAAG
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000509144
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000509144.2:n.140-3458_140-3456delAAG
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000521622
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000521622.1:n.279-3458_279-3456delAAG
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000428720
  ensembl transcript: ENST00000517361
  gene symbol: ZFPM2
  hgvsc: ENST00000517361.1:c.1422_1424delTCT
  hgvsp: ENSP00000428720.1:p.Leu475del
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: true
  consequence: inframe_deletion
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000384179
  ensembl transcript: ENST00000407775
  gene symbol: ZFPM2
  hgvsc: ENST00000407775.2:c.1818_1820delTCT
  hgvsp: ENSP00000384179.2:p.Leu607del
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520594
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520594.1:n.155-3458_155-3456delAAG
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000524045
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000524045.2:n.154-3458_154-3456delAAG
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169946
  ensembl transcript: ENST00000522296
  gene symbol: ZFPM2
  hgvsc: ENST00000522296.1:n.1612_1614delTCT
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000430757
  ensembl transcript: ENST00000520492
  gene symbol: ZFPM2
  hgvsc: ENST00000520492.1:c.1422_1424delTCT
  hgvsp: ENSP00000430757.1:p.Leu475del
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000518932
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000518932.1:n.66-3458_66-3456delAAG
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000367733
  ensembl transcript: ENST00000378472
  gene symbol: ZFPM2
  hgvsc: ENST00000378472.4:c.1011_1013delTCT
  hgvsp: ENSP00000367733.4:p.Leu338del
  variant of: http://identifiers.org/hgnc/16700
canonical: true
consequence: inframe deletion
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2077
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1040
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28303
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8787
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17102
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Leu607del
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
population: African
reference allele: CCTT
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

8-106814141-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 106814141
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 106814141
    reference: chr 8
allele count: 1
allele frequency: 8.306475728477921e-6
allele num: 120388
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000384179
  ensembl transcript: ENST00000407775
  gene symbol: ZFPM2
  hgvsc: ENST00000407775.2:c.1831G>A
  hgvsp: ENSP00000384179.2:p.Ala611Thr
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520078
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520078.1:n.149-3471C>T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000428720
  ensembl transcript: ENST00000517361
  gene symbol: ZFPM2
  hgvsc: ENST00000517361.1:c.1435G>A
  hgvsp: ENSP00000428720.1:p.Ala479Thr
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000524045
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000524045.2:n.154-3471C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520433
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520433.1:n.212-3471C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520594
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520594.1:n.155-3471C>T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000367733
  ensembl transcript: ENST00000378472
  gene symbol: ZFPM2
  hgvsc: ENST00000378472.4:c.1024G>A
  hgvsp: ENSP00000367733.4:p.Ala342Thr
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000518932
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000518932.1:n.66-3471C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000521622
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000521622.1:n.279-3471C>T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000430757
  ensembl transcript: ENST00000520492
  gene symbol: ZFPM2
  hgvsc: ENST00000520492.1:c.1435G>A
  hgvsp: ENSP00000430757.1:p.Ala479Thr
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169946
  ensembl transcript: ENST00000522296
  gene symbol: ZFPM2
  hgvsc: ENST00000522296.1:n.1625G>A
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000509144
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000509144.2:n.140-3471C>T
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17057
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2075
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1040
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28274
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8781
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala611Thr
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: DP
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/8-106814148-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 106814148
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 106814148
    reference: chr 8
allele count: 1
allele frequency: 8.308546170591069e-6
allele num: 120358
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000367733
  ensembl transcript: ENST00000378472
  gene symbol: ZFPM2
  hgvsc: ENST00000378472.4:c.1031C>A
  hgvsp: ENSP00000367733.4:p.Ser344Tyr
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000428720
  ensembl transcript: ENST00000517361
  gene symbol: ZFPM2
  hgvsc: ENST00000517361.1:c.1442C>A
  hgvsp: ENSP00000428720.1:p.Ser481Tyr
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000524045
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000524045.2:n.154-3478G>T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000384179
  ensembl transcript: ENST00000407775
  gene symbol: ZFPM2
  hgvsc: ENST00000407775.2:c.1838C>A
  hgvsp: ENSP00000384179.2:p.Ser613Tyr
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520078
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520078.1:n.149-3478G>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520594
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520594.1:n.155-3478G>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000518932
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000518932.1:n.66-3478G>T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000430757
  ensembl transcript: ENST00000520492
  gene symbol: ZFPM2
  hgvsc: ENST00000520492.1:c.1442C>A
  hgvsp: ENSP00000430757.1:p.Ser481Tyr
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169946
  ensembl transcript: ENST00000522296
  gene symbol: ZFPM2
  hgvsc: ENST00000522296.1:n.1632C>A
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000521622
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000521622.1:n.279-3478G>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520433
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520433.1:n.212-3478G>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000509144
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000509144.2:n.140-3478G>T
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1033
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2073
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8782
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28261
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17008
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser613Tyr
num of homozygotes: 0
population: Other
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
reference allele: C
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ

8-106814161-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 106814161
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 106814161
    reference: chr 8
allele count: 1
allele frequency: 8.314072398942449e-6
allele num: 120278
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000430757
  ensembl transcript: ENST00000520492
  gene symbol: ZFPM2
  hgvsc: ENST00000520492.1:c.1455G>A
  hgvsp: ENST00000520492.1:c.1455G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000521622
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000521622.1:n.279-3491C>T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000384179
  ensembl transcript: ENST00000407775
  gene symbol: ZFPM2
  hgvsc: ENST00000407775.2:c.1851G>A
  hgvsp: ENST00000407775.2:c.1851G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000518932
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000518932.1:n.66-3491C>T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000367733
  ensembl transcript: ENST00000378472
  gene symbol: ZFPM2
  hgvsc: ENST00000378472.4:c.1044G>A
  hgvsp: ENST00000378472.4:c.1044G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000509144
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000509144.2:n.140-3491C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520594
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520594.1:n.155-3491C>T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000428720
  ensembl transcript: ENST00000517361
  gene symbol: ZFPM2
  hgvsc: ENST00000517361.1:c.1455G>A
  hgvsp: ENST00000517361.1:c.1455G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169946
  ensembl transcript: ENST00000522296
  gene symbol: ZFPM2
  hgvsc: ENST00000522296.1:n.1645G>A
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000524045
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000524045.2:n.154-3491C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520078
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520078.1:n.149-3491C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520433
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520433.1:n.212-3491C>T
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28219
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8773
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16955
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1033
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2075
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Glu617Glu
num of homozygotes: 0
population: East Asian
population: Other
population: South Asian
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum

http://identifiers.org/exac.variant/8-106814163-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 106814163
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 106814163
    reference: chr 8
allele count: 1
allele frequency: 8.314348903337379e-6
allele num: 120274
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000518932
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000518932.1:n.66-3493T>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000509144
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000509144.2:n.140-3493T>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520078
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520078.1:n.149-3493T>G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000428720
  ensembl transcript: ENST00000517361
  gene symbol: ZFPM2
  hgvsc: ENST00000517361.1:c.1457A>C
  hgvsp: ENSP00000428720.1:p.Asn486Thr
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520433
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520433.1:n.212-3493T>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169946
  ensembl transcript: ENST00000522296
  gene symbol: ZFPM2
  hgvsc: ENST00000522296.1:n.1647A>C
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000367733
  ensembl transcript: ENST00000378472
  gene symbol: ZFPM2
  hgvsc: ENST00000378472.4:c.1046A>C
  hgvsp: ENSP00000367733.4:p.Asn349Thr
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000384179
  ensembl transcript: ENST00000407775
  gene symbol: ZFPM2
  hgvsc: ENST00000407775.2:c.1853A>C
  hgvsp: ENSP00000384179.2:p.Asn618Thr
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000524045
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000524045.2:n.154-3493T>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520594
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520594.1:n.155-3493T>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000521622
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000521622.1:n.279-3493T>G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000430757
  ensembl transcript: ENST00000520492
  gene symbol: ZFPM2
  hgvsc: ENST00000520492.1:c.1457A>C
  hgvsp: ENSP00000430757.1:p.Asn486Thr
  variant of: http://identifiers.org/hgnc/16700
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8774
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16949
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28212
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 531
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2074
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1032
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn618Thr
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
population: Latino
reference allele: A
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ

8-106814164-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 106814164
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 106814164
    reference: chr 8
allele count: 2
allele frequency: 1.663229326059477e-5
allele num: 120248
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000524045
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000524045.2:n.154-3494A>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520594
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520594.1:n.155-3494A>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520078
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520078.1:n.149-3494A>G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000367733
  ensembl transcript: ENST00000378472
  gene symbol: ZFPM2
  hgvsc: ENST00000378472.4:c.1047T>C
  hgvsp: ENST00000378472.4:c.1047T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000509144
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000509144.2:n.140-3494A>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520433
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520433.1:n.212-3494A>G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000430757
  ensembl transcript: ENST00000520492
  gene symbol: ZFPM2
  hgvsc: ENST00000520492.1:c.1458T>C
  hgvsp: ENST00000520492.1:c.1458T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000384179
  ensembl transcript: ENST00000407775
  gene symbol: ZFPM2
  hgvsc: ENST00000407775.2:c.1854T>C
  hgvsp: ENST00000407775.2:c.1854T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000428720
  ensembl transcript: ENST00000517361
  gene symbol: ZFPM2
  hgvsc: ENST00000517361.1:c.1458T>C
  hgvsp: ENST00000517361.1:c.1458T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169946
  ensembl transcript: ENST00000522296
  gene symbol: ZFPM2
  hgvsc: ENST00000522296.1:n.1648T>C
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000518932
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000518932.1:n.66-3494A>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000521622
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000521622.1:n.279-3494A>G
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16928
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8774
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1031
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28210
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2074
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn618Asn
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum

8-106814165-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 106814165
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 106814165
    reference: chr 8
allele count: 1
allele frequency: 8.315455104857889e-6
allele num: 120258
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000367733
  ensembl transcript: ENST00000378472
  gene symbol: ZFPM2
  hgvsc: ENST00000378472.4:c.1048C>T
  hgvsp: ENSP00000367733.4:p.Pro350Ser
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520594
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520594.1:n.155-3495G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169946
  ensembl transcript: ENST00000522296
  gene symbol: ZFPM2
  hgvsc: ENST00000522296.1:n.1649C>T
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000384179
  ensembl transcript: ENST00000407775
  gene symbol: ZFPM2
  hgvsc: ENST00000407775.2:c.1855C>T
  hgvsp: ENSP00000384179.2:p.Pro619Ser
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520078
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520078.1:n.149-3495G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520433
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520433.1:n.212-3495G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000521622
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000521622.1:n.279-3495G>A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000430757
  ensembl transcript: ENST00000520492
  gene symbol: ZFPM2
  hgvsc: ENST00000520492.1:c.1459C>T
  hgvsp: ENSP00000430757.1:p.Pro487Ser
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000428720
  ensembl transcript: ENST00000517361
  gene symbol: ZFPM2
  hgvsc: ENST00000517361.1:c.1459C>T
  hgvsp: ENSP00000428720.1:p.Pro487Ser
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000518932
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000518932.1:n.66-3495G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000509144
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000509144.2:n.140-3495G>A
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000524045
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000524045.2:n.154-3495G>A
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1032
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28210
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2075
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16926
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8775
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro619Ser
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD

8-106814169-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 106814169
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 106814169
    reference: chr 8
allele count: 1
allele frequency: 8.31766839119658e-6
allele num: 120226
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000509144
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000509144.2:n.140-3499A>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520078
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520078.1:n.149-3499A>C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000430757
  ensembl transcript: ENST00000520492
  gene symbol: ZFPM2
  hgvsc: ENST00000520492.1:c.1463T>G
  hgvsp: ENSP00000430757.1:p.Leu488Arg
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000428720
  ensembl transcript: ENST00000517361
  gene symbol: ZFPM2
  hgvsc: ENST00000517361.1:c.1463T>G
  hgvsp: ENSP00000428720.1:p.Leu488Arg
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520594
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520594.1:n.155-3499A>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169946
  ensembl transcript: ENST00000522296
  gene symbol: ZFPM2
  hgvsc: ENST00000522296.1:n.1653T>G
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520433
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520433.1:n.212-3499A>C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000384179
  ensembl transcript: ENST00000407775
  gene symbol: ZFPM2
  hgvsc: ENST00000407775.2:c.1859T>G
  hgvsp: ENSP00000384179.2:p.Leu620Arg
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000524045
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000524045.2:n.154-3499A>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000521622
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000521622.1:n.279-3499A>C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000367733
  ensembl transcript: ENST00000378472
  gene symbol: ZFPM2
  hgvsc: ENST00000378472.4:c.1052T>G
  hgvsp: ENSP00000367733.4:p.Leu351Arg
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000518932
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000518932.1:n.66-3499A>C
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16908
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1031
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28207
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2075
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8776
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu620Arg
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: T
site quality: MQ
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum

8-106814176-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 106814176
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 106814176
    reference: chr 8
allele count: 3
allele frequency: 2.496214075319099e-5
allele num: 120182
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000518932
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000518932.1:n.66-3506T>C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000367733
  ensembl transcript: ENST00000378472
  gene symbol: ZFPM2
  hgvsc: ENST00000378472.4:c.1059A>G
  hgvsp: ENST00000378472.4:c.1059A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520078
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520078.1:n.149-3506T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000509144
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000509144.2:n.140-3506T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169946
  ensembl transcript: ENST00000522296
  gene symbol: ZFPM2
  hgvsc: ENST00000522296.1:n.1660A>G
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000428720
  ensembl transcript: ENST00000517361
  gene symbol: ZFPM2
  hgvsc: ENST00000517361.1:c.1470A>G
  hgvsp: ENST00000517361.1:c.1470A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000524045
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000524045.2:n.154-3506T>C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000430757
  ensembl transcript: ENST00000520492
  gene symbol: ZFPM2
  hgvsc: ENST00000520492.1:c.1470A>G
  hgvsp: ENST00000520492.1:c.1470A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000521622
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000521622.1:n.279-3506T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520594
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520594.1:n.155-3506T>C
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000384179
  ensembl transcript: ENST00000407775
  gene symbol: ZFPM2
  hgvsc: ENST00000407775.2:c.1866A>G
  hgvsp: ENST00000407775.2:c.1866A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520433
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520433.1:n.212-3506T>C
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2075
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8766
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28199
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1031
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16876
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln622Gln
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
population: Other
population: South Asian
population: European (Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum

8-106814181-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 106814181
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 106814181
    reference: chr 8
allele count: 12
allele frequency: 9.987515605493134e-5
allele num: 120150
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000428720
  ensembl transcript: ENST00000517361
  gene symbol: ZFPM2
  hgvsc: ENST00000517361.1:c.1475C>G
  hgvsp: ENSP00000428720.1:p.Ser492Cys
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000518932
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000518932.1:n.66-3511G>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520594
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520594.1:n.155-3511G>C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000384179
  ensembl transcript: ENST00000407775
  gene symbol: ZFPM2
  hgvsc: ENST00000407775.2:c.1871C>G
  hgvsp: ENSP00000384179.2:p.Ser624Cys
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520078
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520078.1:n.149-3511G>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169946
  ensembl transcript: ENST00000522296
  gene symbol: ZFPM2
  hgvsc: ENST00000522296.1:n.1665C>G
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000367733
  ensembl transcript: ENST00000378472
  gene symbol: ZFPM2
  hgvsc: ENST00000378472.4:c.1064C>G
  hgvsp: ENSP00000367733.4:p.Ser355Cys
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520433
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520433.1:n.212-3511G>C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000430757
  ensembl transcript: ENST00000520492
  gene symbol: ZFPM2
  hgvsc: ENST00000520492.1:c.1475C>G
  hgvsp: ENSP00000430757.1:p.Ser492Cys
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000509144
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000509144.2:n.140-3511G>C
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000524045
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000524045.2:n.154-3511G>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000521622
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000521622.1:n.279-3511G>C
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 605
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16868
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8764
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1032
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28194
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2073
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Ser624Cys
num of homozygotes: 0
population: Latino
population: African
population: Other
population: South Asian
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum

8-106814186-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 106814186
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 106814186
    reference: chr 8
allele count: 1
allele frequency: 8.324315325064513e-6
allele num: 120130
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000518932
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000518932.1:n.66-3516T>C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000367733
  ensembl transcript: ENST00000378472
  gene symbol: ZFPM2
  hgvsc: ENST00000378472.4:c.1069A>G
  hgvsp: ENSP00000367733.4:p.Ile357Val
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000521622
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000521622.1:n.279-3516T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000509144
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000509144.2:n.140-3516T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520433
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520433.1:n.212-3516T>C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000430757
  ensembl transcript: ENST00000520492
  gene symbol: ZFPM2
  hgvsc: ENST00000520492.1:c.1480A>G
  hgvsp: ENSP00000430757.1:p.Ile494Val
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520078
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520078.1:n.149-3516T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520594
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520594.1:n.155-3516T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169946
  ensembl transcript: ENST00000522296
  gene symbol: ZFPM2
  hgvsc: ENST00000522296.1:n.1670A>G
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000384179
  ensembl transcript: ENST00000407775
  gene symbol: ZFPM2
  hgvsc: ENST00000407775.2:c.1876A>G
  hgvsp: ENSP00000384179.2:p.Ile626Val
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000524045
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000524045.2:n.154-3516T>C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000428720
  ensembl transcript: ENST00000517361
  gene symbol: ZFPM2
  hgvsc: ENST00000517361.1:c.1480A>G
  hgvsp: ENSP00000428720.1:p.Ile494Val
  variant of: http://identifiers.org/hgnc/16700
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28183
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16875
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8763
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 531
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2069
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1028
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile626Val
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: South Asian
reference allele: A
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff

8-106814190-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 106814190
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 106814190
    reference: chr 8
allele count: 1
allele frequency: 8.325840077263796e-6
allele num: 120108
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000521622
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000521622.1:n.279-3520T>C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000367733
  ensembl transcript: ENST00000378472
  gene symbol: ZFPM2
  hgvsc: ENST00000378472.4:c.1073A>G
  hgvsp: ENSP00000367733.4:p.Asn358Ser
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000430757
  ensembl transcript: ENST00000520492
  gene symbol: ZFPM2
  hgvsc: ENST00000520492.1:c.1484A>G
  hgvsp: ENSP00000430757.1:p.Asn495Ser
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000524045
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000524045.2:n.154-3520T>C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000384179
  ensembl transcript: ENST00000407775
  gene symbol: ZFPM2
  hgvsc: ENST00000407775.2:c.1880A>G
  hgvsp: ENSP00000384179.2:p.Asn627Ser
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169946
  ensembl transcript: ENST00000522296
  gene symbol: ZFPM2
  hgvsc: ENST00000522296.1:n.1674A>G
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520594
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520594.1:n.155-3520T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000509144
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000509144.2:n.140-3520T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000518932
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000518932.1:n.66-3520T>C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000428720
  ensembl transcript: ENST00000517361
  gene symbol: ZFPM2
  hgvsc: ENST00000517361.1:c.1484A>G
  hgvsp: ENSP00000428720.1:p.Asn495Ser
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520433
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520433.1:n.212-3520T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520078
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520078.1:n.149-3520T>C
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 531
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8759
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16861
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2069
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28184
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1028
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn627Ser
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
population: European (Finnish)
population: African
reference allele: A
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD

http://identifiers.org/exac.variant/8-106814193-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 106814193
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 106814193
    reference: chr 8
allele count: 1
allele frequency: 8.328058896032513e-6
allele num: 120076
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000430757
  ensembl transcript: ENST00000520492
  gene symbol: ZFPM2
  hgvsc: ENST00000520492.1:c.1487C>A
  hgvsp: ENSP00000430757.1:p.Ser496Tyr
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520594
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520594.1:n.155-3523G>T
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000524045
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000524045.2:n.154-3523G>T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000428720
  ensembl transcript: ENST00000517361
  gene symbol: ZFPM2
  hgvsc: ENST00000517361.1:c.1487C>A
  hgvsp: ENSP00000428720.1:p.Ser496Tyr
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520078
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520078.1:n.149-3523G>T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000384179
  ensembl transcript: ENST00000407775
  gene symbol: ZFPM2
  hgvsc: ENST00000407775.2:c.1883C>A
  hgvsp: ENSP00000384179.2:p.Ser628Tyr
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000521622
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000521622.1:n.279-3523G>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169946
  ensembl transcript: ENST00000522296
  gene symbol: ZFPM2
  hgvsc: ENST00000522296.1:n.1677C>A
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000518932
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000518932.1:n.66-3523G>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000509144
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000509144.2:n.140-3523G>T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000367733
  ensembl transcript: ENST00000378472
  gene symbol: ZFPM2
  hgvsc: ENST00000378472.4:c.1076C>A
  hgvsp: ENSP00000367733.4:p.Ser359Tyr
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520433
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520433.1:n.212-3523G>T
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28172
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16830
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2069
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1027
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8760
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser628Tyr
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: BaseQRankSum

8-106814199-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 106814199
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 106814199
    reference: chr 8
allele count: 3
allele frequency: 2.498709000349819e-5
allele num: 120062
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000521622
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000521622.1:n.279-3529G>A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000428720
  ensembl transcript: ENST00000517361
  gene symbol: ZFPM2
  hgvsc: ENST00000517361.1:c.1493C>T
  hgvsp: ENSP00000428720.1:p.Thr498Ile
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000430757
  ensembl transcript: ENST00000520492
  gene symbol: ZFPM2
  hgvsc: ENST00000520492.1:c.1493C>T
  hgvsp: ENSP00000430757.1:p.Thr498Ile
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000384179
  ensembl transcript: ENST00000407775
  gene symbol: ZFPM2
  hgvsc: ENST00000407775.2:c.1889C>T
  hgvsp: ENSP00000384179.2:p.Thr630Ile
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520594
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520594.1:n.155-3529G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520078
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520078.1:n.149-3529G>A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000367733
  ensembl transcript: ENST00000378472
  gene symbol: ZFPM2
  hgvsc: ENST00000378472.4:c.1082C>T
  hgvsp: ENSP00000367733.4:p.Thr361Ile
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169946
  ensembl transcript: ENST00000522296
  gene symbol: ZFPM2
  hgvsc: ENST00000522296.1:n.1683C>T
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000524045
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000524045.2:n.154-3529G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000518932
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000518932.1:n.66-3529G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520433
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520433.1:n.212-3529G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000509144
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000509144.2:n.140-3529G>A
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28166
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2072
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16820
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8755
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1027
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr630Ile
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
population: Other
population: South Asian
population: European (Finnish)
reference allele: C
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ

8-106814203-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 106814203
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 106814203
    reference: chr 8
allele count: 1
allele frequency: 8.331805835596807e-6
allele num: 120022
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000367733
  ensembl transcript: ENST00000378472
  gene symbol: ZFPM2
  hgvsc: ENST00000378472.4:c.1086C>G
  hgvsp: ENST00000378472.4:c.1086C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000524045
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000524045.2:n.154-3533G>C
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000384179
  ensembl transcript: ENST00000407775
  gene symbol: ZFPM2
  hgvsc: ENST00000407775.2:c.1893C>G
  hgvsp: ENST00000407775.2:c.1893C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000521622
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000521622.1:n.279-3533G>C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000428720
  ensembl transcript: ENST00000517361
  gene symbol: ZFPM2
  hgvsc: ENST00000517361.1:c.1497C>G
  hgvsp: ENST00000517361.1:c.1497C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520594
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520594.1:n.155-3533G>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520433
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520433.1:n.212-3533G>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169946
  ensembl transcript: ENST00000522296
  gene symbol: ZFPM2
  hgvsc: ENST00000522296.1:n.1687C>G
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000518932
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000518932.1:n.66-3533G>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520078
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520078.1:n.149-3533G>C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000430757
  ensembl transcript: ENST00000520492
  gene symbol: ZFPM2
  hgvsc: ENST00000520492.1:c.1497C>G
  hgvsp: ENST00000520492.1:c.1497C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000509144
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000509144.2:n.140-3533G>C
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16785
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28166
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2065
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 531
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8749
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1030
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Val631Val
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: South Asian
population: East Asian
population: African
population: Other
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: QD

8-106814214-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 106814214
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 106814214
    reference: chr 8
allele count: 1
allele frequency: 8.335973058135075e-6
allele num: 119962
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000367733
  ensembl transcript: ENST00000378472
  gene symbol: ZFPM2
  hgvsc: ENST00000378472.4:c.1097T>C
  hgvsp: ENSP00000367733.4:p.Ile366Thr
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000509144
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000509144.2:n.140-3544A>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520594
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520594.1:n.155-3544A>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520078
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520078.1:n.149-3544A>G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000384179
  ensembl transcript: ENST00000407775
  gene symbol: ZFPM2
  hgvsc: ENST00000407775.2:c.1904T>C
  hgvsp: ENSP00000384179.2:p.Ile635Thr
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000524045
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000524045.2:n.154-3544A>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000521622
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000521622.1:n.279-3544A>G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000430757
  ensembl transcript: ENST00000520492
  gene symbol: ZFPM2
  hgvsc: ENST00000520492.1:c.1508T>C
  hgvsp: ENSP00000430757.1:p.Ile503Thr
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520433
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520433.1:n.212-3544A>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169946
  ensembl transcript: ENST00000522296
  gene symbol: ZFPM2
  hgvsc: ENST00000522296.1:n.1698T>C
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000428720
  ensembl transcript: ENST00000517361
  gene symbol: ZFPM2
  hgvsc: ENST00000517361.1:c.1508T>C
  hgvsp: ENSP00000428720.1:p.Ile503Thr
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000518932
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000518932.1:n.66-3544A>G
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16697
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8733
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2060
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28105
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1022
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile635Thr
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
population: Other
population: South Asian
population: European (Finnish)
reference allele: T
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: ClippingRankSum

8-106814222-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 106814222
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 106814222
    reference: chr 8
allele count: 1
allele frequency: 8.340422692622062e-6
allele num: 119898
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000367733
  ensembl transcript: ENST00000378472
  gene symbol: ZFPM2
  hgvsc: ENST00000378472.4:c.1105A>G
  hgvsp: ENSP00000367733.4:p.Asn369Asp
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000428720
  ensembl transcript: ENST00000517361
  gene symbol: ZFPM2
  hgvsc: ENST00000517361.1:c.1516A>G
  hgvsp: ENSP00000428720.1:p.Asn506Asp
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000521622
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000521622.1:n.279-3552T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000518932
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000518932.1:n.66-3552T>C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000430757
  ensembl transcript: ENST00000520492
  gene symbol: ZFPM2
  hgvsc: ENST00000520492.1:c.1516A>G
  hgvsp: ENSP00000430757.1:p.Asn506Asp
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520594
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520594.1:n.155-3552T>C
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000524045
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000524045.2:n.154-3552T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520433
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520433.1:n.212-3552T>C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000384179
  ensembl transcript: ENST00000407775
  gene symbol: ZFPM2
  hgvsc: ENST00000407775.2:c.1912A>G
  hgvsp: ENSP00000384179.2:p.Asn638Asp
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169946
  ensembl transcript: ENST00000522296
  gene symbol: ZFPM2
  hgvsc: ENST00000522296.1:n.1706A>G
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520078
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520078.1:n.149-3552T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000509144
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000509144.2:n.140-3552T>C
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16641
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2047
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1017
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28096
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8660
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn638Asp
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Latino
population: African
population: Other
reference allele: A
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: QD

8-106814233-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 106814233
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 106814233
    reference: chr 8
allele count: 1
allele frequency: 8.349893956346754e-6
allele num: 119762
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000428720
  ensembl transcript: ENST00000517361
  gene symbol: ZFPM2
  hgvsc: ENST00000517361.1:c.1527C>T
  hgvsp: ENST00000517361.1:c.1527C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000430757
  ensembl transcript: ENST00000520492
  gene symbol: ZFPM2
  hgvsc: ENST00000520492.1:c.1527C>T
  hgvsp: ENST00000520492.1:c.1527C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520078
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520078.1:n.149-3563G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000509144
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000509144.2:n.140-3563G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520594
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520594.1:n.155-3563G>A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000384179
  ensembl transcript: ENST00000407775
  gene symbol: ZFPM2
  hgvsc: ENST00000407775.2:c.1923C>T
  hgvsp: ENST00000407775.2:c.1923C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520433
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520433.1:n.212-3563G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169946
  ensembl transcript: ENST00000522296
  gene symbol: ZFPM2
  hgvsc: ENST00000522296.1:n.1717C>T
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000367733
  ensembl transcript: ENST00000378472
  gene symbol: ZFPM2
  hgvsc: ENST00000378472.4:c.1116C>T
  hgvsp: ENST00000378472.4:c.1116C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000518932
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000518932.1:n.66-3563G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000521622
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000521622.1:n.279-3563G>A
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000524045
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000524045.2:n.154-3563G>A
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8580
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2044
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 687
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27879
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1021
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16507
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly641Gly
num of homozygotes: 0
population: South Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
population: Latino
reference allele: C
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ

http://identifiers.org/exac.variant/8-106814241-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 106814241
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 106814241
    reference: chr 8
allele count: 1
allele frequency: 8.350312301680083e-6
allele num: 119756
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520433
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520433.1:n.212-3571T>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000518932
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000518932.1:n.66-3571T>G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000428720
  ensembl transcript: ENST00000517361
  gene symbol: ZFPM2
  hgvsc: ENST00000517361.1:c.1535A>C
  hgvsp: ENSP00000428720.1:p.Lys512Thr
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000430757
  ensembl transcript: ENST00000520492
  gene symbol: ZFPM2
  hgvsc: ENST00000520492.1:c.1535A>C
  hgvsp: ENSP00000430757.1:p.Lys512Thr
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169946
  ensembl transcript: ENST00000522296
  gene symbol: ZFPM2
  hgvsc: ENST00000522296.1:n.1725A>C
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000384179
  ensembl transcript: ENST00000407775
  gene symbol: ZFPM2
  hgvsc: ENST00000407775.2:c.1931A>C
  hgvsp: ENSP00000384179.2:p.Lys644Thr
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000367733
  ensembl transcript: ENST00000378472
  gene symbol: ZFPM2
  hgvsc: ENST00000378472.4:c.1124A>C
  hgvsp: ENSP00000367733.4:p.Lys375Thr
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520594
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520594.1:n.155-3571T>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000509144
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000509144.2:n.140-3571T>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000521622
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000521622.1:n.279-3571T>G
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000524045
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000524045.2:n.154-3571T>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520078
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520078.1:n.149-3571T>G
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 797
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2006
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1008
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27698
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16585
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8459
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys644Thr
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
reference allele: A
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: DP

http://identifiers.org/exac.variant/8-106814245-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 106814245
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 106814245
    reference: chr 8
allele count: 1
allele frequency: 8.354637659364713e-6
allele num: 119694
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000384179
  ensembl transcript: ENST00000407775
  gene symbol: ZFPM2
  hgvsc: ENST00000407775.2:c.1935C>A
  hgvsp: ENSP00000384179.2:p.Asp645Glu
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520594
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520594.1:n.155-3575G>T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000367733
  ensembl transcript: ENST00000378472
  gene symbol: ZFPM2
  hgvsc: ENST00000378472.4:c.1128C>A
  hgvsp: ENSP00000367733.4:p.Asp376Glu
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520078
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520078.1:n.149-3575G>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169946
  ensembl transcript: ENST00000522296
  gene symbol: ZFPM2
  hgvsc: ENST00000522296.1:n.1729C>A
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520433
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520433.1:n.212-3575G>T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000430757
  ensembl transcript: ENST00000520492
  gene symbol: ZFPM2
  hgvsc: ENST00000520492.1:c.1539C>A
  hgvsp: ENSP00000430757.1:p.Asp513Glu
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000428720
  ensembl transcript: ENST00000517361
  gene symbol: ZFPM2
  hgvsc: ENST00000517361.1:c.1539C>A
  hgvsp: ENSP00000428720.1:p.Asp513Glu
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000524045
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000524045.2:n.154-3575G>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000521622
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000521622.1:n.279-3575G>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000509144
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000509144.2:n.140-3575G>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000518932
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000518932.1:n.66-3575G>T
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 836
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1994
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27620
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16486
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1007
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8434
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp645Glu
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD

http://identifiers.org/exac.variant/8-106814251-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 106814251
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 106814251
    reference: chr 8
allele count: 3
allele frequency: 2.506433178491462e-5
allele num: 119692
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520078
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520078.1:n.149-3581G>T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000384179
  ensembl transcript: ENST00000407775
  gene symbol: ZFPM2
  hgvsc: ENST00000407775.2:c.1941C>A
  hgvsp: ENST00000407775.2:c.1941C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000428720
  ensembl transcript: ENST00000517361
  gene symbol: ZFPM2
  hgvsc: ENST00000517361.1:c.1545C>A
  hgvsp: ENST00000517361.1:c.1545C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000509144
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000509144.2:n.140-3581G>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169946
  ensembl transcript: ENST00000522296
  gene symbol: ZFPM2
  hgvsc: ENST00000522296.1:n.1735C>A
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520433
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520433.1:n.212-3581G>T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000367733
  ensembl transcript: ENST00000378472
  gene symbol: ZFPM2
  hgvsc: ENST00000378472.4:c.1134C>A
  hgvsp: ENST00000378472.4:c.1134C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000521622
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000521622.1:n.279-3581G>T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000430757
  ensembl transcript: ENST00000520492
  gene symbol: ZFPM2
  hgvsc: ENST00000520492.1:c.1545C>A
  hgvsp: ENST00000520492.1:c.1545C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000518932
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000518932.1:n.66-3581G>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520594
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520594.1:n.155-3581G>T
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000524045
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000524045.2:n.154-3581G>T
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1977
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8364
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 910
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16531
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 954
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 998
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27463
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser647Ser
num of homozygotes: 0
population: East Asian
population: Other
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: DP

8-106814254-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 106814254
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 106814254
    reference: chr 8
allele count: 1
allele frequency: 8.356592515835743e-6
allele num: 119666
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000524045
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000524045.2:n.154-3584A>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000509144
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000509144.2:n.140-3584A>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520594
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520594.1:n.155-3584A>T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000384179
  ensembl transcript: ENST00000407775
  gene symbol: ZFPM2
  hgvsc: ENST00000407775.2:c.1944T>A
  hgvsp: ENST00000407775.2:c.1944T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000518932
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000518932.1:n.66-3584A>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520078
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520078.1:n.149-3584A>T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000428720
  ensembl transcript: ENST00000517361
  gene symbol: ZFPM2
  hgvsc: ENST00000517361.1:c.1548T>A
  hgvsp: ENST00000517361.1:c.1548T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000521622
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000521622.1:n.279-3584A>T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000430757
  ensembl transcript: ENST00000520492
  gene symbol: ZFPM2
  hgvsc: ENST00000520492.1:c.1548T>A
  hgvsp: ENST00000520492.1:c.1548T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000367733
  ensembl transcript: ENST00000378472
  gene symbol: ZFPM2
  hgvsc: ENST00000378472.4:c.1137T>A
  hgvsp: ENST00000378472.4:c.1137T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169946
  ensembl transcript: ENST00000522296
  gene symbol: ZFPM2
  hgvsc: ENST00000522296.1:n.1738T>A
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520433
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520433.1:n.212-3584A>T
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1968
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27405
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 989
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 942
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8301
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1015
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16568
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr648Thr
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: South Asian
population: Other
reference allele: T
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum

8-106814266-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 106814266
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 106814266
    reference: chr 8
allele count: 1
allele frequency: 8.360644772924887e-6
allele num: 119608
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000384179
  ensembl transcript: ENST00000407775
  gene symbol: ZFPM2
  hgvsc: ENST00000407775.2:c.1956G>A
  hgvsp: ENST00000407775.2:c.1956G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000428720
  ensembl transcript: ENST00000517361
  gene symbol: ZFPM2
  hgvsc: ENST00000517361.1:c.1560G>A
  hgvsp: ENST00000517361.1:c.1560G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520433
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520433.1:n.212-3596C>T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000430757
  ensembl transcript: ENST00000520492
  gene symbol: ZFPM2
  hgvsc: ENST00000520492.1:c.1560G>A
  hgvsp: ENST00000520492.1:c.1560G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000367733
  ensembl transcript: ENST00000378472
  gene symbol: ZFPM2
  hgvsc: ENST00000378472.4:c.1149G>A
  hgvsp: ENST00000378472.4:c.1149G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169946
  ensembl transcript: ENST00000522296
  gene symbol: ZFPM2
  hgvsc: ENST00000522296.1:n.1750G>A
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000524045
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000524045.2:n.154-3596C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520594
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520594.1:n.155-3596C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000518932
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000518932.1:n.66-3596C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520078
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520078.1:n.149-3596C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000521622
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000521622.1:n.279-3596C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000509144
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000509144.2:n.140-3596C>T
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1942
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16771
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26979
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1098
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8124
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1268
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 978
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 499
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys652Lys
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: QD

8-106814269-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 106814269
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 106814269
    reference: chr 8
allele count: 2
allele frequency: 1.67238063383226e-5
allele num: 119590
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000509144
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000509144.2:n.140-3599G>A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000367733
  ensembl transcript: ENST00000378472
  gene symbol: ZFPM2
  hgvsc: ENST00000378472.4:c.1152C>T
  hgvsp: ENST00000378472.4:c.1152C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000521622
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000521622.1:n.279-3599G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520433
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520433.1:n.212-3599G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520594
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520594.1:n.155-3599G>A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000430757
  ensembl transcript: ENST00000520492
  gene symbol: ZFPM2
  hgvsc: ENST00000520492.1:c.1563C>T
  hgvsp: ENST00000520492.1:c.1563C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000428720
  ensembl transcript: ENST00000517361
  gene symbol: ZFPM2
  hgvsc: ENST00000517361.1:c.1563C>T
  hgvsp: ENST00000517361.1:c.1563C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000524045
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000524045.2:n.154-3599G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169946
  ensembl transcript: ENST00000522296
  gene symbol: ZFPM2
  hgvsc: ENST00000522296.1:n.1753C>T
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000169946
  ensembl protein: ENSP00000384179
  ensembl transcript: ENST00000407775
  gene symbol: ZFPM2
  hgvsc: ENST00000407775.2:c.1959C>T
  hgvsp: ENST00000407775.2:c.1959C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16700
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000518932
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000518932.1:n.66-3599G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000251003
  ensembl transcript: ENST00000520078
  gene symbol: RP11-152P17.2
  hgvsc: ENST00000520078.1:n.149-3599G>A
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8067
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 975
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26879
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1169
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1387
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16739
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1935
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu653Leu
num of homozygotes: 0
reference allele: C

GenotypeQuality
all individuals: 206
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 124
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1264
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 2856
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 659
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5355
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 217
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37237
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8525
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 583
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 672
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 73
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2387
bin: 7.75e1
variant carriers: 0

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9526
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66314
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.17e-1

QD
type: SiteQuality
SIO_000300: 9.1e0

MQRankSum
type: SiteQuality
SIO_000300: 7.57e-1

FS
type: SiteQuality
SIO_000300: 5.732e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.21e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.662e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -3.29e-1

MQ
type: SiteQuality
SIO_000300: 5.823e1

DP
type: SiteQuality
SIO_000300: 1.818252e6

GenotypeQuality
all individuals: 61
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37228
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 684
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2384
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2853
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 655
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 49
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 203
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5422
bin: 9.75e1
variant carriers: 84

GenotypeQuality
all individuals: 215
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 120
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8526
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1259
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 580
bin: 8.75e1
variant carriers: 0

Other
type: Population
allele count: 3
allele frequency: 3.36322869955157e-3
allele num: 892
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8620
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.056935190793458e-5
allele num: 16510
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 1.049317943336831e-4
allele num: 9530
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: 80
allele frequency: 1.20627261761158e-3
allele num: 66320
num of homozygotes: 1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.67e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.64e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.56e0

DP
type: SiteQuality
SIO_000300: 1.827396e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.95e-1

FS
type: SiteQuality
SIO_000300: 1.115e0

MQ
type: SiteQuality
SIO_000300: 5.974e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.29e-2

QD
type: SiteQuality
SIO_000300: 1.395e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.178e0

GenotypeQuality
all individuals: 42
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 655
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 204
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8533
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 114
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1260
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 38
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37368
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2391
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5342
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 580
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 686
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 196
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2857
bin: 7.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66328
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9536
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.056935190793458e-5
allele num: 16510
num of homozygotes: 0

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

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

QD
type: SiteQuality
SIO_000300: 1.223e1

MQRankSum
type: SiteQuality
SIO_000300: -3.2e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -6.1e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.985e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.634e0

DP
type: SiteQuality
SIO_000300: 1.818481e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.63e-1

FS
type: SiteQuality
SIO_000300: 5.703e0

VQSLOD
type: SiteQuality
SIO_000300: 1.03e0

GenotypeQuality
all individuals: 8529
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 686
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2855
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37362
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 55
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 655
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 113
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5341
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 581
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1261
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2388
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 212
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 198
bin: 2.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9534
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66322
num of homozygotes: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.160092807424594e-4
allele num: 8620
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: 1.84e-1

FS
type: SiteQuality
SIO_000300: 4.442e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.902e0

DP
type: SiteQuality
SIO_000300: 1.818494e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.428e0

VQSLOD
type: SiteQuality
SIO_000300: 3.7e-2

QD
type: SiteQuality
SIO_000300: 1.23e1

MQ
type: SiteQuality
SIO_000300: 5.895e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.86e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.5e-3

GenotypeQuality
all individuals: 31
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 578
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5343
bin: 9.75e1
variant carriers: 4

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

GenotypeQuality
all individuals: 46
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37332
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 201
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 213
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 118
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2856
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 687
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 41
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1261
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8532
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 655
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2387
bin: 7.75e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66322
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9532
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 4
allele frequency: 2.422774076317383e-4
allele num: 16510
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.818755e6

MQRankSum
type: SiteQuality
SIO_000300: 4.21e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.42e0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.494e0

MQ
type: SiteQuality
SIO_000300: 5.989e1

QD
type: SiteQuality
SIO_000300: 1.365e1

VQSLOD
type: SiteQuality
SIO_000300: 8.6e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.8e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -8.77e-1

GenotypeQuality
all individuals: 212
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8520
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 580
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 680
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2392
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 7.5e0
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GenotypeQuality
all individuals: 127
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1261
bin: 8.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 2851
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 655
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5339
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 213
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37275
bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.016136329362087e-5
allele num: 66310
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9524
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 892
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: 16510
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.5e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.3e-3

QD
type: SiteQuality
SIO_000300: 1.256e1

MQ
type: SiteQuality
SIO_000300: 5.971e1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.2e0

MQRankSum
type: SiteQuality
SIO_000300: -5.21e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.44e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.419999999999999e-1

FS
type: SiteQuality
SIO_000300: 1.093e0

DP
type: SiteQuality
SIO_000300: 1.817843e6

GenotypeQuality
all individuals: 94
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1258
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 13
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 8501
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2386
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variant carriers: 0

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

GenotypeQuality
all individuals: 58
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2852
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 655
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 37150
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 139
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 581
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 239
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 88
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 696
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5338
bin: 9.75e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.508386629660915e-5
allele num: 66296
num of homozygotes: 0

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9530
num of homozygotes: 0

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

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -1.192e0

VQSLOD
type: SiteQuality
SIO_000300: 2.45e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.25e-1

FS
type: SiteQuality
SIO_000300: 5.032e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.02e-1

DP
type: SiteQuality
SIO_000300: 1.816902e6

BaseQRankSum
type: SiteQuality
SIO_000300: 5.22e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.7e-3

QD
type: SiteQuality
SIO_000300: 1.368e1

GenotypeQuality
all individuals: 212
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37159
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2853
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 655
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 583
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 86
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variant carriers: 0

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

GenotypeQuality
all individuals: 5338
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 685
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 241
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2385
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variant carriers: 0

GenotypeQuality
all individuals: 8500
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 142
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 90
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1257
bin: 8.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66282
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9518
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8620
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.056935190793458e-5
allele num: 16510
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.48e0

MQRankSum
type: SiteQuality
SIO_000300: -2.65e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.731e0

FS
type: SiteQuality
SIO_000300: 3.383e0

DP
type: SiteQuality
SIO_000300: 1.817003e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.75e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.6e-3

QD
type: SiteQuality
SIO_000300: 1.548e1

VQSLOD
type: SiteQuality
SIO_000300: 3.31e-1

GenotypeQuality
all individuals: 244
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 212
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 142
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8501
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2853
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1261
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2383
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 582
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 655
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5337
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 695
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 88
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37190
bin: 6.25e1
variant carriers: 0

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

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

Latino
type: Population
allele count: 1
allele frequency: 8.64902266043937e-5
allele num: 11562
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66304
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9526
num of homozygotes: 0

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

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

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

QD
type: SiteQuality
SIO_000300: 1.654e1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.92e-1

FS
type: SiteQuality
SIO_000300: 3.068e0

MQRankSum
type: SiteQuality
SIO_000300: -6.68e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.777e0

MQ
type: SiteQuality
SIO_000300: 5.907e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.1e-3

DP
type: SiteQuality
SIO_000300: 1.816926e6

BaseQRankSum
type: SiteQuality
SIO_000300: -4.204e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.776e0

GenotypeQuality
all individuals: 580
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 147
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 208
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variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8493
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2855
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 684
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37203
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1256
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 31
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5356
bin: 9.75e1
variant carriers: 29

GenotypeQuality
all individuals: 652
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2381
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 245
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 7.5e0
variant carriers: 0

South Asian
type: Population
allele count: 22
allele frequency: 1.332525741974561e-3
allele num: 16510
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 2.596053997923157e-4
allele num: 11556
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.035003017501508e-5
allele num: 66280
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9516
num of homozygotes: 0

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

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

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

DP
type: SiteQuality
SIO_000300: 1.819828e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -2.58e-1

QD
type: SiteQuality
SIO_000300: 1.3e1

MQRankSum
type: SiteQuality
SIO_000300: 1.57e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.97e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.52e0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -8.500000000000001e-2

MQ
type: SiteQuality
SIO_000300: 5.971e1

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

GenotypeQuality
all individuals: 2854
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8496
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variant carriers: 0

GenotypeQuality
all individuals: 161
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 248
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variant carriers: 0

GenotypeQuality
all individuals: 1258
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 76
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variant carriers: 0

GenotypeQuality
all individuals: 79
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 199
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37272
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 656
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2384
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 654
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 578
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5330
bin: 9.75e1
variant carriers: 1

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: 11562
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.508568670045861e-5
allele num: 66288
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9524
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8620
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.25e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.38e0

QD
type: SiteQuality
SIO_000300: 1.34e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.1e-3

FS
type: SiteQuality
SIO_000300: 1.876e0

VQSLOD
type: SiteQuality
SIO_000300: 7.05e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.23e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.29e0

MQ
type: SiteQuality
SIO_000300: 5.977e1

DP
type: SiteQuality
SIO_000300: 1.816723e6

GenotypeQuality
all individuals: 86
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 169
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 243
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variant carriers: 0

GenotypeQuality
all individuals: 40
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 25
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variant carriers: 0

GenotypeQuality
all individuals: 74
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GenotypeQuality
all individuals: 2379
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variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 653
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 195
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1262
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5331
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 37235
bin: 6.25e1
variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9522
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 894
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: 1.508932882665379e-5
allele num: 66272
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11556
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 9.1e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.7e-3

DP
type: SiteQuality
SIO_000300: 1.816722e6

QD
type: SiteQuality
SIO_000300: 1.533e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.35e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.59e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.03e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.47e-1

MQ
type: SiteQuality
SIO_000300: 5.913e1

GenotypeDepth
all individuals: 16592
bin: 2.25e1
variant carriers: 2

GenotypeDepth
all individuals: 862
bin: 4.75e1
variant carriers: 2

GenotypeDepth
all individuals: 1268
bin: 4.25e1
variant carriers: 5

GenotypeQuality
all individuals: 556
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 236
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2834
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 627
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37148
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1223
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 69
bin: 7.5e0
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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bin: 5.25e1
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GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
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GenotypeQuality
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bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 5558
bin: 9.75e1
variant carriers: 411

GenotypeQuality
all individuals: 630
bin: 9.25e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 32
allele frequency: 4.838221953432114e-3
allele num: 6614
num of homozygotes: 0

South Asian
type: Population
allele count: 10
allele frequency: 6.056935190793458e-4
allele num: 16510
num of homozygotes: 1

European (Non-Finnish)
type: Population
allele count: 329
allele frequency: 4.963490435097459e-3
allele num: 66284
num of homozygotes: 1

African
type: Population
allele count: 5
allele frequency: 5.255413075467731e-4
allele num: 9514
num of homozygotes: 0

Latino
type: Population
allele count: 35
allele frequency: 3.028205571898252e-3
allele num: 11558
num of homozygotes: 0

Other
type: Population
allele count: 3
allele frequency: 3.355704697986577e-3
allele num: 894
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 6.16e0

MQRankSum
type: SiteQuality
SIO_000300: 2.52e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.03e-1

DP
type: SiteQuality
SIO_000300: 1.852127e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.1e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -5.988e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.69e-1

QD
type: SiteQuality
SIO_000300: 1.298e1

MQ
type: SiteQuality
SIO_000300: 5.971e1

GenotypeDepth
all individuals: 1268
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 862
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 685
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 630
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 91
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 37148
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 2361
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variant carriers: 0

GenotypeQuality
all individuals: 2834
bin: 7.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 894
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: 16510
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66284
num of homozygotes: 0

African
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allele count: 1
allele frequency: 1.051082615093546e-4
allele num: 9514
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11558
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 6.16e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.1e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.69e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.03e-1

MQ
type: SiteQuality
SIO_000300: 5.971e1

MQRankSum
type: SiteQuality
SIO_000300: 2.52e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.852127e6

BaseQRankSum
type: SiteQuality
SIO_000300: -5.988e0

QD
type: SiteQuality
SIO_000300: 1.298e1

GenotypeQuality
all individuals: 1240
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 237
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 8525
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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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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 567
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variant carriers: 0

GenotypeQuality
all individuals: 5215
bin: 9.75e1
variant carriers: 3

South Asian
type: Population
allele count: 3
allele frequency: 1.817080557238038e-4
allele num: 16510
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: 0
allele frequency: 0.0e0
allele num: 66280
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9524
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.7e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -5.659999999999999e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 1.85e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.13e0

MQ
type: SiteQuality
SIO_000300: 5.981e1

DP
type: SiteQuality
SIO_000300: 1.814991e6

BaseQRankSum
type: SiteQuality
SIO_000300: -3.117e0

MQRankSum
type: SiteQuality
SIO_000300: 6.830000000000001e-1

QD
type: SiteQuality
SIO_000300: 1.243e1

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

GenotypeQuality
all individuals: 5213
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 21
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2392
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 619
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 62
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variant carriers: 0

GenotypeQuality
all individuals: 54
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variant carriers: 0

GenotypeQuality
all individuals: 233
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variant carriers: 0

GenotypeQuality
all individuals: 63
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variant carriers: 0

GenotypeQuality
all individuals: 2865
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 32
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 184
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GenotypeQuality
all individuals: 8527
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 643
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1241
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 568
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variant carriers: 0

GenotypeQuality
all individuals: 37429
bin: 6.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11556
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66300
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9530
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8614
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: 1
allele frequency: 6.056935190793458e-5
allele num: 16510
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.9e-3

FS
type: SiteQuality
SIO_000300: 3.833e0

VQSLOD
type: SiteQuality
SIO_000300: 1.48e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.53e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.93e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.62e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.307e0

QD
type: SiteQuality
SIO_000300: 1.379e1

DP
type: SiteQuality
SIO_000300: 1.815151e6

MQ
type: SiteQuality
SIO_000300: 5.924e1

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

GenotypeQuality
all individuals: 2867
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 57
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variant carriers: 0

GenotypeQuality
all individuals: 209
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variant carriers: 0

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

GenotypeQuality
all individuals: 5213
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 610
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
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variant carriers: 0

GenotypeQuality
all individuals: 16
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variant carriers: 0

GenotypeQuality
all individuals: 132
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30
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GenotypeQuality
all individuals: 8534
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variant carriers: 0

GenotypeQuality
all individuals: 8
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GenotypeQuality
all individuals: 645
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variant carriers: 0

GenotypeQuality
all individuals: 37520
bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
all individuals: 2392
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1244
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 569
bin: 8.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8618
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: 0
allele frequency: 0.0e0
allele num: 66318
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.056935190793458e-5
allele num: 16510
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9548
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -8.180999999999999e0

DP
type: SiteQuality
SIO_000300: 1.81625e6

MQ
type: SiteQuality
SIO_000300: 5.975e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.6e-3

MQRankSum
type: SiteQuality
SIO_000300: -4.03e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 1.08e0

QD
type: SiteQuality
SIO_000300: 1.531e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.8e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.869e0

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

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2873
bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9594
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11570
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: 0
allele frequency: 0.0e0
allele num: 66406
num of homozygotes: 0

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

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

MQ
type: SiteQuality
SIO_000300: 5.991e1

MQRankSum
type: SiteQuality
SIO_000300: 2.13e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.75e-1

QD
type: SiteQuality
SIO_000300: 1.254e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.12e0

DP
type: SiteQuality
SIO_000300: 1.821098e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.444e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 6.735e0

VQSLOD
type: SiteQuality
SIO_000300: 7.85e-1

GenotypeQuality
all individuals: 48
bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 3

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2872
bin: 7.25e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.516575833308241e-5
allele num: 66422
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9614
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: 16512
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 7.17e0

DP
type: SiteQuality
SIO_000300: 1.822023e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.867e1

MQRankSum
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SIO_000300: -5.55e-1

ReadPosRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 9.08e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.12e-1

MQ
type: SiteQuality
SIO_000300: 5.944e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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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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GenotypeQuality
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GenotypeQuality
all individuals: 2398
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variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 5.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66426
num of homozygotes: 0

South Asian
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allele count: 0
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African
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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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European (Finnish)
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allele frequency: 4.535833081342606e-4
allele num: 6614
num of homozygotes: 0

East Asian
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ClippingRankSum
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MQ
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DP
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InbreedingCoeff
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ReadPosRankSum
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SIO_000300: -1.03e-1

MQRankSum
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BaseQRankSum
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FS
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QD
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VQSLOD
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SIO_000300: 9.5e-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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

African
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Latino
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allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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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

Other
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MQRankSum
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FS
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InbreedingCoeff
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QD
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VQSLOD
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DP
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ClippingRankSum
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BaseQRankSum
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ReadPosRankSum
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MQ
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SIO_000300: 5.958e1

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

Other
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allele frequency: 0.0e0
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South Asian
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allele frequency: 0.0e0
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African
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allele num: 9668
num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 66524
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East Asian
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allele frequency: 0.0e0
allele num: 8620
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Latino
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allele frequency: 0.0e0
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ClippingRankSum
type: SiteQuality
SIO_000300: -3.42e-1

ReadPosRankSum
type: SiteQuality
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FS
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SIO_000300: 1.093e0

MQ
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VQSLOD
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QD
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MQRankSum
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DP
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SIO_000300: 1.825061e6

InbreedingCoeff
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SIO_000300: 1.0e-4

BaseQRankSum
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SIO_000300: -5.82e0

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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66550
num of homozygotes: 0

South Asian
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allele num: 16512
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East Asian
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Other
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African
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Latino
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European (Finnish)
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InbreedingCoeff
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ReadPosRankSum
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DP
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VQSLOD
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MQRankSum
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BaseQRankSum
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QD
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FS
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ClippingRankSum
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 (Non-Finnish)
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allele num: 66560
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Latino
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Other
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East Asian
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allele frequency: 1.159554730983302e-4
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European (Finnish)
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African
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South Asian
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FS
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QD
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MQ
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ReadPosRankSum
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BaseQRankSum
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InbreedingCoeff
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DP
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VQSLOD
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ClippingRankSum
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MQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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Other
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European (Finnish)
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African
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Latino
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European (Non-Finnish)
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South Asian
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InbreedingCoeff
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ReadPosRankSum
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ClippingRankSum
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BaseQRankSum
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VQSLOD
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MQRankSum
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MQ
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FS
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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East Asian
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European (Finnish)
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European (Non-Finnish)
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allele num: 66618
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South Asian
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Latino
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Other
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BaseQRankSum
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MQRankSum
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QD
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VQSLOD
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InbreedingCoeff
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FS
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DP
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ClippingRankSum
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MQ
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ReadPosRankSum
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SIO_000300: 1.54e0

GenotypeQuality
all individuals: 563
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2892
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 38498
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 657
bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5025
bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2442
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8674
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 2.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9752
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8624
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66636
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

VQSLOD
type: SiteQuality
SIO_000300: 5.69e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.242e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.54e0

MQRankSum
type: SiteQuality
SIO_000300: -6.81e-1

MQ
type: SiteQuality
SIO_000300: 5.951e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.088e0

FS
type: SiteQuality
SIO_000300: 2.064e0

QD
type: SiteQuality
SIO_000300: 1.157e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-3

DP
type: SiteQuality
SIO_000300: 1.824798e6

GenotypeQuality
all individuals: 14
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 126
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
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: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8679
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5024
bin: 9.75e1
variant carriers: 1

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: 16512
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9750
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8624
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.5004651441947e-5
allele num: 66646
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.825096e6

FS
type: SiteQuality
SIO_000300: 5.25e-1

MQRankSum
type: SiteQuality
SIO_000300: 8.51e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.34e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.623e0

QD
type: SiteQuality
SIO_000300: 1.242e1

MQ
type: SiteQuality
SIO_000300: 5.915e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.2e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.24e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.48e-1

GenotypeQuality
all individuals: 18
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5023
bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38507
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8678
bin: 6.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500555205426008e-5
allele num: 66642
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9750
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8624
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.64e0

MQ
type: SiteQuality
SIO_000300: 5.965e1

DP
type: SiteQuality
SIO_000300: 1.825014e6

BaseQRankSum
type: SiteQuality
SIO_000300: -4.343e0

FS
type: SiteQuality
SIO_000300: 2.246e0

MQRankSum
type: SiteQuality
SIO_000300: 4.63e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.6e-3

QD
type: SiteQuality
SIO_000300: 1.323e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.94e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.82e-1

GenotypeQuality
all individuals: 47
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1268
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5023
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 658
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9752
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

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

Latino
type: Population
allele count: 2
allele frequency: 1.728011059270779e-4
allele num: 11574
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8624
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66650
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.953e1

MQRankSum
type: SiteQuality
SIO_000300: -3.31e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 7.23e-1

QD
type: SiteQuality
SIO_000300: 1.26e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.304e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 1.51e-1

DP
type: SiteQuality
SIO_000300: 1.825486e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.89e-1

GenotypeQuality
all individuals: 2
bin: 1.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 46
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variant carriers: 0

GenotypeQuality
all individuals: 2897
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 5.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500195025353296e-5
allele num: 66658
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8624
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9754
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: 11574
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.593e0

MQ
type: SiteQuality
SIO_000300: 5.868e1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.1e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.13e0

QD
type: SiteQuality
SIO_000300: 1.066e1

DP
type: SiteQuality
SIO_000300: 1.825417e6

FS
type: SiteQuality
SIO_000300: 7.558e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.68e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.799999999999999e-2

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 7

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 655
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9756
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500240038406145e-5
allele num: 66656
num of homozygotes: 0

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

South Asian
type: Population
allele count: 6
allele frequency: 3.633720930232558e-4
allele num: 16512
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.298e1

MQ
type: SiteQuality
SIO_000300: 5.974e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.087e0

VQSLOD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 5.2e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.35e0

MQRankSum
type: SiteQuality
SIO_000300: -3.9e-1

DP
type: SiteQuality
SIO_000300: 1.826478e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.85e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 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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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 50
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variant carriers: 0

GenotypeQuality
all individuals: 5022
bin: 9.75e1
variant carriers: 1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9756
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500195025353296e-5
allele num: 66658
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.02e0

FS
type: SiteQuality
SIO_000300: 1.135e0

QD
type: SiteQuality
SIO_000300: 1.413e1

MQ
type: SiteQuality
SIO_000300: 5.992e1

VQSLOD
type: SiteQuality
SIO_000300: 7.66e-1

DP
type: SiteQuality
SIO_000300: 1.825937e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.3e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 3.12e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.23e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.2e-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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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 13
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GenotypeQuality
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GenotypeQuality
all individuals: 41
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GenotypeQuality
all individuals: 1269
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.75e1
variant carriers: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9756
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.500195025353296e-5
allele num: 66658
num of homozygotes: 0

QD
type: SiteQuality
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ReadPosRankSum
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VQSLOD
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DP
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FS
type: SiteQuality
SIO_000300: 1.135e0

BaseQRankSum
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SIO_000300: 3.2e-2

MQ
type: SiteQuality
SIO_000300: 5.992e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.3e-3

MQRankSum
type: SiteQuality
SIO_000300: 1.02e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.12e-1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 898
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 2.051282051282051e-4
allele num: 9750
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66660
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 1.4e0

FS
type: SiteQuality
SIO_000300: 3.216e0

DP
type: SiteQuality
SIO_000300: 1.825945e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.41e-1

VQSLOD
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SIO_000300: 1.52e0

BaseQRankSum
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SIO_000300: -1.872e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.9e-3

MQ
type: SiteQuality
SIO_000300: 5.978e1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.57e-1

QD
type: SiteQuality
SIO_000300: 1.255e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 3.75e1
variant carriers: 2

East Asian
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allele count: 53
allele frequency: 6.147065646021805e-3
allele num: 8622
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 28
allele frequency: 4.233444209253099e-3
allele num: 6614
num of homozygotes: 0

African
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allele count: 1309
allele frequency: 1.342013532909576e-1
allele num: 9754
num of homozygotes: 94

Other
type: Population
allele count: 37
allele frequency: 4.120267260579064e-2
allele num: 898
num of homozygotes: 2

South Asian
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allele count: 553
allele frequency: 3.349079457364341e-2
allele num: 16512
num of homozygotes: 22

Latino
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allele count: 346
allele frequency: 2.992561840512022e-2
allele num: 11562
num of homozygotes: 9

European (Non-Finnish)
type: Population
allele count: 1570
allele frequency: 2.355235523552355e-2
allele num: 66660
num of homozygotes: 25

QD
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SIO_000300: 1.368e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.4e-1

BaseQRankSum
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SIO_000300: -3.131e0

InbreedingCoeff
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SIO_000300: 4.46e-2

DP
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SIO_000300: 2.259311e6

MQ
type: SiteQuality
SIO_000300: 5.969e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.74e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.55e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.17e0

GenotypeQuality
all individuals: 41
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3030
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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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variant carriers: 0

GenotypeQuality
all individuals: 3
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GenotypeQuality
all individuals: 31
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variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9754
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8620
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: 16506
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.000750187546887e-5
allele num: 66650
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 5.5e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -7.679e0

VQSLOD
type: SiteQuality
SIO_000300: 3.35e0

DP
type: SiteQuality
SIO_000300: 1.756965e6

MQ
type: SiteQuality
SIO_000300: 5.955e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.4e-3

FS
type: SiteQuality
SIO_000300: 5.3e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.379999999999999e-1

QD
type: SiteQuality
SIO_000300: 1.221e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.65e-1

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
all individuals: 8
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variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66656
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9758
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16508
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.8e-2

QD
type: SiteQuality
SIO_000300: 1.335e1

MQRankSum
type: SiteQuality
SIO_000300: 5.92e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.36e-1

InbreedingCoeff
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SIO_000300: 4.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 3.43e0

FS
type: SiteQuality
SIO_000300: 8.114000000000001e0

DP
type: SiteQuality
SIO_000300: 1.756506e6

MQ
type: SiteQuality
SIO_000300: 5.976e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.51e-1

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.5008254539997e-5
allele num: 66630
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9750
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16508
num of homozygotes: 0

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

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

Latino
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allele count: 0
allele frequency: 0.0e0
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MQRankSum
type: SiteQuality
SIO_000300: 7.61e-1

BaseQRankSum
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VQSLOD
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FS
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SIO_000300: 2.176e0

ClippingRankSum
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SIO_000300: 1.08e0

InbreedingCoeff
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DP
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ReadPosRankSum
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MQ
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QD
type: SiteQuality
SIO_000300: 1.213e1

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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16502
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11548
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66610
num of homozygotes: 0

African
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allele count: 1
allele frequency: 1.026694045174538e-4
allele num: 9740
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8616
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 2.1248e1

DP
type: SiteQuality
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ClippingRankSum
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InbreedingCoeff
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ReadPosRankSum
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MQ
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BaseQRankSum
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QD
type: SiteQuality
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MQRankSum
type: SiteQuality
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 39644
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GenotypeQuality
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bin: 8.25e1
variant carriers: 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: 16502
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.002822653294096e-5
allele num: 66604
num of homozygotes: 0

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

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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
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VQSLOD
type: SiteQuality
SIO_000300: 1.36e0

MQRankSum
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ClippingRankSum
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SIO_000300: 1.16e0

DP
type: SiteQuality
SIO_000300: 1.754798e6

BaseQRankSum
type: SiteQuality
SIO_000300: 4.28e0

MQ
type: SiteQuality
SIO_000300: 5.986e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.3e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.68e-1

FS
type: SiteQuality
SIO_000300: 3.098e0

QD
type: SiteQuality
SIO_000300: 1.305e1

GenotypeQuality
all individuals: 48
bin: 7.5e0
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
all individuals: 1280
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9742
num of homozygotes: 0

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

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

South Asian
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allele count: 1
allele frequency: 6.059871530723549e-5
allele num: 16502
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66598
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 1.03e0

DP
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SIO_000300: 1.754633e6

ReadPosRankSum
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SIO_000300: 1.77e0

ClippingRankSum
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SIO_000300: 1.94e-1

BaseQRankSum
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SIO_000300: 8.98e0

VQSLOD
type: SiteQuality
SIO_000300: 4.87e-1

FS
type: SiteQuality
SIO_000300: 1.965e0

MQ
type: SiteQuality
SIO_000300: 5.934e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

QD
type: SiteQuality
SIO_000300: 1.428e1

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66598
num of homozygotes: 0

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

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

Other
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allele frequency: 0.0e0
allele num: 898
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.06134076857801e-5
allele num: 16498
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9734
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 7.36e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.75e0

MQ
type: SiteQuality
SIO_000300: 5.672e1

DP
type: SiteQuality
SIO_000300: 1.754193e6

FS
type: SiteQuality
SIO_000300: 3.566e0

QD
type: SiteQuality
SIO_000300: 1.619e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -1.314e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.84e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.03e0

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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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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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 22
bin: 5.75e1
variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9722
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.064281382656155e-5
allele num: 16490
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66548
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 1.385e0

BaseQRankSum
type: SiteQuality
SIO_000300: -6.887e0

VQSLOD
type: SiteQuality
SIO_000300: 2.91e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 8.0e-3

MQRankSum
type: SiteQuality
SIO_000300: 6.7e-2

MQ
type: SiteQuality
SIO_000300: 5.993e1

QD
type: SiteQuality
SIO_000300: 1.353e1

DP
type: SiteQuality
SIO_000300: 1.752914e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.22e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 300
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variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11534
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)
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allele count: 1
allele frequency: 1.503081316699233e-5
allele num: 66530
num of homozygotes: 0

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: 1.8e0

MQRankSum
type: SiteQuality
SIO_000300: 2.82e-1

FS
type: SiteQuality
SIO_000300: 4.603e0

DP
type: SiteQuality
SIO_000300: 1.751925e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.99e-1

InbreedingCoeff
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SIO_000300: 3.3e-3

QD
type: SiteQuality
SIO_000300: 1.351e1

VQSLOD
type: SiteQuality
SIO_000300: 4.88e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.195e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 10
bin: 5.75e1
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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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: 1

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9698
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11522
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: 1
allele frequency: 1.504166541319455e-5
allele num: 66482
num of homozygotes: 0

QD
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: 3.42e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.14e-1

VQSLOD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.945e1

BaseQRankSum
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SIO_000300: -3.163e0

DP
type: SiteQuality
SIO_000300: 1.750403e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.31e-1

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
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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)
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allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9696
num of homozygotes: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.163061177017911e-4
allele num: 8598
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66480
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11518
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 9.99e-1

BaseQRankSum
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ReadPosRankSum
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FS
type: SiteQuality
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QD
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ClippingRankSum
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DP
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InbreedingCoeff
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SIO_000300: -2.0e-4

VQSLOD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.94e1

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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8592
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: 2
allele frequency: 1.736714136853074e-4
allele num: 11516
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9688
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16468
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66474
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.750055e6

VQSLOD
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MQ
type: SiteQuality
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QD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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FS
type: SiteQuality
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InbreedingCoeff
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BaseQRankSum
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MQRankSum
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ClippingRankSum
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SIO_000300: -3.61e-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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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
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GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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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: 26
bin: 5.25e1
variant carriers: 0

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

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

African
type: Population
allele count: 1
allele frequency: 1.031778786628147e-4
allele num: 9692
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16468
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: 11524
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66466
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.9e-2

MQRankSum
type: SiteQuality
SIO_000300: 7.86e-1

MQ
type: SiteQuality
SIO_000300: 5.954e1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.58e-1

DP
type: SiteQuality
SIO_000300: 1.749955e6

FS
type: SiteQuality
SIO_000300: 7.24e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 5.2e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.36e-1

QD
type: SiteQuality
SIO_000300: 1.221e1

GenotypeQuality
all individuals: 109
bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39369
bin: 6.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9686
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: 11516
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16466
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.504800312998465e-5
allele num: 66454
num of homozygotes: 0

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

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

MQ
type: SiteQuality
SIO_000300: 5.928e1

FS
type: SiteQuality
SIO_000300: 1.45e0

QD
type: SiteQuality
SIO_000300: 1.178e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.95e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.600000000000001e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.749523e6

MQRankSum
type: SiteQuality
SIO_000300: 1.74e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.669999999999999e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.5e0

GenotypeQuality
all individuals: 55
bin: 3.75e1
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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 5.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3339
bin: 9.75e1
variant carriers: 3

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.505343971097396e-5
allele num: 66430
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9676
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.736714136853074e-4
allele num: 11516
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16468
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.87e-1

FS
type: SiteQuality
SIO_000300: 9.85e-1

DP
type: SiteQuality
SIO_000300: 1.748886e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 7.33e-1

QD
type: SiteQuality
SIO_000300: 1.292e1

MQRankSum
type: SiteQuality
SIO_000300: 9.64e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.29e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.4e-2

GenotypeQuality
all individuals: 1274
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 12

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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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 7
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 39308
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 3.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11518
num of homozygotes: 0

African
type: Population
allele count: 12
allele frequency: 1.241721854304636e-3
allele num: 9664
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16468
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8582
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: 0
allele frequency: 0.0e0
allele num: 66414
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.28e0

MQRankSum
type: SiteQuality
SIO_000300: -2.27e-1

DP
type: SiteQuality
SIO_000300: 1.749071e6

MQ
type: SiteQuality
SIO_000300: 5.963e1

FS
type: SiteQuality
SIO_000300: 1.296e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

QD
type: SiteQuality
SIO_000300: 1.357e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.2e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 4.1e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.851e0

GenotypeQuality
all individuals: 391
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 22
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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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bin: 9.75e1
variant carriers: 1

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: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 5.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66410
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 1.03498240529911e-4
allele num: 9662
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16466
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 7.62e-1

QD
type: SiteQuality
SIO_000300: 1.512e1

DP
type: SiteQuality
SIO_000300: 1.747727e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.08e0

FS
type: SiteQuality
SIO_000300: 5.085e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.19e-1

MQ
type: SiteQuality
SIO_000300: 5.972e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.36e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.8e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66398
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.073120369245719e-5
allele num: 16466
num of homozygotes: 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: 9660
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 6.13e0

FS
type: SiteQuality
SIO_000300: 2.12e0

QD
type: SiteQuality
SIO_000300: 1.584e1

MQRankSum
type: SiteQuality
SIO_000300: 2.17e0

DP
type: SiteQuality
SIO_000300: 1.747363e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.08e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.999999999999999e-3

VQSLOD
type: SiteQuality
SIO_000300: -1.186e0

GenotypeQuality
all individuals: 537
bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
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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GenotypeQuality
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GenotypeQuality
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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: 2491
bin: 7.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16468
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9658
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.506387081224391e-5
allele num: 66384
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: 7.6e-1

VQSLOD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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FS
type: SiteQuality
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ReadPosRankSum
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MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.746851e6

QD
type: SiteQuality
SIO_000300: 1.051e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.831e0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 573
bin: 9.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.519569736961041e-5
allele num: 66378
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9650
num of homozygotes: 0

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

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

South Asian
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allele count: 0
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European (Finnish)
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allele frequency: 0.0e0
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QD
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ReadPosRankSum
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VQSLOD
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BaseQRankSum
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FS
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DP
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InbreedingCoeff
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SIO_000300: 1.2e-3

MQRankSum
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ClippingRankSum
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 66352
num of homozygotes: 0

Latino
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allele num: 11494
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South Asian
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allele num: 16462
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East Asian
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African
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Other
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European (Finnish)
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VQSLOD
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ClippingRankSum
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InbreedingCoeff
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DP
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BaseQRankSum
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MQRankSum
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FS
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ReadPosRankSum
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MQ
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 66312
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African
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allele frequency: 1.036914143508917e-4
allele num: 9644
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Latino
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Other
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South Asian
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European (Finnish)
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VQSLOD
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MQRankSum
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FS
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BaseQRankSum
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QD
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ReadPosRankSum
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InbreedingCoeff
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DP
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MQ
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 6606
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.508841813024323e-5
allele num: 66276
num of homozygotes: 0

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

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

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

InbreedingCoeff
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ClippingRankSum
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MQRankSum
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FS
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BaseQRankSum
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ReadPosRankSum
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SIO_000300: 6.3e-1

VQSLOD
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MQ
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DP
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele frequency: 0.0e0
allele num: 16444
num of homozygotes: 0

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

European (Non-Finnish)
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allele frequency: 1.510163399679845e-5
allele num: 66218
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European (Finnish)
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African
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East Asian
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allele frequency: 0.0e0
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Latino
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InbreedingCoeff
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ClippingRankSum
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FS
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QD
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DP
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BaseQRankSum
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MQRankSum
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VQSLOD
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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num of homozygotes: 0

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 frequency: 0.0e0
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South Asian
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East Asian
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Latino
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allele num: 11464
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European (Finnish)
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VQSLOD
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QD
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MQRankSum
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InbreedingCoeff
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ReadPosRankSum
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MQ
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BaseQRankSum
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ClippingRankSum
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FS
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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
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GenotypeQuality
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GenotypeQuality
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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 (Non-Finnish)
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African
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European (Finnish)
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Latino
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East Asian
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South Asian
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InbreedingCoeff
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BaseQRankSum
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MQ
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ClippingRankSum
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FS
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DP
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ReadPosRankSum
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MQRankSum
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VQSLOD
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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Other
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African
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Latino
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South Asian
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European (Non-Finnish)
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European (Finnish)
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BaseQRankSum
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ClippingRankSum
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MQRankSum
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InbreedingCoeff
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FS
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ReadPosRankSum
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QD
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MQ
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VQSLOD
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DP
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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: 299
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 356
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 428
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2862
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 193
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 443
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 328
bin: 5.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 1206
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 552
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37684
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 214
bin: 4.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8504
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66148
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9624
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.738203425375742e-5
allele num: 11444
num of homozygotes: 0

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 8.159999999999999e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.01e-1

DP
type: SiteQuality
SIO_000300: 1.7227e6

QD
type: SiteQuality
SIO_000300: 9.779999999999999e0

MQ
type: SiteQuality
SIO_000300: 5.957e1

MQRankSum
type: SiteQuality
SIO_000300: 4.27e-1

FS
type: SiteQuality
SIO_000300: 2.966e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.79e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.12e-1

GenotypeQuality
all individuals: 15
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 531
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 506
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 335
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 906
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 432
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3293
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 83
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 549
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 362
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37455
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2309
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2804
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 251
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 546
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8575
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 186
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1199
bin: 8.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9618
num of homozygotes: 0

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.512172992590352e-5
allele num: 66130
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -3.3e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.289e0

FS
type: SiteQuality
SIO_000300: 2.053e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.79e0

BaseQRankSum
type: SiteQuality
SIO_000300: -8.773999999999999e0

VQSLOD
type: SiteQuality
SIO_000300: -6.4e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

MQ
type: SiteQuality
SIO_000300: 5.971e1

DP
type: SiteQuality
SIO_000300: 1.715418e6

QD
type: SiteQuality
SIO_000300: 1.328e1

GenotypeQuality
all individuals: 8510
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 302
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 937
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2778
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 283
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3293
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 546
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 85
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 591
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 2.5e0
variant carriers: 0