2-220047294-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 220047294
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 220047294
    reference: chr 2
allele count: 1
allele frequency: 8.251097395953662e-6
allele num: 121196
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000144567
  ensembl protein: ENSP00000411247
  ensembl transcript: ENST00000420189
  gene symbol: FAM134A
  hgvsc: ENST00000420189.1:c.553C>T
  hgvsp: ENST00000420189.1:c.553C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28450
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000144567
  ensembl protein: ENSP00000395249
  ensembl transcript: ENST00000430297
  gene symbol: FAM134A
  hgvsc: ENST00000430297.2:c.1575C>T
  hgvsp: ENST00000430297.2:c.1575C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28450
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000144567
  ensembl protein: ENSP00000273048
  ensembl transcript: ENST00000273048
  gene symbol: FAM134A
  hgvsc: ENST00000273048.2:c.*950C>T
  variant of: http://identifiers.org/hgnc/28450
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1139
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5325
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3116
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1985
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 605
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7645
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13962
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12325
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3374
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9893
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5058
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18343
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15217
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 213
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3212
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2245
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3868
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7607
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4601
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Pro525Pro
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: African
population: Latino
population: South Asian
reference allele: C
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: DP

2-220047295-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 220047295
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 220047295
    reference: chr 2
allele count: 293
allele frequency: 2.41773112849457e-3
allele num: 121188
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000144567
  ensembl protein: ENSP00000273048
  ensembl transcript: ENST00000273048
  gene symbol: FAM134A
  hgvsc: ENST00000273048.2:c.*951G>A
  variant of: http://identifiers.org/hgnc/28450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000144567
  ensembl protein: ENSP00000411247
  ensembl transcript: ENST00000420189
  gene symbol: FAM134A
  hgvsc: ENST00000420189.1:c.554G>A
  hgvsp: ENSP00000411247.1:p.Asp186Asn
  variant of: http://identifiers.org/hgnc/28450
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000144567
  ensembl protein: ENSP00000395249
  ensembl transcript: ENST00000430297
  gene symbol: FAM134A
  hgvsc: ENST00000430297.2:c.1576G>A
  hgvsp: ENSP00000395249.2:p.Asp526Asn
  variant of: http://identifiers.org/hgnc/28450
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1133
  bin: 6.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7647
  bin: 4.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 13952
  bin: 3.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 7.75e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 8.25e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 3108
  bin: 2.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 3371
  bin: 5.25e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 1983
  bin: 5.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5322
  bin: 4.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 9.75e1
  variant carriers: 128
genotype depth: GenotypeDepth
  all individuals: 596
  bin: 6.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 9896
  bin: 3.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 12311
  bin: 2.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 7.25e1
  variant carriers: 13
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7588
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15274
  bin: 9.75e1
  variant carriers: 289
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 222
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3207
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4598
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2241
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5053
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3866
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Asp526Asn
num of homozygotes: 4
population: South Asian
population: Other
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD

http://identifiers.org/exac.variant/2-220047298-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 220047298
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 220047298
    reference: chr 2
allele count: 1
allele frequency: 8.251233559417133e-6
allele num: 121194
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000144567
  ensembl protein: ENSP00000395249
  ensembl transcript: ENST00000430297
  gene symbol: FAM134A
  hgvsc: ENST00000430297.2:c.1579A>C
  hgvsp: ENSP00000395249.2:p.Ile527Leu
  variant of: http://identifiers.org/hgnc/28450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000144567
  ensembl protein: ENSP00000411247
  ensembl transcript: ENST00000420189
  gene symbol: FAM134A
  hgvsc: ENST00000420189.1:c.557A>C
  hgvsp: ENSP00000411247.1:p.Ile187Leu
  variant of: http://identifiers.org/hgnc/28450
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000144567
  ensembl protein: ENSP00000273048
  ensembl transcript: ENST00000273048
  gene symbol: FAM134A
  hgvsc: ENST00000273048.2:c.*954A>C
  variant of: http://identifiers.org/hgnc/28450
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1985
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3370
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3125
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14006
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7671
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12369
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9919
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5337
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1122
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4616
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 3.75e1
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genotype quality: GenotypeQuality
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  bin: 4.25e1
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genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
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genotype quality: GenotypeQuality
  all individuals: 22
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 237
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7622
  bin: 6.75e1
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genotype quality: GenotypeQuality
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  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 5.25e1
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genotype quality: GenotypeQuality
  all individuals: 2254
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3217
  bin: 7.25e1
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genotype quality: GenotypeQuality
  all individuals: 5076
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genotype quality: GenotypeQuality
  all individuals: 18443
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15058
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Ile527Leu
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: Other
population: South Asian
population: European (Non-Finnish)
population: African
reference allele: A
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: ClippingRankSum

2-220047302-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 220047302
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 220047302
    reference: chr 2
allele count: 1
allele frequency: 8.255456856982466e-6
allele num: 121132
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000144567
  ensembl protein: ENSP00000395249
  ensembl transcript: ENST00000430297
  gene symbol: FAM134A
  hgvsc: ENST00000430297.2:c.1583A>G
  hgvsp: ENSP00000395249.2:p.His528Arg
  variant of: http://identifiers.org/hgnc/28450
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000144567
  ensembl protein: ENSP00000273048
  ensembl transcript: ENST00000273048
  gene symbol: FAM134A
  hgvsc: ENST00000273048.2:c.*958A>G
  variant of: http://identifiers.org/hgnc/28450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000144567
  ensembl protein: ENSP00000411247
  ensembl transcript: ENST00000420189
  gene symbol: FAM134A
  hgvsc: ENST00000420189.1:c.561A>G
  hgvsp: ENSP00000411247.1:p.His188Arg
  variant of: http://identifiers.org/hgnc/28450
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3104
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3370
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12325
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1985
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9921
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1122
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7668
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5337
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13992
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7621
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15055
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 2.75e1
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genotype quality: GenotypeQuality
  all individuals: 3875
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genotype quality: GenotypeQuality
  all individuals: 3215
  bin: 7.25e1
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genotype quality: GenotypeQuality
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  bin: 1.75e1
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genotype quality: GenotypeQuality
  all individuals: 29
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18367
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 294
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 5.25e1
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genotype quality: GenotypeQuality
  all individuals: 4616
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5079
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2251
  bin: 8.75e1
  variant carriers: 0
hgvs: p.His528Arg
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
reference allele: A
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum

2-220047307-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 220047307
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 220047307
    reference: chr 2
allele count: 2
allele frequency: 1.65180046250413e-5
allele num: 121080
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000144567
  ensembl protein: ENSP00000273048
  ensembl transcript: ENST00000273048
  gene symbol: FAM134A
  hgvsc: ENST00000273048.2:c.*963C>T
  variant of: http://identifiers.org/hgnc/28450
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000144567
  ensembl protein: ENSP00000395249
  ensembl transcript: ENST00000430297
  gene symbol: FAM134A
  hgvsc: ENST00000430297.2:c.1588C>T
  hgvsp: ENST00000430297.2:c.1588C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000144567
  ensembl protein: ENSP00000411247
  ensembl transcript: ENST00000420189
  gene symbol: FAM134A
  hgvsc: ENST00000420189.1:c.566C>T
  hgvsp: ENST00000420189.1:c.566C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28450
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7666
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12273
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1985
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3072
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13975
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3369
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9917
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5339
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1121
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4611
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3212
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7598
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 359
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18282
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3874
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15053
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5074
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2249
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Leu530Leu
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
population: African
population: European (Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff

2-220047314-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 220047314
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 220047314
    reference: chr 2
allele count: 1
allele frequency: 8.267742575567167e-6
allele num: 120952
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000144567
  ensembl protein: ENSP00000395249
  ensembl transcript: ENST00000430297
  gene symbol: FAM134A
  hgvsc: ENST00000430297.2:c.1595A>G
  hgvsp: ENSP00000395249.2:p.Gln532Arg
  variant of: http://identifiers.org/hgnc/28450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000144567
  ensembl protein: ENSP00000411247
  ensembl transcript: ENST00000420189
  gene symbol: FAM134A
  hgvsc: ENST00000420189.1:c.573A>G
  hgvsp: ENSP00000411247.1:p.Gln192Arg
  variant of: http://identifiers.org/hgnc/28450
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000144567
  ensembl protein: ENSP00000273048
  ensembl transcript: ENST00000273048
  gene symbol: FAM134A
  hgvsc: ENST00000273048.2:c.*970A>G
  variant of: http://identifiers.org/hgnc/28450
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2978
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1119
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9905
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7662
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12110
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5335
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3368
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13933
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1986
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18019
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7559
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3872
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 116
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3202
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4609
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5060
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 580
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 133
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2246
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15049
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Gln532Arg
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
reference allele: A
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum

2-220047323-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 220047323
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 220047323
    reference: chr 2
allele count: 7
allele frequency: 5.792592102214425e-5
allele num: 120844
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000144567
  ensembl protein: ENSP00000395249
  ensembl transcript: ENST00000430297
  gene symbol: FAM134A
  hgvsc: ENST00000430297.2:c.1604A>G
  hgvsp: ENSP00000395249.2:p.Gln535Arg
  variant of: http://identifiers.org/hgnc/28450
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000144567
  ensembl protein: ENSP00000273048
  ensembl transcript: ENST00000273048
  gene symbol: FAM134A
  hgvsc: ENST00000273048.2:c.*979A>G
  variant of: http://identifiers.org/hgnc/28450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000144567
  ensembl protein: ENSP00000411247
  ensembl transcript: ENST00000420189
  gene symbol: FAM134A
  hgvsc: ENST00000420189.1:c.582A>G
  hgvsp: ENSP00000411247.1:p.Gln195Arg
  variant of: http://identifiers.org/hgnc/28450
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3367
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2914
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9862
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11884
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 810
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13800
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7652
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1984
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5334
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1119
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4602
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 199
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 179
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7482
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 105
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 896
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5035
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3176
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2246
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3868
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15040
  bin: 9.75e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 17737
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Gln535Arg
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
population: East Asian
reference allele: A
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: QD

2-220047331-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 220047331
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 220047331
    reference: chr 2
allele count: 1
allele frequency: 8.293799555452344e-6
allele num: 120572
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000144567
  ensembl protein: ENSP00000395249
  ensembl transcript: ENST00000430297
  gene symbol: FAM134A
  hgvsc: ENST00000430297.2:c.1612C>T
  hgvsp: ENSP00000395249.2:p.Gln538Ter
  variant of: http://identifiers.org/hgnc/28450
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000144567
  ensembl protein: ENSP00000273048
  ensembl transcript: ENST00000273048
  gene symbol: FAM134A
  hgvsc: ENST00000273048.2:c.*987C>T
  variant of: http://identifiers.org/hgnc/28450
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000144567
  ensembl protein: ENSP00000411247
  ensembl transcript: ENST00000420189
  gene symbol: FAM134A
  hgvsc: ENST00000420189.1:c.590C>T
  hgvsp: ENSP00000411247.1:p.Gln198Ter
  variant of: http://identifiers.org/hgnc/28450
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11326
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2924
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1226
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9728
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13389
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7623
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 938
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1986
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1120
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3367
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5329
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4587
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3865
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 390
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 196
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 231
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 100
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1431
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3118
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15033
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4999
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16453
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 231
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7221
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 428
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2243
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Gln538Ter
num of homozygotes: 0
population: South Asian
population: Latino
population: Other
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD

2-220047335-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 220047335
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 220047335
    reference: chr 2
allele count: 1
allele frequency: 8.297240337863626e-6
allele num: 120522
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000144567
  ensembl protein: ENSP00000411247
  ensembl transcript: ENST00000420189
  gene symbol: FAM134A
  hgvsc: ENST00000420189.1:c.594C>T
  hgvsp: ENSP00000411247.1:p.Ala199Val
  variant of: http://identifiers.org/hgnc/28450
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000144567
  ensembl protein: ENSP00000273048
  ensembl transcript: ENST00000273048
  gene symbol: FAM134A
  hgvsc: ENST00000273048.2:c.*991C>T
  variant of: http://identifiers.org/hgnc/28450
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000144567
  ensembl protein: ENSP00000395249
  ensembl transcript: ENST00000430297
  gene symbol: FAM134A
  hgvsc: ENST00000430297.2:c.1616C>T
  hgvsp: ENSP00000395249.2:p.Ala539Val
  variant of: http://identifiers.org/hgnc/28450
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1986
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5326
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7610
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13302
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1257
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9707
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2990
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 963
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11311
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1120
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3367
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2238
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15031
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3104
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1501
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7190
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 228
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16731
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4986
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3865
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 446
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4578
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 95
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 402
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Ala539Val
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
reference allele: C
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum

2-220047336-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 220047336
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 220047336
    reference: chr 2
allele count: 1
allele frequency: 8.303854649328218e-6
allele num: 120426
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000144567
  ensembl protein: ENSP00000273048
  ensembl transcript: ENST00000273048
  gene symbol: FAM134A
  hgvsc: ENST00000273048.2:c.*992C>T
  variant of: http://identifiers.org/hgnc/28450
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000144567
  ensembl protein: ENSP00000395249
  ensembl transcript: ENST00000430297
  gene symbol: FAM134A
  hgvsc: ENST00000430297.2:c.1617C>T
  hgvsp: ENST00000430297.2:c.1617C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000144567
  ensembl protein: ENSP00000411247
  ensembl transcript: ENST00000420189
  gene symbol: FAM134A
  hgvsc: ENST00000420189.1:c.595C>T
  hgvsp: ENST00000420189.1:c.595C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28450
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5323
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9679
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13217
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7600
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1986
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3366
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3035
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1276
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1120
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1059
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11238
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 154
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7158
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 260
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 494
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16454
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4974
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 439
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4574
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2237
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 97
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1546
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3082
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3861
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 119
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Ala539Ala
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: MQ

2-220047337-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 220047337
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 220047337
    reference: chr 2
allele count: 1
allele frequency: 8.304820117596252e-6
allele num: 120412
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000144567
  ensembl protein: ENSP00000273048
  ensembl transcript: ENST00000273048
  gene symbol: FAM134A
  hgvsc: ENST00000273048.2:c.*993G>A
  variant of: http://identifiers.org/hgnc/28450
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000144567
  ensembl protein: ENSP00000395249
  ensembl transcript: ENST00000430297
  gene symbol: FAM134A
  hgvsc: ENST00000430297.2:c.1618G>A
  hgvsp: ENSP00000395249.2:p.Val540Met
  variant of: http://identifiers.org/hgnc/28450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000144567
  ensembl protein: ENSP00000411247
  ensembl transcript: ENST00000420189
  gene symbol: FAM134A
  hgvsc: ENST00000420189.1:c.596G>A
  hgvsp: ENSP00000411247.1:p.Val200Met
  variant of: http://identifiers.org/hgnc/28450
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5322
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3061
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1044
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13197
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1120
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11252
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9667
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1281
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7597
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3368
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1986
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4980
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1569
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2239
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3087
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16596
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15027
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 252
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3861
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 479
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 439
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7149
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Val540Met
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: Other
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum

2-220047341-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 220047341
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 220047341
    reference: chr 2
allele count: 0
allele frequency: 0.0e0
allele num: 120090
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000144567
  ensembl protein: ENSP00000411247
  ensembl transcript: ENST00000420189
  gene symbol: FAM134A
  hgvsc: ENST00000420189.1:c.600C>G
  hgvsp: ENSP00000411247.1:p.Ala201Gly
  variant of: http://identifiers.org/hgnc/28450
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000144567
  ensembl protein: ENSP00000395249
  ensembl transcript: ENST00000430297
  gene symbol: FAM134A
  hgvsc: ENST00000430297.2:c.1622C>G
  hgvsp: ENSP00000395249.2:p.Ala541Gly
  variant of: http://identifiers.org/hgnc/28450
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000144567
  ensembl protein: ENSP00000273048
  ensembl transcript: ENST00000273048
  gene symbol: FAM134A
  hgvsc: ENST00000273048.2:c.*997C>G
  variant of: http://identifiers.org/hgnc/28450
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 1987
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1119
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5321
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1345
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3363
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7581
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9611
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1150
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12958
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11044
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3279
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7050
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1668
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15017
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2230
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3860
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4567
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 127
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 612
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 495
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 153
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4937
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 113
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 352
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 151
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16130
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Ala541Gly
num of homozygotes: 0
population: East Asian
population: South Asian
population: Other
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD

2-220047345-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 220047345
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 220047345
    reference: chr 2
allele count: 1
allele frequency: 8.364840900726069e-6
allele num: 119548
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000144567
  ensembl protein: ENSP00000411247
  ensembl transcript: ENST00000420189
  gene symbol: FAM134A
  hgvsc: ENST00000420189.1:c.604G>A
  hgvsp: ENST00000420189.1:c.604G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28450
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000144567
  ensembl protein: ENSP00000395249
  ensembl transcript: ENST00000430297
  gene symbol: FAM134A
  hgvsc: ENST00000430297.2:c.1626G>A
  hgvsp: ENST00000430297.2:c.1626G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28450
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000144567
  ensembl protein: ENSP00000273048
  ensembl transcript: ENST00000273048
  gene symbol: FAM134A
  hgvsc: ENST00000273048.2:c.*1001G>A
  variant of: http://identifiers.org/hgnc/28450
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5314
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3431
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12724
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1987
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1522
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1115
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7534
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3357
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9504
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10972
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1120
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 321
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 287
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2228
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15020
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 186
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 479
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 514
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 677
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6836
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1688
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2993
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 256
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 100
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4901
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15478
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3856
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 199
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Glu542Glu
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
population: Latino
population: European (Finnish)
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum

2-220047345-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 220047345
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 220047345
    reference: chr 2
allele count: 17
allele frequency: 1.422022953123431e-4
allele num: 119548
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000144567
  ensembl protein: ENSP00000411247
  ensembl transcript: ENST00000420189
  gene symbol: FAM134A
  hgvsc: ENST00000420189.1:c.604G>T
  hgvsp: ENSP00000411247.1:p.Glu202Asp
  variant of: http://identifiers.org/hgnc/28450
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000144567
  ensembl protein: ENSP00000395249
  ensembl transcript: ENST00000430297
  gene symbol: FAM134A
  hgvsc: ENST00000430297.2:c.1626G>T
  hgvsp: ENSP00000395249.2:p.Glu542Asp
  variant of: http://identifiers.org/hgnc/28450
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000144567
  ensembl protein: ENSP00000273048
  ensembl transcript: ENST00000273048
  gene symbol: FAM134A
  hgvsc: ENST00000273048.2:c.*1001G>T
  variant of: http://identifiers.org/hgnc/28450
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9504
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3431
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3357
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1522
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1987
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1115
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7534
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5314
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10972
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12724
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1120
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4901
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 479
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 186
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 100
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6836
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4555
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2993
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 514
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 287
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 321
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 199
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 677
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1688
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3856
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2228
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15478
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 256
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Glu542Asp
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
reference allele: G
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum

2-220047352-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 220047352
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 220047352
    reference: chr 2
allele count: 1
allele frequency: 8.41779184484326e-6
allele num: 118796
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000144567
  ensembl protein: ENSP00000395249
  ensembl transcript: ENST00000430297
  gene symbol: FAM134A
  hgvsc: ENST00000430297.2:c.*1G>A
  variant of: http://identifiers.org/hgnc/28450
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000144567
  ensembl protein: ENSP00000411247
  ensembl transcript: ENST00000420189
  gene symbol: FAM134A
  hgvsc: ENST00000420189.1:c.*1G>A
  variant of: http://identifiers.org/hgnc/28450
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000144567
  ensembl protein: ENSP00000273048
  ensembl transcript: ENST00000273048
  gene symbol: FAM134A
  hgvsc: ENST00000273048.2:c.*1008G>A
  variant of: http://identifiers.org/hgnc/28450
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1126
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1987
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5306
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7499
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1117
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 809
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9444
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12589
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10781
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1813
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3379
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3359
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 731
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 154
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 201
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 209
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2960
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 307
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 282
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2222
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 163
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1752
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 522
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6714
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 560
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 288
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4536
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15141
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4868
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3850
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 219
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD

2-220047358-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 220047358
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 220047358
    reference: chr 2
allele count: 3
allele frequency: 2.511889610824569e-5
allele num: 119432
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000144567
  ensembl protein: ENSP00000395249
  ensembl transcript: ENST00000430297
  gene symbol: FAM134A
  hgvsc: ENST00000430297.2:c.*7C>T
  variant of: http://identifiers.org/hgnc/28450
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000144567
  ensembl protein: ENSP00000411247
  ensembl transcript: ENST00000420189
  gene symbol: FAM134A
  hgvsc: ENST00000420189.1:c.*7C>T
  variant of: http://identifiers.org/hgnc/28450
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000144567
  ensembl protein: ENSP00000273048
  ensembl transcript: ENST00000273048
  gene symbol: FAM134A
  hgvsc: ENST00000273048.2:c.*1014C>T
  variant of: http://identifiers.org/hgnc/28450
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5357
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11030
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3380
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3131
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1999
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7545
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1861
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 778
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12791
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9535
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1119
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 224
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16212
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1855
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3891
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3015
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2236
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6880
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 103
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 282
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 450
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4594
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 491
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15096
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 4931
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
population: East Asian
reference allele: C
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: ReadPosRankSum

2-220047359-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 220047359
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 220047359
    reference: chr 2
allele count: 22
allele frequency: 1.842330045053344e-4
allele num: 119414
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000144567
  ensembl protein: ENSP00000273048
  ensembl transcript: ENST00000273048
  gene symbol: FAM134A
  hgvsc: ENST00000273048.2:c.*1015G>A
  variant of: http://identifiers.org/hgnc/28450
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000144567
  ensembl protein: ENSP00000411247
  ensembl transcript: ENST00000420189
  gene symbol: FAM134A
  hgvsc: ENST00000420189.1:c.*8G>A
  variant of: http://identifiers.org/hgnc/28450
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000144567
  ensembl protein: ENSP00000395249
  ensembl transcript: ENST00000430297
  gene symbol: FAM134A
  hgvsc: ENST00000430297.2:c.*8G>A
  variant of: http://identifiers.org/hgnc/28450
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10917
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12737
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 807
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3106
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5354
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 9534
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 6.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1118
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1979
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3380
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1995
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 725
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7544
  bin: 4.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 140
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3001
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16049
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4588
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 487
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 544
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4925
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 297
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 215
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 127
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15094
  bin: 9.75e1
  variant carriers: 22
genotype quality: GenotypeQuality
  all individuals: 6854
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1938
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3891
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
reference allele: G
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff

2-220047363-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 220047363
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 220047363
    reference: chr 2
allele count: 1
allele frequency: 8.378437253883405e-6
allele num: 119354
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000144567
  ensembl protein: ENSP00000411247
  ensembl transcript: ENST00000420189
  gene symbol: FAM134A
  hgvsc: ENST00000420189.1:c.*12A>G
  variant of: http://identifiers.org/hgnc/28450
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000144567
  ensembl protein: ENSP00000395249
  ensembl transcript: ENST00000430297
  gene symbol: FAM134A
  hgvsc: ENST00000430297.2:c.*12A>G
  variant of: http://identifiers.org/hgnc/28450
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000144567
  ensembl protein: ENSP00000273048
  ensembl transcript: ENST00000273048
  gene symbol: FAM134A
  hgvsc: ENST00000273048.2:c.*1019A>G
  variant of: http://identifiers.org/hgnc/28450
canonical: true
consequence: 3' UTR
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12644
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2222
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3380
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2952
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 887
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10751
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9520
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5358
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7542
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 859
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1993
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1114
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4913
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15075
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 368
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2179
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 178
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2989
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 569
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15841
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 638
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 100
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4576
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6808
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3889
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
population: African
population: Other
reference allele: A
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP

2-220047366-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 220047366
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 220047366
    reference: chr 2
allele count: 4
allele frequency: 3.35418518456404e-5
allele num: 119254
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000144567
  ensembl protein: ENSP00000411247
  ensembl transcript: ENST00000420189
  gene symbol: FAM134A
  hgvsc: ENST00000420189.1:c.*15A>T
  variant of: http://identifiers.org/hgnc/28450
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000144567
  ensembl protein: ENSP00000273048
  ensembl transcript: ENST00000273048
  gene symbol: FAM134A
  hgvsc: ENST00000273048.2:c.*1022A>T
  variant of: http://identifiers.org/hgnc/28450
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000144567
  ensembl protein: ENSP00000395249
  ensembl transcript: ENST00000430297
  gene symbol: FAM134A
  hgvsc: ENST00000430297.2:c.*15A>T
  variant of: http://identifiers.org/hgnc/28450
canonical: true
consequence: 3' UTR
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 1991
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1202
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7542
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 911
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10394
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9508
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2561
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5355
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2762
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1114
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12512
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3377
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 123
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 136
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6720
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 813
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 676
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 166
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15065
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 498
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 101
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 109
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2232
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3887
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2974
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2430
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4576
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4897
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
population: African
population: Other
reference allele: A
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum

2-220047369-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 220047369
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 220047369
    reference: chr 2
allele count: 78
allele frequency: 6.544063359957044e-4
allele num: 119192
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000144567
  ensembl protein: ENSP00000411247
  ensembl transcript: ENST00000420189
  gene symbol: FAM134A
  hgvsc: ENST00000420189.1:c.*18G>T
  variant of: http://identifiers.org/hgnc/28450
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000144567
  ensembl protein: ENSP00000273048
  ensembl transcript: ENST00000273048
  gene symbol: FAM134A
  hgvsc: ENST00000273048.2:c.*1025G>T
  variant of: http://identifiers.org/hgnc/28450
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000144567
  ensembl protein: ENSP00000395249
  ensembl transcript: ENST00000430297
  gene symbol: FAM134A
  hgvsc: ENST00000430297.2:c.*18G>T
  variant of: http://identifiers.org/hgnc/28450
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1394
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2709
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5358
  bin: 4.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 934
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 9505
  bin: 3.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 2731
  bin: 2.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 8.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 3377
  bin: 5.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10183
  bin: 2.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 12414
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1990
  bin: 5.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 584
  bin: 6.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1114
  bin: 6.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 7538
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 7.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 97
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 14970
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 736
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 137
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 142
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 544
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6645
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2557
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4572
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 916
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15085
  bin: 9.75e1
  variant carriers: 79
genotype quality: GenotypeQuality
  all individuals: 3883
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2232
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 105
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2960
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 1
population: South Asian
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: G
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum

2-220047370-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 220047370
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 220047370
    reference: chr 2
allele count: 79
allele frequency: 6.626960825434107e-4
allele num: 119210
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000144567
  ensembl protein: ENSP00000273048
  ensembl transcript: ENST00000273048
  gene symbol: FAM134A
  hgvsc: ENST00000273048.2:c.*1026A>T
  variant of: http://identifiers.org/hgnc/28450
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000144567
  ensembl protein: ENSP00000395249
  ensembl transcript: ENST00000430297
  gene symbol: FAM134A
  hgvsc: ENST00000430297.2:c.*19A>T
  variant of: http://identifiers.org/hgnc/28450
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000144567
  ensembl protein: ENSP00000411247
  ensembl transcript: ENST00000420189
  gene symbol: FAM134A
  hgvsc: ENST00000420189.1:c.*19A>T
  variant of: http://identifiers.org/hgnc/28450
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5358
  bin: 4.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 8.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 7538
  bin: 4.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 3374
  bin: 5.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 10023
  bin: 2.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2817
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 958
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1580
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12329
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1991
  bin: 5.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 1117
  bin: 6.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 2684
  bin: 2.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 9491
  bin: 3.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 15087
  bin: 9.75e1
  variant carriers: 79
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2631
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 151
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 134
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 104
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 149
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14645
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 993
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 629
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 127
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4880
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6617
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 794
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2232
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2969
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3883
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 1
population: Latino
population: East Asian
population: South Asian
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: QD

2-220047384-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 220047384
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 220047384
    reference: chr 2
allele count: 193
allele frequency: 1.629847317930009e-3
allele num: 118416
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000144567
  ensembl protein: ENSP00000411247
  ensembl transcript: ENST00000420189
  gene symbol: FAM134A
  hgvsc: ENST00000420189.1:c.*33T>C
  variant of: http://identifiers.org/hgnc/28450
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000144567
  ensembl protein: ENSP00000395249
  ensembl transcript: ENST00000430297
  gene symbol: FAM134A
  hgvsc: ENST00000430297.2:c.*33T>C
  variant of: http://identifiers.org/hgnc/28450
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000144567
  ensembl protein: ENSP00000273048
  ensembl transcript: ENST00000273048
  gene symbol: FAM134A
  hgvsc: ENST00000273048.2:c.*1040T>C
  variant of: http://identifiers.org/hgnc/28450
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9171
  bin: 3.75e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 1108
  bin: 6.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1986
  bin: 5.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 7961
  bin: 2.75e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 10951
  bin: 3.25e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 7484
  bin: 4.25e1
  variant carriers: 29
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3644
  bin: 1.75e1
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 3356
  bin: 5.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3212
  bin: 1.25e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 1223
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3853
  bin: 2.25e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5330
  bin: 4.75e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 251
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15130
  bin: 9.75e1
  variant carriers: 187
genotype quality: GenotypeQuality
  all individuals: 3843
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1166
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2732
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1794
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 5736
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 651
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4502
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 209
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1154
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 176
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4737
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 345
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1720
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2215
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2753
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 892
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 4
population: African
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
population: European (Finnish)
population: East Asian
reference allele: T
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP

2-220047393-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 220047393
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 220047393
    reference: chr 2
allele count: 64786
allele frequency: 5.504426583289436e-1
allele num: 117698
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000144567
  ensembl protein: ENSP00000273048
  ensembl transcript: ENST00000273048
  gene symbol: FAM134A
  hgvsc: ENST00000273048.2:c.*1049C>T
  variant of: http://identifiers.org/hgnc/28450
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000144567
  ensembl protein: ENSP00000411247
  ensembl transcript: ENST00000420189
  gene symbol: FAM134A
  hgvsc: ENST00000420189.1:c.*42C>T
  variant of: http://identifiers.org/hgnc/28450
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000144567
  ensembl protein: ENSP00000395249
  ensembl transcript: ENST00000430297
  gene symbol: FAM134A
  hgvsc: ENST00000430297.2:c.*42C>T
  variant of: http://identifiers.org/hgnc/28450
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 7.25e1
  variant carriers: 336
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 2.5e0
  variant carriers: 48
genotype depth: GenotypeDepth
  all individuals: 8821
  bin: 3.75e1
  variant carriers: 6881
genotype depth: GenotypeDepth
  all individuals: 4888
  bin: 2.25e1
  variant carriers: 3940
genotype depth: GenotypeDepth
  all individuals: 1319
  bin: 7.5e0
  variant carriers: 860
genotype depth: GenotypeDepth
  all individuals: 1792
  bin: 5.75e1
  variant carriers: 1590
genotype depth: GenotypeDepth
  all individuals: 8125
  bin: 2.75e1
  variant carriers: 5596
genotype depth: GenotypeDepth
  all individuals: 3162
  bin: 5.25e1
  variant carriers: 2781
genotype depth: GenotypeDepth
  all individuals: 4438
  bin: 1.75e1
  variant carriers: 3318
genotype depth: GenotypeDepth
  all individuals: 3344
  bin: 1.25e1
  variant carriers: 2487
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 7.75e1
  variant carriers: 202
genotype depth: GenotypeDepth
  all individuals: 9697
  bin: 3.25e1
  variant carriers: 6802
genotype depth: GenotypeDepth
  all individuals: 4965
  bin: 4.75e1
  variant carriers: 4185
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 9.75e1
  variant carriers: 261
genotype depth: GenotypeDepth
  all individuals: 612
  bin: 6.75e1
  variant carriers: 575
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 9.25e1
  variant carriers: 68
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 8.25e1
  variant carriers: 138
genotype depth: GenotypeDepth
  all individuals: 1089
  bin: 6.25e1
  variant carriers: 993
genotype depth: GenotypeDepth
  all individuals: 7157
  bin: 4.25e1
  variant carriers: 5870
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.75e1
  variant carriers: 103
genotype quality: GenotypeQuality
  all individuals: 575
  bin: 5.75e1
  variant carriers: 442
genotype quality: GenotypeQuality
  all individuals: 148
  bin: 7.5e0
  variant carriers: 60
genotype quality: GenotypeQuality
  all individuals: 274
  bin: 2.5e0
  variant carriers: 38
genotype quality: GenotypeQuality
  all individuals: 538
  bin: 2.75e1
  variant carriers: 228
genotype quality: GenotypeQuality
  all individuals: 1004
  bin: 2.25e1
  variant carriers: 288
genotype quality: GenotypeQuality
  all individuals: 245
  bin: 1.75e1
  variant carriers: 158
genotype quality: GenotypeQuality
  all individuals: 2239
  bin: 6.75e1
  variant carriers: 817
genotype quality: GenotypeQuality
  all individuals: 638
  bin: 4.25e1
  variant carriers: 371
genotype quality: GenotypeQuality
  all individuals: 2010
  bin: 7.75e1
  variant carriers: 926
genotype quality: GenotypeQuality
  all individuals: 932
  bin: 5.25e1
  variant carriers: 749
genotype quality: GenotypeQuality
  all individuals: 164
  bin: 1.25e1
  variant carriers: 83
genotype quality: GenotypeQuality
  all individuals: 1000
  bin: 4.75e1
  variant carriers: 662
genotype quality: GenotypeQuality
  all individuals: 1066
  bin: 8.75e1
  variant carriers: 655
genotype quality: GenotypeQuality
  all individuals: 957
  bin: 3.25e1
  variant carriers: 474
genotype quality: GenotypeQuality
  all individuals: 1798
  bin: 9.25e1
  variant carriers: 1090
genotype quality: GenotypeQuality
  all individuals: 3674
  bin: 6.25e1
  variant carriers: 754
genotype quality: GenotypeQuality
  all individuals: 39158
  bin: 9.75e1
  variant carriers: 37090
genotype quality: GenotypeQuality
  all individuals: 1033
  bin: 3.75e1
  variant carriers: 550
genotype quality: GenotypeQuality
  all individuals: 1230
  bin: 7.25e1
  variant carriers: 518
num of homozygotes: 18849
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
population: Other
population: South Asian
population: European (Finnish)
reference allele: C
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: QD

2-220047396-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 220047396
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 220047396
    reference: chr 2
allele count: 1
allele frequency: 8.592837011067574e-6
allele num: 116376
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000144567
  ensembl protein: ENSP00000273048
  ensembl transcript: ENST00000273048
  gene symbol: FAM134A
  hgvsc: ENST00000273048.2:c.*1052G>T
  variant of: http://identifiers.org/hgnc/28450
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000144567
  ensembl protein: ENSP00000395249
  ensembl transcript: ENST00000430297
  gene symbol: FAM134A
  hgvsc: ENST00000430297.2:c.*45G>T
  variant of: http://identifiers.org/hgnc/28450
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000144567
  ensembl protein: ENSP00000411247
  ensembl transcript: ENST00000420189
  gene symbol: FAM134A
  hgvsc: ENST00000420189.1:c.*45G>T
  variant of: http://identifiers.org/hgnc/28450
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4675
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7684
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11638
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2037
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1308
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6175
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11651
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6145
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2655
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4729
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 424
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4713
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1785
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4072
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1226
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 541
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6144
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 332
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 333
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2932
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3195
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2544
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2810
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2791
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1549
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1513
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12183
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8693
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: G
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: FS

2-220047398-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 220047398
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 220047398
    reference: chr 2
allele count: 2
allele frequency: 1.722741916033559e-5
allele num: 116094
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000144567
  ensembl protein: ENSP00000273048
  ensembl transcript: ENST00000273048
  gene symbol: FAM134A
  hgvsc: ENST00000273048.2:c.*1054T>C
  variant of: http://identifiers.org/hgnc/28450
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000144567
  ensembl protein: ENSP00000411247
  ensembl transcript: ENST00000420189
  gene symbol: FAM134A
  hgvsc: ENST00000420189.1:c.*47T>C
  variant of: http://identifiers.org/hgnc/28450
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000144567
  ensembl protein: ENSP00000395249
  ensembl transcript: ENST00000430297
  gene symbol: FAM134A
  hgvsc: ENST00000430297.2:c.*47T>C
  variant of: http://identifiers.org/hgnc/28450
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 661
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7286
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2152
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6103
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4650
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11092
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7637
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2650
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11094
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4722
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1308
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3113
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8684
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 2822
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1851
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3044
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3062
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10765
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2826
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4057
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1786
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 657
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1655
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 104
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 364
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1568
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 433
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2781
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4683
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6004
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP

2-220071667-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 220071667
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 220071667
    reference: chr 2
allele count: 1
allele frequency: 9.723275577076405e-6
allele num: 102846
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000400760
  ensembl transcript: ENST00000436556
  gene symbol: ZFAND2B
  hgvsc: ENST00000436556.1:c.-21-22C>G
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000489197
  gene symbol: ZFAND2B
  hgvsc: ENST00000489197.1:n.66C>G
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386847
  ensembl transcript: ENST00000409412
  gene symbol: ZFAND2B
  hgvsc: ENST00000409412.1:c.-18-25C>G
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000388773
  ensembl transcript: ENST00000448496
  gene symbol: ZFAND2B
  hgvsc: ENST00000448496.1:c.-43C>G
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386898
  ensembl transcript: ENST00000409336
  gene symbol: ZFAND2B
  hgvsc: ENST00000409336.1:c.-21-22C>G
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000387312
  ensembl transcript: ENST00000409319
  gene symbol: ZFAND2B
  hgvsc: ENST00000409319.1:c.-43C>G
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386399
  ensembl transcript: ENST00000409594
  gene symbol: ZFAND2B
  hgvsc: ENST00000409594.1:c.-43C>G
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000486734
  gene symbol: ZFAND2B
  hgvsc: ENST00000486734.1:n.35-25C>G
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000289528
  ensembl transcript: ENST00000289528
  gene symbol: ZFAND2B
  hgvsc: ENST00000289528.5:c.-43C>G
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000468301
  gene symbol: ZFAND2B
  hgvsc: ENST00000468301.1:n.98C>G
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386824
  ensembl transcript: ENST00000409206
  gene symbol: ZFAND2B
  hgvsc: ENST00000409206.1:c.-18-25C>G
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000409931
  ensembl transcript: ENST00000422255
  gene symbol: ZFAND2B
  hgvsc: ENST00000422255.1:c.-21-22C>G
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000476713
  gene symbol: ZFAND2B
  hgvsc: ENST00000476713.1:n.40-25C>G
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386370
  ensembl transcript: ENST00000409217
  gene symbol: ZFAND2B
  hgvsc: ENST00000409217.1:c.-43C>G
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000387179
  ensembl transcript: ENST00000409097
  gene symbol: ZFAND2B
  hgvsc: ENST00000409097.1:c.-18-25C>G
  variant of: http://identifiers.org/hgnc/25206
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18042
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8230
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 931
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9818
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12008
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: QD

http://identifiers.org/exac.variant/2-220071674-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 220071674
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 220071674
    reference: chr 2
allele count: 2
allele frequency: 1.941370607649e-5
allele num: 103020
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000289528
  ensembl transcript: ENST00000289528
  gene symbol: ZFAND2B
  hgvsc: ENST00000289528.5:c.-36C>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386824
  ensembl transcript: ENST00000409206
  gene symbol: ZFAND2B
  hgvsc: ENST00000409206.1:c.-18-18C>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000476713
  gene symbol: ZFAND2B
  hgvsc: ENST00000476713.1:n.40-18C>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386370
  ensembl transcript: ENST00000409217
  gene symbol: ZFAND2B
  hgvsc: ENST00000409217.1:c.-36C>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000387179
  ensembl transcript: ENST00000409097
  gene symbol: ZFAND2B
  hgvsc: ENST00000409097.1:c.-18-18C>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000388773
  ensembl transcript: ENST00000448496
  gene symbol: ZFAND2B
  hgvsc: ENST00000448496.1:c.-36C>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000468301
  gene symbol: ZFAND2B
  hgvsc: ENST00000468301.1:n.105C>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386399
  ensembl transcript: ENST00000409594
  gene symbol: ZFAND2B
  hgvsc: ENST00000409594.1:c.-36C>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386898
  ensembl transcript: ENST00000409336
  gene symbol: ZFAND2B
  hgvsc: ENST00000409336.1:c.-21-15C>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000387312
  ensembl transcript: ENST00000409319
  gene symbol: ZFAND2B
  hgvsc: ENST00000409319.1:c.-36C>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000400760
  ensembl transcript: ENST00000436556
  gene symbol: ZFAND2B
  hgvsc: ENST00000436556.1:c.-21-15C>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000486734
  gene symbol: ZFAND2B
  hgvsc: ENST00000486734.1:n.35-18C>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386847
  ensembl transcript: ENST00000409412
  gene symbol: ZFAND2B
  hgvsc: ENST00000409412.1:c.-18-18C>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000409931
  ensembl transcript: ENST00000422255
  gene symbol: ZFAND2B
  hgvsc: ENST00000422255.1:c.-21-15C>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000489197
  gene symbol: ZFAND2B
  hgvsc: ENST00000489197.1:n.73C>A
  variant of: http://identifiers.org/hgnc/25206
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10334
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 511
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2766
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7988
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10856
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 863
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Other
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
reference allele: C
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum

2-220071678-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 220071678
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 220071678
    reference: chr 2
allele count: 1
allele frequency: 9.701202949165697e-6
allele num: 103080
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000409931
  ensembl transcript: ENST00000422255
  gene symbol: ZFAND2B
  hgvsc: ENST00000422255.1:c.-21-11G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000387179
  ensembl transcript: ENST00000409097
  gene symbol: ZFAND2B
  hgvsc: ENST00000409097.1:c.-18-14G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386399
  ensembl transcript: ENST00000409594
  gene symbol: ZFAND2B
  hgvsc: ENST00000409594.1:c.-32G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000489197
  gene symbol: ZFAND2B
  hgvsc: ENST00000489197.1:n.77G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386370
  ensembl transcript: ENST00000409217
  gene symbol: ZFAND2B
  hgvsc: ENST00000409217.1:c.-32G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000486734
  gene symbol: ZFAND2B
  hgvsc: ENST00000486734.1:n.35-14G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000289528
  ensembl transcript: ENST00000289528
  gene symbol: ZFAND2B
  hgvsc: ENST00000289528.5:c.-32G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000400760
  ensembl transcript: ENST00000436556
  gene symbol: ZFAND2B
  hgvsc: ENST00000436556.1:c.-21-11G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000387312
  ensembl transcript: ENST00000409319
  gene symbol: ZFAND2B
  hgvsc: ENST00000409319.1:c.-32G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000468301
  gene symbol: ZFAND2B
  hgvsc: ENST00000468301.1:n.109G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386898
  ensembl transcript: ENST00000409336
  gene symbol: ZFAND2B
  hgvsc: ENST00000409336.1:c.-21-11G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000388773
  ensembl transcript: ENST00000448496
  gene symbol: ZFAND2B
  hgvsc: ENST00000448496.1:c.-32G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386824
  ensembl transcript: ENST00000409206
  gene symbol: ZFAND2B
  hgvsc: ENST00000409206.1:c.-18-14G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386847
  ensembl transcript: ENST00000409412
  gene symbol: ZFAND2B
  hgvsc: ENST00000409412.1:c.-18-14G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000476713
  gene symbol: ZFAND2B
  hgvsc: ENST00000476713.1:n.40-14G>A
  variant of: http://identifiers.org/hgnc/25206
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23774
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 801
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8057
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9796
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3758
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: African
population: Latino
population: Other
population: European (Finnish)
reference allele: G
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

2-220071697-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 220071697
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 220071697
    reference: chr 2
allele count: 3
allele frequency: 2.902701447480455e-5
allele num: 103352
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000387179
  ensembl transcript: ENST00000409097
  gene symbol: ZFAND2B
  hgvsc: ENST00000409097.1:c.-13G>T
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000289528
  ensembl transcript: ENST00000289528
  gene symbol: ZFAND2B
  hgvsc: ENST00000289528.5:c.-13G>T
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000400760
  ensembl transcript: ENST00000436556
  gene symbol: ZFAND2B
  hgvsc: ENST00000436556.1:c.-13G>T
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000486734
  gene symbol: ZFAND2B
  hgvsc: ENST00000486734.1:n.40G>T
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386370
  ensembl transcript: ENST00000409217
  gene symbol: ZFAND2B
  hgvsc: ENST00000409217.1:c.-13G>T
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000388773
  ensembl transcript: ENST00000448496
  gene symbol: ZFAND2B
  hgvsc: ENST00000448496.1:c.-13G>T
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000411334
  ensembl transcript: ENST00000444522
  gene symbol: ZFAND2B
  hgvsc: ENST00000444522.2:c.-13G>T
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000387312
  ensembl transcript: ENST00000409319
  gene symbol: ZFAND2B
  hgvsc: ENST00000409319.1:c.-13G>T
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386847
  ensembl transcript: ENST00000409412
  gene symbol: ZFAND2B
  hgvsc: ENST00000409412.1:c.-13G>T
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386399
  ensembl transcript: ENST00000409594
  gene symbol: ZFAND2B
  hgvsc: ENST00000409594.1:c.-13G>T
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386898
  ensembl transcript: ENST00000409336
  gene symbol: ZFAND2B
  hgvsc: ENST00000409336.1:c.-13G>T
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000476713
  gene symbol: ZFAND2B
  hgvsc: ENST00000476713.1:n.45G>T
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000489197
  gene symbol: ZFAND2B
  hgvsc: ENST00000489197.1:n.96G>T
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000468301
  gene symbol: ZFAND2B
  hgvsc: ENST00000468301.1:n.128G>T
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386824
  ensembl transcript: ENST00000409206
  gene symbol: ZFAND2B
  hgvsc: ENST00000409206.1:c.-13G>T
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000409931
  ensembl transcript: ENST00000422255
  gene symbol: ZFAND2B
  hgvsc: ENST00000422255.1:c.-13G>T
  variant of: http://identifiers.org/hgnc/25206
canonical: true
consequence: 5' UTR
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 726
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27384
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11847
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
population: Latino
reference allele: G
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: ReadPosRankSum

2-220071698-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 220071698
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 220071698
    reference: chr 2
allele count: 2
allele frequency: 1.936108422071636e-5
allele num: 103300
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000388773
  ensembl transcript: ENST00000448496
  gene symbol: ZFAND2B
  hgvsc: ENST00000448496.1:c.-12C>T
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000468301
  gene symbol: ZFAND2B
  hgvsc: ENST00000468301.1:n.129C>T
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386370
  ensembl transcript: ENST00000409217
  gene symbol: ZFAND2B
  hgvsc: ENST00000409217.1:c.-12C>T
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386898
  ensembl transcript: ENST00000409336
  gene symbol: ZFAND2B
  hgvsc: ENST00000409336.1:c.-12C>T
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000387179
  ensembl transcript: ENST00000409097
  gene symbol: ZFAND2B
  hgvsc: ENST00000409097.1:c.-12C>T
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000289528
  ensembl transcript: ENST00000289528
  gene symbol: ZFAND2B
  hgvsc: ENST00000289528.5:c.-12C>T
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386824
  ensembl transcript: ENST00000409206
  gene symbol: ZFAND2B
  hgvsc: ENST00000409206.1:c.-12C>T
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000489197
  gene symbol: ZFAND2B
  hgvsc: ENST00000489197.1:n.97C>T
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000411334
  ensembl transcript: ENST00000444522
  gene symbol: ZFAND2B
  hgvsc: ENST00000444522.2:c.-12C>T
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000476713
  gene symbol: ZFAND2B
  hgvsc: ENST00000476713.1:n.46C>T
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386399
  ensembl transcript: ENST00000409594
  gene symbol: ZFAND2B
  hgvsc: ENST00000409594.1:c.-12C>T
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000409931
  ensembl transcript: ENST00000422255
  gene symbol: ZFAND2B
  hgvsc: ENST00000422255.1:c.-12C>T
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386847
  ensembl transcript: ENST00000409412
  gene symbol: ZFAND2B
  hgvsc: ENST00000409412.1:c.-12C>T
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000400760
  ensembl transcript: ENST00000436556
  gene symbol: ZFAND2B
  hgvsc: ENST00000436556.1:c.-12C>T
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000486734
  gene symbol: ZFAND2B
  hgvsc: ENST00000486734.1:n.41C>T
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000387312
  ensembl transcript: ENST00000409319
  gene symbol: ZFAND2B
  hgvsc: ENST00000409319.1:c.-12C>T
  variant of: http://identifiers.org/hgnc/25206
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1861
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 727
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27430
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6720
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2923
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum

2-220071700-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 220071700
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 220071700
    reference: chr 2
allele count: 1
allele frequency: 9.673425166382914e-6
allele num: 103376
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386847
  ensembl transcript: ENST00000409412
  gene symbol: ZFAND2B
  hgvsc: ENST00000409412.1:c.-10C>T
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386898
  ensembl transcript: ENST00000409336
  gene symbol: ZFAND2B
  hgvsc: ENST00000409336.1:c.-10C>T
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000476713
  gene symbol: ZFAND2B
  hgvsc: ENST00000476713.1:n.48C>T
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386399
  ensembl transcript: ENST00000409594
  gene symbol: ZFAND2B
  hgvsc: ENST00000409594.1:c.-10C>T
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000289528
  ensembl transcript: ENST00000289528
  gene symbol: ZFAND2B
  hgvsc: ENST00000289528.5:c.-10C>T
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000400760
  ensembl transcript: ENST00000436556
  gene symbol: ZFAND2B
  hgvsc: ENST00000436556.1:c.-10C>T
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000411334
  ensembl transcript: ENST00000444522
  gene symbol: ZFAND2B
  hgvsc: ENST00000444522.2:c.-10C>T
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000387312
  ensembl transcript: ENST00000409319
  gene symbol: ZFAND2B
  hgvsc: ENST00000409319.1:c.-10C>T
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000388773
  ensembl transcript: ENST00000448496
  gene symbol: ZFAND2B
  hgvsc: ENST00000448496.1:c.-10C>T
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386824
  ensembl transcript: ENST00000409206
  gene symbol: ZFAND2B
  hgvsc: ENST00000409206.1:c.-10C>T
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000409931
  ensembl transcript: ENST00000422255
  gene symbol: ZFAND2B
  hgvsc: ENST00000422255.1:c.-10C>T
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000387179
  ensembl transcript: ENST00000409097
  gene symbol: ZFAND2B
  hgvsc: ENST00000409097.1:c.-10C>T
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000489197
  gene symbol: ZFAND2B
  hgvsc: ENST00000489197.1:n.99C>T
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386370
  ensembl transcript: ENST00000409217
  gene symbol: ZFAND2B
  hgvsc: ENST00000409217.1:c.-10C>T
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000486734
  gene symbol: ZFAND2B
  hgvsc: ENST00000486734.1:n.43C>T
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000468301
  gene symbol: ZFAND2B
  hgvsc: ENST00000468301.1:n.131C>T
  variant of: http://identifiers.org/hgnc/25206
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27660
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 717
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8010
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12133
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
population: Other
population: African
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ

http://identifiers.org/exac.variant/2-220071700-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 220071700
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 220071700
    reference: chr 2
allele count: 2
allele frequency: 1.934685033276583e-5
allele num: 103376
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386847
  ensembl transcript: ENST00000409412
  gene symbol: ZFAND2B
  hgvsc: ENST00000409412.1:c.-10C>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000387179
  ensembl transcript: ENST00000409097
  gene symbol: ZFAND2B
  hgvsc: ENST00000409097.1:c.-10C>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386898
  ensembl transcript: ENST00000409336
  gene symbol: ZFAND2B
  hgvsc: ENST00000409336.1:c.-10C>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000476713
  gene symbol: ZFAND2B
  hgvsc: ENST00000476713.1:n.48C>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000489197
  gene symbol: ZFAND2B
  hgvsc: ENST00000489197.1:n.99C>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000486734
  gene symbol: ZFAND2B
  hgvsc: ENST00000486734.1:n.43C>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000468301
  gene symbol: ZFAND2B
  hgvsc: ENST00000468301.1:n.131C>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000400760
  ensembl transcript: ENST00000436556
  gene symbol: ZFAND2B
  hgvsc: ENST00000436556.1:c.-10C>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000289528
  ensembl transcript: ENST00000289528
  gene symbol: ZFAND2B
  hgvsc: ENST00000289528.5:c.-10C>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000387312
  ensembl transcript: ENST00000409319
  gene symbol: ZFAND2B
  hgvsc: ENST00000409319.1:c.-10C>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000388773
  ensembl transcript: ENST00000448496
  gene symbol: ZFAND2B
  hgvsc: ENST00000448496.1:c.-10C>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000411334
  ensembl transcript: ENST00000444522
  gene symbol: ZFAND2B
  hgvsc: ENST00000444522.2:c.-10C>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386824
  ensembl transcript: ENST00000409206
  gene symbol: ZFAND2B
  hgvsc: ENST00000409206.1:c.-10C>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386399
  ensembl transcript: ENST00000409594
  gene symbol: ZFAND2B
  hgvsc: ENST00000409594.1:c.-10C>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386370
  ensembl transcript: ENST00000409217
  gene symbol: ZFAND2B
  hgvsc: ENST00000409217.1:c.-10C>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000409931
  ensembl transcript: ENST00000422255
  gene symbol: ZFAND2B
  hgvsc: ENST00000422255.1:c.-10C>A
  variant of: http://identifiers.org/hgnc/25206
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8010
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27660
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1710
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 717
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2901
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Latino
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: C
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum

2-220071709-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 220071709
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 220071709
    reference: chr 2
allele count: 1
allele frequency: 9.71722864639005e-6
allele num: 102910
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000387179
  ensembl transcript: ENST00000409097
  gene symbol: ZFAND2B
  hgvsc: ENST00000409097.1:c.-1G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386370
  ensembl transcript: ENST00000409217
  gene symbol: ZFAND2B
  hgvsc: ENST00000409217.1:c.-1G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386898
  ensembl transcript: ENST00000409336
  gene symbol: ZFAND2B
  hgvsc: ENST00000409336.1:c.-1G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386824
  ensembl transcript: ENST00000409206
  gene symbol: ZFAND2B
  hgvsc: ENST00000409206.1:c.-1G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000400760
  ensembl transcript: ENST00000436556
  gene symbol: ZFAND2B
  hgvsc: ENST00000436556.1:c.-1G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386399
  ensembl transcript: ENST00000409594
  gene symbol: ZFAND2B
  hgvsc: ENST00000409594.1:c.-1G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000289528
  ensembl transcript: ENST00000289528
  gene symbol: ZFAND2B
  hgvsc: ENST00000289528.5:c.-1G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386847
  ensembl transcript: ENST00000409412
  gene symbol: ZFAND2B
  hgvsc: ENST00000409412.1:c.-1G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000387312
  ensembl transcript: ENST00000409319
  gene symbol: ZFAND2B
  hgvsc: ENST00000409319.1:c.-1G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000409931
  ensembl transcript: ENST00000422255
  gene symbol: ZFAND2B
  hgvsc: ENST00000422255.1:c.-1G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000388773
  ensembl transcript: ENST00000448496
  gene symbol: ZFAND2B
  hgvsc: ENST00000448496.1:c.-1G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000468301
  gene symbol: ZFAND2B
  hgvsc: ENST00000468301.1:n.140G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000489197
  gene symbol: ZFAND2B
  hgvsc: ENST00000489197.1:n.108G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000476713
  gene symbol: ZFAND2B
  hgvsc: ENST00000476713.1:n.57G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000411334
  ensembl transcript: ENST00000444522
  gene symbol: ZFAND2B
  hgvsc: ENST00000444522.2:c.-1G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000486734
  gene symbol: ZFAND2B
  hgvsc: ENST00000486734.1:n.52G>A
  variant of: http://identifiers.org/hgnc/25206
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 729
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum

2-220071721-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 220071721
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 220071721
    reference: chr 2
allele count: 9
allele frequency: 9.00756635573882e-5
allele num: 99916
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386370
  ensembl transcript: ENST00000409217
  gene symbol: ZFAND2B
  hgvsc: ENST00000409217.1:c.12G>C
  hgvsp: ENST00000409217.1:c.12G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000409931
  ensembl transcript: ENST00000422255
  gene symbol: ZFAND2B
  hgvsc: ENST00000422255.1:c.12G>C
  hgvsp: ENST00000422255.1:c.12G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000289528
  ensembl transcript: ENST00000289528
  gene symbol: ZFAND2B
  hgvsc: ENST00000289528.5:c.12G>C
  hgvsp: ENST00000289528.5:c.12G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000388773
  ensembl transcript: ENST00000448496
  gene symbol: ZFAND2B
  hgvsc: ENST00000448496.1:c.12G>C
  hgvsp: ENST00000448496.1:c.12G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386399
  ensembl transcript: ENST00000409594
  gene symbol: ZFAND2B
  hgvsc: ENST00000409594.1:c.12G>C
  hgvsp: ENST00000409594.1:c.12G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000468301
  gene symbol: ZFAND2B
  hgvsc: ENST00000468301.1:n.152G>C
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386847
  ensembl transcript: ENST00000409412
  gene symbol: ZFAND2B
  hgvsc: ENST00000409412.1:c.12G>C
  hgvsp: ENST00000409412.1:c.12G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000400760
  ensembl transcript: ENST00000436556
  gene symbol: ZFAND2B
  hgvsc: ENST00000436556.1:c.12G>C
  hgvsp: ENST00000436556.1:c.12G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386898
  ensembl transcript: ENST00000409336
  gene symbol: ZFAND2B
  hgvsc: ENST00000409336.1:c.12G>C
  hgvsp: ENST00000409336.1:c.12G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000387179
  ensembl transcript: ENST00000409097
  gene symbol: ZFAND2B
  hgvsc: ENST00000409097.1:c.12G>C
  hgvsp: ENST00000409097.1:c.12G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000476713
  gene symbol: ZFAND2B
  hgvsc: ENST00000476713.1:n.69G>C
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000411334
  ensembl transcript: ENST00000444522
  gene symbol: ZFAND2B
  hgvsc: ENST00000444522.2:c.12G>C
  hgvsp: ENST00000444522.2:c.12G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386824
  ensembl transcript: ENST00000409206
  gene symbol: ZFAND2B
  hgvsc: ENST00000409206.1:c.12G>C
  hgvsp: ENST00000409206.1:c.12G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000486734
  gene symbol: ZFAND2B
  hgvsc: ENST00000486734.1:n.64G>C
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000387312
  ensembl transcript: ENST00000409319
  gene symbol: ZFAND2B
  hgvsc: ENST00000409319.1:c.12G>C
  hgvsp: ENST00000409319.1:c.12G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000489197
  gene symbol: ZFAND2B
  hgvsc: ENST00000489197.1:n.120G>C
  variant of: http://identifiers.org/hgnc/25206
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9560
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23099
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro4Pro
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
population: Other
population: East Asian
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: VQSLOD

2-220071725-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 220071725
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 220071725
    reference: chr 2
allele count: 1
allele frequency: 1.006745192791704e-5
allele num: 99330
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000411334
  ensembl transcript: ENST00000444522
  gene symbol: ZFAND2B
  hgvsc: ENST00000444522.2:c.16C>G
  hgvsp: ENSP00000411334.2:p.Leu6Val
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000387312
  ensembl transcript: ENST00000409319
  gene symbol: ZFAND2B
  hgvsc: ENST00000409319.1:c.16C>G
  hgvsp: ENSP00000387312.1:p.Leu6Val
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386898
  ensembl transcript: ENST00000409336
  gene symbol: ZFAND2B
  hgvsc: ENST00000409336.1:c.16C>G
  hgvsp: ENSP00000386898.1:p.Leu6Val
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000400760
  ensembl transcript: ENST00000436556
  gene symbol: ZFAND2B
  hgvsc: ENST00000436556.1:c.16C>G
  hgvsp: ENSP00000400760.1:p.Leu6Val
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000468301
  gene symbol: ZFAND2B
  hgvsc: ENST00000468301.1:n.156C>G
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386399
  ensembl transcript: ENST00000409594
  gene symbol: ZFAND2B
  hgvsc: ENST00000409594.1:c.16C>G
  hgvsp: ENSP00000386399.1:p.Leu6Val
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386370
  ensembl transcript: ENST00000409217
  gene symbol: ZFAND2B
  hgvsc: ENST00000409217.1:c.16C>G
  hgvsp: ENSP00000386370.1:p.Leu6Val
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386824
  ensembl transcript: ENST00000409206
  gene symbol: ZFAND2B
  hgvsc: ENST00000409206.1:c.16C>G
  hgvsp: ENSP00000386824.1:p.Leu6Val
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000476713
  gene symbol: ZFAND2B
  hgvsc: ENST00000476713.1:n.73C>G
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000289528
  ensembl transcript: ENST00000289528
  gene symbol: ZFAND2B
  hgvsc: ENST00000289528.5:c.16C>G
  hgvsp: ENSP00000289528.5:p.Leu6Val
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386847
  ensembl transcript: ENST00000409412
  gene symbol: ZFAND2B
  hgvsc: ENST00000409412.1:c.16C>G
  hgvsp: ENSP00000386847.1:p.Leu6Val
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000388773
  ensembl transcript: ENST00000448496
  gene symbol: ZFAND2B
  hgvsc: ENST00000448496.1:c.16C>G
  hgvsp: ENSP00000388773.1:p.Leu6Val
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000387179
  ensembl transcript: ENST00000409097
  gene symbol: ZFAND2B
  hgvsc: ENST00000409097.1:c.16C>G
  hgvsp: ENSP00000387179.1:p.Leu6Val
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000489197
  gene symbol: ZFAND2B
  hgvsc: ENST00000489197.1:n.124C>G
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000486734
  gene symbol: ZFAND2B
  hgvsc: ENST00000486734.1:n.68C>G
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000409931
  ensembl transcript: ENST00000422255
  gene symbol: ZFAND2B
  hgvsc: ENST00000422255.1:c.16C>G
  hgvsp: ENSP00000409931.1:p.Leu6Val
  variant of: http://identifiers.org/hgnc/25206
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22453
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu6Val
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum

2-220071728-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 220071728
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 220071728
    reference: chr 2
allele count: 1
allele frequency: 1.01909789454375e-5
allele num: 98126
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000387179
  ensembl transcript: ENST00000409097
  gene symbol: ZFAND2B
  hgvsc: ENST00000409097.1:c.19G>A
  hgvsp: ENSP00000387179.1:p.Gly7Ser
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386898
  ensembl transcript: ENST00000409336
  gene symbol: ZFAND2B
  hgvsc: ENST00000409336.1:c.19G>A
  hgvsp: ENSP00000386898.1:p.Gly7Ser
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000400760
  ensembl transcript: ENST00000436556
  gene symbol: ZFAND2B
  hgvsc: ENST00000436556.1:c.19G>A
  hgvsp: ENSP00000400760.1:p.Gly7Ser
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000476713
  gene symbol: ZFAND2B
  hgvsc: ENST00000476713.1:n.76G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000387312
  ensembl transcript: ENST00000409319
  gene symbol: ZFAND2B
  hgvsc: ENST00000409319.1:c.19G>A
  hgvsp: ENSP00000387312.1:p.Gly7Ser
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000489197
  gene symbol: ZFAND2B
  hgvsc: ENST00000489197.1:n.127G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386399
  ensembl transcript: ENST00000409594
  gene symbol: ZFAND2B
  hgvsc: ENST00000409594.1:c.19G>A
  hgvsp: ENSP00000386399.1:p.Gly7Ser
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386847
  ensembl transcript: ENST00000409412
  gene symbol: ZFAND2B
  hgvsc: ENST00000409412.1:c.19G>A
  hgvsp: ENSP00000386847.1:p.Gly7Ser
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000289528
  ensembl transcript: ENST00000289528
  gene symbol: ZFAND2B
  hgvsc: ENST00000289528.5:c.19G>A
  hgvsp: ENSP00000289528.5:p.Gly7Ser
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000409931
  ensembl transcript: ENST00000422255
  gene symbol: ZFAND2B
  hgvsc: ENST00000422255.1:c.19G>A
  hgvsp: ENSP00000409931.1:p.Gly7Ser
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386824
  ensembl transcript: ENST00000409206
  gene symbol: ZFAND2B
  hgvsc: ENST00000409206.1:c.19G>A
  hgvsp: ENSP00000386824.1:p.Gly7Ser
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000388773
  ensembl transcript: ENST00000448496
  gene symbol: ZFAND2B
  hgvsc: ENST00000448496.1:c.19G>A
  hgvsp: ENSP00000388773.1:p.Gly7Ser
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000486734
  gene symbol: ZFAND2B
  hgvsc: ENST00000486734.1:n.71G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386370
  ensembl transcript: ENST00000409217
  gene symbol: ZFAND2B
  hgvsc: ENST00000409217.1:c.19G>A
  hgvsp: ENSP00000386370.1:p.Gly7Ser
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000411334
  ensembl transcript: ENST00000444522
  gene symbol: ZFAND2B
  hgvsc: ENST00000444522.2:c.19G>A
  hgvsp: ENSP00000411334.2:p.Gly7Ser
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000468301
  gene symbol: ZFAND2B
  hgvsc: ENST00000468301.1:n.159G>A
  variant of: http://identifiers.org/hgnc/25206
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 495
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10304
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2130
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12271
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2788
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly7Ser
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum

2-220071742-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 220071742
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 220071742
    reference: chr 2
allele count: 2
allele frequency: 2.150583883524377e-5
allele num: 92998
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386847
  ensembl transcript: ENST00000409412
  gene symbol: ZFAND2B
  hgvsc: ENST00000409412.1:c.33G>A
  hgvsp: ENST00000409412.1:c.33G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386824
  ensembl transcript: ENST00000409206
  gene symbol: ZFAND2B
  hgvsc: ENST00000409206.1:c.33G>A
  hgvsp: ENST00000409206.1:c.33G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000387179
  ensembl transcript: ENST00000409097
  gene symbol: ZFAND2B
  hgvsc: ENST00000409097.1:c.33G>A
  hgvsp: ENST00000409097.1:c.33G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000411334
  ensembl transcript: ENST00000444522
  gene symbol: ZFAND2B
  hgvsc: ENST00000444522.2:c.33G>A
  hgvsp: ENST00000444522.2:c.33G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000489197
  gene symbol: ZFAND2B
  hgvsc: ENST00000489197.1:n.141G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000388773
  ensembl transcript: ENST00000448496
  gene symbol: ZFAND2B
  hgvsc: ENST00000448496.1:c.33G>A
  hgvsp: ENST00000448496.1:c.33G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000289528
  ensembl transcript: ENST00000289528
  gene symbol: ZFAND2B
  hgvsc: ENST00000289528.5:c.33G>A
  hgvsp: ENST00000289528.5:c.33G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000387312
  ensembl transcript: ENST00000409319
  gene symbol: ZFAND2B
  hgvsc: ENST00000409319.1:c.33G>A
  hgvsp: ENST00000409319.1:c.33G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000486734
  gene symbol: ZFAND2B
  hgvsc: ENST00000486734.1:n.85G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000476713
  gene symbol: ZFAND2B
  hgvsc: ENST00000476713.1:n.90G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000400760
  ensembl transcript: ENST00000436556
  gene symbol: ZFAND2B
  hgvsc: ENST00000436556.1:c.33G>A
  hgvsp: ENST00000436556.1:c.33G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386898
  ensembl transcript: ENST00000409336
  gene symbol: ZFAND2B
  hgvsc: ENST00000409336.1:c.33G>A
  hgvsp: ENST00000409336.1:c.33G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000468301
  gene symbol: ZFAND2B
  hgvsc: ENST00000468301.1:n.173G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386370
  ensembl transcript: ENST00000409217
  gene symbol: ZFAND2B
  hgvsc: ENST00000409217.1:c.33G>A
  hgvsp: ENST00000409217.1:c.33G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000409931
  ensembl transcript: ENST00000422255
  gene symbol: ZFAND2B
  hgvsc: ENST00000422255.1:c.33G>A
  hgvsp: ENST00000422255.1:c.33G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386399
  ensembl transcript: ENST00000409594
  gene symbol: ZFAND2B
  hgvsc: ENST00000409594.1:c.33G>A
  hgvsp: ENST00000409594.1:c.33G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25206
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15290
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2696
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser11Ser
num of homozygotes: 0
population: South Asian
population: Other
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD

2-220071750-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 220071750
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 220071750
    reference: chr 2
allele count: 1
allele frequency: 1.122158134524317e-5
allele num: 89114
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000387179
  ensembl transcript: ENST00000409097
  gene symbol: ZFAND2B
  hgvsc: ENST00000409097.1:c.41G>A
  hgvsp: ENSP00000387179.1:p.Ser14Asn
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000289528
  ensembl transcript: ENST00000289528
  gene symbol: ZFAND2B
  hgvsc: ENST00000289528.5:c.41G>A
  hgvsp: ENSP00000289528.5:p.Ser14Asn
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000476713
  gene symbol: ZFAND2B
  hgvsc: ENST00000476713.1:n.98G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000411334
  ensembl transcript: ENST00000444522
  gene symbol: ZFAND2B
  hgvsc: ENST00000444522.2:c.41G>A
  hgvsp: ENSP00000411334.2:p.Ser14Asn
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386898
  ensembl transcript: ENST00000409336
  gene symbol: ZFAND2B
  hgvsc: ENST00000409336.1:c.41G>A
  hgvsp: ENSP00000386898.1:p.Ser14Asn
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000409931
  ensembl transcript: ENST00000422255
  gene symbol: ZFAND2B
  hgvsc: ENST00000422255.1:c.41G>A
  hgvsp: ENSP00000409931.1:p.Ser14Asn
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386399
  ensembl transcript: ENST00000409594
  gene symbol: ZFAND2B
  hgvsc: ENST00000409594.1:c.41G>A
  hgvsp: ENSP00000386399.1:p.Ser14Asn
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000486734
  gene symbol: ZFAND2B
  hgvsc: ENST00000486734.1:n.93G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000387312
  ensembl transcript: ENST00000409319
  gene symbol: ZFAND2B
  hgvsc: ENST00000409319.1:c.41G>A
  hgvsp: ENSP00000387312.1:p.Ser14Asn
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000388773
  ensembl transcript: ENST00000448496
  gene symbol: ZFAND2B
  hgvsc: ENST00000448496.1:c.41G>A
  hgvsp: ENSP00000388773.1:p.Ser14Asn
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000468301
  gene symbol: ZFAND2B
  hgvsc: ENST00000468301.1:n.181G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000400760
  ensembl transcript: ENST00000436556
  gene symbol: ZFAND2B
  hgvsc: ENST00000436556.1:c.41G>A
  hgvsp: ENSP00000400760.1:p.Ser14Asn
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386370
  ensembl transcript: ENST00000409217
  gene symbol: ZFAND2B
  hgvsc: ENST00000409217.1:c.41G>A
  hgvsp: ENSP00000386370.1:p.Ser14Asn
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000489197
  gene symbol: ZFAND2B
  hgvsc: ENST00000489197.1:n.149G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386847
  ensembl transcript: ENST00000409412
  gene symbol: ZFAND2B
  hgvsc: ENST00000409412.1:c.41G>A
  hgvsp: ENSP00000386847.1:p.Ser14Asn
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386824
  ensembl transcript: ENST00000409206
  gene symbol: ZFAND2B
  hgvsc: ENST00000409206.1:c.41G>A
  hgvsp: ENSP00000386824.1:p.Ser14Asn
  variant of: http://identifiers.org/hgnc/25206
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1882
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser14Asn
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
population: East Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD

2-220071757-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 220071757
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 220071757
    reference: chr 2
allele count: 1
allele frequency: 1.152711176687569e-5
allele num: 86752
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000387179
  ensembl transcript: ENST00000409097
  gene symbol: ZFAND2B
  hgvsc: ENST00000409097.1:c.48G>C
  hgvsp: ENSP00000387179.1:p.Gln16His
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000387312
  ensembl transcript: ENST00000409319
  gene symbol: ZFAND2B
  hgvsc: ENST00000409319.1:c.48G>C
  hgvsp: ENSP00000387312.1:p.Gln16His
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000476713
  gene symbol: ZFAND2B
  hgvsc: ENST00000476713.1:n.105G>C
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000411334
  ensembl transcript: ENST00000444522
  gene symbol: ZFAND2B
  hgvsc: ENST00000444522.2:c.48G>C
  hgvsp: ENSP00000411334.2:p.Gln16His
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000489197
  gene symbol: ZFAND2B
  hgvsc: ENST00000489197.1:n.156G>C
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000388773
  ensembl transcript: ENST00000448496
  gene symbol: ZFAND2B
  hgvsc: ENST00000448496.1:c.48G>C
  hgvsp: ENSP00000388773.1:p.Gln16His
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386847
  ensembl transcript: ENST00000409412
  gene symbol: ZFAND2B
  hgvsc: ENST00000409412.1:c.48G>C
  hgvsp: ENSP00000386847.1:p.Gln16His
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000486734
  gene symbol: ZFAND2B
  hgvsc: ENST00000486734.1:n.100G>C
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386898
  ensembl transcript: ENST00000409336
  gene symbol: ZFAND2B
  hgvsc: ENST00000409336.1:c.48G>C
  hgvsp: ENSP00000386898.1:p.Gln16His
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000289528
  ensembl transcript: ENST00000289528
  gene symbol: ZFAND2B
  hgvsc: ENST00000289528.5:c.48G>C
  hgvsp: ENSP00000289528.5:p.Gln16His
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000400760
  ensembl transcript: ENST00000436556
  gene symbol: ZFAND2B
  hgvsc: ENST00000436556.1:c.48G>C
  hgvsp: ENSP00000400760.1:p.Gln16His
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386399
  ensembl transcript: ENST00000409594
  gene symbol: ZFAND2B
  hgvsc: ENST00000409594.1:c.48G>C
  hgvsp: ENSP00000386399.1:p.Gln16His
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000409931
  ensembl transcript: ENST00000422255
  gene symbol: ZFAND2B
  hgvsc: ENST00000422255.1:c.48G>C
  hgvsp: ENSP00000409931.1:p.Gln16His
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386370
  ensembl transcript: ENST00000409217
  gene symbol: ZFAND2B
  hgvsc: ENST00000409217.1:c.48G>C
  hgvsp: ENSP00000386370.1:p.Gln16His
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386824
  ensembl transcript: ENST00000409206
  gene symbol: ZFAND2B
  hgvsc: ENST00000409206.1:c.48G>C
  hgvsp: ENSP00000386824.1:p.Gln16His
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000468301
  gene symbol: ZFAND2B
  hgvsc: ENST00000468301.1:n.188G>C
  variant of: http://identifiers.org/hgnc/25206
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8859
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3679
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln16His
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS

http://identifiers.org/exac.variant/2-220071758-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 220071758
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 220071758
    reference: chr 2
allele count: 1
allele frequency: 1.157219894924434e-5
allele num: 86414
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000409931
  ensembl transcript: ENST00000422255
  gene symbol: ZFAND2B
  hgvsc: ENST00000422255.1:c.49C>A
  hgvsp: ENSP00000409931.1:p.Arg17Ser
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000400760
  ensembl transcript: ENST00000436556
  gene symbol: ZFAND2B
  hgvsc: ENST00000436556.1:c.49C>A
  hgvsp: ENSP00000400760.1:p.Arg17Ser
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386847
  ensembl transcript: ENST00000409412
  gene symbol: ZFAND2B
  hgvsc: ENST00000409412.1:c.49C>A
  hgvsp: ENSP00000386847.1:p.Arg17Ser
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000387179
  ensembl transcript: ENST00000409097
  gene symbol: ZFAND2B
  hgvsc: ENST00000409097.1:c.49C>A
  hgvsp: ENSP00000387179.1:p.Arg17Ser
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000387312
  ensembl transcript: ENST00000409319
  gene symbol: ZFAND2B
  hgvsc: ENST00000409319.1:c.49C>A
  hgvsp: ENSP00000387312.1:p.Arg17Ser
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000289528
  ensembl transcript: ENST00000289528
  gene symbol: ZFAND2B
  hgvsc: ENST00000289528.5:c.49C>A
  hgvsp: ENSP00000289528.5:p.Arg17Ser
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386399
  ensembl transcript: ENST00000409594
  gene symbol: ZFAND2B
  hgvsc: ENST00000409594.1:c.49C>A
  hgvsp: ENSP00000386399.1:p.Arg17Ser
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000468301
  gene symbol: ZFAND2B
  hgvsc: ENST00000468301.1:n.189C>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386824
  ensembl transcript: ENST00000409206
  gene symbol: ZFAND2B
  hgvsc: ENST00000409206.1:c.49C>A
  hgvsp: ENSP00000386824.1:p.Arg17Ser
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000388773
  ensembl transcript: ENST00000448496
  gene symbol: ZFAND2B
  hgvsc: ENST00000448496.1:c.49C>A
  hgvsp: ENSP00000388773.1:p.Arg17Ser
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386898
  ensembl transcript: ENST00000409336
  gene symbol: ZFAND2B
  hgvsc: ENST00000409336.1:c.49C>A
  hgvsp: ENSP00000386898.1:p.Arg17Ser
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000476713
  gene symbol: ZFAND2B
  hgvsc: ENST00000476713.1:n.106C>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000486734
  gene symbol: ZFAND2B
  hgvsc: ENST00000486734.1:n.101C>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386370
  ensembl transcript: ENST00000409217
  gene symbol: ZFAND2B
  hgvsc: ENST00000409217.1:c.49C>A
  hgvsp: ENSP00000386370.1:p.Arg17Ser
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000411334
  ensembl transcript: ENST00000444522
  gene symbol: ZFAND2B
  hgvsc: ENST00000444522.2:c.49C>A
  hgvsp: ENSP00000411334.2:p.Arg17Ser
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000489197
  gene symbol: ZFAND2B
  hgvsc: ENST00000489197.1:n.157C>A
  variant of: http://identifiers.org/hgnc/25206
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8845
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19967
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3625
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14487
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8025
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg17Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: Other
reference allele: C
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: MQRankSum

http://identifiers.org/exac.variant/2-220071760-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 220071760
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 220071760
    reference: chr 2
allele count: 1
allele frequency: 1.164578189779662e-5
allele num: 85868
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000409931
  ensembl transcript: ENST00000422255
  gene symbol: ZFAND2B
  hgvsc: ENST00000422255.1:c.51C>A
  hgvsp: ENST00000422255.1:c.51C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000468301
  gene symbol: ZFAND2B
  hgvsc: ENST00000468301.1:n.191C>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386847
  ensembl transcript: ENST00000409412
  gene symbol: ZFAND2B
  hgvsc: ENST00000409412.1:c.51C>A
  hgvsp: ENST00000409412.1:c.51C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000289528
  ensembl transcript: ENST00000289528
  gene symbol: ZFAND2B
  hgvsc: ENST00000289528.5:c.51C>A
  hgvsp: ENST00000289528.5:c.51C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000411334
  ensembl transcript: ENST00000444522
  gene symbol: ZFAND2B
  hgvsc: ENST00000444522.2:c.51C>A
  hgvsp: ENST00000444522.2:c.51C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000387179
  ensembl transcript: ENST00000409097
  gene symbol: ZFAND2B
  hgvsc: ENST00000409097.1:c.51C>A
  hgvsp: ENST00000409097.1:c.51C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000489197
  gene symbol: ZFAND2B
  hgvsc: ENST00000489197.1:n.159C>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386824
  ensembl transcript: ENST00000409206
  gene symbol: ZFAND2B
  hgvsc: ENST00000409206.1:c.51C>A
  hgvsp: ENST00000409206.1:c.51C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000400760
  ensembl transcript: ENST00000436556
  gene symbol: ZFAND2B
  hgvsc: ENST00000436556.1:c.51C>A
  hgvsp: ENST00000436556.1:c.51C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386898
  ensembl transcript: ENST00000409336
  gene symbol: ZFAND2B
  hgvsc: ENST00000409336.1:c.51C>A
  hgvsp: ENST00000409336.1:c.51C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000388773
  ensembl transcript: ENST00000448496
  gene symbol: ZFAND2B
  hgvsc: ENST00000448496.1:c.51C>A
  hgvsp: ENST00000448496.1:c.51C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000476713
  gene symbol: ZFAND2B
  hgvsc: ENST00000476713.1:n.108C>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000387312
  ensembl transcript: ENST00000409319
  gene symbol: ZFAND2B
  hgvsc: ENST00000409319.1:c.51C>A
  hgvsp: ENST00000409319.1:c.51C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000486734
  gene symbol: ZFAND2B
  hgvsc: ENST00000486734.1:n.103C>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386399
  ensembl transcript: ENST00000409594
  gene symbol: ZFAND2B
  hgvsc: ENST00000409594.1:c.51C>A
  hgvsp: ENST00000409594.1:c.51C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386370
  ensembl transcript: ENST00000409217
  gene symbol: ZFAND2B
  hgvsc: ENST00000409217.1:c.51C>A
  hgvsp: ENST00000409217.1:c.51C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25206
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7819
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3606
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8241
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2492
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg17Arg
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
population: Other
reference allele: C
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: ClippingRankSum

2-220071767-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 220071767
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 220071767
    reference: chr 2
allele count: 1
allele frequency: 1.233684522193985e-5
allele num: 81058
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000387312
  ensembl transcript: ENST00000409319
  gene symbol: ZFAND2B
  hgvsc: ENST00000409319.1:c.55+3G>C
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000409931
  ensembl transcript: ENST00000422255
  gene symbol: ZFAND2B
  hgvsc: ENST00000422255.1:c.55+3G>C
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386898
  ensembl transcript: ENST00000409336
  gene symbol: ZFAND2B
  hgvsc: ENST00000409336.1:c.55+3G>C
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000468301
  gene symbol: ZFAND2B
  hgvsc: ENST00000468301.1:n.195+3G>C
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386847
  ensembl transcript: ENST00000409412
  gene symbol: ZFAND2B
  hgvsc: ENST00000409412.1:c.55+3G>C
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386399
  ensembl transcript: ENST00000409594
  gene symbol: ZFAND2B
  hgvsc: ENST00000409594.1:c.55+3G>C
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000476713
  gene symbol: ZFAND2B
  hgvsc: ENST00000476713.1:n.112+3G>C
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386370
  ensembl transcript: ENST00000409217
  gene symbol: ZFAND2B
  hgvsc: ENST00000409217.1:c.55+3G>C
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000489197
  gene symbol: ZFAND2B
  hgvsc: ENST00000489197.1:n.163+3G>C
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000411334
  ensembl transcript: ENST00000444522
  gene symbol: ZFAND2B
  hgvsc: ENST00000444522.2:c.55+3G>C
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000289528
  ensembl transcript: ENST00000289528
  gene symbol: ZFAND2B
  hgvsc: ENST00000289528.5:c.55+3G>C
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000400760
  ensembl transcript: ENST00000436556
  gene symbol: ZFAND2B
  hgvsc: ENST00000436556.1:c.55+3G>C
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000486734
  gene symbol: ZFAND2B
  hgvsc: ENST00000486734.1:n.107+3G>C
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386824
  ensembl transcript: ENST00000409206
  gene symbol: ZFAND2B
  hgvsc: ENST00000409206.1:c.55+3G>C
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000387179
  ensembl transcript: ENST00000409097
  gene symbol: ZFAND2B
  hgvsc: ENST00000409097.1:c.55+3G>C
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000388773
  ensembl transcript: ENST00000448496
  gene symbol: ZFAND2B
  hgvsc: ENST00000448496.1:c.55+3G>C
  variant of: http://identifiers.org/hgnc/25206
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23079
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15502
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.55+3G>C
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: DP

2-220071777-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 220071777
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 220071777
    reference: chr 2
allele count: 1
allele frequency: 1.366979249254996e-5
allele num: 73154
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386824
  ensembl transcript: ENST00000409206
  gene symbol: ZFAND2B
  hgvsc: ENST00000409206.1:c.55+13G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000388773
  ensembl transcript: ENST00000448496
  gene symbol: ZFAND2B
  hgvsc: ENST00000448496.1:c.55+13G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386370
  ensembl transcript: ENST00000409217
  gene symbol: ZFAND2B
  hgvsc: ENST00000409217.1:c.55+13G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000289528
  ensembl transcript: ENST00000289528
  gene symbol: ZFAND2B
  hgvsc: ENST00000289528.5:c.55+13G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000387179
  ensembl transcript: ENST00000409097
  gene symbol: ZFAND2B
  hgvsc: ENST00000409097.1:c.55+13G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000411334
  ensembl transcript: ENST00000444522
  gene symbol: ZFAND2B
  hgvsc: ENST00000444522.2:c.55+13G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000489197
  gene symbol: ZFAND2B
  hgvsc: ENST00000489197.1:n.163+13G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386898
  ensembl transcript: ENST00000409336
  gene symbol: ZFAND2B
  hgvsc: ENST00000409336.1:c.55+13G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000468301
  gene symbol: ZFAND2B
  hgvsc: ENST00000468301.1:n.195+13G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000387312
  ensembl transcript: ENST00000409319
  gene symbol: ZFAND2B
  hgvsc: ENST00000409319.1:c.55+13G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000476713
  gene symbol: ZFAND2B
  hgvsc: ENST00000476713.1:n.112+13G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000400760
  ensembl transcript: ENST00000436556
  gene symbol: ZFAND2B
  hgvsc: ENST00000436556.1:c.55+13G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000409931
  ensembl transcript: ENST00000422255
  gene symbol: ZFAND2B
  hgvsc: ENST00000422255.1:c.55+13G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000486734
  gene symbol: ZFAND2B
  hgvsc: ENST00000486734.1:n.107+13G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386399
  ensembl transcript: ENST00000409594
  gene symbol: ZFAND2B
  hgvsc: ENST00000409594.1:c.55+13G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386847
  ensembl transcript: ENST00000409412
  gene symbol: ZFAND2B
  hgvsc: ENST00000409412.1:c.55+13G>A
  variant of: http://identifiers.org/hgnc/25206
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17268
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2507
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3766
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
population: African
reference allele: G
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum

2-220071780-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 220071780
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 220071780
    reference: chr 2
allele count: 0
allele frequency: 0.0e0
allele num: 70202
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000411334
  ensembl transcript: ENST00000444522
  gene symbol: ZFAND2B
  hgvsc: ENST00000444522.2:c.55+16C>T
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000289528
  ensembl transcript: ENST00000289528
  gene symbol: ZFAND2B
  hgvsc: ENST00000289528.5:c.55+16C>T
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000387179
  ensembl transcript: ENST00000409097
  gene symbol: ZFAND2B
  hgvsc: ENST00000409097.1:c.55+16C>T
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386370
  ensembl transcript: ENST00000409217
  gene symbol: ZFAND2B
  hgvsc: ENST00000409217.1:c.55+16C>T
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000476713
  gene symbol: ZFAND2B
  hgvsc: ENST00000476713.1:n.112+16C>T
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000400760
  ensembl transcript: ENST00000436556
  gene symbol: ZFAND2B
  hgvsc: ENST00000436556.1:c.55+16C>T
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386824
  ensembl transcript: ENST00000409206
  gene symbol: ZFAND2B
  hgvsc: ENST00000409206.1:c.55+16C>T
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386399
  ensembl transcript: ENST00000409594
  gene symbol: ZFAND2B
  hgvsc: ENST00000409594.1:c.55+16C>T
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386898
  ensembl transcript: ENST00000409336
  gene symbol: ZFAND2B
  hgvsc: ENST00000409336.1:c.55+16C>T
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000409931
  ensembl transcript: ENST00000422255
  gene symbol: ZFAND2B
  hgvsc: ENST00000422255.1:c.55+16C>T
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386847
  ensembl transcript: ENST00000409412
  gene symbol: ZFAND2B
  hgvsc: ENST00000409412.1:c.55+16C>T
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000387312
  ensembl transcript: ENST00000409319
  gene symbol: ZFAND2B
  hgvsc: ENST00000409319.1:c.55+16C>T
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000489197
  gene symbol: ZFAND2B
  hgvsc: ENST00000489197.1:n.163+16C>T
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000388773
  ensembl transcript: ENST00000448496
  gene symbol: ZFAND2B
  hgvsc: ENST00000448496.1:c.55+16C>T
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000468301
  gene symbol: ZFAND2B
  hgvsc: ENST00000468301.1:n.195+16C>T
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000486734
  gene symbol: ZFAND2B
  hgvsc: ENST00000486734.1:n.107+16C>T
  variant of: http://identifiers.org/hgnc/25206
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3188
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6099
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22344
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
reference allele: C
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD

2-220071781-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 220071781
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 220071781
    reference: chr 2
allele count: 1
allele frequency: 1.469723691945914e-5
allele num: 68040
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000289528
  ensembl transcript: ENST00000289528
  gene symbol: ZFAND2B
  hgvsc: ENST00000289528.5:c.55+17G>C
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386370
  ensembl transcript: ENST00000409217
  gene symbol: ZFAND2B
  hgvsc: ENST00000409217.1:c.55+17G>C
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000489197
  gene symbol: ZFAND2B
  hgvsc: ENST00000489197.1:n.163+17G>C
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386399
  ensembl transcript: ENST00000409594
  gene symbol: ZFAND2B
  hgvsc: ENST00000409594.1:c.55+17G>C
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000400760
  ensembl transcript: ENST00000436556
  gene symbol: ZFAND2B
  hgvsc: ENST00000436556.1:c.55+17G>C
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386824
  ensembl transcript: ENST00000409206
  gene symbol: ZFAND2B
  hgvsc: ENST00000409206.1:c.55+17G>C
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386898
  ensembl transcript: ENST00000409336
  gene symbol: ZFAND2B
  hgvsc: ENST00000409336.1:c.55+17G>C
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000476713
  gene symbol: ZFAND2B
  hgvsc: ENST00000476713.1:n.112+17G>C
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386847
  ensembl transcript: ENST00000409412
  gene symbol: ZFAND2B
  hgvsc: ENST00000409412.1:c.55+17G>C
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000409931
  ensembl transcript: ENST00000422255
  gene symbol: ZFAND2B
  hgvsc: ENST00000422255.1:c.55+17G>C
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000486734
  gene symbol: ZFAND2B
  hgvsc: ENST00000486734.1:n.107+17G>C
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000388773
  ensembl transcript: ENST00000448496
  gene symbol: ZFAND2B
  hgvsc: ENST00000448496.1:c.55+17G>C
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000387312
  ensembl transcript: ENST00000409319
  gene symbol: ZFAND2B
  hgvsc: ENST00000409319.1:c.55+17G>C
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000411334
  ensembl transcript: ENST00000444522
  gene symbol: ZFAND2B
  hgvsc: ENST00000444522.2:c.55+17G>C
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000387179
  ensembl transcript: ENST00000409097
  gene symbol: ZFAND2B
  hgvsc: ENST00000409097.1:c.55+17G>C
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000468301
  gene symbol: ZFAND2B
  hgvsc: ENST00000468301.1:n.195+17G>C
  variant of: http://identifiers.org/hgnc/25206
canonical: true
consequence: intron
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18307
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6416
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21822
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1247
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2029
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
reference allele: G
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum

2-220071781-GC-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 220071781
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 220071780
    reference: chr 2
allele count: 0
allele frequency: 0.0e0
allele num: 68040
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000468301
  gene symbol: ZFAND2B
  hgvsc: ENST00000468301.1:n.195+18delC
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000411334
  ensembl transcript: ENST00000444522
  gene symbol: ZFAND2B
  hgvsc: ENST00000444522.2:c.55+18delC
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386898
  ensembl transcript: ENST00000409336
  gene symbol: ZFAND2B
  hgvsc: ENST00000409336.1:c.55+18delC
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000489197
  gene symbol: ZFAND2B
  hgvsc: ENST00000489197.1:n.163+18delC
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000387179
  ensembl transcript: ENST00000409097
  gene symbol: ZFAND2B
  hgvsc: ENST00000409097.1:c.55+18delC
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386824
  ensembl transcript: ENST00000409206
  gene symbol: ZFAND2B
  hgvsc: ENST00000409206.1:c.55+18delC
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000400760
  ensembl transcript: ENST00000436556
  gene symbol: ZFAND2B
  hgvsc: ENST00000436556.1:c.55+18delC
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000388773
  ensembl transcript: ENST00000448496
  gene symbol: ZFAND2B
  hgvsc: ENST00000448496.1:c.55+18delC
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000409931
  ensembl transcript: ENST00000422255
  gene symbol: ZFAND2B
  hgvsc: ENST00000422255.1:c.55+18delC
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000289528
  ensembl transcript: ENST00000289528
  gene symbol: ZFAND2B
  hgvsc: ENST00000289528.5:c.55+18delC
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000486734
  gene symbol: ZFAND2B
  hgvsc: ENST00000486734.1:n.107+18delC
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386370
  ensembl transcript: ENST00000409217
  gene symbol: ZFAND2B
  hgvsc: ENST00000409217.1:c.55+18delC
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386847
  ensembl transcript: ENST00000409412
  gene symbol: ZFAND2B
  hgvsc: ENST00000409412.1:c.55+18delC
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000387312
  ensembl transcript: ENST00000409319
  gene symbol: ZFAND2B
  hgvsc: ENST00000409319.1:c.55+18delC
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000476713
  gene symbol: ZFAND2B
  hgvsc: ENST00000476713.1:n.112+18delC
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386399
  ensembl transcript: ENST00000409594
  gene symbol: ZFAND2B
  hgvsc: ENST00000409594.1:c.55+18delC
  variant of: http://identifiers.org/hgnc/25206
canonical: true
consequence: intron
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18307
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1247
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2029
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6416
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: Other
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: GC
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP

2-220071782-C-CG
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 220071782
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 220071783
    reference: chr 2
allele count: 60
allele frequency: 8.946944618412812e-4
allele num: 67062
alternate allele: CG
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386847
  ensembl transcript: ENST00000409412
  gene symbol: ZFAND2B
  hgvsc: ENST00000409412.1:c.55+24dupG
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000409931
  ensembl transcript: ENST00000422255
  gene symbol: ZFAND2B
  hgvsc: ENST00000422255.1:c.55+24dupG
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386399
  ensembl transcript: ENST00000409594
  gene symbol: ZFAND2B
  hgvsc: ENST00000409594.1:c.55+24dupG
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000289528
  ensembl transcript: ENST00000289528
  gene symbol: ZFAND2B
  hgvsc: ENST00000289528.5:c.55+24dupG
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000388773
  ensembl transcript: ENST00000448496
  gene symbol: ZFAND2B
  hgvsc: ENST00000448496.1:c.55+24dupG
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386824
  ensembl transcript: ENST00000409206
  gene symbol: ZFAND2B
  hgvsc: ENST00000409206.1:c.55+24dupG
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386370
  ensembl transcript: ENST00000409217
  gene symbol: ZFAND2B
  hgvsc: ENST00000409217.1:c.55+24dupG
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000489197
  gene symbol: ZFAND2B
  hgvsc: ENST00000489197.1:n.163+24dupG
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000468301
  gene symbol: ZFAND2B
  hgvsc: ENST00000468301.1:n.195+24dupG
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000400760
  ensembl transcript: ENST00000436556
  gene symbol: ZFAND2B
  hgvsc: ENST00000436556.1:c.55+24dupG
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386898
  ensembl transcript: ENST00000409336
  gene symbol: ZFAND2B
  hgvsc: ENST00000409336.1:c.55+24dupG
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000486734
  gene symbol: ZFAND2B
  hgvsc: ENST00000486734.1:n.107+24dupG
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000387312
  ensembl transcript: ENST00000409319
  gene symbol: ZFAND2B
  hgvsc: ENST00000409319.1:c.55+24dupG
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000411334
  ensembl transcript: ENST00000444522
  gene symbol: ZFAND2B
  hgvsc: ENST00000444522.2:c.55+24dupG
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000476713
  gene symbol: ZFAND2B
  hgvsc: ENST00000476713.1:n.112+24dupG
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000387179
  ensembl transcript: ENST00000409097
  gene symbol: ZFAND2B
  hgvsc: ENST00000409097.1:c.55+24dupG
  variant of: http://identifiers.org/hgnc/25206
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18375
  bin: 7.5e0
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 21850
  bin: 1.25e1
  variant carriers: 33
genotype depth: GenotypeDepth
  all individuals: 1227
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2039
  bin: 2.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2837
  bin: 2.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 1
population: Latino
population: Other
population: South Asian
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ

2-220071783-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 220071783
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 220071783
    reference: chr 2
allele count: 0
allele frequency: 0.0e0
allele num: 67206
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386370
  ensembl transcript: ENST00000409217
  gene symbol: ZFAND2B
  hgvsc: ENST00000409217.1:c.55+19G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000489197
  gene symbol: ZFAND2B
  hgvsc: ENST00000489197.1:n.163+19G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000486734
  gene symbol: ZFAND2B
  hgvsc: ENST00000486734.1:n.107+19G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386898
  ensembl transcript: ENST00000409336
  gene symbol: ZFAND2B
  hgvsc: ENST00000409336.1:c.55+19G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386399
  ensembl transcript: ENST00000409594
  gene symbol: ZFAND2B
  hgvsc: ENST00000409594.1:c.55+19G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000409931
  ensembl transcript: ENST00000422255
  gene symbol: ZFAND2B
  hgvsc: ENST00000422255.1:c.55+19G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000289528
  ensembl transcript: ENST00000289528
  gene symbol: ZFAND2B
  hgvsc: ENST00000289528.5:c.55+19G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386824
  ensembl transcript: ENST00000409206
  gene symbol: ZFAND2B
  hgvsc: ENST00000409206.1:c.55+19G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000400760
  ensembl transcript: ENST00000436556
  gene symbol: ZFAND2B
  hgvsc: ENST00000436556.1:c.55+19G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386847
  ensembl transcript: ENST00000409412
  gene symbol: ZFAND2B
  hgvsc: ENST00000409412.1:c.55+19G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000476713
  gene symbol: ZFAND2B
  hgvsc: ENST00000476713.1:n.112+19G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000388773
  ensembl transcript: ENST00000448496
  gene symbol: ZFAND2B
  hgvsc: ENST00000448496.1:c.55+19G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000468301
  gene symbol: ZFAND2B
  hgvsc: ENST00000468301.1:n.195+19G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000387179
  ensembl transcript: ENST00000409097
  gene symbol: ZFAND2B
  hgvsc: ENST00000409097.1:c.55+19G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000387312
  ensembl transcript: ENST00000409319
  gene symbol: ZFAND2B
  hgvsc: ENST00000409319.1:c.55+19G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000411334
  ensembl transcript: ENST00000444522
  gene symbol: ZFAND2B
  hgvsc: ENST00000444522.2:c.55+19G>A
  variant of: http://identifiers.org/hgnc/25206
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 6190
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21820
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18477
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1201
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2845
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: Other
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum

2-220071785-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 220071785
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 220071785
    reference: chr 2
allele count: 0
allele frequency: 0.0e0
allele num: 68006
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386370
  ensembl transcript: ENST00000409217
  gene symbol: ZFAND2B
  hgvsc: ENST00000409217.1:c.55+21G>T
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000489197
  gene symbol: ZFAND2B
  hgvsc: ENST00000489197.1:n.163+21G>T
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000409931
  ensembl transcript: ENST00000422255
  gene symbol: ZFAND2B
  hgvsc: ENST00000422255.1:c.55+21G>T
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000468301
  gene symbol: ZFAND2B
  hgvsc: ENST00000468301.1:n.195+21G>T
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000400760
  ensembl transcript: ENST00000436556
  gene symbol: ZFAND2B
  hgvsc: ENST00000436556.1:c.55+21G>T
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386399
  ensembl transcript: ENST00000409594
  gene symbol: ZFAND2B
  hgvsc: ENST00000409594.1:c.55+21G>T
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000289528
  ensembl transcript: ENST00000289528
  gene symbol: ZFAND2B
  hgvsc: ENST00000289528.5:c.55+21G>T
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386824
  ensembl transcript: ENST00000409206
  gene symbol: ZFAND2B
  hgvsc: ENST00000409206.1:c.55+21G>T
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386898
  ensembl transcript: ENST00000409336
  gene symbol: ZFAND2B
  hgvsc: ENST00000409336.1:c.55+21G>T
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000476713
  gene symbol: ZFAND2B
  hgvsc: ENST00000476713.1:n.112+21G>T
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000486734
  gene symbol: ZFAND2B
  hgvsc: ENST00000486734.1:n.107+21G>T
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000387312
  ensembl transcript: ENST00000409319
  gene symbol: ZFAND2B
  hgvsc: ENST00000409319.1:c.55+21G>T
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000388773
  ensembl transcript: ENST00000448496
  gene symbol: ZFAND2B
  hgvsc: ENST00000448496.1:c.55+21G>T
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000387179
  ensembl transcript: ENST00000409097
  gene symbol: ZFAND2B
  hgvsc: ENST00000409097.1:c.55+21G>T
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000411334
  ensembl transcript: ENST00000444522
  gene symbol: ZFAND2B
  hgvsc: ENST00000444522.2:c.55+21G>T
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386847
  ensembl transcript: ENST00000409412
  gene symbol: ZFAND2B
  hgvsc: ENST00000409412.1:c.55+21G>T
  variant of: http://identifiers.org/hgnc/25206
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 1155
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18764
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1990
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6655
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6028
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2784
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum

2-220071787-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 220071787
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 220071787
    reference: chr 2
allele count: 1
allele frequency: 1.490312965722802e-5
allele num: 67100
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000409931
  ensembl transcript: ENST00000422255
  gene symbol: ZFAND2B
  hgvsc: ENST00000422255.1:c.55+23G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386824
  ensembl transcript: ENST00000409206
  gene symbol: ZFAND2B
  hgvsc: ENST00000409206.1:c.55+23G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000400760
  ensembl transcript: ENST00000436556
  gene symbol: ZFAND2B
  hgvsc: ENST00000436556.1:c.55+23G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386898
  ensembl transcript: ENST00000409336
  gene symbol: ZFAND2B
  hgvsc: ENST00000409336.1:c.55+23G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000289528
  ensembl transcript: ENST00000289528
  gene symbol: ZFAND2B
  hgvsc: ENST00000289528.5:c.55+23G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386399
  ensembl transcript: ENST00000409594
  gene symbol: ZFAND2B
  hgvsc: ENST00000409594.1:c.55+23G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000489197
  gene symbol: ZFAND2B
  hgvsc: ENST00000489197.1:n.163+23G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000387179
  ensembl transcript: ENST00000409097
  gene symbol: ZFAND2B
  hgvsc: ENST00000409097.1:c.55+23G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000468301
  gene symbol: ZFAND2B
  hgvsc: ENST00000468301.1:n.195+23G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386847
  ensembl transcript: ENST00000409412
  gene symbol: ZFAND2B
  hgvsc: ENST00000409412.1:c.55+23G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000388773
  ensembl transcript: ENST00000448496
  gene symbol: ZFAND2B
  hgvsc: ENST00000448496.1:c.55+23G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000486734
  gene symbol: ZFAND2B
  hgvsc: ENST00000486734.1:n.107+23G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000476713
  gene symbol: ZFAND2B
  hgvsc: ENST00000476713.1:n.112+23G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000411334
  ensembl transcript: ENST00000444522
  gene symbol: ZFAND2B
  hgvsc: ENST00000444522.2:c.55+23G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000387312
  ensembl transcript: ENST00000409319
  gene symbol: ZFAND2B
  hgvsc: ENST00000409319.1:c.55+23G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386370
  ensembl transcript: ENST00000409217
  gene symbol: ZFAND2B
  hgvsc: ENST00000409217.1:c.55+23G>A
  variant of: http://identifiers.org/hgnc/25206
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1822
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1123
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21481
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6302
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
population: African
population: East Asian
reference allele: G
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: DP

2-220071791-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 220071791
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 220071791
    reference: chr 2
allele count: 0
allele frequency: 0.0e0
allele num: 60898
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000411334
  ensembl transcript: ENST00000444522
  gene symbol: ZFAND2B
  hgvsc: ENST00000444522.2:c.55+27G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000489197
  gene symbol: ZFAND2B
  hgvsc: ENST00000489197.1:n.163+27G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000289528
  ensembl transcript: ENST00000289528
  gene symbol: ZFAND2B
  hgvsc: ENST00000289528.5:c.55+27G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000486734
  gene symbol: ZFAND2B
  hgvsc: ENST00000486734.1:n.107+27G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000387179
  ensembl transcript: ENST00000409097
  gene symbol: ZFAND2B
  hgvsc: ENST00000409097.1:c.55+27G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386824
  ensembl transcript: ENST00000409206
  gene symbol: ZFAND2B
  hgvsc: ENST00000409206.1:c.55+27G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000476713
  gene symbol: ZFAND2B
  hgvsc: ENST00000476713.1:n.112+27G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000468301
  gene symbol: ZFAND2B
  hgvsc: ENST00000468301.1:n.195+27G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386370
  ensembl transcript: ENST00000409217
  gene symbol: ZFAND2B
  hgvsc: ENST00000409217.1:c.55+27G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000400760
  ensembl transcript: ENST00000436556
  gene symbol: ZFAND2B
  hgvsc: ENST00000436556.1:c.55+27G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386399
  ensembl transcript: ENST00000409594
  gene symbol: ZFAND2B
  hgvsc: ENST00000409594.1:c.55+27G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000409931
  ensembl transcript: ENST00000422255
  gene symbol: ZFAND2B
  hgvsc: ENST00000422255.1:c.55+27G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386898
  ensembl transcript: ENST00000409336
  gene symbol: ZFAND2B
  hgvsc: ENST00000409336.1:c.55+27G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000388773
  ensembl transcript: ENST00000448496
  gene symbol: ZFAND2B
  hgvsc: ENST00000448496.1:c.55+27G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386847
  ensembl transcript: ENST00000409412
  gene symbol: ZFAND2B
  hgvsc: ENST00000409412.1:c.55+27G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000387312
  ensembl transcript: ENST00000409319
  gene symbol: ZFAND2B
  hgvsc: ENST00000409319.1:c.55+27G>A
  variant of: http://identifiers.org/hgnc/25206
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7091
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19259
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21253
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: MQ

2-220071792-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 220071792
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 220071792
    reference: chr 2
allele count: 1
allele frequency: 1.636018585171127e-5
allele num: 61124
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386824
  ensembl transcript: ENST00000409206
  gene symbol: ZFAND2B
  hgvsc: ENST00000409206.1:c.55+28G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000289528
  ensembl transcript: ENST00000289528
  gene symbol: ZFAND2B
  hgvsc: ENST00000289528.5:c.55+28G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000387179
  ensembl transcript: ENST00000409097
  gene symbol: ZFAND2B
  hgvsc: ENST00000409097.1:c.55+28G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000411334
  ensembl transcript: ENST00000444522
  gene symbol: ZFAND2B
  hgvsc: ENST00000444522.2:c.55+28G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000400760
  ensembl transcript: ENST00000436556
  gene symbol: ZFAND2B
  hgvsc: ENST00000436556.1:c.55+28G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000409931
  ensembl transcript: ENST00000422255
  gene symbol: ZFAND2B
  hgvsc: ENST00000422255.1:c.55+28G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000387312
  ensembl transcript: ENST00000409319
  gene symbol: ZFAND2B
  hgvsc: ENST00000409319.1:c.55+28G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000486734
  gene symbol: ZFAND2B
  hgvsc: ENST00000486734.1:n.107+28G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386898
  ensembl transcript: ENST00000409336
  gene symbol: ZFAND2B
  hgvsc: ENST00000409336.1:c.55+28G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000476713
  gene symbol: ZFAND2B
  hgvsc: ENST00000476713.1:n.112+28G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386399
  ensembl transcript: ENST00000409594
  gene symbol: ZFAND2B
  hgvsc: ENST00000409594.1:c.55+28G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000489197
  gene symbol: ZFAND2B
  hgvsc: ENST00000489197.1:n.163+28G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000388773
  ensembl transcript: ENST00000448496
  gene symbol: ZFAND2B
  hgvsc: ENST00000448496.1:c.55+28G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000468301
  gene symbol: ZFAND2B
  hgvsc: ENST00000468301.1:n.195+28G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386370
  ensembl transcript: ENST00000409217
  gene symbol: ZFAND2B
  hgvsc: ENST00000409217.1:c.55+28G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386847
  ensembl transcript: ENST00000409412
  gene symbol: ZFAND2B
  hgvsc: ENST00000409412.1:c.55+28G>A
  variant of: http://identifiers.org/hgnc/25206
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7116
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1841
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19268
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 863
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: G
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum

2-220071793-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 220071793
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 220071793
    reference: chr 2
allele count: 0
allele frequency: 0.0e0
allele num: 58840
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000387179
  ensembl transcript: ENST00000409097
  gene symbol: ZFAND2B
  hgvsc: ENST00000409097.1:c.55+29G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386824
  ensembl transcript: ENST00000409206
  gene symbol: ZFAND2B
  hgvsc: ENST00000409206.1:c.55+29G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386847
  ensembl transcript: ENST00000409412
  gene symbol: ZFAND2B
  hgvsc: ENST00000409412.1:c.55+29G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386898
  ensembl transcript: ENST00000409336
  gene symbol: ZFAND2B
  hgvsc: ENST00000409336.1:c.55+29G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000400760
  ensembl transcript: ENST00000436556
  gene symbol: ZFAND2B
  hgvsc: ENST00000436556.1:c.55+29G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000468301
  gene symbol: ZFAND2B
  hgvsc: ENST00000468301.1:n.195+29G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386399
  ensembl transcript: ENST00000409594
  gene symbol: ZFAND2B
  hgvsc: ENST00000409594.1:c.55+29G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000486734
  gene symbol: ZFAND2B
  hgvsc: ENST00000486734.1:n.107+29G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000289528
  ensembl transcript: ENST00000289528
  gene symbol: ZFAND2B
  hgvsc: ENST00000289528.5:c.55+29G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000409931
  ensembl transcript: ENST00000422255
  gene symbol: ZFAND2B
  hgvsc: ENST00000422255.1:c.55+29G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386370
  ensembl transcript: ENST00000409217
  gene symbol: ZFAND2B
  hgvsc: ENST00000409217.1:c.55+29G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000388773
  ensembl transcript: ENST00000448496
  gene symbol: ZFAND2B
  hgvsc: ENST00000448496.1:c.55+29G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000476713
  gene symbol: ZFAND2B
  hgvsc: ENST00000476713.1:n.112+29G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000387312
  ensembl transcript: ENST00000409319
  gene symbol: ZFAND2B
  hgvsc: ENST00000409319.1:c.55+29G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000489197
  gene symbol: ZFAND2B
  hgvsc: ENST00000489197.1:n.163+29G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000411334
  ensembl transcript: ENST00000444522
  gene symbol: ZFAND2B
  hgvsc: ENST00000444522.2:c.55+29G>A
  variant of: http://identifiers.org/hgnc/25206
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6629
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 795
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2061
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18516
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
population: African
population: East Asian
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/2-220071794-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 220071794
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 220071794
    reference: chr 2
allele count: 1
allele frequency: 1.699986400108799e-5
allele num: 58824
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000476713
  gene symbol: ZFAND2B
  hgvsc: ENST00000476713.1:n.112+30C>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000387179
  ensembl transcript: ENST00000409097
  gene symbol: ZFAND2B
  hgvsc: ENST00000409097.1:c.55+30C>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000409931
  ensembl transcript: ENST00000422255
  gene symbol: ZFAND2B
  hgvsc: ENST00000422255.1:c.55+30C>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000489197
  gene symbol: ZFAND2B
  hgvsc: ENST00000489197.1:n.163+30C>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000486734
  gene symbol: ZFAND2B
  hgvsc: ENST00000486734.1:n.107+30C>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000289528
  ensembl transcript: ENST00000289528
  gene symbol: ZFAND2B
  hgvsc: ENST00000289528.5:c.55+30C>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000400760
  ensembl transcript: ENST00000436556
  gene symbol: ZFAND2B
  hgvsc: ENST00000436556.1:c.55+30C>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000411334
  ensembl transcript: ENST00000444522
  gene symbol: ZFAND2B
  hgvsc: ENST00000444522.2:c.55+30C>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386399
  ensembl transcript: ENST00000409594
  gene symbol: ZFAND2B
  hgvsc: ENST00000409594.1:c.55+30C>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386370
  ensembl transcript: ENST00000409217
  gene symbol: ZFAND2B
  hgvsc: ENST00000409217.1:c.55+30C>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386847
  ensembl transcript: ENST00000409412
  gene symbol: ZFAND2B
  hgvsc: ENST00000409412.1:c.55+30C>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000468301
  gene symbol: ZFAND2B
  hgvsc: ENST00000468301.1:n.195+30C>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000387312
  ensembl transcript: ENST00000409319
  gene symbol: ZFAND2B
  hgvsc: ENST00000409319.1:c.55+30C>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000388773
  ensembl transcript: ENST00000448496
  gene symbol: ZFAND2B
  hgvsc: ENST00000448496.1:c.55+30C>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386898
  ensembl transcript: ENST00000409336
  gene symbol: ZFAND2B
  hgvsc: ENST00000409336.1:c.55+30C>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386824
  ensembl transcript: ENST00000409206
  gene symbol: ZFAND2B
  hgvsc: ENST00000409206.1:c.55+30C>A
  variant of: http://identifiers.org/hgnc/25206
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7112
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18459
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 792
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2085
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1607
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Latino
population: African
population: Other
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum

2-220071795-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 220071795
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 220071795
    reference: chr 2
allele count: 1
allele frequency: 1.710863986313088e-5
allele num: 58450
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386370
  ensembl transcript: ENST00000409217
  gene symbol: ZFAND2B
  hgvsc: ENST00000409217.1:c.55+31C>T
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000289528
  ensembl transcript: ENST00000289528
  gene symbol: ZFAND2B
  hgvsc: ENST00000289528.5:c.55+31C>T
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000387312
  ensembl transcript: ENST00000409319
  gene symbol: ZFAND2B
  hgvsc: ENST00000409319.1:c.55+31C>T
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000468301
  gene symbol: ZFAND2B
  hgvsc: ENST00000468301.1:n.195+31C>T
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000388773
  ensembl transcript: ENST00000448496
  gene symbol: ZFAND2B
  hgvsc: ENST00000448496.1:c.55+31C>T
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386399
  ensembl transcript: ENST00000409594
  gene symbol: ZFAND2B
  hgvsc: ENST00000409594.1:c.55+31C>T
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000476713
  gene symbol: ZFAND2B
  hgvsc: ENST00000476713.1:n.112+31C>T
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000400760
  ensembl transcript: ENST00000436556
  gene symbol: ZFAND2B
  hgvsc: ENST00000436556.1:c.55+31C>T
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000409931
  ensembl transcript: ENST00000422255
  gene symbol: ZFAND2B
  hgvsc: ENST00000422255.1:c.55+31C>T
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000486734
  gene symbol: ZFAND2B
  hgvsc: ENST00000486734.1:n.107+31C>T
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386847
  ensembl transcript: ENST00000409412
  gene symbol: ZFAND2B
  hgvsc: ENST00000409412.1:c.55+31C>T
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386824
  ensembl transcript: ENST00000409206
  gene symbol: ZFAND2B
  hgvsc: ENST00000409206.1:c.55+31C>T
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000489197
  gene symbol: ZFAND2B
  hgvsc: ENST00000489197.1:n.163+31C>T
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000411334
  ensembl transcript: ENST00000444522
  gene symbol: ZFAND2B
  hgvsc: ENST00000444522.2:c.55+31C>T
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000387179
  ensembl transcript: ENST00000409097
  gene symbol: ZFAND2B
  hgvsc: ENST00000409097.1:c.55+31C>T
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386898
  ensembl transcript: ENST00000409336
  gene symbol: ZFAND2B
  hgvsc: ENST00000409336.1:c.55+31C>T
  variant of: http://identifiers.org/hgnc/25206
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 22408
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6509
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18269
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: Latino
reference allele: C
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ

2-220071797-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 220071797
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 220071797
    reference: chr 2
allele count: 0
allele frequency: 0.0e0
allele num: 56222
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000409931
  ensembl transcript: ENST00000422255
  gene symbol: ZFAND2B
  hgvsc: ENST00000422255.1:c.55+33A>G
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386370
  ensembl transcript: ENST00000409217
  gene symbol: ZFAND2B
  hgvsc: ENST00000409217.1:c.55+33A>G
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000489197
  gene symbol: ZFAND2B
  hgvsc: ENST00000489197.1:n.163+33A>G
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000486734
  gene symbol: ZFAND2B
  hgvsc: ENST00000486734.1:n.107+33A>G
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000400760
  ensembl transcript: ENST00000436556
  gene symbol: ZFAND2B
  hgvsc: ENST00000436556.1:c.55+33A>G
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000476713
  gene symbol: ZFAND2B
  hgvsc: ENST00000476713.1:n.112+33A>G
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386824
  ensembl transcript: ENST00000409206
  gene symbol: ZFAND2B
  hgvsc: ENST00000409206.1:c.55+33A>G
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386898
  ensembl transcript: ENST00000409336
  gene symbol: ZFAND2B
  hgvsc: ENST00000409336.1:c.55+33A>G
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000388773
  ensembl transcript: ENST00000448496
  gene symbol: ZFAND2B
  hgvsc: ENST00000448496.1:c.55+33A>G
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000411334
  ensembl transcript: ENST00000444522
  gene symbol: ZFAND2B
  hgvsc: ENST00000444522.2:c.55+33A>G
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000289528
  ensembl transcript: ENST00000289528
  gene symbol: ZFAND2B
  hgvsc: ENST00000289528.5:c.55+33A>G
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386847
  ensembl transcript: ENST00000409412
  gene symbol: ZFAND2B
  hgvsc: ENST00000409412.1:c.55+33A>G
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000468301
  gene symbol: ZFAND2B
  hgvsc: ENST00000468301.1:n.195+33A>G
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000387179
  ensembl transcript: ENST00000409097
  gene symbol: ZFAND2B
  hgvsc: ENST00000409097.1:c.55+33A>G
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386399
  ensembl transcript: ENST00000409594
  gene symbol: ZFAND2B
  hgvsc: ENST00000409594.1:c.55+33A>G
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000387312
  ensembl transcript: ENST00000409319
  gene symbol: ZFAND2B
  hgvsc: ENST00000409319.1:c.55+33A>G
  variant of: http://identifiers.org/hgnc/25206
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6387
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1356
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2417
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7040
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23114
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: East Asian
reference allele: A
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum

http://identifiers.org/exac.variant/2-220071799-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 220071799
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 220071799
    reference: chr 2
allele count: 2
allele frequency: 3.730508095202566e-5
allele num: 53612
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386824
  ensembl transcript: ENST00000409206
  gene symbol: ZFAND2B
  hgvsc: ENST00000409206.1:c.55+35C>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000400760
  ensembl transcript: ENST00000436556
  gene symbol: ZFAND2B
  hgvsc: ENST00000436556.1:c.55+35C>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000409931
  ensembl transcript: ENST00000422255
  gene symbol: ZFAND2B
  hgvsc: ENST00000422255.1:c.55+35C>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000387179
  ensembl transcript: ENST00000409097
  gene symbol: ZFAND2B
  hgvsc: ENST00000409097.1:c.55+35C>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000388773
  ensembl transcript: ENST00000448496
  gene symbol: ZFAND2B
  hgvsc: ENST00000448496.1:c.55+35C>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386370
  ensembl transcript: ENST00000409217
  gene symbol: ZFAND2B
  hgvsc: ENST00000409217.1:c.55+35C>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000289528
  ensembl transcript: ENST00000289528
  gene symbol: ZFAND2B
  hgvsc: ENST00000289528.5:c.55+35C>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000489197
  gene symbol: ZFAND2B
  hgvsc: ENST00000489197.1:n.163+35C>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000468301
  gene symbol: ZFAND2B
  hgvsc: ENST00000468301.1:n.195+35C>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000387312
  ensembl transcript: ENST00000409319
  gene symbol: ZFAND2B
  hgvsc: ENST00000409319.1:c.55+35C>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000486734
  gene symbol: ZFAND2B
  hgvsc: ENST00000486734.1:n.107+35C>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000411334
  ensembl transcript: ENST00000444522
  gene symbol: ZFAND2B
  hgvsc: ENST00000444522.2:c.55+35C>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386847
  ensembl transcript: ENST00000409412
  gene symbol: ZFAND2B
  hgvsc: ENST00000409412.1:c.55+35C>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386399
  ensembl transcript: ENST00000409594
  gene symbol: ZFAND2B
  hgvsc: ENST00000409594.1:c.55+35C>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386898
  ensembl transcript: ENST00000409336
  gene symbol: ZFAND2B
  hgvsc: ENST00000409336.1:c.55+35C>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000476713
  gene symbol: ZFAND2B
  hgvsc: ENST00000476713.1:n.112+35C>A
  variant of: http://identifiers.org/hgnc/25206
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6311
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 657
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1272
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2534
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6955
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD

2-220071803-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 220071803
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 220071803
    reference: chr 2
allele count: 48716
allele frequency: 8.652315998863314e-1
allele num: 56304
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000387312
  ensembl transcript: ENST00000409319
  gene symbol: ZFAND2B
  hgvsc: ENST00000409319.1:c.55+39C>G
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386370
  ensembl transcript: ENST00000409217
  gene symbol: ZFAND2B
  hgvsc: ENST00000409217.1:c.55+39C>G
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000409931
  ensembl transcript: ENST00000422255
  gene symbol: ZFAND2B
  hgvsc: ENST00000422255.1:c.55+39C>G
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000388773
  ensembl transcript: ENST00000448496
  gene symbol: ZFAND2B
  hgvsc: ENST00000448496.1:c.55+39C>G
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386399
  ensembl transcript: ENST00000409594
  gene symbol: ZFAND2B
  hgvsc: ENST00000409594.1:c.55+39C>G
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000289528
  ensembl transcript: ENST00000289528
  gene symbol: ZFAND2B
  hgvsc: ENST00000289528.5:c.55+39C>G
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386824
  ensembl transcript: ENST00000409206
  gene symbol: ZFAND2B
  hgvsc: ENST00000409206.1:c.55+39C>G
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000411334
  ensembl transcript: ENST00000444522
  gene symbol: ZFAND2B
  hgvsc: ENST00000444522.2:c.55+39C>G
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000486734
  gene symbol: ZFAND2B
  hgvsc: ENST00000486734.1:n.107+39C>G
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000400760
  ensembl transcript: ENST00000436556
  gene symbol: ZFAND2B
  hgvsc: ENST00000436556.1:c.55+39C>G
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000387179
  ensembl transcript: ENST00000409097
  gene symbol: ZFAND2B
  hgvsc: ENST00000409097.1:c.55+39C>G
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000468301
  gene symbol: ZFAND2B
  hgvsc: ENST00000468301.1:n.195+39C>G
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000489197
  gene symbol: ZFAND2B
  hgvsc: ENST00000489197.1:n.163+39C>G
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000476713
  gene symbol: ZFAND2B
  hgvsc: ENST00000476713.1:n.112+39C>G
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386898
  ensembl transcript: ENST00000409336
  gene symbol: ZFAND2B
  hgvsc: ENST00000409336.1:c.55+39C>G
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386847
  ensembl transcript: ENST00000409412
  gene symbol: ZFAND2B
  hgvsc: ENST00000409412.1:c.55+39C>G
  variant of: http://identifiers.org/hgnc/25206
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5308
  bin: 2.5e0
  variant carriers: 3937
genotype depth: GenotypeDepth
  all individuals: 6454
  bin: 1.75e1
  variant carriers: 6334
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 4.75e1
  variant carriers: 79
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 4.25e1
  variant carriers: 145
genotype depth: GenotypeDepth
  all individuals: 556
  bin: 3.25e1
  variant carriers: 520
genotype depth: GenotypeDepth
  all individuals: 2465
  bin: 2.25e1
  variant carriers: 2421
genotype depth: GenotypeDepth
  all individuals: 24023
  bin: 7.5e0
  variant carriers: 21985
genotype depth: GenotypeDepth
  all individuals: 1204
  bin: 2.75e1
  variant carriers: 1144
genotype quality: GenotypeQuality
num of homozygotes: 21218
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Latino
population: Other
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum

2-220071806-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 220071806
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 220071806
    reference: chr 2
allele count: 1
allele frequency: 2.425300737291424e-5
allele num: 41232
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000289528
  ensembl transcript: ENST00000289528
  gene symbol: ZFAND2B
  hgvsc: ENST00000289528.5:c.55+42G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000388773
  ensembl transcript: ENST00000448496
  gene symbol: ZFAND2B
  hgvsc: ENST00000448496.1:c.55+42G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000476713
  gene symbol: ZFAND2B
  hgvsc: ENST00000476713.1:n.112+42G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000486734
  gene symbol: ZFAND2B
  hgvsc: ENST00000486734.1:n.107+42G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386824
  ensembl transcript: ENST00000409206
  gene symbol: ZFAND2B
  hgvsc: ENST00000409206.1:c.55+42G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000468301
  gene symbol: ZFAND2B
  hgvsc: ENST00000468301.1:n.195+42G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000409931
  ensembl transcript: ENST00000422255
  gene symbol: ZFAND2B
  hgvsc: ENST00000422255.1:c.55+42G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386898
  ensembl transcript: ENST00000409336
  gene symbol: ZFAND2B
  hgvsc: ENST00000409336.1:c.55+42G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000400760
  ensembl transcript: ENST00000436556
  gene symbol: ZFAND2B
  hgvsc: ENST00000436556.1:c.55+42G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000489197
  gene symbol: ZFAND2B
  hgvsc: ENST00000489197.1:n.163+42G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386370
  ensembl transcript: ENST00000409217
  gene symbol: ZFAND2B
  hgvsc: ENST00000409217.1:c.55+42G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000411334
  ensembl transcript: ENST00000444522
  gene symbol: ZFAND2B
  hgvsc: ENST00000444522.2:c.55+42G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386847
  ensembl transcript: ENST00000409412
  gene symbol: ZFAND2B
  hgvsc: ENST00000409412.1:c.55+42G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000387312
  ensembl transcript: ENST00000409319
  gene symbol: ZFAND2B
  hgvsc: ENST00000409319.1:c.55+42G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000387179
  ensembl transcript: ENST00000409097
  gene symbol: ZFAND2B
  hgvsc: ENST00000409097.1:c.55+42G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386399
  ensembl transcript: ENST00000409594
  gene symbol: ZFAND2B
  hgvsc: ENST00000409594.1:c.55+42G>A
  variant of: http://identifiers.org/hgnc/25206
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 919
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11706
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1131
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4051
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26053
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: MQ

2-220071999-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 220071999
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 220071999
    reference: chr 2
allele count: 1
allele frequency: 8.244566830458728e-6
allele num: 121292
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386847
  ensembl transcript: ENST00000409412
  gene symbol: ZFAND2B
  hgvsc: ENST00000409412.1:c.56-50G>C
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000388773
  ensembl transcript: ENST00000448496
  gene symbol: ZFAND2B
  hgvsc: ENST00000448496.1:c.56-50G>C
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000400760
  ensembl transcript: ENST00000436556
  gene symbol: ZFAND2B
  hgvsc: ENST00000436556.1:c.56-50G>C
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000387312
  ensembl transcript: ENST00000409319
  gene symbol: ZFAND2B
  hgvsc: ENST00000409319.1:c.56-50G>C
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000469596
  gene symbol: ZFAND2B
  hgvsc: ENST00000469596.1:n.60G>C
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000475533
  gene symbol: ZFAND2B
  hgvsc: ENST00000475533.1:n.15G>C
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000464902
  gene symbol: ZFAND2B
  hgvsc: ENST00000464902.1:n.193G>C
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000289528
  ensembl transcript: ENST00000289528
  gene symbol: ZFAND2B
  hgvsc: ENST00000289528.5:c.56-50G>C
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000409931
  ensembl transcript: ENST00000422255
  gene symbol: ZFAND2B
  hgvsc: ENST00000422255.1:c.56-50G>C
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000489197
  gene symbol: ZFAND2B
  hgvsc: ENST00000489197.1:n.164-50G>C
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386898
  ensembl transcript: ENST00000409336
  gene symbol: ZFAND2B
  hgvsc: ENST00000409336.1:c.56-50G>C
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386399
  ensembl transcript: ENST00000409594
  gene symbol: ZFAND2B
  hgvsc: ENST00000409594.1:c.56-50G>C
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000476713
  gene symbol: ZFAND2B
  hgvsc: ENST00000476713.1:n.113-50G>C
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000486734
  gene symbol: ZFAND2B
  hgvsc: ENST00000486734.1:n.108-50G>C
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000411334
  ensembl transcript: ENST00000444522
  gene symbol: ZFAND2B
  hgvsc: ENST00000444522.2:c.56-50G>C
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000468301
  gene symbol: ZFAND2B
  hgvsc: ENST00000468301.1:n.196-50G>C
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386370
  ensembl transcript: ENST00000409217
  gene symbol: ZFAND2B
  hgvsc: ENST00000409217.1:c.56-50G>C
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386824
  ensembl transcript: ENST00000409206
  gene symbol: ZFAND2B
  hgvsc: ENST00000409206.1:c.56-50G>C
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000387179
  ensembl transcript: ENST00000409097
  gene symbol: ZFAND2B
  hgvsc: ENST00000409097.1:c.56-50G>C
  variant of: http://identifiers.org/hgnc/25206
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21091
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3968
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Other
population: African
population: East Asian
population: Latino
reference allele: G
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: ClippingRankSum

2-220072000-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 220072000
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 220072000
    reference: chr 2
allele count: 3
allele frequency: 2.473288484368817e-5
allele num: 121296
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386399
  ensembl transcript: ENST00000409594
  gene symbol: ZFAND2B
  hgvsc: ENST00000409594.1:c.56-49A>G
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000475533
  gene symbol: ZFAND2B
  hgvsc: ENST00000475533.1:n.16A>G
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000468301
  gene symbol: ZFAND2B
  hgvsc: ENST00000468301.1:n.196-49A>G
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000387312
  ensembl transcript: ENST00000409319
  gene symbol: ZFAND2B
  hgvsc: ENST00000409319.1:c.56-49A>G
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000387179
  ensembl transcript: ENST00000409097
  gene symbol: ZFAND2B
  hgvsc: ENST00000409097.1:c.56-49A>G
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000464902
  gene symbol: ZFAND2B
  hgvsc: ENST00000464902.1:n.194A>G
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000411334
  ensembl transcript: ENST00000444522
  gene symbol: ZFAND2B
  hgvsc: ENST00000444522.2:c.56-49A>G
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386824
  ensembl transcript: ENST00000409206
  gene symbol: ZFAND2B
  hgvsc: ENST00000409206.1:c.56-49A>G
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000486734
  gene symbol: ZFAND2B
  hgvsc: ENST00000486734.1:n.108-49A>G
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000469596
  gene symbol: ZFAND2B
  hgvsc: ENST00000469596.1:n.61A>G
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000489197
  gene symbol: ZFAND2B
  hgvsc: ENST00000489197.1:n.164-49A>G
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000400760
  ensembl transcript: ENST00000436556
  gene symbol: ZFAND2B
  hgvsc: ENST00000436556.1:c.56-49A>G
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000388773
  ensembl transcript: ENST00000448496
  gene symbol: ZFAND2B
  hgvsc: ENST00000448496.1:c.56-49A>G
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000409931
  ensembl transcript: ENST00000422255
  gene symbol: ZFAND2B
  hgvsc: ENST00000422255.1:c.56-49A>G
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386898
  ensembl transcript: ENST00000409336
  gene symbol: ZFAND2B
  hgvsc: ENST00000409336.1:c.56-49A>G
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386847
  ensembl transcript: ENST00000409412
  gene symbol: ZFAND2B
  hgvsc: ENST00000409412.1:c.56-49A>G
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000476713
  gene symbol: ZFAND2B
  hgvsc: ENST00000476713.1:n.113-49A>G
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000289528
  ensembl transcript: ENST00000289528
  gene symbol: ZFAND2B
  hgvsc: ENST00000289528.5:c.56-49A>G
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386370
  ensembl transcript: ENST00000409217
  gene symbol: ZFAND2B
  hgvsc: ENST00000409217.1:c.56-49A>G
  variant of: http://identifiers.org/hgnc/25206
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4058
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 1
population: South Asian
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: QD

2-220072003-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 220072003
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 220072003
    reference: chr 2
allele count: 4
allele frequency: 3.297717979158422e-5
allele num: 121296
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000475533
  gene symbol: ZFAND2B
  hgvsc: ENST00000475533.1:n.19G>C
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000486734
  gene symbol: ZFAND2B
  hgvsc: ENST00000486734.1:n.108-46G>C
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386824
  ensembl transcript: ENST00000409206
  gene symbol: ZFAND2B
  hgvsc: ENST00000409206.1:c.56-46G>C
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000411334
  ensembl transcript: ENST00000444522
  gene symbol: ZFAND2B
  hgvsc: ENST00000444522.2:c.56-46G>C
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000476713
  gene symbol: ZFAND2B
  hgvsc: ENST00000476713.1:n.113-46G>C
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386370
  ensembl transcript: ENST00000409217
  gene symbol: ZFAND2B
  hgvsc: ENST00000409217.1:c.56-46G>C
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000468301
  gene symbol: ZFAND2B
  hgvsc: ENST00000468301.1:n.196-46G>C
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000289528
  ensembl transcript: ENST00000289528
  gene symbol: ZFAND2B
  hgvsc: ENST00000289528.5:c.56-46G>C
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000400760
  ensembl transcript: ENST00000436556
  gene symbol: ZFAND2B
  hgvsc: ENST00000436556.1:c.56-46G>C
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000469596
  gene symbol: ZFAND2B
  hgvsc: ENST00000469596.1:n.64G>C
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000387312
  ensembl transcript: ENST00000409319
  gene symbol: ZFAND2B
  hgvsc: ENST00000409319.1:c.56-46G>C
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000489197
  gene symbol: ZFAND2B
  hgvsc: ENST00000489197.1:n.164-46G>C
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000464902
  gene symbol: ZFAND2B
  hgvsc: ENST00000464902.1:n.197G>C
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000409931
  ensembl transcript: ENST00000422255
  gene symbol: ZFAND2B
  hgvsc: ENST00000422255.1:c.56-46G>C
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386898
  ensembl transcript: ENST00000409336
  gene symbol: ZFAND2B
  hgvsc: ENST00000409336.1:c.56-46G>C
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386847
  ensembl transcript: ENST00000409412
  gene symbol: ZFAND2B
  hgvsc: ENST00000409412.1:c.56-46G>C
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386399
  ensembl transcript: ENST00000409594
  gene symbol: ZFAND2B
  hgvsc: ENST00000409594.1:c.56-46G>C
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000388773
  ensembl transcript: ENST00000448496
  gene symbol: ZFAND2B
  hgvsc: ENST00000448496.1:c.56-46G>C
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000387179
  ensembl transcript: ENST00000409097
  gene symbol: ZFAND2B
  hgvsc: ENST00000409097.1:c.56-46G>C
  variant of: http://identifiers.org/hgnc/25206
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4020
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2326
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
population: African
population: East Asian
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: DP

2-220072004-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 220072004
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 220072004
    reference: chr 2
allele count: 1
allele frequency: 8.244294947896055e-6
allele num: 121296
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000469596
  gene symbol: ZFAND2B
  hgvsc: ENST00000469596.1:n.65A>G
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386399
  ensembl transcript: ENST00000409594
  gene symbol: ZFAND2B
  hgvsc: ENST00000409594.1:c.56-45A>G
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000400760
  ensembl transcript: ENST00000436556
  gene symbol: ZFAND2B
  hgvsc: ENST00000436556.1:c.56-45A>G
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000475533
  gene symbol: ZFAND2B
  hgvsc: ENST00000475533.1:n.20A>G
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386847
  ensembl transcript: ENST00000409412
  gene symbol: ZFAND2B
  hgvsc: ENST00000409412.1:c.56-45A>G
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000486734
  gene symbol: ZFAND2B
  hgvsc: ENST00000486734.1:n.108-45A>G
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000388773
  ensembl transcript: ENST00000448496
  gene symbol: ZFAND2B
  hgvsc: ENST00000448496.1:c.56-45A>G
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000411334
  ensembl transcript: ENST00000444522
  gene symbol: ZFAND2B
  hgvsc: ENST00000444522.2:c.56-45A>G
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000464902
  gene symbol: ZFAND2B
  hgvsc: ENST00000464902.1:n.198A>G
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000387312
  ensembl transcript: ENST00000409319
  gene symbol: ZFAND2B
  hgvsc: ENST00000409319.1:c.56-45A>G
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386824
  ensembl transcript: ENST00000409206
  gene symbol: ZFAND2B
  hgvsc: ENST00000409206.1:c.56-45A>G
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386898
  ensembl transcript: ENST00000409336
  gene symbol: ZFAND2B
  hgvsc: ENST00000409336.1:c.56-45A>G
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000387179
  ensembl transcript: ENST00000409097
  gene symbol: ZFAND2B
  hgvsc: ENST00000409097.1:c.56-45A>G
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000468301
  gene symbol: ZFAND2B
  hgvsc: ENST00000468301.1:n.196-45A>G
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000476713
  gene symbol: ZFAND2B
  hgvsc: ENST00000476713.1:n.113-45A>G
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000489197
  gene symbol: ZFAND2B
  hgvsc: ENST00000489197.1:n.164-45A>G
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000289528
  ensembl transcript: ENST00000289528
  gene symbol: ZFAND2B
  hgvsc: ENST00000289528.5:c.56-45A>G
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386370
  ensembl transcript: ENST00000409217
  gene symbol: ZFAND2B
  hgvsc: ENST00000409217.1:c.56-45A>G
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000409931
  ensembl transcript: ENST00000422255
  gene symbol: ZFAND2B
  hgvsc: ENST00000422255.1:c.56-45A>G
  variant of: http://identifiers.org/hgnc/25206
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4056
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16441
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
population: European (Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum

2-220072020-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 220072020
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 220072020
    reference: chr 2
allele count: 1
allele frequency: 8.243887157672586e-6
allele num: 121302
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000289528
  ensembl transcript: ENST00000289528
  gene symbol: ZFAND2B
  hgvsc: ENST00000289528.5:c.56-29G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386370
  ensembl transcript: ENST00000409217
  gene symbol: ZFAND2B
  hgvsc: ENST00000409217.1:c.56-29G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000388773
  ensembl transcript: ENST00000448496
  gene symbol: ZFAND2B
  hgvsc: ENST00000448496.1:c.56-29G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000475533
  gene symbol: ZFAND2B
  hgvsc: ENST00000475533.1:n.36G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386847
  ensembl transcript: ENST00000409412
  gene symbol: ZFAND2B
  hgvsc: ENST00000409412.1:c.56-29G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000400760
  ensembl transcript: ENST00000436556
  gene symbol: ZFAND2B
  hgvsc: ENST00000436556.1:c.56-29G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000464902
  gene symbol: ZFAND2B
  hgvsc: ENST00000464902.1:n.214G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000469596
  gene symbol: ZFAND2B
  hgvsc: ENST00000469596.1:n.81G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000489197
  gene symbol: ZFAND2B
  hgvsc: ENST00000489197.1:n.164-29G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000486734
  gene symbol: ZFAND2B
  hgvsc: ENST00000486734.1:n.108-29G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000387179
  ensembl transcript: ENST00000409097
  gene symbol: ZFAND2B
  hgvsc: ENST00000409097.1:c.56-29G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000411334
  ensembl transcript: ENST00000444522
  gene symbol: ZFAND2B
  hgvsc: ENST00000444522.2:c.56-29G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000409931
  ensembl transcript: ENST00000422255
  gene symbol: ZFAND2B
  hgvsc: ENST00000422255.1:c.56-29G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000468301
  gene symbol: ZFAND2B
  hgvsc: ENST00000468301.1:n.196-29G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386824
  ensembl transcript: ENST00000409206
  gene symbol: ZFAND2B
  hgvsc: ENST00000409206.1:c.56-29G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000387312
  ensembl transcript: ENST00000409319
  gene symbol: ZFAND2B
  hgvsc: ENST00000409319.1:c.56-29G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386399
  ensembl transcript: ENST00000409594
  gene symbol: ZFAND2B
  hgvsc: ENST00000409594.1:c.56-29G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386898
  ensembl transcript: ENST00000409336
  gene symbol: ZFAND2B
  hgvsc: ENST00000409336.1:c.56-29G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000476713
  gene symbol: ZFAND2B
  hgvsc: ENST00000476713.1:n.113-29G>A
  variant of: http://identifiers.org/hgnc/25206
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2324
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: BaseQRankSum

2-220072026-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 220072026
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 220072026
    reference: chr 2
allele count: 1
allele frequency: 8.243207596940122e-6
allele num: 121312
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386824
  ensembl transcript: ENST00000409206
  gene symbol: ZFAND2B
  hgvsc: ENST00000409206.1:c.56-23G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000475533
  gene symbol: ZFAND2B
  hgvsc: ENST00000475533.1:n.42G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000411334
  ensembl transcript: ENST00000444522
  gene symbol: ZFAND2B
  hgvsc: ENST00000444522.2:c.56-23G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000464902
  gene symbol: ZFAND2B
  hgvsc: ENST00000464902.1:n.220G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000486734
  gene symbol: ZFAND2B
  hgvsc: ENST00000486734.1:n.108-23G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000387179
  ensembl transcript: ENST00000409097
  gene symbol: ZFAND2B
  hgvsc: ENST00000409097.1:c.56-23G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000489197
  gene symbol: ZFAND2B
  hgvsc: ENST00000489197.1:n.164-23G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000476713
  gene symbol: ZFAND2B
  hgvsc: ENST00000476713.1:n.113-23G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386847
  ensembl transcript: ENST00000409412
  gene symbol: ZFAND2B
  hgvsc: ENST00000409412.1:c.56-23G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000469596
  gene symbol: ZFAND2B
  hgvsc: ENST00000469596.1:n.87G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000289528
  ensembl transcript: ENST00000289528
  gene symbol: ZFAND2B
  hgvsc: ENST00000289528.5:c.56-23G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000468301
  gene symbol: ZFAND2B
  hgvsc: ENST00000468301.1:n.196-23G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000400760
  ensembl transcript: ENST00000436556
  gene symbol: ZFAND2B
  hgvsc: ENST00000436556.1:c.56-23G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000409931
  ensembl transcript: ENST00000422255
  gene symbol: ZFAND2B
  hgvsc: ENST00000422255.1:c.56-23G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386370
  ensembl transcript: ENST00000409217
  gene symbol: ZFAND2B
  hgvsc: ENST00000409217.1:c.56-23G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000388773
  ensembl transcript: ENST00000448496
  gene symbol: ZFAND2B
  hgvsc: ENST00000448496.1:c.56-23G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386898
  ensembl transcript: ENST00000409336
  gene symbol: ZFAND2B
  hgvsc: ENST00000409336.1:c.56-23G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386399
  ensembl transcript: ENST00000409594
  gene symbol: ZFAND2B
  hgvsc: ENST00000409594.1:c.56-23G>A
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000387312
  ensembl transcript: ENST00000409319
  gene symbol: ZFAND2B
  hgvsc: ENST00000409319.1:c.56-23G>A
  variant of: http://identifiers.org/hgnc/25206
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4049
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1417
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP

2-220072026-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 220072026
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 220072026
    reference: chr 2
allele count: 1
allele frequency: 8.243207596940122e-6
allele num: 121312
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000464902
  gene symbol: ZFAND2B
  hgvsc: ENST00000464902.1:n.220G>C
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000411334
  ensembl transcript: ENST00000444522
  gene symbol: ZFAND2B
  hgvsc: ENST00000444522.2:c.56-23G>C
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386370
  ensembl transcript: ENST00000409217
  gene symbol: ZFAND2B
  hgvsc: ENST00000409217.1:c.56-23G>C
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000388773
  ensembl transcript: ENST00000448496
  gene symbol: ZFAND2B
  hgvsc: ENST00000448496.1:c.56-23G>C
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000387179
  ensembl transcript: ENST00000409097
  gene symbol: ZFAND2B
  hgvsc: ENST00000409097.1:c.56-23G>C
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000469596
  gene symbol: ZFAND2B
  hgvsc: ENST00000469596.1:n.87G>C
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000289528
  ensembl transcript: ENST00000289528
  gene symbol: ZFAND2B
  hgvsc: ENST00000289528.5:c.56-23G>C
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386824
  ensembl transcript: ENST00000409206
  gene symbol: ZFAND2B
  hgvsc: ENST00000409206.1:c.56-23G>C
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000468301
  gene symbol: ZFAND2B
  hgvsc: ENST00000468301.1:n.196-23G>C
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000400760
  ensembl transcript: ENST00000436556
  gene symbol: ZFAND2B
  hgvsc: ENST00000436556.1:c.56-23G>C
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000409931
  ensembl transcript: ENST00000422255
  gene symbol: ZFAND2B
  hgvsc: ENST00000422255.1:c.56-23G>C
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000475533
  gene symbol: ZFAND2B
  hgvsc: ENST00000475533.1:n.42G>C
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386399
  ensembl transcript: ENST00000409594
  gene symbol: ZFAND2B
  hgvsc: ENST00000409594.1:c.56-23G>C
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000486734
  gene symbol: ZFAND2B
  hgvsc: ENST00000486734.1:n.108-23G>C
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000387312
  ensembl transcript: ENST00000409319
  gene symbol: ZFAND2B
  hgvsc: ENST00000409319.1:c.56-23G>C
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386847
  ensembl transcript: ENST00000409412
  gene symbol: ZFAND2B
  hgvsc: ENST00000409412.1:c.56-23G>C
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000476713
  gene symbol: ZFAND2B
  hgvsc: ENST00000476713.1:n.113-23G>C
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386898
  ensembl transcript: ENST00000409336
  gene symbol: ZFAND2B
  hgvsc: ENST00000409336.1:c.56-23G>C
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000489197
  gene symbol: ZFAND2B
  hgvsc: ENST00000489197.1:n.164-23G>C
  variant of: http://identifiers.org/hgnc/25206
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16448
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4275
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: Other
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD

2-220072027-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 220072027
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 220072027
    reference: chr 2
allele count: 1
allele frequency: 8.243071698237632e-6
allele num: 121314
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000489197
  gene symbol: ZFAND2B
  hgvsc: ENST00000489197.1:n.164-22C>G
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000464902
  gene symbol: ZFAND2B
  hgvsc: ENST00000464902.1:n.221C>G
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000476713
  gene symbol: ZFAND2B
  hgvsc: ENST00000476713.1:n.113-22C>G
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386399
  ensembl transcript: ENST00000409594
  gene symbol: ZFAND2B
  hgvsc: ENST00000409594.1:c.56-22C>G
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000468301
  gene symbol: ZFAND2B
  hgvsc: ENST00000468301.1:n.196-22C>G
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386824
  ensembl transcript: ENST00000409206
  gene symbol: ZFAND2B
  hgvsc: ENST00000409206.1:c.56-22C>G
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000411334
  ensembl transcript: ENST00000444522
  gene symbol: ZFAND2B
  hgvsc: ENST00000444522.2:c.56-22C>G
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386898
  ensembl transcript: ENST00000409336
  gene symbol: ZFAND2B
  hgvsc: ENST00000409336.1:c.56-22C>G
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000387312
  ensembl transcript: ENST00000409319
  gene symbol: ZFAND2B
  hgvsc: ENST00000409319.1:c.56-22C>G
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000289528
  ensembl transcript: ENST00000289528
  gene symbol: ZFAND2B
  hgvsc: ENST00000289528.5:c.56-22C>G
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000469596
  gene symbol: ZFAND2B
  hgvsc: ENST00000469596.1:n.88C>G
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000475533
  gene symbol: ZFAND2B
  hgvsc: ENST00000475533.1:n.43C>G
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000388773
  ensembl transcript: ENST00000448496
  gene symbol: ZFAND2B
  hgvsc: ENST00000448496.1:c.56-22C>G
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000409931
  ensembl transcript: ENST00000422255
  gene symbol: ZFAND2B
  hgvsc: ENST00000422255.1:c.56-22C>G
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000486734
  gene symbol: ZFAND2B
  hgvsc: ENST00000486734.1:n.108-22C>G
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000400760
  ensembl transcript: ENST00000436556
  gene symbol: ZFAND2B
  hgvsc: ENST00000436556.1:c.56-22C>G
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000387179
  ensembl transcript: ENST00000409097
  gene symbol: ZFAND2B
  hgvsc: ENST00000409097.1:c.56-22C>G
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386370
  ensembl transcript: ENST00000409217
  gene symbol: ZFAND2B
  hgvsc: ENST00000409217.1:c.56-22C>G
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386847
  ensembl transcript: ENST00000409412
  gene symbol: ZFAND2B
  hgvsc: ENST00000409412.1:c.56-22C>G
  variant of: http://identifiers.org/hgnc/25206
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4285
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
population: East Asian
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP

2-220072029-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 220072029
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 220072029
    reference: chr 2
allele count: 1
allele frequency: 8.242935804015958e-6
allele num: 121316
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386847
  ensembl transcript: ENST00000409412
  gene symbol: ZFAND2B
  hgvsc: ENST00000409412.1:c.56-20A>G
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000409931
  ensembl transcript: ENST00000422255
  gene symbol: ZFAND2B
  hgvsc: ENST00000422255.1:c.56-20A>G
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000386399
  ensembl transcript: ENST00000409594
  gene symbol: ZFAND2B
  hgvsc: ENST00000409594.1:c.56-20A>G
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000411334
  ensembl transcript: ENST00000444522
  gene symbol: ZFAND2B
  hgvsc: ENST00000444522.2:c.56-20A>G
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158552
  ensembl protein: ENSP00000400760
  ensembl transcript: ENST00000436556
  gene symbol: ZFAND2B
  hgvsc: ENST00000436556.1:c.56-20A>G
  variant of: http://identifiers.org/hgnc/25206
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158552
  ensembl transcript: ENST00000464902
  gene symbol: ZFAND2B
  hgvsc: ENST00000464902.1:n.223A>G
  variant of: http://identifiers.org/hgnc/25206
canonical: false
consequence: non coding transcript exon
filter: PASS
num of homozygotes: 0
reference allele: A

GenotypeQuality
all individuals: 56
bin: 2.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66590
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: 904
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10362
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.05766900896535e-5
allele num: 16508
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.5e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 1.43e0

VQSLOD
type: SiteQuality
SIO_000300: 6.45e-1

MQRankSum
type: SiteQuality
SIO_000300: -9.5e-2

QD
type: SiteQuality
SIO_000300: 1.345e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.259e0

DP
type: SiteQuality
SIO_000300: 2.2689e6

GenotypeQuality
all individuals: 18300
bin: 6.25e1
variant carriers: 0

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

Other
type: Population
allele count: 1
allele frequency: 1.106194690265487e-3
allele num: 904
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: 276
allele frequency: 2.664092664092664e-2
allele num: 10360
num of homozygotes: 4

Latino
type: Population
allele count: 8
allele frequency: 6.912044237083118e-4
allele num: 11574
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 7
allele frequency: 1.051303616484441e-4
allele num: 66584
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.5e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.4e-2

DP
type: SiteQuality
SIO_000300: 2.273235e6

MQRankSum
type: SiteQuality
SIO_000300: 2.98e-1

QD
type: SiteQuality
SIO_000300: 1.344e1

MQ
type: SiteQuality
SIO_000300: 5.958e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.21e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.59e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.3e0

GenotypeQuality
all individuals: 3875
bin: 9.25e1
variant carriers: 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

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501681883709755e-5
allele num: 66592
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10356
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.37e0

MQRankSum
type: SiteQuality
SIO_000300: -6.12e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 1.603e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.72e0

VQSLOD
type: SiteQuality
SIO_000300: -4.375e-1

QD
type: SiteQuality
SIO_000300: 1.093e1

DP
type: SiteQuality
SIO_000300: 2.257499e6

ClippingRankSum
type: SiteQuality
SIO_000300: -2.548e0

GenotypeQuality
all individuals: 45
bin: 3.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10354
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 902
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.502494140272853e-5
allele num: 66556
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: 8630
num of homozygotes: 0

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

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

VQSLOD
type: SiteQuality
SIO_000300: -3.221e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.38e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-3

DP
type: SiteQuality
SIO_000300: 2.256076e6

BaseQRankSum
type: SiteQuality
SIO_000300: 9.69e-1

MQ
type: SiteQuality
SIO_000300: 5.904e1

MQRankSum
type: SiteQuality
SIO_000300: 1.29e0

FS
type: SiteQuality
SIO_000300: 5.174e0

QD
type: SiteQuality
SIO_000300: 1.193e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.43e-1

GenotypeQuality
all individuals: 87
bin: 3.25e1
variant carriers: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.21197430614471e-4
allele num: 16502
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11564
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66526
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8630
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 902
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10344
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -1.451e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.933e1

DP
type: SiteQuality
SIO_000300: 2.254312e6

QD
type: SiteQuality
SIO_000300: 1.436e1

VQSLOD
type: SiteQuality
SIO_000300: 9.96e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.625e0

MQRankSum
type: SiteQuality
SIO_000300: 6.29e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.55e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

GenotypeQuality
all individuals: 23
bin: 4.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11554
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: 1
allele frequency: 6.066488716330988e-5
allele num: 16484
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 902
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: 10324
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 2.21e-1

QD
type: SiteQuality
SIO_000300: 1.216e1

FS
type: SiteQuality
SIO_000300: 3.395e0

DP
type: SiteQuality
SIO_000300: 2.249402e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -2.746e0

BaseQRankSum
type: SiteQuality
SIO_000300: -8.139999999999999e-1

MQ
type: SiteQuality
SIO_000300: 5.929e1

VQSLOD
type: SiteQuality
SIO_000300: 7.71e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.4e-1

GenotypeQuality
all individuals: 9
bin: 1.75e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 7
allele frequency: 1.054343896855043e-4
allele num: 66392
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10304
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 902
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8612
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.22e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.06e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.93e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.81e-1

DP
type: SiteQuality
SIO_000300: 2.241613e6

FS
type: SiteQuality
SIO_000300: 5.93e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.25e0

QD
type: SiteQuality
SIO_000300: 1.31e1

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16424
num of homozygotes: 0

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

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

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

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

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

African
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East Asian
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European (Non-Finnish)
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South Asian
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Other
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Latino
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European (Finnish)
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FS
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BaseQRankSum
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QD
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MQ
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ReadPosRankSum
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VQSLOD
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InbreedingCoeff
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MQRankSum
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DP
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ClippingRankSum
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GenotypeQuality
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African
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East Asian
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South Asian
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European (Non-Finnish)
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Latino
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Other
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European (Finnish)
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MQ
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MQRankSum
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DP
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BaseQRankSum
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QD
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ReadPosRankSum
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VQSLOD
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InbreedingCoeff
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FS
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ClippingRankSum
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GenotypeQuality
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East Asian
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Latino
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African
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European (Non-Finnish)
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South Asian
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European (Finnish)
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Other
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BaseQRankSum
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MQ
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ReadPosRankSum
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MQRankSum
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ClippingRankSum
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FS
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DP
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InbreedingCoeff
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QD
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VQSLOD
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GenotypeQuality
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South Asian
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Latino
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European (Non-Finnish)
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European (Finnish)
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African
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Other
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East Asian
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InbreedingCoeff
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QD
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MQRankSum
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ClippingRankSum
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VQSLOD
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BaseQRankSum
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FS
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MQ
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DP
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ReadPosRankSum
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GenotypeQuality
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South Asian
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European (Finnish)
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Latino
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Other
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European (Non-Finnish)
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African
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East Asian
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FS
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ReadPosRankSum
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DP
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ClippingRankSum
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VQSLOD
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MQRankSum
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MQ
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BaseQRankSum
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QD
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InbreedingCoeff
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GenotypeQuality
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European (Non-Finnish)
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East Asian
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Latino
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European (Finnish)
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South Asian
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African
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Other
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MQ
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VQSLOD
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FS
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QD
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InbreedingCoeff
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MQRankSum
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ReadPosRankSum
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BaseQRankSum
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ClippingRankSum
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DP
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GenotypeQuality
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European (Non-Finnish)
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East Asian
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European (Finnish)
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Latino
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South Asian
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African
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Other
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FS
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ClippingRankSum
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MQRankSum
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QD
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DP
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InbreedingCoeff
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ReadPosRankSum
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VQSLOD
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MQ
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BaseQRankSum
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GenotypeQuality
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South Asian
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African
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East Asian
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Latino
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European (Non-Finnish)
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European (Finnish)
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MQ
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VQSLOD
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FS
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DP
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QD
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MQRankSum
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InbreedingCoeff
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ClippingRankSum
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BaseQRankSum
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ReadPosRankSum
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GenotypeQuality
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East Asian
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South Asian
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African
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Other
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European (Non-Finnish)
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European (Finnish)
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MQ
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InbreedingCoeff
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DP
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ReadPosRankSum
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BaseQRankSum
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ClippingRankSum
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MQRankSum
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FS
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VQSLOD
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QD
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GenotypeQuality
all individuals: 10653
bin: 6.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10008
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 9.193429762196617e-5
allele num: 65264
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11514
num of homozygotes: 0

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

South Asian
type: Population
allele count: 187
allele frequency: 1.197796566743531e-2
allele num: 15612
num of homozygotes: 4

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

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

QD
type: SiteQuality
SIO_000300: 1.629e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.4e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 4.75e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.52e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.01e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.99e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.74e-1

DP
type: SiteQuality
SIO_000300: 2.120227e6

GenotypeQuality
all individuals: 2004
bin: 8.25e1
variant carriers: 1081

European (Non-Finnish)
type: Population
allele count: 41078
allele frequency: 6.315999876994988e-1
allele num: 65038
num of homozygotes: 12884

Latino
type: Population
allele count: 4395
allele frequency: 3.865435356200528e-1
allele num: 11370
num of homozygotes: 860

East Asian
type: Population
allele count: 2408
allele frequency: 2.842304060434372e-1
allele num: 8472
num of homozygotes: 349

African
type: Population
allele count: 2832
allele frequency: 2.816789337577084e-1
allele num: 10054
num of homozygotes: 418

Other
type: Population
allele count: 518
allele frequency: 5.91324200913242e-1
allele num: 876
num of homozygotes: 149

South Asian
type: Population
allele count: 9233
allele frequency: 6.020474700052165e-1
allele num: 15336
num of homozygotes: 2782

European (Finnish)
type: Population
allele count: 4322
allele frequency: 6.596459096459096e-1
allele num: 6552
num of homozygotes: 1407

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 5.4e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.37e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.32e-1

DP
type: SiteQuality
SIO_000300: 2.100875e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.716e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.23e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 5.36e0

QD
type: SiteQuality
SIO_000300: 2.307e1

GenotypeQuality
all individuals: 2823
bin: 9.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.745845723281441e-5
allele num: 11434
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10016
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64538
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14470
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 856
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -2.269e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.19e-1

MQ
type: SiteQuality
SIO_000300: 5.864e1

MQRankSum
type: SiteQuality
SIO_000300: 1.79e0

QD
type: SiteQuality
SIO_000300: 7.65e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.8e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 9.02e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.771e0

DP
type: SiteQuality
SIO_000300: 1.799459e6

FS
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
all individuals: 435
bin: 7.5e0
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9998
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11422
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 856
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.103565997330933e-5
allele num: 64442
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14328
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6556
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.44e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.42e0

QD
type: SiteQuality
SIO_000300: 1.845e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.7e-3

VQSLOD
type: SiteQuality
SIO_000300: -6.1e-1

FS
type: SiteQuality
SIO_000300: 1.78e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 9.97e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.788998e6

GenotypeDepth
all individuals: 2702
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7934
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 98
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variant carriers: 0

GenotypeDepth
all individuals: 4
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variant carriers: 0

GenotypeDepth
all individuals: 52
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variant carriers: 0

GenotypeDepth
all individuals: 5
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variant carriers: 0

GenotypeDepth
all individuals: 3
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variant carriers: 0

GenotypeDepth
all individuals: 9
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variant carriers: 0

GenotypeQuality
all individuals: 179
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2336
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variant carriers: 0

GenotypeQuality
all individuals: 431
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4265
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variant carriers: 0

GenotypeQuality
all individuals: 509
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variant carriers: 0

GenotypeQuality
all individuals: 3781
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variant carriers: 0

GenotypeQuality
all individuals: 367
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 801
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variant carriers: 0

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

GenotypeQuality
all individuals: 9547
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 643
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3981
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 358
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 23411
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 890
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1715
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2408
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 881
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3846
bin: 3.25e1
variant carriers: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 740
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7462
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8208
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10298
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5062
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14520
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.768158992856638e-5
allele num: 56556
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.19e-1

FS
type: SiteQuality
SIO_000300: 7.925e0

MQRankSum
type: SiteQuality
SIO_000300: -1.85e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 1.33e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.12e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.5e-3

DP
type: SiteQuality
SIO_000300: 1.123107e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.733e0

QD
type: SiteQuality
SIO_000300: 1.37e1

GenotypeDepth
all individuals: 52
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 13
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 21918
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variant carriers: 0

GenotypeDepth
all individuals: 4937
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variant carriers: 0

GenotypeDepth
all individuals: 3
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variant carriers: 0

GenotypeDepth
all individuals: 21
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 99
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variant carriers: 1

GenotypeQuality
all individuals: 860
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 123
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 455
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variant carriers: 0

GenotypeQuality
all individuals: 3967
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variant carriers: 0

GenotypeQuality
all individuals: 2062
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1046
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 480
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variant carriers: 0

GenotypeQuality
all individuals: 334
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variant carriers: 0

GenotypeQuality
all individuals: 1746
bin: 4.25e1
variant carriers: 1

GenotypeQuality
all individuals: 3533
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 120
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variant carriers: 0

GenotypeQuality
all individuals: 3554
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9872
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2184
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 789
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variant carriers: 0

GenotypeQuality
all individuals: 883
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27763
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 352
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variant carriers: 1

GenotypeQuality
all individuals: 349
bin: 8.25e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5064
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14514
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 740
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8220
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.764166255027874e-5
allele num: 56684
num of homozygotes: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.333688983728994e-4
allele num: 7498
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.64e-1

FS
type: SiteQuality
SIO_000300: 1.0569e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.983e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.4e-3

QD
type: SiteQuality
SIO_000300: 1.76e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -1.901e0

MQRankSum
type: SiteQuality
SIO_000300: 4.12e-1

DP
type: SiteQuality
SIO_000300: 1.153927e6

ClippingRankSum
type: SiteQuality
SIO_000300: -2.54e-1

GenotypeDepth
all individuals: 21
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2811
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 10669
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7
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variant carriers: 0

GenotypeDepth
all individuals: 5
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variant carriers: 0

GenotypeDepth
all individuals: 199
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variant carriers: 0

GenotypeDepth
all individuals: 4
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variant carriers: 0

GenotypeDepth
all individuals: 3
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variant carriers: 0

GenotypeQuality
all individuals: 267
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4013
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variant carriers: 0

GenotypeQuality
all individuals: 108
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2095
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variant carriers: 0

GenotypeQuality
all individuals: 757
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GenotypeQuality
all individuals: 1297
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 353
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variant carriers: 1

GenotypeQuality
all individuals: 897
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GenotypeQuality
all individuals: 847
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variant carriers: 0

GenotypeQuality
all individuals: 3209
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GenotypeQuality
all individuals: 380
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variant carriers: 0

GenotypeQuality
all individuals: 829
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GenotypeQuality
all individuals: 2917
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GenotypeQuality
all individuals: 29583
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GenotypeQuality
all individuals: 360
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GenotypeQuality
all individuals: 1465
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GenotypeQuality
all individuals: 926
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GenotypeQuality
all individuals: 10050
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variant carriers: 0

GenotypeQuality
all individuals: 120
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variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7520
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 56690
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14516
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8210
num of homozygotes: 0

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

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

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.973164956590371e-4
allele num: 5068
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.133e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.78e0

FS
type: SiteQuality
SIO_000300: 4.84e0

MQRankSum
type: SiteQuality
SIO_000300: 7.6e-1

DP
type: SiteQuality
SIO_000300: 1.172447e6

VQSLOD
type: SiteQuality
SIO_000300: 5.659999999999999e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.47e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.2e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 7.6e-1

GenotypeDepth
all individuals: 2869
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6876
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variant carriers: 0

GenotypeDepth
all individuals: 8034
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variant carriers: 0

GenotypeDepth
all individuals: 199
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variant carriers: 0

GenotypeDepth
all individuals: 4
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GenotypeDepth
all individuals: 99
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GenotypeDepth
all individuals: 5
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GenotypeDepth
all individuals: 9
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GenotypeDepth
all individuals: 1918
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GenotypeDepth
all individuals: 3
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GenotypeQuality
all individuals: 904
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GenotypeQuality
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GenotypeQuality
all individuals: 358
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 4075
bin: 6.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5038
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 2.443195699975568e-4
allele num: 8186
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7578
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14570
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 56864
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 756
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -1.885e0

QD
type: SiteQuality
SIO_000300: 1.99e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.4e-3

MQRankSum
type: SiteQuality
SIO_000300: 1.07e-1

MQ
type: SiteQuality
SIO_000300: 5.911e1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.76e-1

VQSLOD
type: SiteQuality
SIO_000300: -4.095e0

DP
type: SiteQuality
SIO_000300: 1.219738e6

FS
type: SiteQuality
SIO_000300: 4.067e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.561e0

GenotypeDepth
all individuals: 205
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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South Asian
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East Asian
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European (Finnish)
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European (Non-Finnish)
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Latino
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ClippingRankSum
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MQ
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InbreedingCoeff
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DP
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VQSLOD
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FS
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MQRankSum
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BaseQRankSum
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QD
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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Latino
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East Asian
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European (Finnish)
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Other
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African
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European (Non-Finnish)
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BaseQRankSum
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MQRankSum
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InbreedingCoeff
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FS
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QD
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ClippingRankSum
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ReadPosRankSum
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VQSLOD
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DP
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MQ
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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African
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European (Non-Finnish)
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European (Finnish)
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South Asian
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FS
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QD
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BaseQRankSum
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MQ
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ReadPosRankSum
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VQSLOD
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MQRankSum
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DP
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InbreedingCoeff
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ClippingRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 56752
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Latino
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African
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South Asian
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European (Finnish)
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East Asian
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Other
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MQRankSum
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VQSLOD
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ReadPosRankSum
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DP
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InbreedingCoeff
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FS
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MQ
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BaseQRankSum
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QD
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ClippingRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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Latino
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European (Finnish)
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Other
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East Asian
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South Asian
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MQRankSum
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QD
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ClippingRankSum
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ReadPosRankSum
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FS
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BaseQRankSum
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InbreedingCoeff
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MQ
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DP
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VQSLOD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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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East Asian
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South Asian
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European (Finnish)
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Other
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VQSLOD
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ClippingRankSum
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DP
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QD
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MQRankSum
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MQ
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InbreedingCoeff
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FS
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ReadPosRankSum
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BaseQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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allele frequency: 0.0e0
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South Asian
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Latino
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allele frequency: 0.0e0
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African
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East Asian
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European (Non-Finnish)
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allele num: 54276
num of homozygotes: 0

Other
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FS
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VQSLOD
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InbreedingCoeff
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ReadPosRankSum
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MQRankSum
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MQ
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DP
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ClippingRankSum
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QD
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BaseQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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African
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European (Finnish)
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Latino
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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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BaseQRankSum
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MQRankSum
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DP
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FS
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MQ
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ClippingRankSum
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VQSLOD
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InbreedingCoeff
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ReadPosRankSum
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 49536
num of homozygotes: 0

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

DP
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SIO_000300: 9.18454e5

InbreedingCoeff
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SIO_000300: -7.900000000000001e-3

MQRankSum
type: SiteQuality
SIO_000300: 1.55e0

VQSLOD
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SIO_000300: -1.27e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.2e0

FS
type: SiteQuality
SIO_000300: 4.27e0

BaseQRankSum
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SIO_000300: -3.533e0

MQ
type: SiteQuality
SIO_000300: 5.939e1

QD
type: SiteQuality
SIO_000300: 8.44e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.06e-1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

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

Latino
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allele frequency: 0.0e0
allele num: 7798
num of homozygotes: 0

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

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

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 5672
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 2.222024708914763e-5
allele num: 45004
num of homozygotes: 0

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 600
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.92e-1

InbreedingCoeff
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SIO_000300: -1.07e-2

MQRankSum
type: SiteQuality
SIO_000300: 6.34e-1

BaseQRankSum
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QD
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ReadPosRankSum
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FS
type: SiteQuality
SIO_000300: 1.425e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
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SIO_000300: 1.02e0

DP
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SIO_000300: 8.35905e5

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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variant carriers: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 6932
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 40666
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 3158
num of homozygotes: 0

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

South Asian
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allele count: 1
allele frequency: 8.287750704458811e-5
allele num: 12066
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 564
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4822
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
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SIO_000300: 3.72e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.31e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.67e-1

DP
type: SiteQuality
SIO_000300: 7.46478e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.46e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.84e-1

MQRankSum
type: SiteQuality
SIO_000300: -6.19e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.344e0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 2962
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 4478
num of homozygotes: 0

Latino
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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 count: 0
allele frequency: 0.0e0
allele num: 39102
num of homozygotes: 0

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

South Asian
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allele count: 0
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num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
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MQRankSum
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DP
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InbreedingCoeff
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MQ
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ReadPosRankSum
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QD
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ClippingRankSum
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SIO_000300: -3.61e-1

VQSLOD
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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allele count: 0
allele frequency: 0.0e0
allele num: 4302
num of homozygotes: 0

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

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

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

European (Finnish)
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allele frequency: 0.0e0
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Latino
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allele num: 6344
num of homozygotes: 0

QD
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InbreedingCoeff
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MQ
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BaseQRankSum
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VQSLOD
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DP
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MQRankSum
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FS
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ClippingRankSum
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ReadPosRankSum
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 6344
num of homozygotes: 0

African
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allele frequency: 0.0e0
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East Asian
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Other
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South Asian
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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

European (Non-Finnish)
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allele frequency: 0.0e0
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MQ
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ReadPosRankSum
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MQRankSum
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QD
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ClippingRankSum
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FS
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VQSLOD
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BaseQRankSum
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InbreedingCoeff
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DP
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GenotypeDepth
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variant carriers: 2

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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: 50

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

Latino
type: Population
allele count: 6
allele frequency: 9.637006103437199e-4
allele num: 6226
num of homozygotes: 0

Other
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allele count: 0
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num of homozygotes: 0

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

African
type: Population
allele count: 54
allele frequency: 1.248843663274746e-2
allele num: 4324
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European (Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

FS
type: SiteQuality
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DP
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SIO_000300: 7.08413e5

VQSLOD
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ReadPosRankSum
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InbreedingCoeff
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BaseQRankSum
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QD
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MQRankSum
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SIO_000300: 3.46e-1

ClippingRankSum
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MQ
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

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

ClippingRankSum
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MQRankSum
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VQSLOD
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QD
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InbreedingCoeff
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MQ
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FS
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DP
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BaseQRankSum
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 frequency: 0.0e0
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num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

European (Non-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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num of homozygotes: 0

DP
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SIO_000300: 7.00778e5

InbreedingCoeff
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ClippingRankSum
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FS
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QD
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MQ
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VQSLOD
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BaseQRankSum
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SIO_000300: 9.56e-1

ReadPosRankSum
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SIO_000300: -6.840000000000001e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.52e0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

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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Latino
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Other
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African
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East Asian
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QD
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InbreedingCoeff
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FS
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BaseQRankSum
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ReadPosRankSum
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VQSLOD
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MQRankSum
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MQ
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ClippingRankSum
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DP
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GenotypeDepth
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variant carriers: 0

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

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

East Asian
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allele num: 3716
num of homozygotes: 0

South Asian
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num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

African
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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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num of homozygotes: 0

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

MQRankSum
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FS
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BaseQRankSum
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QD
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ClippingRankSum
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DP
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VQSLOD
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InbreedingCoeff
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MQ
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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allele frequency: 0.0e0
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num of homozygotes: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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East Asian
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African
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allele frequency: 2.745744096650192e-4
allele num: 3642
num of homozygotes: 0

South Asian
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num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

DP
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ReadPosRankSum
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FS
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VQSLOD
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ClippingRankSum
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InbreedingCoeff
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QD
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BaseQRankSum
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SIO_000300: 8.04e-1

MQRankSum
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MQ
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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African
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num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 0.0e0
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European (Finnish)
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South Asian
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East Asian
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InbreedingCoeff
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VQSLOD
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QD
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FS
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MQRankSum
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DP
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MQ
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BaseQRankSum
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ReadPosRankSum
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ClippingRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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East Asian
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European (Non-Finnish)
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Latino
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African
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European (Finnish)
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Other
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ReadPosRankSum
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DP
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MQ
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ClippingRankSum
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VQSLOD
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FS
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MQRankSum
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InbreedingCoeff
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BaseQRankSum
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QD
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GenotypeDepth
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variant carriers: 16798

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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allele frequency: 5.264565992865636e-1
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European (Finnish)
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allele frequency: 9.631396357328708e-1
allele num: 2306
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European (Non-Finnish)
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allele num: 31334
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East Asian
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South Asian
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allele frequency: 8.17148182665424e-1
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num of homozygotes: 3578

Latino
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allele frequency: 8.887252839713925e-1
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Other
type: Population
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allele num: 436
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VQSLOD
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InbreedingCoeff
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DP
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ReadPosRankSum
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QD
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MQRankSum
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MQ
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FS
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BaseQRankSum
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ClippingRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1480
num of homozygotes: 0

Latino
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allele frequency: 3.51123595505618e-4
allele num: 2848
num of homozygotes: 0

South Asian
type: Population
allele count: 0
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MQRankSum
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FS
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VQSLOD
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ClippingRankSum
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InbreedingCoeff
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DP
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QD
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MQ
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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African
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East Asian
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Latino
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MQRankSum
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MQ
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DP
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InbreedingCoeff
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VQSLOD
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FS
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QD
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ClippingRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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European (Finnish)
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Latino
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East Asian
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European (Non-Finnish)
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BaseQRankSum
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MQRankSum
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ReadPosRankSum
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DP
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MQ
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InbreedingCoeff
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VQSLOD
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ClippingRankSum
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FS
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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African
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East Asian
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South Asian
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BaseQRankSum
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MQRankSum
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InbreedingCoeff
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QD
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ReadPosRankSum
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FS
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MQ
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ClippingRankSum
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DP
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GenotypeQuality
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South Asian
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European (Non-Finnish)
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East Asian
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DP
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VQSLOD
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MQ
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GenotypeQuality
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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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VQSLOD
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ReadPosRankSum
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FS
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InbreedingCoeff
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MQ
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GenotypeDepth
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bin: 1.25e1
variant carriers: 0

GenotypeDepth
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bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 45
bin: 7.5e0
variant carriers: 0

GenotypeDepth
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bin: 9.75e1
variant carriers: 1

GenotypeDepth
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bin: 8.75e1
variant carriers: 0

GenotypeDepth
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bin: 3.75e1
variant carriers: 0

GenotypeDepth
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bin: 1.75e1
variant carriers: 0

GenotypeDepth
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bin: 2.25e1
variant carriers: 0

GenotypeDepth
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bin: 3.25e1
variant carriers: 0

GenotypeDepth
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bin: 2.75e1
variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 111
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2324
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 544
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 221
bin: 7.75e1
variant carriers: 0

GenotypeDepth
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9557
bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
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: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 46
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variant carriers: 0

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.500015000150001e-5
allele num: 66666
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10392
num of homozygotes: 0

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

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

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

VQSLOD
type: SiteQuality
SIO_000300: -8.751e-1

InbreedingCoeff
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SIO_000300: 1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -3.52e-1

QD
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SIO_000300: 1.595e1

BaseQRankSum
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SIO_000300: -5.629999999999999e-1

MQ
type: SiteQuality
SIO_000300: 5.971e1

MQRankSum
type: SiteQuality
SIO_000300: 9.79e-1

FS
type: SiteQuality
SIO_000300: 1.3958e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.45e-1

DP
type: SiteQuality
SIO_000300: 2.067193e6

GenotypeDepth
all individuals: 1417
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 441
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 4
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 2324
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 897
bin: 5.75e1
variant carriers: 0

GenotypeDepth
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bin: 1.25e1
variant carriers: 0

GenotypeDepth
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bin: 2.75e1
variant carriers: 0

GenotypeDepth
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bin: 9.25e1
variant carriers: 0

GenotypeDepth
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bin: 4.25e1
variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
all individuals: 68
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variant carriers: 0

GenotypeDepth
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bin: 3.75e1
variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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bin: 6.25e1
variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
all individuals: 4911
bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 62
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3
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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: 9.25e1
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
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 46
bin: 3.75e1
variant carriers: 0

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66666
num of homozygotes: 0

African
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allele count: 1
allele frequency: 9.622786759045419e-5
allele num: 10392
num of homozygotes: 0

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

BaseQRankSum
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SIO_000300: -5.629999999999999e-1

MQRankSum
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SIO_000300: 9.79e-1

DP
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SIO_000300: 2.067193e6

MQ
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SIO_000300: 5.971e1

ReadPosRankSum
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SIO_000300: 7.45e-1

ClippingRankSum
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SIO_000300: -3.52e-1

QD
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SIO_000300: 1.595e1

FS
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SIO_000300: 1.3958e1

InbreedingCoeff
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SIO_000300: 1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -8.751e-1

GenotypeDepth
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bin: 4.75e1
variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
all individuals: 152
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
all individuals: 111
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variant carriers: 0

GenotypeQuality
all individuals: 3
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variant carriers: 0

GenotypeQuality
all individuals: 78
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variant carriers: 0

GenotypeQuality
all individuals: 14
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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: 2.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 4.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
all individuals: 4
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4915
bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3635
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1629
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10392
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66668
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.05766900896535e-5
allele num: 16508
num of homozygotes: 0

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

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: -1.463e0

MQRankSum
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SIO_000300: 2.66e0

MQ
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SIO_000300: 5.965e1

QD
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SIO_000300: 1.064e1

VQSLOD
type: SiteQuality
SIO_000300: -1.39e0

InbreedingCoeff
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SIO_000300: 0.0e0

ClippingRankSum
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SIO_000300: 1.8e-2

FS
type: SiteQuality
SIO_000300: 3.321e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.53e0

DP
type: SiteQuality
SIO_000300: 2.067103e6