16-3433599-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3433599
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3433599
    reference: chr 16
allele count: 3
allele frequency: 2.47255464345762e-5
allele num: 121332
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262621
  ensembl transcript: ENST00000576906
  gene symbol: NAA60
  hgvsc: ENST00000576906.1:n.85-411A>G
  variant of: http://identifiers.org/hgnc/25875
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000302502
  ensembl transcript: ENST00000304926
  gene symbol: ZSCAN32
  hgvsc: ENST00000304926.3:c.711T>C
  hgvsp: ENST00000304926.3:c.711T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000380057
  ensembl transcript: ENST00000396846
  gene symbol: ZSCAN32
  hgvsc: ENST00000396846.3:c.1347T>C
  hgvsp: ENST00000396846.3:c.1347T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000391787
  ensembl transcript: ENST00000439568
  gene symbol: ZSCAN32
  hgvsc: ENST00000439568.2:c.480T>C
  hgvsp: ENST00000439568.2:c.480T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140987
  ensembl transcript: ENST00000571285
  gene symbol: ZSCAN32
  hgvsc: ENST00000571285.1:n.463T>C
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000380061
  ensembl transcript: ENST00000396852
  gene symbol: ZSCAN32
  hgvsc: ENST00000396852.4:c.1347T>C
  hgvsp: ENST00000396852.4:c.1347T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000459069
  ensembl transcript: ENST00000576500
  gene symbol: ZSCAN32
  hgvsc: ENST00000576500.1:c.*401T>C
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262621
  ensembl protein: ENSP00000477472
  ensembl transcript: ENST00000575785
  gene symbol: NAA60
  hgvsc: ENST00000575785.1:c.-13+18417A>G
  variant of: http://identifiers.org/hgnc/25875
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1341
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13166
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8446
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 6449
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 806
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3881
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21741
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2181
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31760
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7320
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Ser237Ser
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
population: Other
population: European (Finnish)
population: South Asian
reference allele: A
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: BaseQRankSum

16-3433608-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3433608
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3433608
    reference: chr 16
allele count: 1
allele frequency: 8.244974687927709e-6
allele num: 121286
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262621
  ensembl transcript: ENST00000576906
  gene symbol: NAA60
  hgvsc: ENST00000576906.1:n.85-402A>G
  variant of: http://identifiers.org/hgnc/25875
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000380057
  ensembl transcript: ENST00000396846
  gene symbol: ZSCAN32
  hgvsc: ENST00000396846.3:c.1338T>C
  hgvsp: ENST00000396846.3:c.1338T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140987
  ensembl transcript: ENST00000571285
  gene symbol: ZSCAN32
  hgvsc: ENST00000571285.1:n.454T>C
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262621
  ensembl protein: ENSP00000477472
  ensembl transcript: ENST00000575785
  gene symbol: NAA60
  hgvsc: ENST00000575785.1:c.-13+18426A>G
  variant of: http://identifiers.org/hgnc/25875
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000459069
  ensembl transcript: ENST00000576500
  gene symbol: ZSCAN32
  hgvsc: ENST00000576500.1:c.*392T>C
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000302502
  ensembl transcript: ENST00000304926
  gene symbol: ZSCAN32
  hgvsc: ENST00000304926.3:c.702T>C
  hgvsp: ENST00000304926.3:c.702T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000380061
  ensembl transcript: ENST00000396852
  gene symbol: ZSCAN32
  hgvsc: ENST00000396852.4:c.1338T>C
  hgvsp: ENST00000396852.4:c.1338T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000391787
  ensembl transcript: ENST00000439568
  gene symbol: ZSCAN32
  hgvsc: ENST00000439568.2:c.471T>C
  hgvsp: ENST00000439568.2:c.471T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20812
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3883
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21716
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13153
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6443
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2182
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 806
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8430
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1341
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1378
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1770
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Tyr234Tyr
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: A
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: MQ

16-3433613-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3433613
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3433613
    reference: chr 16
allele count: 2
allele frequency: 1.649838315845047e-5
allele num: 121224
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000302502
  ensembl transcript: ENST00000304926
  gene symbol: ZSCAN32
  hgvsc: ENST00000304926.3:c.697G>A
  hgvsp: ENSP00000302502.3:p.Val233Ile
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000380057
  ensembl transcript: ENST00000396846
  gene symbol: ZSCAN32
  hgvsc: ENST00000396846.3:c.1333G>A
  hgvsp: ENSP00000380057.3:p.Val445Ile
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000380061
  ensembl transcript: ENST00000396852
  gene symbol: ZSCAN32
  hgvsc: ENST00000396852.4:c.1333G>A
  hgvsp: ENSP00000380061.4:p.Val445Ile
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000459069
  ensembl transcript: ENST00000576500
  gene symbol: ZSCAN32
  hgvsc: ENST00000576500.1:c.*387G>A
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000391787
  ensembl transcript: ENST00000439568
  gene symbol: ZSCAN32
  hgvsc: ENST00000439568.2:c.466G>A
  hgvsp: ENSP00000391787.2:p.Val156Ile
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262621
  ensembl protein: ENSP00000477472
  ensembl transcript: ENST00000575785
  gene symbol: NAA60
  hgvsc: ENST00000575785.1:c.-13+18431C>T
  variant of: http://identifiers.org/hgnc/25875
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262621
  ensembl transcript: ENST00000576906
  gene symbol: NAA60
  hgvsc: ENST00000576906.1:n.85-397C>T
  variant of: http://identifiers.org/hgnc/25875
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140987
  ensembl transcript: ENST00000571285
  gene symbol: ZSCAN32
  hgvsc: ENST00000571285.1:n.449G>A
  variant of: http://identifiers.org/hgnc/20812
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8406
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 807
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13158
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2182
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3882
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6442
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21674
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1341
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7317
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2713
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31637
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Val233Ile
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: Other
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: QD

16-3433622-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3433622
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3433622
    reference: chr 16
allele count: 51
allele frequency: 4.209448974875367e-4
allele num: 121156
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000302502
  ensembl transcript: ENST00000304926
  gene symbol: ZSCAN32
  hgvsc: ENST00000304926.3:c.688T>C
  hgvsp: ENSP00000302502.3:p.Ser230Pro
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262621
  ensembl transcript: ENST00000576906
  gene symbol: NAA60
  hgvsc: ENST00000576906.1:n.85-388A>G
  variant of: http://identifiers.org/hgnc/25875
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140987
  ensembl transcript: ENST00000571285
  gene symbol: ZSCAN32
  hgvsc: ENST00000571285.1:n.440T>C
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262621
  ensembl protein: ENSP00000477472
  ensembl transcript: ENST00000575785
  gene symbol: NAA60
  hgvsc: ENST00000575785.1:c.-13+18440A>G
  variant of: http://identifiers.org/hgnc/25875
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000380061
  ensembl transcript: ENST00000396852
  gene symbol: ZSCAN32
  hgvsc: ENST00000396852.4:c.1324T>C
  hgvsp: ENSP00000380061.4:p.Ser442Pro
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000380057
  ensembl transcript: ENST00000396846
  gene symbol: ZSCAN32
  hgvsc: ENST00000396846.3:c.1324T>C
  hgvsp: ENSP00000380057.3:p.Ser442Pro
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000459069
  ensembl transcript: ENST00000576500
  gene symbol: ZSCAN32
  hgvsc: ENST00000576500.1:c.*378T>C
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000391787
  ensembl transcript: ENST00000439568
  gene symbol: ZSCAN32
  hgvsc: ENST00000439568.2:c.457T>C
  hgvsp: ENSP00000391787.2:p.Ser153Pro
  variant of: http://identifiers.org/hgnc/20812
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3878
  bin: 4.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 9.75e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 1346
  bin: 5.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13135
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 596
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2175
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8370
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21593
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 807
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 6438
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 6.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3221
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1767
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Ser230Pro
num of homozygotes: 1
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
reference allele: A
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff

16-3433636-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3433636
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3433636
    reference: chr 16
allele count: 1
allele frequency: 8.277323444690924e-6
allele num: 120812
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140987
  ensembl transcript: ENST00000571285
  gene symbol: ZSCAN32
  hgvsc: ENST00000571285.1:n.426C>T
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000380057
  ensembl transcript: ENST00000396846
  gene symbol: ZSCAN32
  hgvsc: ENST00000396846.3:c.1310C>T
  hgvsp: ENSP00000380057.3:p.Ala437Val
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262621
  ensembl transcript: ENST00000576906
  gene symbol: NAA60
  hgvsc: ENST00000576906.1:n.85-374G>A
  variant of: http://identifiers.org/hgnc/25875
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000380061
  ensembl transcript: ENST00000396852
  gene symbol: ZSCAN32
  hgvsc: ENST00000396852.4:c.1310C>T
  hgvsp: ENSP00000380061.4:p.Ala437Val
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000302502
  ensembl transcript: ENST00000304926
  gene symbol: ZSCAN32
  hgvsc: ENST00000304926.3:c.674C>T
  hgvsp: ENSP00000302502.3:p.Ala225Val
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000459069
  ensembl transcript: ENST00000576500
  gene symbol: ZSCAN32
  hgvsc: ENST00000576500.1:c.*364C>T
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262621
  ensembl protein: ENSP00000477472
  ensembl transcript: ENST00000575785
  gene symbol: NAA60
  hgvsc: ENST00000575785.1:c.-13+18454G>A
  variant of: http://identifiers.org/hgnc/25875
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000391787
  ensembl transcript: ENST00000439568
  gene symbol: ZSCAN32
  hgvsc: ENST00000439568.2:c.443C>T
  hgvsp: ENSP00000391787.2:p.Ala148Val
  variant of: http://identifiers.org/hgnc/20812
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3868
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1341
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8277
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13049
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6410
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 807
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21347
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2176
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 590
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7296
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 31123
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3784
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Ala225Val
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
population: African
reference allele: G
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff

16-3433636-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3433636
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3433636
    reference: chr 16
allele count: 1
allele frequency: 8.277323444690924e-6
allele num: 120812
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000459069
  ensembl transcript: ENST00000576500
  gene symbol: ZSCAN32
  hgvsc: ENST00000576500.1:c.*364C>G
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000302502
  ensembl transcript: ENST00000304926
  gene symbol: ZSCAN32
  hgvsc: ENST00000304926.3:c.674C>G
  hgvsp: ENSP00000302502.3:p.Ala225Gly
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000380061
  ensembl transcript: ENST00000396852
  gene symbol: ZSCAN32
  hgvsc: ENST00000396852.4:c.1310C>G
  hgvsp: ENSP00000380061.4:p.Ala437Gly
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000391787
  ensembl transcript: ENST00000439568
  gene symbol: ZSCAN32
  hgvsc: ENST00000439568.2:c.443C>G
  hgvsp: ENSP00000391787.2:p.Ala148Gly
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000380057
  ensembl transcript: ENST00000396846
  gene symbol: ZSCAN32
  hgvsc: ENST00000396846.3:c.1310C>G
  hgvsp: ENSP00000380057.3:p.Ala437Gly
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140987
  ensembl transcript: ENST00000571285
  gene symbol: ZSCAN32
  hgvsc: ENST00000571285.1:n.426C>G
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262621
  ensembl transcript: ENST00000576906
  gene symbol: NAA60
  hgvsc: ENST00000576906.1:n.85-374G>C
  variant of: http://identifiers.org/hgnc/25875
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262621
  ensembl protein: ENSP00000477472
  ensembl transcript: ENST00000575785
  gene symbol: NAA60
  hgvsc: ENST00000575785.1:c.-13+18454G>C
  variant of: http://identifiers.org/hgnc/25875
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 807
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8277
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13049
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3868
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21347
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6410
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2176
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1341
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7296
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 590
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31123
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Ala225Gly
num of homozygotes: 0
population: East Asian
population: Other
population: European (Non-Finnish)
population: South Asian
population: African
population: Latino
population: European (Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: QD

16-3433637-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3433637
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3433637
    reference: chr 16
allele count: 1
allele frequency: 8.279105194310599e-6
allele num: 120786
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000391787
  ensembl transcript: ENST00000439568
  gene symbol: ZSCAN32
  hgvsc: ENST00000439568.2:c.442G>C
  hgvsp: ENSP00000391787.2:p.Ala148Pro
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000459069
  ensembl transcript: ENST00000576500
  gene symbol: ZSCAN32
  hgvsc: ENST00000576500.1:c.*363G>C
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000302502
  ensembl transcript: ENST00000304926
  gene symbol: ZSCAN32
  hgvsc: ENST00000304926.3:c.673G>C
  hgvsp: ENSP00000302502.3:p.Ala225Pro
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000380061
  ensembl transcript: ENST00000396852
  gene symbol: ZSCAN32
  hgvsc: ENST00000396852.4:c.1309G>C
  hgvsp: ENSP00000380061.4:p.Ala437Pro
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140987
  ensembl transcript: ENST00000571285
  gene symbol: ZSCAN32
  hgvsc: ENST00000571285.1:n.425G>C
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262621
  ensembl transcript: ENST00000576906
  gene symbol: NAA60
  hgvsc: ENST00000576906.1:n.85-373C>G
  variant of: http://identifiers.org/hgnc/25875
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262621
  ensembl protein: ENSP00000477472
  ensembl transcript: ENST00000575785
  gene symbol: NAA60
  hgvsc: ENST00000575785.1:c.-13+18455C>G
  variant of: http://identifiers.org/hgnc/25875
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000380057
  ensembl transcript: ENST00000396846
  gene symbol: ZSCAN32
  hgvsc: ENST00000396846.3:c.1309G>C
  hgvsp: ENSP00000380057.3:p.Ala437Pro
  variant of: http://identifiers.org/hgnc/20812
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3864
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21324
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6406
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8279
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13033
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2175
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1341
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 808
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1368
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 618
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7297
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3779
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Ala225Pro
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: Other
population: East Asian
population: European (Non-Finnish)
population: African
reference allele: C
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: DP

16-3433637-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3433637
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3433637
    reference: chr 16
allele count: 1
allele frequency: 8.279105194310599e-6
allele num: 120786
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000380057
  ensembl transcript: ENST00000396846
  gene symbol: ZSCAN32
  hgvsc: ENST00000396846.3:c.1309G>A
  hgvsp: ENSP00000380057.3:p.Ala437Thr
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000459069
  ensembl transcript: ENST00000576500
  gene symbol: ZSCAN32
  hgvsc: ENST00000576500.1:c.*363G>A
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140987
  ensembl transcript: ENST00000571285
  gene symbol: ZSCAN32
  hgvsc: ENST00000571285.1:n.425G>A
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000391787
  ensembl transcript: ENST00000439568
  gene symbol: ZSCAN32
  hgvsc: ENST00000439568.2:c.442G>A
  hgvsp: ENSP00000391787.2:p.Ala148Thr
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000302502
  ensembl transcript: ENST00000304926
  gene symbol: ZSCAN32
  hgvsc: ENST00000304926.3:c.673G>A
  hgvsp: ENSP00000302502.3:p.Ala225Thr
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262621
  ensembl protein: ENSP00000477472
  ensembl transcript: ENST00000575785
  gene symbol: NAA60
  hgvsc: ENST00000575785.1:c.-13+18455C>T
  variant of: http://identifiers.org/hgnc/25875
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000380061
  ensembl transcript: ENST00000396852
  gene symbol: ZSCAN32
  hgvsc: ENST00000396852.4:c.1309G>A
  hgvsp: ENSP00000380061.4:p.Ala437Thr
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262621
  ensembl transcript: ENST00000576906
  gene symbol: NAA60
  hgvsc: ENST00000576906.1:n.85-373C>T
  variant of: http://identifiers.org/hgnc/25875
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21324
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3864
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6406
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13033
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8279
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1341
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2175
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 808
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31116
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 618
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Ala225Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
population: East Asian
population: African
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum

16-3433638-CTTG-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3433638
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3433635
    reference: chr 16
allele count: 36
allele frequency: 2.980971465478694e-4
allele num: 120766
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000459069
  ensembl transcript: ENST00000576500
  gene symbol: ZSCAN32
  hgvsc: ENST00000576500.1:c.*359_*361delCAA
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000380057
  ensembl transcript: ENST00000396846
  gene symbol: ZSCAN32
  hgvsc: ENST00000396846.3:c.1305_1307delCAA
  hgvsp: ENSP00000380057.3:p.Asn435del
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140987
  ensembl transcript: ENST00000571285
  gene symbol: ZSCAN32
  hgvsc: ENST00000571285.1:n.421_423delCAA
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000391787
  ensembl transcript: ENST00000439568
  gene symbol: ZSCAN32
  hgvsc: ENST00000439568.2:c.438_440delCAA
  hgvsp: ENSP00000391787.2:p.Asn146del
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000380061
  ensembl transcript: ENST00000396852
  gene symbol: ZSCAN32
  hgvsc: ENST00000396852.4:c.1305_1307delCAA
  hgvsp: ENSP00000380061.4:p.Asn435del
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262621
  ensembl transcript: ENST00000576906
  gene symbol: NAA60
  hgvsc: ENST00000576906.1:n.85-369_85-367delGTT
  variant of: http://identifiers.org/hgnc/25875
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262621
  ensembl protein: ENSP00000477472
  ensembl transcript: ENST00000575785
  gene symbol: NAA60
  hgvsc: ENST00000575785.1:c.-13+18459_-13+18461delGTT
  variant of: http://identifiers.org/hgnc/25875
annotation: Annotation
  canonical: true
  consequence: inframe_deletion
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000302502
  ensembl transcript: ENST00000304926
  gene symbol: ZSCAN32
  hgvsc: ENST00000304926.3:c.669_671delCAA
  hgvsp: ENSP00000302502.3:p.Asn223del
  variant of: http://identifiers.org/hgnc/20812
canonical: true
consequence: inframe deletion
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1342
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2176
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 21323
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 596
  bin: 6.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 806
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 9.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 13009
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3864
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6403
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8272
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7317
  bin: 9.75e1
  variant carriers: 36
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1368
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Asn223del
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: CTTG
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: BaseQRankSum

16-3433651-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3433651
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3433651
    reference: chr 16
allele count: 3
allele frequency: 2.494470590191741e-5
allele num: 120266
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000380061
  ensembl transcript: ENST00000396852
  gene symbol: ZSCAN32
  hgvsc: ENST00000396852.4:c.1295T>C
  hgvsp: ENSP00000380061.4:p.Val432Ala
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000459069
  ensembl transcript: ENST00000576500
  gene symbol: ZSCAN32
  hgvsc: ENST00000576500.1:c.*349T>C
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000380057
  ensembl transcript: ENST00000396846
  gene symbol: ZSCAN32
  hgvsc: ENST00000396846.3:c.1295T>C
  hgvsp: ENSP00000380057.3:p.Val432Ala
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000391787
  ensembl transcript: ENST00000439568
  gene symbol: ZSCAN32
  hgvsc: ENST00000439568.2:c.428T>C
  hgvsp: ENSP00000391787.2:p.Val143Ala
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262621
  ensembl protein: ENSP00000477472
  ensembl transcript: ENST00000575785
  gene symbol: NAA60
  hgvsc: ENST00000575785.1:c.-13+18469A>G
  variant of: http://identifiers.org/hgnc/25875
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140987
  ensembl transcript: ENST00000571285
  gene symbol: ZSCAN32
  hgvsc: ENST00000571285.1:n.411T>C
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262621
  ensembl transcript: ENST00000576906
  gene symbol: NAA60
  hgvsc: ENST00000576906.1:n.85-359A>G
  variant of: http://identifiers.org/hgnc/25875
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000302502
  ensembl transcript: ENST00000304926
  gene symbol: ZSCAN32
  hgvsc: ENST00000304926.3:c.659T>C
  hgvsp: ENSP00000302502.3:p.Val220Ala
  variant of: http://identifiers.org/hgnc/20812
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8151
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1342
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20742
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 946
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12819
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 805
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6377
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2175
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3855
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 207
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3156
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 132
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2683
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Val220Ala
num of homozygotes: 0
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
reference allele: A
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum

16-3433687-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3433687
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3433687
    reference: chr 16
allele count: 1
allele frequency: 8.47687508476875e-6
allele num: 117968
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000459069
  ensembl transcript: ENST00000576500
  gene symbol: ZSCAN32
  hgvsc: ENST00000576500.1:c.*313A>G
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000391787
  ensembl transcript: ENST00000439568
  gene symbol: ZSCAN32
  hgvsc: ENST00000439568.2:c.392A>G
  hgvsp: ENSP00000391787.2:p.Lys131Arg
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262621
  ensembl protein: ENSP00000477472
  ensembl transcript: ENST00000575785
  gene symbol: NAA60
  hgvsc: ENST00000575785.1:c.-13+18505T>C
  variant of: http://identifiers.org/hgnc/25875
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000302502
  ensembl transcript: ENST00000304926
  gene symbol: ZSCAN32
  hgvsc: ENST00000304926.3:c.623A>G
  hgvsp: ENSP00000302502.3:p.Lys208Arg
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000380061
  ensembl transcript: ENST00000396852
  gene symbol: ZSCAN32
  hgvsc: ENST00000396852.4:c.1259A>G
  hgvsp: ENSP00000380061.4:p.Lys420Arg
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000460487
  ensembl transcript: ENST00000573327
  gene symbol: ZSCAN32
  hgvsc: ENST00000573327.1:c.1259A>G
  hgvsp: ENSP00000460487.1:p.Lys420Arg
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000380057
  ensembl transcript: ENST00000396846
  gene symbol: ZSCAN32
  hgvsc: ENST00000396846.3:c.1259A>G
  hgvsp: ENSP00000380057.3:p.Lys420Arg
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140987
  ensembl transcript: ENST00000571285
  gene symbol: ZSCAN32
  hgvsc: ENST00000571285.1:n.375A>G
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262621
  ensembl transcript: ENST00000576906
  gene symbol: NAA60
  hgvsc: ENST00000576906.1:n.85-323T>C
  variant of: http://identifiers.org/hgnc/25875
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4177
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7766
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1259
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2166
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 805
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15560
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10794
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1344
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3808
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3864
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6170
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1346
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1371
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4113
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6592
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Lys208Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: Other
reference allele: T
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ

16-3433688-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3433688
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3433688
    reference: chr 16
allele count: 1
allele frequency: 8.4774499830451e-6
allele num: 117960
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000459069
  ensembl transcript: ENST00000576500
  gene symbol: ZSCAN32
  hgvsc: ENST00000576500.1:c.*312A>C
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262621
  ensembl transcript: ENST00000576906
  gene symbol: NAA60
  hgvsc: ENST00000576906.1:n.85-322T>G
  variant of: http://identifiers.org/hgnc/25875
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140987
  ensembl transcript: ENST00000571285
  gene symbol: ZSCAN32
  hgvsc: ENST00000571285.1:n.374A>C
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000391787
  ensembl transcript: ENST00000439568
  gene symbol: ZSCAN32
  hgvsc: ENST00000439568.2:c.391A>C
  hgvsp: ENSP00000391787.2:p.Lys131Gln
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262621
  ensembl protein: ENSP00000477472
  ensembl transcript: ENST00000575785
  gene symbol: NAA60
  hgvsc: ENST00000575785.1:c.-13+18506T>G
  variant of: http://identifiers.org/hgnc/25875
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000380057
  ensembl transcript: ENST00000396846
  gene symbol: ZSCAN32
  hgvsc: ENST00000396846.3:c.1258A>C
  hgvsp: ENSP00000380057.3:p.Lys420Gln
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000302502
  ensembl transcript: ENST00000304926
  gene symbol: ZSCAN32
  hgvsc: ENST00000304926.3:c.622A>C
  hgvsp: ENSP00000302502.3:p.Lys208Gln
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000380061
  ensembl transcript: ENST00000396852
  gene symbol: ZSCAN32
  hgvsc: ENST00000396852.4:c.1258A>C
  hgvsp: ENSP00000380061.4:p.Lys420Gln
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000460487
  ensembl transcript: ENST00000573327
  gene symbol: ZSCAN32
  hgvsc: ENST00000573327.1:c.1258A>C
  hgvsp: ENSP00000460487.1:p.Lys420Gln
  variant of: http://identifiers.org/hgnc/20812
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6169
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4173
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2166
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1259
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 805
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7805
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3808
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15564
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3861
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10756
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1344
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1857
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1346
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 452
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Lys208Gln
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: Other
reference allele: T
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: QD

16-3433691-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3433691
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3433691
    reference: chr 16
allele count: 1
allele frequency: 8.498342823149486e-6
allele num: 117670
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140987
  ensembl transcript: ENST00000571285
  gene symbol: ZSCAN32
  hgvsc: ENST00000571285.1:n.371A>T
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000459069
  ensembl transcript: ENST00000576500
  gene symbol: ZSCAN32
  hgvsc: ENST00000576500.1:c.*309A>T
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000302502
  ensembl transcript: ENST00000304926
  gene symbol: ZSCAN32
  hgvsc: ENST00000304926.3:c.619A>T
  hgvsp: ENSP00000302502.3:p.Ile207Phe
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000380057
  ensembl transcript: ENST00000396846
  gene symbol: ZSCAN32
  hgvsc: ENST00000396846.3:c.1255A>T
  hgvsp: ENSP00000380057.3:p.Ile419Phe
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000460487
  ensembl transcript: ENST00000573327
  gene symbol: ZSCAN32
  hgvsc: ENST00000573327.1:c.1255A>T
  hgvsp: ENSP00000460487.1:p.Ile419Phe
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262621
  ensembl transcript: ENST00000576906
  gene symbol: NAA60
  hgvsc: ENST00000576906.1:n.85-319T>A
  variant of: http://identifiers.org/hgnc/25875
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262621
  ensembl protein: ENSP00000477472
  ensembl transcript: ENST00000575785
  gene symbol: NAA60
  hgvsc: ENST00000575785.1:c.-13+18509T>A
  variant of: http://identifiers.org/hgnc/25875
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000391787
  ensembl transcript: ENST00000439568
  gene symbol: ZSCAN32
  hgvsc: ENST00000439568.2:c.388A>T
  hgvsp: ENSP00000391787.2:p.Ile130Phe
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000380061
  ensembl transcript: ENST00000396852
  gene symbol: ZSCAN32
  hgvsc: ENST00000396852.4:c.1255A>T
  hgvsp: ENSP00000380061.4:p.Ile419Phe
  variant of: http://identifiers.org/hgnc/20812
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7809
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 805
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4084
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2165
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14735
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4950
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1323
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6148
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1344
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3803
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10493
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 764
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1553
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2835
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1347
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Ile207Phe
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum

16-3433693-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3433693
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3433693
    reference: chr 16
allele count: 1
allele frequency: 8.508465923593976e-6
allele num: 117530
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000380057
  ensembl transcript: ENST00000396846
  gene symbol: ZSCAN32
  hgvsc: ENST00000396846.3:c.1253A>G
  hgvsp: ENSP00000380057.3:p.Glu418Gly
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000459069
  ensembl transcript: ENST00000576500
  gene symbol: ZSCAN32
  hgvsc: ENST00000576500.1:c.*307A>G
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000460487
  ensembl transcript: ENST00000573327
  gene symbol: ZSCAN32
  hgvsc: ENST00000573327.1:c.1253A>G
  hgvsp: ENSP00000460487.1:p.Glu418Gly
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000302502
  ensembl transcript: ENST00000304926
  gene symbol: ZSCAN32
  hgvsc: ENST00000304926.3:c.617A>G
  hgvsp: ENSP00000302502.3:p.Glu206Gly
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262621
  ensembl protein: ENSP00000477472
  ensembl transcript: ENST00000575785
  gene symbol: NAA60
  hgvsc: ENST00000575785.1:c.-13+18511T>C
  variant of: http://identifiers.org/hgnc/25875
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262621
  ensembl transcript: ENST00000576906
  gene symbol: NAA60
  hgvsc: ENST00000576906.1:n.85-317T>C
  variant of: http://identifiers.org/hgnc/25875
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140987
  ensembl transcript: ENST00000571285
  gene symbol: ZSCAN32
  hgvsc: ENST00000571285.1:n.369A>G
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000380061
  ensembl transcript: ENST00000396852
  gene symbol: ZSCAN32
  hgvsc: ENST00000396852.4:c.1253A>G
  hgvsp: ENSP00000380061.4:p.Glu418Gly
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000391787
  ensembl transcript: ENST00000439568
  gene symbol: ZSCAN32
  hgvsc: ENST00000439568.2:c.386A>G
  hgvsp: ENSP00000391787.2:p.Glu129Gly
  variant of: http://identifiers.org/hgnc/20812
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1361
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4204
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14263
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5410
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10314
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2165
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6130
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3801
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1344
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7838
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 805
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1675
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20896
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 423
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Glu206Gly
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
reference allele: T
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP

16-3433694-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3433694
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3433694
    reference: chr 16
allele count: 5
allele frequency: 4.262792640714785e-5
allele num: 117294
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000380057
  ensembl transcript: ENST00000396846
  gene symbol: ZSCAN32
  hgvsc: ENST00000396846.3:c.1252G>A
  hgvsp: ENSP00000380057.3:p.Glu418Lys
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262621
  ensembl protein: ENSP00000477472
  ensembl transcript: ENST00000575785
  gene symbol: NAA60
  hgvsc: ENST00000575785.1:c.-13+18512C>T
  variant of: http://identifiers.org/hgnc/25875
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000380061
  ensembl transcript: ENST00000396852
  gene symbol: ZSCAN32
  hgvsc: ENST00000396852.4:c.1252G>A
  hgvsp: ENSP00000380061.4:p.Glu418Lys
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000302502
  ensembl transcript: ENST00000304926
  gene symbol: ZSCAN32
  hgvsc: ENST00000304926.3:c.616G>A
  hgvsp: ENSP00000302502.3:p.Glu206Lys
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000460487
  ensembl transcript: ENST00000573327
  gene symbol: ZSCAN32
  hgvsc: ENST00000573327.1:c.1252G>A
  hgvsp: ENSP00000460487.1:p.Glu418Lys
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140987
  ensembl transcript: ENST00000571285
  gene symbol: ZSCAN32
  hgvsc: ENST00000571285.1:n.368G>A
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262621
  ensembl transcript: ENST00000576906
  gene symbol: NAA60
  hgvsc: ENST00000576906.1:n.85-316C>T
  variant of: http://identifiers.org/hgnc/25875
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000391787
  ensembl transcript: ENST00000439568
  gene symbol: ZSCAN32
  hgvsc: ENST00000439568.2:c.385G>A
  hgvsp: ENSP00000391787.2:p.Glu129Lys
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000459069
  ensembl transcript: ENST00000576500
  gene symbol: ZSCAN32
  hgvsc: ENST00000576500.1:c.*306G>A
  variant of: http://identifiers.org/hgnc/20812
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1393
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7868
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6115
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 807
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4270
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10186
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5782
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3804
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2168
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1343
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13851
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 158
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 941
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1775
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2789
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Glu206Lys
num of homozygotes: 0
population: Latino
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
population: East Asian
reference allele: C
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum

16-3433695-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3433695
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3433695
    reference: chr 16
allele count: 4
allele frequency: 3.411921252857484e-5
allele num: 117236
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140987
  ensembl transcript: ENST00000571285
  gene symbol: ZSCAN32
  hgvsc: ENST00000571285.1:n.367C>T
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262621
  ensembl transcript: ENST00000576906
  gene symbol: NAA60
  hgvsc: ENST00000576906.1:n.85-315G>A
  variant of: http://identifiers.org/hgnc/25875
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000302502
  ensembl transcript: ENST00000304926
  gene symbol: ZSCAN32
  hgvsc: ENST00000304926.3:c.615C>T
  hgvsp: ENST00000304926.3:c.615C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262621
  ensembl protein: ENSP00000477472
  ensembl transcript: ENST00000575785
  gene symbol: NAA60
  hgvsc: ENST00000575785.1:c.-13+18513G>A
  variant of: http://identifiers.org/hgnc/25875
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000391787
  ensembl transcript: ENST00000439568
  gene symbol: ZSCAN32
  hgvsc: ENST00000439568.2:c.384C>T
  hgvsp: ENST00000439568.2:c.384C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000380061
  ensembl transcript: ENST00000396852
  gene symbol: ZSCAN32
  hgvsc: ENST00000396852.4:c.1251C>T
  hgvsp: ENST00000396852.4:c.1251C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000380057
  ensembl transcript: ENST00000396846
  gene symbol: ZSCAN32
  hgvsc: ENST00000396846.3:c.1251C>T
  hgvsp: ENST00000396846.3:c.1251C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000460487
  ensembl transcript: ENST00000573327
  gene symbol: ZSCAN32
  hgvsc: ENST00000573327.1:c.1251C>T
  hgvsp: ENST00000573327.1:c.1251C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000459069
  ensembl transcript: ENST00000576500
  gene symbol: ZSCAN32
  hgvsc: ENST00000576500.1:c.*305C>T
  variant of: http://identifiers.org/hgnc/20812
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 806
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7909
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3800
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10110
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1396
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13886
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6114
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5768
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4288
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2160
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1345
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2125
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 617
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2524
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1738
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Asn205Asn
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
population: African
reference allele: G
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff

16-3433699-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3433699
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3433699
    reference: chr 16
allele count: 1
allele frequency: 8.554759012438619e-6
allele num: 116894
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000459069
  ensembl transcript: ENST00000576500
  gene symbol: ZSCAN32
  hgvsc: ENST00000576500.1:c.*301A>G
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000380057
  ensembl transcript: ENST00000396846
  gene symbol: ZSCAN32
  hgvsc: ENST00000396846.3:c.1247A>G
  hgvsp: ENSP00000380057.3:p.Lys416Arg
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000302502
  ensembl transcript: ENST00000304926
  gene symbol: ZSCAN32
  hgvsc: ENST00000304926.3:c.611A>G
  hgvsp: ENSP00000302502.3:p.Lys204Arg
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262621
  ensembl protein: ENSP00000477472
  ensembl transcript: ENST00000575785
  gene symbol: NAA60
  hgvsc: ENST00000575785.1:c.-13+18517T>C
  variant of: http://identifiers.org/hgnc/25875
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000460487
  ensembl transcript: ENST00000573327
  gene symbol: ZSCAN32
  hgvsc: ENST00000573327.1:c.1247A>G
  hgvsp: ENSP00000460487.1:p.Lys416Arg
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000380061
  ensembl transcript: ENST00000396852
  gene symbol: ZSCAN32
  hgvsc: ENST00000396852.4:c.1247A>G
  hgvsp: ENSP00000380061.4:p.Lys416Arg
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262621
  ensembl transcript: ENST00000576906
  gene symbol: NAA60
  hgvsc: ENST00000576906.1:n.85-311T>C
  variant of: http://identifiers.org/hgnc/25875
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000391787
  ensembl transcript: ENST00000439568
  gene symbol: ZSCAN32
  hgvsc: ENST00000439568.2:c.380A>G
  hgvsp: ENSP00000391787.2:p.Lys127Arg
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140987
  ensembl transcript: ENST00000571285
  gene symbol: ZSCAN32
  hgvsc: ENST00000571285.1:n.363A>G
  variant of: http://identifiers.org/hgnc/20812
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3792
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12728
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 806
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2159
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8336
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1503
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4444
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9758
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6059
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6549
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1346
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1737
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1275
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2964
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Lys204Arg
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
population: African
population: East Asian
population: European (Finnish)
reference allele: T
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff

16-3433714-G-GA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3433714
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3433715
    reference: chr 16
allele count: 6246
allele frequency: 1.084676298971937e-1
allele num: 57584
alternate allele: GA
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000459772
  ensembl transcript: ENST00000574940
  gene symbol: ZSCAN32
  hgvsc: ENST00000574940.1:c.*694dupT
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000391787
  ensembl transcript: ENST00000439568
  gene symbol: ZSCAN32
  hgvsc: ENST00000439568.2:c.368-4dupT
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000302502
  ensembl transcript: ENST00000304926
  gene symbol: ZSCAN32
  hgvsc: ENST00000304926.3:c.599-4dupT
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262621
  ensembl transcript: ENST00000576906
  gene symbol: NAA60
  hgvsc: ENST00000576906.1:n.85-285dupA
  variant of: http://identifiers.org/hgnc/25875
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262621
  ensembl protein: ENSP00000477472
  ensembl transcript: ENST00000575785
  gene symbol: NAA60
  hgvsc: ENST00000575785.1:c.-13+18543dupA
  variant of: http://identifiers.org/hgnc/25875
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000459069
  ensembl transcript: ENST00000576500
  gene symbol: ZSCAN32
  hgvsc: ENST00000576500.1:c.*289-4dupT
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000380057
  ensembl transcript: ENST00000396846
  gene symbol: ZSCAN32
  hgvsc: ENST00000396846.3:c.1235-4dupT
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000380061
  ensembl transcript: ENST00000396852
  gene symbol: ZSCAN32
  hgvsc: ENST00000396852.4:c.1235-4dupT
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140987
  ensembl transcript: ENST00000571285
  gene symbol: ZSCAN32
  hgvsc: ENST00000571285.1:n.347dupT
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000460487
  ensembl transcript: ENST00000573327
  gene symbol: ZSCAN32
  hgvsc: ENST00000573327.1:c.1235-4dupT
  variant of: http://identifiers.org/hgnc/20812
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 764
  bin: 5.75e1
  variant carriers: 76
genotype depth: GenotypeDepth
  all individuals: 10189
  bin: 2.25e1
  variant carriers: 2137
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 719
  bin: 2.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8253
  bin: 1.75e1
  variant carriers: 1721
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.25e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 8196
  bin: 3.25e1
  variant carriers: 1229
genotype depth: GenotypeDepth
  all individuals: 3370
  bin: 4.25e1
  variant carriers: 395
genotype depth: GenotypeDepth
  all individuals: 5174
  bin: 1.25e1
  variant carriers: 588
genotype depth: GenotypeDepth
  all individuals: 2083
  bin: 4.75e1
  variant carriers: 207
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 7.25e1
  variant carriers: 31
genotype depth: GenotypeDepth
  all individuals: 2043
  bin: 7.5e0
  variant carriers: 76
genotype depth: GenotypeDepth
  all individuals: 10585
  bin: 2.75e1
  variant carriers: 1675
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 7.75e1
  variant carriers: 27
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 9.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 9.75e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 6.75e1
  variant carriers: 56
genotype depth: GenotypeDepth
  all individuals: 1333
  bin: 5.25e1
  variant carriers: 139
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 6.25e1
  variant carriers: 61
genotype depth: GenotypeDepth
  all individuals: 5310
  bin: 3.75e1
  variant carriers: 669
genotype quality: GenotypeQuality
  all individuals: 1490
  bin: 5.25e1
  variant carriers: 378
genotype quality: GenotypeQuality
  all individuals: 2450
  bin: 3.75e1
  variant carriers: 561
hgvs: c.599-4dupT
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
reference allele: G
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum

16-3433714-G-GAA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3433714
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3433716
    reference: chr 16
allele count: 297
allele frequency: 5.15768268963601e-3
allele num: 57584
alternate allele: GAA
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000380061
  ensembl transcript: ENST00000396852
  gene symbol: ZSCAN32
  hgvsc: ENST00000396852.4:c.1235-5_1235-4dupTT
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000459772
  ensembl transcript: ENST00000574940
  gene symbol: ZSCAN32
  hgvsc: ENST00000574940.1:c.*693_*694dupTT
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000459069
  ensembl transcript: ENST00000576500
  gene symbol: ZSCAN32
  hgvsc: ENST00000576500.1:c.*289-5_*289-4dupTT
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000380057
  ensembl transcript: ENST00000396846
  gene symbol: ZSCAN32
  hgvsc: ENST00000396846.3:c.1235-5_1235-4dupTT
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262621
  ensembl protein: ENSP00000477472
  ensembl transcript: ENST00000575785
  gene symbol: NAA60
  hgvsc: ENST00000575785.1:c.-13+18542_-13+18543dupAA
  variant of: http://identifiers.org/hgnc/25875
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000460487
  ensembl transcript: ENST00000573327
  gene symbol: ZSCAN32
  hgvsc: ENST00000573327.1:c.1235-5_1235-4dupTT
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000391787
  ensembl transcript: ENST00000439568
  gene symbol: ZSCAN32
  hgvsc: ENST00000439568.2:c.368-5_368-4dupTT
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000302502
  ensembl transcript: ENST00000304926
  gene symbol: ZSCAN32
  hgvsc: ENST00000304926.3:c.599-5_599-4dupTT
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262621
  ensembl transcript: ENST00000576906
  gene symbol: NAA60
  hgvsc: ENST00000576906.1:n.85-286_85-285dupAA
  variant of: http://identifiers.org/hgnc/25875
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140987
  ensembl transcript: ENST00000571285
  gene symbol: ZSCAN32
  hgvsc: ENST00000571285.1:n.346_347dupTT
  variant of: http://identifiers.org/hgnc/20812
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5174
  bin: 1.25e1
  variant carriers: 50
genotype depth: GenotypeDepth
  all individuals: 2043
  bin: 7.5e0
  variant carriers: 35
genotype depth: GenotypeDepth
  all individuals: 5310
  bin: 3.75e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 10585
  bin: 2.75e1
  variant carriers: 53
genotype depth: GenotypeDepth
  all individuals: 1333
  bin: 5.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10189
  bin: 2.25e1
  variant carriers: 62
genotype depth: GenotypeDepth
  all individuals: 719
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3370
  bin: 4.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 764
  bin: 5.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 8253
  bin: 1.75e1
  variant carriers: 73
genotype depth: GenotypeDepth
  all individuals: 2083
  bin: 4.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8196
  bin: 3.25e1
  variant carriers: 26
genotype quality: GenotypeQuality
  all individuals: 19007
  bin: 2.5e0
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 2450
  bin: 3.75e1
  variant carriers: 7
hgvs: c.599-5_599-4dupTT
num of homozygotes: 1
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff

16-3433714-G-GAAA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3433714
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3433717
    reference: chr 16
allele count: 7
allele frequency: 1.21561544873576e-4
allele num: 57584
alternate allele: GAAA
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262621
  ensembl transcript: ENST00000576906
  gene symbol: NAA60
  hgvsc: ENST00000576906.1:n.85-287_85-285dupAAA
  variant of: http://identifiers.org/hgnc/25875
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000302502
  ensembl transcript: ENST00000304926
  gene symbol: ZSCAN32
  hgvsc: ENST00000304926.3:c.599-6_599-4dupTTT
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000391787
  ensembl transcript: ENST00000439568
  gene symbol: ZSCAN32
  hgvsc: ENST00000439568.2:c.368-6_368-4dupTTT
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000459772
  ensembl transcript: ENST00000574940
  gene symbol: ZSCAN32
  hgvsc: ENST00000574940.1:c.*692_*694dupTTT
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000380057
  ensembl transcript: ENST00000396846
  gene symbol: ZSCAN32
  hgvsc: ENST00000396846.3:c.1235-6_1235-4dupTTT
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262621
  ensembl protein: ENSP00000477472
  ensembl transcript: ENST00000575785
  gene symbol: NAA60
  hgvsc: ENST00000575785.1:c.-13+18541_-13+18543dupAAA
  variant of: http://identifiers.org/hgnc/25875
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000459069
  ensembl transcript: ENST00000576500
  gene symbol: ZSCAN32
  hgvsc: ENST00000576500.1:c.*289-6_*289-4dupTTT
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000460487
  ensembl transcript: ENST00000573327
  gene symbol: ZSCAN32
  hgvsc: ENST00000573327.1:c.1235-6_1235-4dupTTT
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140987
  ensembl transcript: ENST00000571285
  gene symbol: ZSCAN32
  hgvsc: ENST00000571285.1:n.345_347dupTTT
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000380061
  ensembl transcript: ENST00000396852
  gene symbol: ZSCAN32
  hgvsc: ENST00000396852.4:c.1235-6_1235-4dupTTT
  variant of: http://identifiers.org/hgnc/20812
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 764
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5310
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2083
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10585
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3370
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8196
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5174
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 719
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2043
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1333
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10189
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8253
  bin: 1.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 5724
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3784
  bin: 1.25e1
  variant carriers: 0
hgvs: c.599-6_599-4dupTTT
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: Other
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff

16-3433714-GA-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3433714
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3433713
    reference: chr 16
allele count: 3845
allele frequency: 6.67720200055571e-2
allele num: 57584
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000459069
  ensembl transcript: ENST00000576500
  gene symbol: ZSCAN32
  hgvsc: ENST00000576500.1:c.*289-4delT
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000380061
  ensembl transcript: ENST00000396852
  gene symbol: ZSCAN32
  hgvsc: ENST00000396852.4:c.1235-4delT
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140987
  ensembl transcript: ENST00000571285
  gene symbol: ZSCAN32
  hgvsc: ENST00000571285.1:n.347delT
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000460487
  ensembl transcript: ENST00000573327
  gene symbol: ZSCAN32
  hgvsc: ENST00000573327.1:c.1235-4delT
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000391787
  ensembl transcript: ENST00000439568
  gene symbol: ZSCAN32
  hgvsc: ENST00000439568.2:c.368-4delT
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262621
  ensembl transcript: ENST00000576906
  gene symbol: NAA60
  hgvsc: ENST00000576906.1:n.85-285delA
  variant of: http://identifiers.org/hgnc/25875
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000302502
  ensembl transcript: ENST00000304926
  gene symbol: ZSCAN32
  hgvsc: ENST00000304926.3:c.599-4delT
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262621
  ensembl protein: ENSP00000477472
  ensembl transcript: ENST00000575785
  gene symbol: NAA60
  hgvsc: ENST00000575785.1:c.-13+18543delA
  variant of: http://identifiers.org/hgnc/25875
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000459772
  ensembl transcript: ENST00000574940
  gene symbol: ZSCAN32
  hgvsc: ENST00000574940.1:c.*694delT
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000380057
  ensembl transcript: ENST00000396846
  gene symbol: ZSCAN32
  hgvsc: ENST00000396846.3:c.1235-4delT
  variant of: http://identifiers.org/hgnc/20812
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2043
  bin: 7.5e0
  variant carriers: 29
genotype depth: GenotypeDepth
  all individuals: 8196
  bin: 3.25e1
  variant carriers: 724
genotype depth: GenotypeDepth
  all individuals: 5174
  bin: 1.25e1
  variant carriers: 234
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 7.25e1
  variant carriers: 39
genotype depth: GenotypeDepth
  all individuals: 2083
  bin: 4.75e1
  variant carriers: 140
genotype depth: GenotypeDepth
  all individuals: 3370
  bin: 4.25e1
  variant carriers: 228
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 9.25e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 10585
  bin: 2.75e1
  variant carriers: 1218
genotype depth: GenotypeDepth
  all individuals: 10189
  bin: 2.25e1
  variant carriers: 1313
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 6.75e1
  variant carriers: 29
genotype depth: GenotypeDepth
  all individuals: 719
  bin: 2.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8253
  bin: 1.75e1
  variant carriers: 808
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.25e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 9.75e1
  variant carriers: 74
genotype depth: GenotypeDepth
  all individuals: 1333
  bin: 5.25e1
  variant carriers: 104
genotype depth: GenotypeDepth
  all individuals: 5310
  bin: 3.75e1
  variant carriers: 518
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 7.75e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 6.25e1
  variant carriers: 42
genotype depth: GenotypeDepth
  all individuals: 764
  bin: 5.75e1
  variant carriers: 62
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.75e1
  variant carriers: 24
genotype quality: GenotypeQuality
  all individuals: 1226
  bin: 6.75e1
  variant carriers: 119
genotype quality: GenotypeQuality
  all individuals: 452
  bin: 8.25e1
  variant carriers: 63
hgvs: c.599-4delT
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: GA
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP

16-3433714-GAA-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3433714
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3433712
    reference: chr 16
allele count: 7
allele frequency: 1.21561544873576e-4
allele num: 57584
alternate allele: G
canonical: false
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1333
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2083
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10189
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 764
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2043
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8253
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 719
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10585
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3370
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5174
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8196
  bin: 3.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 5310
  bin: 3.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3585
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3126
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1226
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3043
  bin: 6.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 3784
  bin: 1.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 452
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1794
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 323
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3257
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2450
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5724
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4527
  bin: 7.5e0
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 19007
  bin: 2.5e0
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1161
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1901
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 598
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 281
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2040
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1490
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 730
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
  type: Population
  allele count: 1
  allele frequency: 2.398081534772182e-4
  allele num: 4170
  num of homozygotes: 0
population: European (Finnish)
  type: Population
  allele count: 1
  allele frequency: 2.561475409836066e-4
  allele num: 3904
  num of homozygotes: 0
population: South Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 7344
  num of homozygotes: 0
population: European (Non-Finnish)
  type: Population
  allele count: 4
  allele frequency: 1.279754287176862e-4
  allele num: 31256
  num of homozygotes: 0
population: African
population: Latino
population: Other
reference allele: GAA
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: DP

16-3433714-GAAAA-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3433714
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3433710
    reference: chr 16
allele count: 5
allele frequency: 8.682967490969714e-5
allele num: 57584
alternate allele: G
canonical: false
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8253
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8196
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10189
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1333
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5174
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 719
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 764
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2043
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2083
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5310
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10585
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3370
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19007
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1794
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3257
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5724
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1226
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3784
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1161
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 323
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 598
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 452
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2450
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3126
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3043
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 281
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2040
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4527
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3585
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1490
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 730
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1901
  bin: 9.75e1
  variant carriers: 5
num of homozygotes: 0
population: Latino
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 5300
  num of homozygotes: 0
population: South Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 7344
  num of homozygotes: 0
population: African
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 5146
  num of homozygotes: 0
population: European (Non-Finnish)
  type: Population
  allele count: 5
  allele frequency: 1.599692858971078e-4
  allele num: 31256
  num of homozygotes: 0
population: East Asian
population: Other
population: European (Finnish)
reference allele: GAAAA
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: DP

16-3433722-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3433722
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3433722
    reference: chr 16
allele count: 2
allele frequency: 1.817983492709886e-5
allele num: 110012
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140987
  ensembl transcript: ENST00000571285
  gene symbol: ZSCAN32
  hgvsc: ENST00000571285.1:n.340T>C
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000380061
  ensembl transcript: ENST00000396852
  gene symbol: ZSCAN32
  hgvsc: ENST00000396852.4:c.1235-11T>C
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000391787
  ensembl transcript: ENST00000439568
  gene symbol: ZSCAN32
  hgvsc: ENST00000439568.2:c.368-11T>C
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000380057
  ensembl transcript: ENST00000396846
  gene symbol: ZSCAN32
  hgvsc: ENST00000396846.3:c.1235-11T>C
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000460487
  ensembl transcript: ENST00000573327
  gene symbol: ZSCAN32
  hgvsc: ENST00000573327.1:c.1235-11T>C
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000302502
  ensembl transcript: ENST00000304926
  gene symbol: ZSCAN32
  hgvsc: ENST00000304926.3:c.599-11T>C
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000459772
  ensembl transcript: ENST00000574940
  gene symbol: ZSCAN32
  hgvsc: ENST00000574940.1:c.*687T>C
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262621
  ensembl transcript: ENST00000576906
  gene symbol: NAA60
  hgvsc: ENST00000576906.1:n.85-288A>G
  variant of: http://identifiers.org/hgnc/25875
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000459069
  ensembl transcript: ENST00000576500
  gene symbol: ZSCAN32
  hgvsc: ENST00000576500.1:c.*289-11T>C
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262621
  ensembl protein: ENSP00000477472
  ensembl transcript: ENST00000575785
  gene symbol: NAA60
  hgvsc: ENST00000575785.1:c.-13+18540A>G
  variant of: http://identifiers.org/hgnc/25875
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1494
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6792
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 869
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9995
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2806
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4512
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10456
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4169
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1075
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16087
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 760
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1696
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 481
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: South Asian
reference allele: A
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: QD

http://identifiers.org/exac.variant/16-3433725-A-AC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3433725
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3433726
    reference: chr 16
allele count: 1
allele frequency: 9.248298313110388e-6
allele num: 108128
alternate allele: AC
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000380057
  ensembl transcript: ENST00000396846
  gene symbol: ZSCAN32
  hgvsc: ENST00000396846.3:c.1235-15dupG
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000391787
  ensembl transcript: ENST00000439568
  gene symbol: ZSCAN32
  hgvsc: ENST00000439568.2:c.368-15dupG
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262621
  ensembl transcript: ENST00000576906
  gene symbol: NAA60
  hgvsc: ENST00000576906.1:n.85-281dupC
  variant of: http://identifiers.org/hgnc/25875
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000459772
  ensembl transcript: ENST00000574940
  gene symbol: ZSCAN32
  hgvsc: ENST00000574940.1:c.*683dupG
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000302502
  ensembl transcript: ENST00000304926
  gene symbol: ZSCAN32
  hgvsc: ENST00000304926.3:c.599-15dupG
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262621
  ensembl protein: ENSP00000477472
  ensembl transcript: ENST00000575785
  gene symbol: NAA60
  hgvsc: ENST00000575785.1:c.-13+18547dupC
  variant of: http://identifiers.org/hgnc/25875
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000459069
  ensembl transcript: ENST00000576500
  gene symbol: ZSCAN32
  hgvsc: ENST00000576500.1:c.*289-15dupG
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140987
  ensembl transcript: ENST00000571285
  gene symbol: ZSCAN32
  hgvsc: ENST00000571285.1:n.336dupG
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000380061
  ensembl transcript: ENST00000396852
  gene symbol: ZSCAN32
  hgvsc: ENST00000396852.4:c.1235-15dupG
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000460487
  ensembl transcript: ENST00000573327
  gene symbol: ZSCAN32
  hgvsc: ENST00000573327.1:c.1235-15dupG
  variant of: http://identifiers.org/hgnc/20812
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9916
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10552
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4914
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1142
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 868
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2793
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4227
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6767
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1482
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15577
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3124
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5830
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 727
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: South Asian
population: African
population: Latino
population: European (Finnish)
population: East Asian
reference allele: A
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum

http://identifiers.org/exac.variant/16-3433725-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3433725
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3433725
    reference: chr 16
allele count: 57
allele frequency: 5.271530038472921e-4
allele num: 108128
alternate allele: C
canonical: false
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1142
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4227
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9916
  bin: 2.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 10552
  bin: 1.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15577
  bin: 2.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 868
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4914
  bin: 1.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 1482
  bin: 4.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 2793
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 6767
  bin: 3.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3167
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1332
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3124
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 510
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 711
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 906
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5830
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 759
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 506
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 636
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1923
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 742
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 727
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1360
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 10079
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 369
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2156
  bin: 7.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 2068
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20499
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3020
  bin: 9.75e1
  variant carriers: 53
num of homozygotes: 0
population: South Asian
  type: Population
  allele count: 34
  allele frequency: 2.43378668575519e-3
  allele num: 13970
  num of homozygotes: 0
population: East Asian
  type: Population
  allele count: 19
  allele frequency: 2.416687865683032e-3
  allele num: 7862
  num of homozygotes: 0
population: African
  type: Population
  allele count: 1
  allele frequency: 1.174536058256989e-4
  allele num: 8514
  num of homozygotes: 0
population: Other
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 824
  num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP

http://identifiers.org/exac.variant/16-3433725-AC-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3433725
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3433724
    reference: chr 16
allele count: 14
allele frequency: 1.294761763835454e-4
allele num: 108128
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000380061
  ensembl transcript: ENST00000396852
  gene symbol: ZSCAN32
  hgvsc: ENST00000396852.4:c.1235-15delG
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000302502
  ensembl transcript: ENST00000304926
  gene symbol: ZSCAN32
  hgvsc: ENST00000304926.3:c.599-15delG
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000391787
  ensembl transcript: ENST00000439568
  gene symbol: ZSCAN32
  hgvsc: ENST00000439568.2:c.368-15delG
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262621
  ensembl transcript: ENST00000576906
  gene symbol: NAA60
  hgvsc: ENST00000576906.1:n.85-281delC
  variant of: http://identifiers.org/hgnc/25875
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262621
  ensembl protein: ENSP00000477472
  ensembl transcript: ENST00000575785
  gene symbol: NAA60
  hgvsc: ENST00000575785.1:c.-13+18547delC
  variant of: http://identifiers.org/hgnc/25875
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000459772
  ensembl transcript: ENST00000574940
  gene symbol: ZSCAN32
  hgvsc: ENST00000574940.1:c.*683delG
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000460487
  ensembl transcript: ENST00000573327
  gene symbol: ZSCAN32
  hgvsc: ENST00000573327.1:c.1235-15delG
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140987
  ensembl transcript: ENST00000571285
  gene symbol: ZSCAN32
  hgvsc: ENST00000571285.1:n.336delG
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000380057
  ensembl transcript: ENST00000396846
  gene symbol: ZSCAN32
  hgvsc: ENST00000396846.3:c.1235-15delG
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000459069
  ensembl transcript: ENST00000576500
  gene symbol: ZSCAN32
  hgvsc: ENST00000576500.1:c.*289-15delG
  variant of: http://identifiers.org/hgnc/20812
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 868
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4914
  bin: 1.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 6767
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4227
  bin: 7.5e0
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15577
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1482
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9916
  bin: 2.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 2793
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10552
  bin: 1.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1142
  bin: 2.5e0
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 369
  bin: 1.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 5830
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3020
  bin: 9.75e1
  variant carriers: 5
num of homozygotes: 0
population: Latino
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: AC
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD

http://identifiers.org/exac.variant/16-3433726-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3433726
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3433726
    reference: chr 16
allele count: 311
allele frequency: 2.943403369297748e-3
allele num: 105660
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000380057
  ensembl transcript: ENST00000396846
  gene symbol: ZSCAN32
  hgvsc: ENST00000396846.3:c.1235-15G>T
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000459772
  ensembl transcript: ENST00000574940
  gene symbol: ZSCAN32
  hgvsc: ENST00000574940.1:c.*683G>T
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000302502
  ensembl transcript: ENST00000304926
  gene symbol: ZSCAN32
  hgvsc: ENST00000304926.3:c.599-15G>T
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140987
  ensembl transcript: ENST00000571285
  gene symbol: ZSCAN32
  hgvsc: ENST00000571285.1:n.336G>T
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000380061
  ensembl transcript: ENST00000396852
  gene symbol: ZSCAN32
  hgvsc: ENST00000396852.4:c.1235-15G>T
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262621
  ensembl protein: ENSP00000477472
  ensembl transcript: ENST00000575785
  gene symbol: NAA60
  hgvsc: ENST00000575785.1:c.-13+18544C>A
  variant of: http://identifiers.org/hgnc/25875
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000459069
  ensembl transcript: ENST00000576500
  gene symbol: ZSCAN32
  hgvsc: ENST00000576500.1:c.*289-15G>T
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000460487
  ensembl transcript: ENST00000573327
  gene symbol: ZSCAN32
  hgvsc: ENST00000573327.1:c.1235-15G>T
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262621
  ensembl transcript: ENST00000576906
  gene symbol: NAA60
  hgvsc: ENST00000576906.1:n.85-284C>A
  variant of: http://identifiers.org/hgnc/25875
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000391787
  ensembl transcript: ENST00000439568
  gene symbol: ZSCAN32
  hgvsc: ENST00000439568.2:c.368-15G>T
  variant of: http://identifiers.org/hgnc/20812
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 854
  bin: 4.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 6.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1448
  bin: 4.25e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 7.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6549
  bin: 3.25e1
  variant carriers: 45
genotype depth: GenotypeDepth
  all individuals: 4360
  bin: 7.5e0
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 2695
  bin: 3.75e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10600
  bin: 1.25e1
  variant carriers: 40
genotype depth: GenotypeDepth
  all individuals: 10173
  bin: 2.25e1
  variant carriers: 39
genotype depth: GenotypeDepth
  all individuals: 1162
  bin: 2.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 15542
  bin: 2.75e1
  variant carriers: 54
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 5.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 5.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 4829
  bin: 1.75e1
  variant carriers: 65
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1051
  bin: 2.5e0
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 10183
  bin: 2.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 802
  bin: 4.75e1
  variant carriers: 5
num of homozygotes: 5
population: South Asian
population: Latino
population: Other
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: QD

16-3433749-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3433749
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3433749
    reference: chr 16
allele count: 10
allele frequency: 9.631684388965942e-5
allele num: 103824
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000380061
  ensembl transcript: ENST00000396852
  gene symbol: ZSCAN32
  hgvsc: ENST00000396852.4:c.1235-38A>G
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000391787
  ensembl transcript: ENST00000439568
  gene symbol: ZSCAN32
  hgvsc: ENST00000439568.2:c.368-38A>G
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140987
  ensembl transcript: ENST00000571285
  gene symbol: ZSCAN32
  hgvsc: ENST00000571285.1:n.313A>G
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000459772
  ensembl transcript: ENST00000574940
  gene symbol: ZSCAN32
  hgvsc: ENST00000574940.1:c.*660A>G
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000459069
  ensembl transcript: ENST00000576500
  gene symbol: ZSCAN32
  hgvsc: ENST00000576500.1:c.*289-38A>G
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000460487
  ensembl transcript: ENST00000573327
  gene symbol: ZSCAN32
  hgvsc: ENST00000573327.1:c.1235-38A>G
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000380057
  ensembl transcript: ENST00000396846
  gene symbol: ZSCAN32
  hgvsc: ENST00000396846.3:c.1235-38A>G
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000302502
  ensembl transcript: ENST00000304926
  gene symbol: ZSCAN32
  hgvsc: ENST00000304926.3:c.599-38A>G
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262621
  ensembl transcript: ENST00000576906
  gene symbol: NAA60
  hgvsc: ENST00000576906.1:n.85-261T>C
  variant of: http://identifiers.org/hgnc/25875
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262621
  ensembl protein: ENSP00000477472
  ensembl transcript: ENST00000575785
  gene symbol: NAA60
  hgvsc: ENST00000575785.1:c.-13+18567T>C
  variant of: http://identifiers.org/hgnc/25875
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12425
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4836
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2030
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2336
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10707
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6161
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10078
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1271
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7539
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 810
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1415
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1603
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 717
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
population: Other
population: South Asian
population: European (Finnish)
reference allele: T
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum

16-3433752-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3433752
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3433752
    reference: chr 16
allele count: 75
allele frequency: 7.260547154833588e-4
allele num: 103298
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000459069
  ensembl transcript: ENST00000576500
  gene symbol: ZSCAN32
  hgvsc: ENST00000576500.1:c.*289-41T>C
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262621
  ensembl protein: ENSP00000477472
  ensembl transcript: ENST00000575785
  gene symbol: NAA60
  hgvsc: ENST00000575785.1:c.-13+18570A>G
  variant of: http://identifiers.org/hgnc/25875
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000380061
  ensembl transcript: ENST00000396852
  gene symbol: ZSCAN32
  hgvsc: ENST00000396852.4:c.1235-41T>C
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000391787
  ensembl transcript: ENST00000439568
  gene symbol: ZSCAN32
  hgvsc: ENST00000439568.2:c.368-41T>C
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000302502
  ensembl transcript: ENST00000304926
  gene symbol: ZSCAN32
  hgvsc: ENST00000304926.3:c.599-41T>C
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000459772
  ensembl transcript: ENST00000574940
  gene symbol: ZSCAN32
  hgvsc: ENST00000574940.1:c.*657T>C
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140987
  ensembl transcript: ENST00000571285
  gene symbol: ZSCAN32
  hgvsc: ENST00000571285.1:n.310T>C
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262621
  ensembl transcript: ENST00000576906
  gene symbol: NAA60
  hgvsc: ENST00000576906.1:n.85-258A>G
  variant of: http://identifiers.org/hgnc/25875
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000380057
  ensembl transcript: ENST00000396846
  gene symbol: ZSCAN32
  hgvsc: ENST00000396846.3:c.1235-41T>C
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000460487
  ensembl transcript: ENST00000573327
  gene symbol: ZSCAN32
  hgvsc: ENST00000573327.1:c.1235-41T>C
  variant of: http://identifiers.org/hgnc/20812
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 810
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4731
  bin: 3.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12255
  bin: 1.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 9347
  bin: 2.75e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 11839
  bin: 1.75e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1270
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2056
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7173
  bin: 2.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2325
  bin: 3.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 551
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6379
  bin: 7.5e0
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 1668
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 648
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 941
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
population: East Asian
population: Other
population: South Asian
reference allele: A
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: InbreedingCoeff

16-3434359-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3434359
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3434359
    reference: chr 16
allele count: 1
allele frequency: 8.961055253866696e-6
allele num: 111594
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000459960
  ensembl transcript: ENST00000573830
  gene symbol: ZSCAN32
  hgvsc: ENST00000573830.1:c.*50A>G
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000302502
  ensembl transcript: ENST00000304926
  gene symbol: ZSCAN32
  hgvsc: ENST00000304926.3:c.598+100A>G
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000460487
  ensembl transcript: ENST00000573327
  gene symbol: ZSCAN32
  hgvsc: ENST00000573327.1:c.1234+100A>G
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000459772
  ensembl transcript: ENST00000574940
  gene symbol: ZSCAN32
  hgvsc: ENST00000574940.1:c.*50A>G
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000380057
  ensembl transcript: ENST00000396846
  gene symbol: ZSCAN32
  hgvsc: ENST00000396846.3:c.1234+100A>G
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000262621
  ensembl transcript: ENST00000576906
  gene symbol: NAA60
  hgvsc: ENST00000576906.1:n.434T>C
  variant of: http://identifiers.org/hgnc/25875
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000391787
  ensembl transcript: ENST00000439568
  gene symbol: ZSCAN32
  hgvsc: ENST00000439568.2:c.367+100A>G
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000380061
  ensembl transcript: ENST00000396852
  gene symbol: ZSCAN32
  hgvsc: ENST00000396852.4:c.1234+100A>G
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262621
  ensembl protein: ENSP00000477472
  ensembl transcript: ENST00000575785
  gene symbol: NAA60
  hgvsc: ENST00000575785.1:c.-13+19177T>C
  variant of: http://identifiers.org/hgnc/25875
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140987
  ensembl transcript: ENST00000574084
  gene symbol: ZSCAN32
  hgvsc: ENST00000574084.1:n.783A>G
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000459069
  ensembl transcript: ENST00000576500
  gene symbol: ZSCAN32
  hgvsc: ENST00000576500.1:c.*288+100A>G
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000407312
  ensembl transcript: ENST00000422427
  gene symbol: ZSCAN32
  hgvsc: ENST00000422427.2:c.*50A>G
  variant of: http://identifiers.org/hgnc/20812
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8100
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3192
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1979
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3111
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1228
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4754
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1371
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 499
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8156
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3106
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 793
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1697
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1169
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7048
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1223
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6556
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum

16-3434391-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3434391
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3434391
    reference: chr 16
allele count: 1
allele frequency: 8.892208646783689e-6
allele num: 112458
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262621
  ensembl protein: ENSP00000477472
  ensembl transcript: ENST00000575785
  gene symbol: NAA60
  hgvsc: ENST00000575785.1:c.-13+19209C>G
  variant of: http://identifiers.org/hgnc/25875
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000391787
  ensembl transcript: ENST00000439568
  gene symbol: ZSCAN32
  hgvsc: ENST00000439568.2:c.367+68G>C
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000459960
  ensembl transcript: ENST00000573830
  gene symbol: ZSCAN32
  hgvsc: ENST00000573830.1:c.*18G>C
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000380057
  ensembl transcript: ENST00000396846
  gene symbol: ZSCAN32
  hgvsc: ENST00000396846.3:c.1234+68G>C
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140987
  ensembl transcript: ENST00000574084
  gene symbol: ZSCAN32
  hgvsc: ENST00000574084.1:n.751G>C
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000459069
  ensembl transcript: ENST00000576500
  gene symbol: ZSCAN32
  hgvsc: ENST00000576500.1:c.*288+68G>C
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000380061
  ensembl transcript: ENST00000396852
  gene symbol: ZSCAN32
  hgvsc: ENST00000396852.4:c.1234+68G>C
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000407312
  ensembl transcript: ENST00000422427
  gene symbol: ZSCAN32
  hgvsc: ENST00000422427.2:c.*18G>C
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000262621
  ensembl transcript: ENST00000576906
  gene symbol: NAA60
  hgvsc: ENST00000576906.1:n.466C>G
  variant of: http://identifiers.org/hgnc/25875
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000459772
  ensembl transcript: ENST00000574940
  gene symbol: ZSCAN32
  hgvsc: ENST00000574940.1:c.*18G>C
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000302502
  ensembl transcript: ENST00000304926
  gene symbol: ZSCAN32
  hgvsc: ENST00000304926.3:c.598+68G>C
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000460487
  ensembl transcript: ENST00000573327
  gene symbol: ZSCAN32
  hgvsc: ENST00000573327.1:c.1234+68G>C
  variant of: http://identifiers.org/hgnc/20812
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1170
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4031
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3196
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3601
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4756
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 776
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8219
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1168
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 795
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8148
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7431
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5640
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6580
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1976
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1223
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum

16-3434416-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3434416
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3434416
    reference: chr 16
allele count: 0
allele frequency: 0.0e0
allele num: 115498
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000459069
  ensembl transcript: ENST00000576500
  gene symbol: ZSCAN32
  hgvsc: ENST00000576500.1:c.*288+43C>G
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000407312
  ensembl transcript: ENST00000422427
  gene symbol: ZSCAN32
  hgvsc: ENST00000422427.2:c.641C>G
  hgvsp: ENSP00000407312.2:p.Pro214Arg
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262621
  ensembl protein: ENSP00000477472
  ensembl transcript: ENST00000575785
  gene symbol: NAA60
  hgvsc: ENST00000575785.1:c.-13+19234G>C
  variant of: http://identifiers.org/hgnc/25875
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140987
  ensembl transcript: ENST00000574084
  gene symbol: ZSCAN32
  hgvsc: ENST00000574084.1:n.726C>G
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000262621
  ensembl transcript: ENST00000576906
  gene symbol: NAA60
  hgvsc: ENST00000576906.1:n.491G>C
  variant of: http://identifiers.org/hgnc/25875
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000302502
  ensembl transcript: ENST00000304926
  gene symbol: ZSCAN32
  hgvsc: ENST00000304926.3:c.598+43C>G
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000380057
  ensembl transcript: ENST00000396846
  gene symbol: ZSCAN32
  hgvsc: ENST00000396846.3:c.1234+43C>G
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000460487
  ensembl transcript: ENST00000573327
  gene symbol: ZSCAN32
  hgvsc: ENST00000573327.1:c.1234+43C>G
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000459960
  ensembl transcript: ENST00000573830
  gene symbol: ZSCAN32
  hgvsc: ENST00000573830.1:c.410C>G
  hgvsp: ENSP00000459960.1:p.Pro137Arg
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000459772
  ensembl transcript: ENST00000574940
  gene symbol: ZSCAN32
  hgvsc: ENST00000574940.1:c.1277C>G
  hgvsp: ENSP00000459772.1:p.Pro426Arg
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000380061
  ensembl transcript: ENST00000396852
  gene symbol: ZSCAN32
  hgvsc: ENST00000396852.4:c.1234+43C>G
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000391787
  ensembl transcript: ENST00000439568
  gene symbol: ZSCAN32
  hgvsc: ENST00000439568.2:c.367+43C>G
  variant of: http://identifiers.org/hgnc/20812
canonical: false
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 5493
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 808
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8238
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3197
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4758
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 796
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2786
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6582
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 499
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5922
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1170
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1223
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7511
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro137Arg
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: Other
reference allele: G
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum

16-3434417-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3434417
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3434417
    reference: chr 16
allele count: 1
allele frequency: 8.643938870064311e-6
allele num: 115688
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000407312
  ensembl transcript: ENST00000422427
  gene symbol: ZSCAN32
  hgvsc: ENST00000422427.2:c.640C>T
  hgvsp: ENSP00000407312.2:p.Pro214Ser
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000459960
  ensembl transcript: ENST00000573830
  gene symbol: ZSCAN32
  hgvsc: ENST00000573830.1:c.409C>T
  hgvsp: ENSP00000459960.1:p.Pro137Ser
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000459772
  ensembl transcript: ENST00000574940
  gene symbol: ZSCAN32
  hgvsc: ENST00000574940.1:c.1276C>T
  hgvsp: ENSP00000459772.1:p.Pro426Ser
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140987
  ensembl transcript: ENST00000574084
  gene symbol: ZSCAN32
  hgvsc: ENST00000574084.1:n.725C>T
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000380057
  ensembl transcript: ENST00000396846
  gene symbol: ZSCAN32
  hgvsc: ENST00000396846.3:c.1234+42C>T
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000302502
  ensembl transcript: ENST00000304926
  gene symbol: ZSCAN32
  hgvsc: ENST00000304926.3:c.598+42C>T
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000459069
  ensembl transcript: ENST00000576500
  gene symbol: ZSCAN32
  hgvsc: ENST00000576500.1:c.*288+42C>T
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000391787
  ensembl transcript: ENST00000439568
  gene symbol: ZSCAN32
  hgvsc: ENST00000439568.2:c.367+42C>T
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262621
  ensembl protein: ENSP00000477472
  ensembl transcript: ENST00000575785
  gene symbol: NAA60
  hgvsc: ENST00000575785.1:c.-13+19235G>A
  variant of: http://identifiers.org/hgnc/25875
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000380061
  ensembl transcript: ENST00000396852
  gene symbol: ZSCAN32
  hgvsc: ENST00000396852.4:c.1234+42C>T
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000262621
  ensembl transcript: ENST00000576906
  gene symbol: NAA60
  hgvsc: ENST00000576906.1:n.492G>A
  variant of: http://identifiers.org/hgnc/25875
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000460487
  ensembl transcript: ENST00000573327
  gene symbol: ZSCAN32
  hgvsc: ENST00000573327.1:c.1234+42C>T
  variant of: http://identifiers.org/hgnc/20812
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3197
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1976
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 499
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8147
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5937
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4758
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2716
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7508
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 796
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1170
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8239
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5565
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro137Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Other
population: European (Finnish)
population: African
population: East Asian
population: Latino
reference allele: G
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP

16-3434426-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3434426
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3434426
    reference: chr 16
allele count: 1
allele frequency: 8.508755509419192e-6
allele num: 117526
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140987
  ensembl transcript: ENST00000574084
  gene symbol: ZSCAN32
  hgvsc: ENST00000574084.1:n.716T>C
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000302502
  ensembl transcript: ENST00000304926
  gene symbol: ZSCAN32
  hgvsc: ENST00000304926.3:c.598+33T>C
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000460487
  ensembl transcript: ENST00000573327
  gene symbol: ZSCAN32
  hgvsc: ENST00000573327.1:c.1234+33T>C
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000380061
  ensembl transcript: ENST00000396852
  gene symbol: ZSCAN32
  hgvsc: ENST00000396852.4:c.1234+33T>C
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000459960
  ensembl transcript: ENST00000573830
  gene symbol: ZSCAN32
  hgvsc: ENST00000573830.1:c.400T>C
  hgvsp: ENSP00000459960.1:p.Trp134Arg
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000407312
  ensembl transcript: ENST00000422427
  gene symbol: ZSCAN32
  hgvsc: ENST00000422427.2:c.631T>C
  hgvsp: ENSP00000407312.2:p.Trp211Arg
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000459772
  ensembl transcript: ENST00000574940
  gene symbol: ZSCAN32
  hgvsc: ENST00000574940.1:c.1267T>C
  hgvsp: ENSP00000459772.1:p.Trp423Arg
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262621
  ensembl protein: ENSP00000477472
  ensembl transcript: ENST00000575785
  gene symbol: NAA60
  hgvsc: ENST00000575785.1:c.-13+19244A>G
  variant of: http://identifiers.org/hgnc/25875
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000380057
  ensembl transcript: ENST00000396846
  gene symbol: ZSCAN32
  hgvsc: ENST00000396846.3:c.1234+33T>C
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000459069
  ensembl transcript: ENST00000576500
  gene symbol: ZSCAN32
  hgvsc: ENST00000576500.1:c.*288+33T>C
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000262621
  ensembl transcript: ENST00000576906
  gene symbol: NAA60
  hgvsc: ENST00000576906.1:n.501A>G
  variant of: http://identifiers.org/hgnc/25875
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000391787
  ensembl transcript: ENST00000439568
  gene symbol: ZSCAN32
  hgvsc: ENST00000439568.2:c.367+33T>C
  variant of: http://identifiers.org/hgnc/20812
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3197
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1867
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1170
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4758
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1976
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8151
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6153
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6582
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 796
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8241
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6430
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7538
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1225
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Trp134Arg
num of homozygotes: 0
population: Latino
population: African
population: Other
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: ClippingRankSum

16-3434434-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3434434
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3434434
    reference: chr 16
allele count: 1
allele frequency: 8.414391976035812e-6
allele num: 118844
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000391787
  ensembl transcript: ENST00000439568
  gene symbol: ZSCAN32
  hgvsc: ENST00000439568.2:c.367+25T>C
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262621
  ensembl protein: ENSP00000477472
  ensembl transcript: ENST00000575785
  gene symbol: NAA60
  hgvsc: ENST00000575785.1:c.-13+19252A>G
  variant of: http://identifiers.org/hgnc/25875
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000459069
  ensembl transcript: ENST00000576500
  gene symbol: ZSCAN32
  hgvsc: ENST00000576500.1:c.*288+25T>C
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000459960
  ensembl transcript: ENST00000573830
  gene symbol: ZSCAN32
  hgvsc: ENST00000573830.1:c.392T>C
  hgvsp: ENSP00000459960.1:p.Val131Ala
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000262621
  ensembl transcript: ENST00000576906
  gene symbol: NAA60
  hgvsc: ENST00000576906.1:n.509A>G
  variant of: http://identifiers.org/hgnc/25875
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000459772
  ensembl transcript: ENST00000574940
  gene symbol: ZSCAN32
  hgvsc: ENST00000574940.1:c.1259T>C
  hgvsp: ENSP00000459772.1:p.Val420Ala
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000407312
  ensembl transcript: ENST00000422427
  gene symbol: ZSCAN32
  hgvsc: ENST00000422427.2:c.623T>C
  hgvsp: ENSP00000407312.2:p.Val208Ala
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000380061
  ensembl transcript: ENST00000396852
  gene symbol: ZSCAN32
  hgvsc: ENST00000396852.4:c.1234+25T>C
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000302502
  ensembl transcript: ENST00000304926
  gene symbol: ZSCAN32
  hgvsc: ENST00000304926.3:c.598+25T>C
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140987
  ensembl transcript: ENST00000574084
  gene symbol: ZSCAN32
  hgvsc: ENST00000574084.1:n.708T>C
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000380057
  ensembl transcript: ENST00000396846
  gene symbol: ZSCAN32
  hgvsc: ENST00000396846.3:c.1234+25T>C
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000460487
  ensembl transcript: ENST00000573327
  gene symbol: ZSCAN32
  hgvsc: ENST00000573327.1:c.1234+25T>C
  variant of: http://identifiers.org/hgnc/20812
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6315
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6583
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4758
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 797
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1231
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1976
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 499
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8151
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7572
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7131
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8244
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1225
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val131Ala
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
population: European (Finnish)
population: African
reference allele: A
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD

16-3434439-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3434439
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3434439
    reference: chr 16
allele count: 2
allele frequency: 1.672968180145214e-5
allele num: 119548
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000460487
  ensembl transcript: ENST00000573327
  gene symbol: ZSCAN32
  hgvsc: ENST00000573327.1:c.1234+20G>A
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000459960
  ensembl transcript: ENST00000573830
  gene symbol: ZSCAN32
  hgvsc: ENST00000573830.1:c.387G>A
  hgvsp: ENST00000573830.1:c.387G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000380057
  ensembl transcript: ENST00000396846
  gene symbol: ZSCAN32
  hgvsc: ENST00000396846.3:c.1234+20G>A
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000459069
  ensembl transcript: ENST00000576500
  gene symbol: ZSCAN32
  hgvsc: ENST00000576500.1:c.*288+20G>A
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000459772
  ensembl transcript: ENST00000574940
  gene symbol: ZSCAN32
  hgvsc: ENST00000574940.1:c.1254G>A
  hgvsp: ENST00000574940.1:c.1254G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140987
  ensembl transcript: ENST00000574084
  gene symbol: ZSCAN32
  hgvsc: ENST00000574084.1:n.703G>A
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262621
  ensembl protein: ENSP00000477472
  ensembl transcript: ENST00000575785
  gene symbol: NAA60
  hgvsc: ENST00000575785.1:c.-13+19257C>T
  variant of: http://identifiers.org/hgnc/25875
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000302502
  ensembl transcript: ENST00000304926
  gene symbol: ZSCAN32
  hgvsc: ENST00000304926.3:c.598+20G>A
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000262621
  ensembl transcript: ENST00000576906
  gene symbol: NAA60
  hgvsc: ENST00000576906.1:n.514C>T
  variant of: http://identifiers.org/hgnc/25875
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000407312
  ensembl transcript: ENST00000422427
  gene symbol: ZSCAN32
  hgvsc: ENST00000422427.2:c.618G>A
  hgvsp: ENST00000422427.2:c.618G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000380061
  ensembl transcript: ENST00000396852
  gene symbol: ZSCAN32
  hgvsc: ENST00000396852.4:c.1234+20G>A
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000391787
  ensembl transcript: ENST00000439568
  gene symbol: ZSCAN32
  hgvsc: ENST00000439568.2:c.367+20G>A
  variant of: http://identifiers.org/hgnc/20812
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1976
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7350
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6583
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 796
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 877
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7633
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3197
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6503
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8150
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1170
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8249
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1227
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu129Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: FS
site quality: DP
site quality: ClippingRankSum

16-3434441-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3434441
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3434441
    reference: chr 16
allele count: 1
allele frequency: 8.345294922722569e-6
allele num: 119828
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000302502
  ensembl transcript: ENST00000304926
  gene symbol: ZSCAN32
  hgvsc: ENST00000304926.3:c.598+18C>T
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000380057
  ensembl transcript: ENST00000396846
  gene symbol: ZSCAN32
  hgvsc: ENST00000396846.3:c.1234+18C>T
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000262621
  ensembl transcript: ENST00000576906
  gene symbol: NAA60
  hgvsc: ENST00000576906.1:n.516G>A
  variant of: http://identifiers.org/hgnc/25875
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262621
  ensembl protein: ENSP00000477472
  ensembl transcript: ENST00000575785
  gene symbol: NAA60
  hgvsc: ENST00000575785.1:c.-13+19259G>A
  variant of: http://identifiers.org/hgnc/25875
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000459960
  ensembl transcript: ENST00000573830
  gene symbol: ZSCAN32
  hgvsc: ENST00000573830.1:c.385C>T
  hgvsp: ENST00000573830.1:c.385C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000460487
  ensembl transcript: ENST00000573327
  gene symbol: ZSCAN32
  hgvsc: ENST00000573327.1:c.1234+18C>T
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000459772
  ensembl transcript: ENST00000574940
  gene symbol: ZSCAN32
  hgvsc: ENST00000574940.1:c.1252C>T
  hgvsp: ENST00000574940.1:c.1252C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000391787
  ensembl transcript: ENST00000439568
  gene symbol: ZSCAN32
  hgvsc: ENST00000439568.2:c.367+18C>T
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000459069
  ensembl transcript: ENST00000576500
  gene symbol: ZSCAN32
  hgvsc: ENST00000576500.1:c.*288+18C>T
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000407312
  ensembl transcript: ENST00000422427
  gene symbol: ZSCAN32
  hgvsc: ENST00000422427.2:c.616C>T
  hgvsp: ENST00000422427.2:c.616C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000380061
  ensembl transcript: ENST00000396852
  gene symbol: ZSCAN32
  hgvsc: ENST00000396852.4:c.1234+18C>T
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140987
  ensembl transcript: ENST00000574084
  gene symbol: ZSCAN32
  hgvsc: ENST00000574084.1:n.701C>T
  variant of: http://identifiers.org/hgnc/20812
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7626
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1170
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3197
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8151
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6570
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1976
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 796
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 751
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7466
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1228
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8249
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4757
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu129Leu
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
population: African
population: European (Finnish)
population: Latino
reference allele: G
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD

16-3434447-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3434447
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3434447
    reference: chr 16
allele count: 1
allele frequency: 8.300408380092301e-6
allele num: 120476
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262621
  ensembl protein: ENSP00000477472
  ensembl transcript: ENST00000575785
  gene symbol: NAA60
  hgvsc: ENST00000575785.1:c.-13+19265A>G
  variant of: http://identifiers.org/hgnc/25875
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000380061
  ensembl transcript: ENST00000396852
  gene symbol: ZSCAN32
  hgvsc: ENST00000396852.4:c.1234+12T>C
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000391787
  ensembl transcript: ENST00000439568
  gene symbol: ZSCAN32
  hgvsc: ENST00000439568.2:c.367+12T>C
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000459772
  ensembl transcript: ENST00000574940
  gene symbol: ZSCAN32
  hgvsc: ENST00000574940.1:c.1246T>C
  hgvsp: ENST00000574940.1:c.1246T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000459960
  ensembl transcript: ENST00000573830
  gene symbol: ZSCAN32
  hgvsc: ENST00000573830.1:c.379T>C
  hgvsp: ENST00000573830.1:c.379T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140987
  ensembl transcript: ENST00000574084
  gene symbol: ZSCAN32
  hgvsc: ENST00000574084.1:n.695T>C
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000407312
  ensembl transcript: ENST00000422427
  gene symbol: ZSCAN32
  hgvsc: ENST00000422427.2:c.610T>C
  hgvsp: ENST00000422427.2:c.610T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000460487
  ensembl transcript: ENST00000573327
  gene symbol: ZSCAN32
  hgvsc: ENST00000573327.1:c.1234+12T>C
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000459069
  ensembl transcript: ENST00000576500
  gene symbol: ZSCAN32
  hgvsc: ENST00000576500.1:c.*288+12T>C
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000380057
  ensembl transcript: ENST00000396846
  gene symbol: ZSCAN32
  hgvsc: ENST00000396846.3:c.1234+12T>C
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000262621
  ensembl transcript: ENST00000576906
  gene symbol: NAA60
  hgvsc: ENST00000576906.1:n.522A>G
  variant of: http://identifiers.org/hgnc/25875
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000302502
  ensembl transcript: ENST00000304926
  gene symbol: ZSCAN32
  hgvsc: ENST00000304926.3:c.598+12T>C
  variant of: http://identifiers.org/hgnc/20812
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1170
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7680
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1976
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6731
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4757
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 499
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6584
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3197
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8152
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7688
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1228
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 796
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu127Leu
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: A
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP

16-3434451-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3434451
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3434451
    reference: chr 16
allele count: 2
allele frequency: 1.656918463042434e-5
allele num: 120706
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140987
  ensembl transcript: ENST00000574084
  gene symbol: ZSCAN32
  hgvsc: ENST00000574084.1:n.691T>C
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000262621
  ensembl transcript: ENST00000576906
  gene symbol: NAA60
  hgvsc: ENST00000576906.1:n.526A>G
  variant of: http://identifiers.org/hgnc/25875
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000380057
  ensembl transcript: ENST00000396846
  gene symbol: ZSCAN32
  hgvsc: ENST00000396846.3:c.1234+8T>C
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000391787
  ensembl transcript: ENST00000439568
  gene symbol: ZSCAN32
  hgvsc: ENST00000439568.2:c.367+8T>C
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000459069
  ensembl transcript: ENST00000576500
  gene symbol: ZSCAN32
  hgvsc: ENST00000576500.1:c.*288+8T>C
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000302502
  ensembl transcript: ENST00000304926
  gene symbol: ZSCAN32
  hgvsc: ENST00000304926.3:c.598+8T>C
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000460487
  ensembl transcript: ENST00000573327
  gene symbol: ZSCAN32
  hgvsc: ENST00000573327.1:c.1234+8T>C
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000459772
  ensembl transcript: ENST00000574940
  gene symbol: ZSCAN32
  hgvsc: ENST00000574940.1:c.1242T>C
  hgvsp: ENST00000574940.1:c.1242T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000407312
  ensembl transcript: ENST00000422427
  gene symbol: ZSCAN32
  hgvsc: ENST00000422427.2:c.606T>C
  hgvsp: ENST00000422427.2:c.606T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262621
  ensembl protein: ENSP00000477472
  ensembl transcript: ENST00000575785
  gene symbol: NAA60
  hgvsc: ENST00000575785.1:c.-13+19269A>G
  variant of: http://identifiers.org/hgnc/25875
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000380061
  ensembl transcript: ENST00000396852
  gene symbol: ZSCAN32
  hgvsc: ENST00000396852.4:c.1234+8T>C
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000459960
  ensembl transcript: ENST00000573830
  gene symbol: ZSCAN32
  hgvsc: ENST00000573830.1:c.375T>C
  hgvsp: ENST00000573830.1:c.375T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20812
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 797
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7750
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1229
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6584
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4757
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8153
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6834
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 499
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1170
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7691
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3198
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.598+8T>C
num of homozygotes: 0
population: Latino
population: Other
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: DP

16-3434476-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3434476
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3434476
    reference: chr 16
allele count: 1
allele frequency: 8.243751236562685e-6
allele num: 121304
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000380057
  ensembl transcript: ENST00000396846
  gene symbol: ZSCAN32
  hgvsc: ENST00000396846.3:c.1217T>C
  hgvsp: ENSP00000380057.3:p.Leu406Pro
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000459772
  ensembl transcript: ENST00000574940
  gene symbol: ZSCAN32
  hgvsc: ENST00000574940.1:c.1217T>C
  hgvsp: ENSP00000459772.1:p.Leu406Pro
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000459069
  ensembl transcript: ENST00000576500
  gene symbol: ZSCAN32
  hgvsc: ENST00000576500.1:c.*271T>C
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000459960
  ensembl transcript: ENST00000573830
  gene symbol: ZSCAN32
  hgvsc: ENST00000573830.1:c.350T>C
  hgvsp: ENSP00000459960.1:p.Leu117Pro
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000302502
  ensembl transcript: ENST00000304926
  gene symbol: ZSCAN32
  hgvsc: ENST00000304926.3:c.581T>C
  hgvsp: ENSP00000302502.3:p.Leu194Pro
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000407312
  ensembl transcript: ENST00000422427
  gene symbol: ZSCAN32
  hgvsc: ENST00000422427.2:c.581T>C
  hgvsp: ENSP00000407312.2:p.Leu194Pro
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000262621
  ensembl transcript: ENST00000576906
  gene symbol: NAA60
  hgvsc: ENST00000576906.1:n.551A>G
  variant of: http://identifiers.org/hgnc/25875
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000391787
  ensembl transcript: ENST00000439568
  gene symbol: ZSCAN32
  hgvsc: ENST00000439568.2:c.350T>C
  hgvsp: ENSP00000391787.2:p.Leu117Pro
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000380061
  ensembl transcript: ENST00000396852
  gene symbol: ZSCAN32
  hgvsc: ENST00000396852.4:c.1217T>C
  hgvsp: ENSP00000380061.4:p.Leu406Pro
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140987
  ensembl transcript: ENST00000574084
  gene symbol: ZSCAN32
  hgvsc: ENST00000574084.1:n.666T>C
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000460487
  ensembl transcript: ENST00000573327
  gene symbol: ZSCAN32
  hgvsc: ENST00000573327.1:c.1217T>C
  hgvsp: ENSP00000460487.1:p.Leu406Pro
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262621
  ensembl protein: ENSP00000477472
  ensembl transcript: ENST00000575785
  gene symbol: NAA60
  hgvsc: ENST00000575785.1:c.-13+19294A>G
  variant of: http://identifiers.org/hgnc/25875
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8154
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7770
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 797
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1976
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1228
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7847
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6585
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 499
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8261
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1170
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7121
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu194Pro
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
population: Other
population: East Asian
reference allele: A
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP

16-3434477-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3434477
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3434477
    reference: chr 16
allele count: 1
allele frequency: 8.24347940778844e-6
allele num: 121308
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000380061
  ensembl transcript: ENST00000396852
  gene symbol: ZSCAN32
  hgvsc: ENST00000396852.4:c.1216C>T
  hgvsp: ENST00000396852.4:c.1216C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000302502
  ensembl transcript: ENST00000304926
  gene symbol: ZSCAN32
  hgvsc: ENST00000304926.3:c.580C>T
  hgvsp: ENST00000304926.3:c.580C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000459772
  ensembl transcript: ENST00000574940
  gene symbol: ZSCAN32
  hgvsc: ENST00000574940.1:c.1216C>T
  hgvsp: ENST00000574940.1:c.1216C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000380057
  ensembl transcript: ENST00000396846
  gene symbol: ZSCAN32
  hgvsc: ENST00000396846.3:c.1216C>T
  hgvsp: ENST00000396846.3:c.1216C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262621
  ensembl protein: ENSP00000477472
  ensembl transcript: ENST00000575785
  gene symbol: NAA60
  hgvsc: ENST00000575785.1:c.-13+19295G>A
  variant of: http://identifiers.org/hgnc/25875
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000459960
  ensembl transcript: ENST00000573830
  gene symbol: ZSCAN32
  hgvsc: ENST00000573830.1:c.349C>T
  hgvsp: ENST00000573830.1:c.349C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000459069
  ensembl transcript: ENST00000576500
  gene symbol: ZSCAN32
  hgvsc: ENST00000576500.1:c.*270C>T
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000391787
  ensembl transcript: ENST00000439568
  gene symbol: ZSCAN32
  hgvsc: ENST00000439568.2:c.349C>T
  hgvsp: ENST00000439568.2:c.349C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000460487
  ensembl transcript: ENST00000573327
  gene symbol: ZSCAN32
  hgvsc: ENST00000573327.1:c.1216C>T
  hgvsp: ENST00000573327.1:c.1216C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000407312
  ensembl transcript: ENST00000422427
  gene symbol: ZSCAN32
  hgvsc: ENST00000422427.2:c.580C>T
  hgvsp: ENST00000422427.2:c.580C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140987
  ensembl transcript: ENST00000574084
  gene symbol: ZSCAN32
  hgvsc: ENST00000574084.1:n.665C>T
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000262621
  ensembl transcript: ENST00000576906
  gene symbol: NAA60
  hgvsc: ENST00000576906.1:n.552G>A
  variant of: http://identifiers.org/hgnc/25875
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6609
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8175
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7771
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3208
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7077
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 804
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7774
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8267
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1229
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1179
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu194Leu
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Latino
population: Other
reference allele: G
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum

16-3434485-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3434485
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3434485
    reference: chr 16
allele count: 1
allele frequency: 8.241441263248117e-6
allele num: 121338
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000380057
  ensembl transcript: ENST00000396846
  gene symbol: ZSCAN32
  hgvsc: ENST00000396846.3:c.1208T>C
  hgvsp: ENSP00000380057.3:p.Leu403Pro
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000459960
  ensembl transcript: ENST00000573830
  gene symbol: ZSCAN32
  hgvsc: ENST00000573830.1:c.341T>C
  hgvsp: ENSP00000459960.1:p.Leu114Pro
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000460487
  ensembl transcript: ENST00000573327
  gene symbol: ZSCAN32
  hgvsc: ENST00000573327.1:c.1208T>C
  hgvsp: ENSP00000460487.1:p.Leu403Pro
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000459069
  ensembl transcript: ENST00000576500
  gene symbol: ZSCAN32
  hgvsc: ENST00000576500.1:c.*262T>C
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000391787
  ensembl transcript: ENST00000439568
  gene symbol: ZSCAN32
  hgvsc: ENST00000439568.2:c.341T>C
  hgvsp: ENSP00000391787.2:p.Leu114Pro
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000407312
  ensembl transcript: ENST00000422427
  gene symbol: ZSCAN32
  hgvsc: ENST00000422427.2:c.572T>C
  hgvsp: ENSP00000407312.2:p.Leu191Pro
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140987
  ensembl transcript: ENST00000574084
  gene symbol: ZSCAN32
  hgvsc: ENST00000574084.1:n.657T>C
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262621
  ensembl protein: ENSP00000477472
  ensembl transcript: ENST00000575785
  gene symbol: NAA60
  hgvsc: ENST00000575785.1:c.-13+19303A>G
  variant of: http://identifiers.org/hgnc/25875
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000380061
  ensembl transcript: ENST00000396852
  gene symbol: ZSCAN32
  hgvsc: ENST00000396852.4:c.1208T>C
  hgvsp: ENSP00000380061.4:p.Leu403Pro
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000302502
  ensembl transcript: ENST00000304926
  gene symbol: ZSCAN32
  hgvsc: ENST00000304926.3:c.572T>C
  hgvsp: ENSP00000302502.3:p.Leu191Pro
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000262621
  ensembl transcript: ENST00000576906
  gene symbol: NAA60
  hgvsc: ENST00000576906.1:n.560A>G
  variant of: http://identifiers.org/hgnc/25875
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000459772
  ensembl transcript: ENST00000574940
  gene symbol: ZSCAN32
  hgvsc: ENST00000574940.1:c.1208T>C
  hgvsp: ENSP00000459772.1:p.Leu403Pro
  variant of: http://identifiers.org/hgnc/20812
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8273
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7778
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7102
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1186
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4782
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 802
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7748
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8169
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1993
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu191Pro
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD

16-3434488-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3434488
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3434488
    reference: chr 16
allele count: 230
allele frequency: 1.931507079393339e-3
allele num: 119078
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000380057
  ensembl transcript: ENST00000396846
  gene symbol: ZSCAN32
  hgvsc: ENST00000396846.3:c.1205A>C
  hgvsp: ENSP00000380057.3:p.Asp402Ala
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000302502
  ensembl transcript: ENST00000304926
  gene symbol: ZSCAN32
  hgvsc: ENST00000304926.3:c.569A>C
  hgvsp: ENSP00000302502.3:p.Asp190Ala
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000459772
  ensembl transcript: ENST00000574940
  gene symbol: ZSCAN32
  hgvsc: ENST00000574940.1:c.1205A>C
  hgvsp: ENSP00000459772.1:p.Asp402Ala
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000460487
  ensembl transcript: ENST00000573327
  gene symbol: ZSCAN32
  hgvsc: ENST00000573327.1:c.1205A>C
  hgvsp: ENSP00000460487.1:p.Asp402Ala
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000391787
  ensembl transcript: ENST00000439568
  gene symbol: ZSCAN32
  hgvsc: ENST00000439568.2:c.338A>C
  hgvsp: ENSP00000391787.2:p.Asp113Ala
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140987
  ensembl transcript: ENST00000574084
  gene symbol: ZSCAN32
  hgvsc: ENST00000574084.1:n.654A>C
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000459960
  ensembl transcript: ENST00000573830
  gene symbol: ZSCAN32
  hgvsc: ENST00000573830.1:c.338A>C
  hgvsp: ENSP00000459960.1:p.Asp113Ala
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000459069
  ensembl transcript: ENST00000576500
  gene symbol: ZSCAN32
  hgvsc: ENST00000576500.1:c.*259A>C
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000380061
  ensembl transcript: ENST00000396852
  gene symbol: ZSCAN32
  hgvsc: ENST00000396852.4:c.1205A>C
  hgvsp: ENSP00000380061.4:p.Asp402Ala
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262621
  ensembl protein: ENSP00000477472
  ensembl transcript: ENST00000575785
  gene symbol: NAA60
  hgvsc: ENST00000575785.1:c.-13+19306T>G
  variant of: http://identifiers.org/hgnc/25875
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000407312
  ensembl transcript: ENST00000422427
  gene symbol: ZSCAN32
  hgvsc: ENST00000422427.2:c.569A>C
  hgvsp: ENSP00000407312.2:p.Asp190Ala
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000262621
  ensembl transcript: ENST00000576906
  gene symbol: NAA60
  hgvsc: ENST00000576906.1:n.563T>G
  variant of: http://identifiers.org/hgnc/25875
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.95to100.00
genotype depth: GenotypeDepth
  all individuals: 4872
  bin: 5.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8227
  bin: 3.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 9.25e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 7601
  bin: 3.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 857
  bin: 7.25e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 1261
  bin: 6.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 8.75e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 2034
  bin: 6.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 6699
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7355
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 596
  bin: 7.75e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 1732
  bin: 9.75e1
  variant carriers: 94
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 8.25e1
  variant carriers: 9
genotype quality: GenotypeQuality
hgvs: p.Asp190Ala
num of homozygotes: 0
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
population: European (Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: MQ

16-3434491-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3434491
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3434491
    reference: chr 16
allele count: 14
allele frequency: 1.15363064042981e-4
allele num: 121356
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000262621
  ensembl transcript: ENST00000576906
  gene symbol: NAA60
  hgvsc: ENST00000576906.1:n.566A>G
  variant of: http://identifiers.org/hgnc/25875
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262621
  ensembl protein: ENSP00000477472
  ensembl transcript: ENST00000575785
  gene symbol: NAA60
  hgvsc: ENST00000575785.1:c.-13+19309A>G
  variant of: http://identifiers.org/hgnc/25875
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000460487
  ensembl transcript: ENST00000573327
  gene symbol: ZSCAN32
  hgvsc: ENST00000573327.1:c.1202T>C
  hgvsp: ENSP00000460487.1:p.Leu401Pro
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000459069
  ensembl transcript: ENST00000576500
  gene symbol: ZSCAN32
  hgvsc: ENST00000576500.1:c.*256T>C
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000391787
  ensembl transcript: ENST00000439568
  gene symbol: ZSCAN32
  hgvsc: ENST00000439568.2:c.335T>C
  hgvsp: ENSP00000391787.2:p.Leu112Pro
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000380057
  ensembl transcript: ENST00000396846
  gene symbol: ZSCAN32
  hgvsc: ENST00000396846.3:c.1202T>C
  hgvsp: ENSP00000380057.3:p.Leu401Pro
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000459772
  ensembl transcript: ENST00000574940
  gene symbol: ZSCAN32
  hgvsc: ENST00000574940.1:c.1202T>C
  hgvsp: ENSP00000459772.1:p.Leu401Pro
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000380061
  ensembl transcript: ENST00000396852
  gene symbol: ZSCAN32
  hgvsc: ENST00000396852.4:c.1202T>C
  hgvsp: ENSP00000380061.4:p.Leu401Pro
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000459960
  ensembl transcript: ENST00000573830
  gene symbol: ZSCAN32
  hgvsc: ENST00000573830.1:c.335T>C
  hgvsp: ENSP00000459960.1:p.Leu112Pro
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000407312
  ensembl transcript: ENST00000422427
  gene symbol: ZSCAN32
  hgvsc: ENST00000422427.2:c.566T>C
  hgvsp: ENSP00000407312.2:p.Leu189Pro
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000302502
  ensembl transcript: ENST00000304926
  gene symbol: ZSCAN32
  hgvsc: ENST00000304926.3:c.566T>C
  hgvsp: ENSP00000302502.3:p.Leu189Pro
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140987
  ensembl transcript: ENST00000574084
  gene symbol: ZSCAN32
  hgvsc: ENST00000574084.1:n.651T>C
  variant of: http://identifiers.org/hgnc/20812
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7793
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1512
  bin: 9.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8151
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3200
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6606
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7185
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7453
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4787
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8222
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Leu189Pro
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum

16-3434508-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3434508
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3434508
    reference: chr 16
allele count: 12
allele frequency: 9.885004448252002e-5
allele num: 121396
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000380057
  ensembl transcript: ENST00000396846
  gene symbol: ZSCAN32
  hgvsc: ENST00000396846.3:c.1185C>A
  hgvsp: ENST00000396846.3:c.1185C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000460487
  ensembl transcript: ENST00000573327
  gene symbol: ZSCAN32
  hgvsc: ENST00000573327.1:c.1185C>A
  hgvsp: ENST00000573327.1:c.1185C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000459960
  ensembl transcript: ENST00000573830
  gene symbol: ZSCAN32
  hgvsc: ENST00000573830.1:c.318C>A
  hgvsp: ENST00000573830.1:c.318C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000262621
  ensembl transcript: ENST00000576906
  gene symbol: NAA60
  hgvsc: ENST00000576906.1:n.583G>T
  variant of: http://identifiers.org/hgnc/25875
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000302502
  ensembl transcript: ENST00000304926
  gene symbol: ZSCAN32
  hgvsc: ENST00000304926.3:c.549C>A
  hgvsp: ENST00000304926.3:c.549C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000459772
  ensembl transcript: ENST00000574940
  gene symbol: ZSCAN32
  hgvsc: ENST00000574940.1:c.1185C>A
  hgvsp: ENST00000574940.1:c.1185C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000407312
  ensembl transcript: ENST00000422427
  gene symbol: ZSCAN32
  hgvsc: ENST00000422427.2:c.549C>A
  hgvsp: ENST00000422427.2:c.549C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000459069
  ensembl transcript: ENST00000576500
  gene symbol: ZSCAN32
  hgvsc: ENST00000576500.1:c.*239C>A
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000458899
  ensembl transcript: ENST00000575350
  gene symbol: ZSCAN32
  hgvsc: ENST00000575350.1:c.549C>A
  hgvsp: ENST00000575350.1:c.549C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000380061
  ensembl transcript: ENST00000396852
  gene symbol: ZSCAN32
  hgvsc: ENST00000396852.4:c.1185C>A
  hgvsp: ENST00000396852.4:c.1185C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000391787
  ensembl transcript: ENST00000439568
  gene symbol: ZSCAN32
  hgvsc: ENST00000439568.2:c.318C>A
  hgvsp: ENST00000439568.2:c.318C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262621
  ensembl protein: ENSP00000477472
  ensembl transcript: ENST00000575785
  gene symbol: NAA60
  hgvsc: ENST00000575785.1:c.-13+19326G>T
  variant of: http://identifiers.org/hgnc/25875
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140987
  ensembl transcript: ENST00000574084
  gene symbol: ZSCAN32
  hgvsc: ENST00000574084.1:n.634C>A
  variant of: http://identifiers.org/hgnc/20812
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7208
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7799
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7464
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1514
  bin: 9.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1193
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 795
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4788
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8152
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3197
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly183Gly
num of homozygotes: 0
population: African
population: Other
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum

16-3434523-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3434523
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3434523
    reference: chr 16
allele count: 1
allele frequency: 8.236960890909689e-6
allele num: 121404
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000460487
  ensembl transcript: ENST00000573327
  gene symbol: ZSCAN32
  hgvsc: ENST00000573327.1:c.1170C>T
  hgvsp: ENST00000573327.1:c.1170C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000459960
  ensembl transcript: ENST00000573830
  gene symbol: ZSCAN32
  hgvsc: ENST00000573830.1:c.303C>T
  hgvsp: ENST00000573830.1:c.303C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000380061
  ensembl transcript: ENST00000396852
  gene symbol: ZSCAN32
  hgvsc: ENST00000396852.4:c.1170C>T
  hgvsp: ENST00000396852.4:c.1170C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000459069
  ensembl transcript: ENST00000576500
  gene symbol: ZSCAN32
  hgvsc: ENST00000576500.1:c.*224C>T
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000262621
  ensembl transcript: ENST00000576906
  gene symbol: NAA60
  hgvsc: ENST00000576906.1:n.598G>A
  variant of: http://identifiers.org/hgnc/25875
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000407312
  ensembl transcript: ENST00000422427
  gene symbol: ZSCAN32
  hgvsc: ENST00000422427.2:c.534C>T
  hgvsp: ENST00000422427.2:c.534C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000380057
  ensembl transcript: ENST00000396846
  gene symbol: ZSCAN32
  hgvsc: ENST00000396846.3:c.1170C>T
  hgvsp: ENST00000396846.3:c.1170C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000391787
  ensembl transcript: ENST00000439568
  gene symbol: ZSCAN32
  hgvsc: ENST00000439568.2:c.303C>T
  hgvsp: ENST00000439568.2:c.303C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140987
  ensembl transcript: ENST00000574084
  gene symbol: ZSCAN32
  hgvsc: ENST00000574084.1:n.619C>T
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000459772
  ensembl transcript: ENST00000574940
  gene symbol: ZSCAN32
  hgvsc: ENST00000574940.1:c.1170C>T
  hgvsp: ENST00000574940.1:c.1170C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000302502
  ensembl transcript: ENST00000304926
  gene symbol: ZSCAN32
  hgvsc: ENST00000304926.3:c.534C>T
  hgvsp: ENST00000304926.3:c.534C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000458899
  ensembl transcript: ENST00000575350
  gene symbol: ZSCAN32
  hgvsc: ENST00000575350.1:c.534C>T
  hgvsp: ENST00000575350.1:c.534C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262621
  ensembl protein: ENSP00000477472
  ensembl transcript: ENST00000575785
  gene symbol: NAA60
  hgvsc: ENST00000575785.1:c.-13+19341G>A
  variant of: http://identifiers.org/hgnc/25875
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8226
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1194
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7211
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4789
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7799
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1509
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7466
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3198
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp178Asp
num of homozygotes: 0
population: South Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/16-3434525-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3434525
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3434525
    reference: chr 16
allele count: 1
allele frequency: 8.236553825879253e-6
allele num: 121410
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140987
  ensembl transcript: ENST00000574084
  gene symbol: ZSCAN32
  hgvsc: ENST00000574084.1:n.617G>T
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000459960
  ensembl transcript: ENST00000573830
  gene symbol: ZSCAN32
  hgvsc: ENST00000573830.1:c.301G>T
  hgvsp: ENSP00000459960.1:p.Asp101Tyr
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000302502
  ensembl transcript: ENST00000304926
  gene symbol: ZSCAN32
  hgvsc: ENST00000304926.3:c.532G>T
  hgvsp: ENSP00000302502.3:p.Asp178Tyr
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000407312
  ensembl transcript: ENST00000422427
  gene symbol: ZSCAN32
  hgvsc: ENST00000422427.2:c.532G>T
  hgvsp: ENSP00000407312.2:p.Asp178Tyr
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000458899
  ensembl transcript: ENST00000575350
  gene symbol: ZSCAN32
  hgvsc: ENST00000575350.1:c.532G>T
  hgvsp: ENSP00000458899.1:p.Asp178Tyr
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000262621
  ensembl transcript: ENST00000576906
  gene symbol: NAA60
  hgvsc: ENST00000576906.1:n.600C>A
  variant of: http://identifiers.org/hgnc/25875
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000380057
  ensembl transcript: ENST00000396846
  gene symbol: ZSCAN32
  hgvsc: ENST00000396846.3:c.1168G>T
  hgvsp: ENSP00000380057.3:p.Asp390Tyr
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262621
  ensembl protein: ENSP00000477472
  ensembl transcript: ENST00000575785
  gene symbol: NAA60
  hgvsc: ENST00000575785.1:c.-13+19343C>A
  variant of: http://identifiers.org/hgnc/25875
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000459772
  ensembl transcript: ENST00000574940
  gene symbol: ZSCAN32
  hgvsc: ENST00000574940.1:c.1168G>T
  hgvsp: ENSP00000459772.1:p.Asp390Tyr
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000380061
  ensembl transcript: ENST00000396852
  gene symbol: ZSCAN32
  hgvsc: ENST00000396852.4:c.1168G>T
  hgvsp: ENSP00000380061.4:p.Asp390Tyr
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000460487
  ensembl transcript: ENST00000573327
  gene symbol: ZSCAN32
  hgvsc: ENST00000573327.1:c.1168G>T
  hgvsp: ENSP00000460487.1:p.Asp390Tyr
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000391787
  ensembl transcript: ENST00000439568
  gene symbol: ZSCAN32
  hgvsc: ENST00000439568.2:c.301G>T
  hgvsp: ENSP00000391787.2:p.Asp101Tyr
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000459069
  ensembl transcript: ENST00000576500
  gene symbol: ZSCAN32
  hgvsc: ENST00000576500.1:c.*222G>T
  variant of: http://identifiers.org/hgnc/20812
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8226
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7801
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6606
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1974
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1510
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1194
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7465
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8152
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp178Tyr
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: C
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff

16-3434540-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3434540
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3434540
    reference: chr 16
allele count: 3
allele frequency: 2.471006852925672e-5
allele num: 121408
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000380061
  ensembl transcript: ENST00000396852
  gene symbol: ZSCAN32
  hgvsc: ENST00000396852.4:c.1153G>C
  hgvsp: ENSP00000380061.4:p.Asp385His
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000380057
  ensembl transcript: ENST00000396846
  gene symbol: ZSCAN32
  hgvsc: ENST00000396846.3:c.1153G>C
  hgvsp: ENSP00000380057.3:p.Asp385His
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000460487
  ensembl transcript: ENST00000573327
  gene symbol: ZSCAN32
  hgvsc: ENST00000573327.1:c.1153G>C
  hgvsp: ENSP00000460487.1:p.Asp385His
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140987
  ensembl transcript: ENST00000574084
  gene symbol: ZSCAN32
  hgvsc: ENST00000574084.1:n.602G>C
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000459960
  ensembl transcript: ENST00000573830
  gene symbol: ZSCAN32
  hgvsc: ENST00000573830.1:c.286G>C
  hgvsp: ENSP00000459960.1:p.Asp96His
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000458899
  ensembl transcript: ENST00000575350
  gene symbol: ZSCAN32
  hgvsc: ENST00000575350.1:c.517G>C
  hgvsp: ENSP00000458899.1:p.Asp173His
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000459772
  ensembl transcript: ENST00000574940
  gene symbol: ZSCAN32
  hgvsc: ENST00000574940.1:c.1153G>C
  hgvsp: ENSP00000459772.1:p.Asp385His
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262621
  ensembl protein: ENSP00000477472
  ensembl transcript: ENST00000575785
  gene symbol: NAA60
  hgvsc: ENST00000575785.1:c.-13+19358C>G
  variant of: http://identifiers.org/hgnc/25875
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000262621
  ensembl transcript: ENST00000576906
  gene symbol: NAA60
  hgvsc: ENST00000576906.1:n.615C>G
  variant of: http://identifiers.org/hgnc/25875
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000391787
  ensembl transcript: ENST00000439568
  gene symbol: ZSCAN32
  hgvsc: ENST00000439568.2:c.286G>C
  hgvsp: ENSP00000391787.2:p.Asp96His
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000302502
  ensembl transcript: ENST00000304926
  gene symbol: ZSCAN32
  hgvsc: ENST00000304926.3:c.517G>C
  hgvsp: ENSP00000302502.3:p.Asp173His
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000407312
  ensembl transcript: ENST00000422427
  gene symbol: ZSCAN32
  hgvsc: ENST00000422427.2:c.517G>C
  hgvsp: ENSP00000407312.2:p.Asp173His
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000459069
  ensembl transcript: ENST00000576500
  gene symbol: ZSCAN32
  hgvsc: ENST00000576500.1:c.*207G>C
  variant of: http://identifiers.org/hgnc/20812
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7462
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4788
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1975
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8230
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7213
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8152
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1511
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Asp173His
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: QD

16-3434558-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3434558
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3434558
    reference: chr 16
allele count: 2
allele frequency: 1.647310765175851e-5
allele num: 121410
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000459069
  ensembl transcript: ENST00000576500
  gene symbol: ZSCAN32
  hgvsc: ENST00000576500.1:c.*189G>A
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000459960
  ensembl transcript: ENST00000573830
  gene symbol: ZSCAN32
  hgvsc: ENST00000573830.1:c.268G>A
  hgvsp: ENSP00000459960.1:p.Gly90Ser
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000391787
  ensembl transcript: ENST00000439568
  gene symbol: ZSCAN32
  hgvsc: ENST00000439568.2:c.268G>A
  hgvsp: ENSP00000391787.2:p.Gly90Ser
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000460487
  ensembl transcript: ENST00000573327
  gene symbol: ZSCAN32
  hgvsc: ENST00000573327.1:c.1135G>A
  hgvsp: ENSP00000460487.1:p.Gly379Ser
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000459772
  ensembl transcript: ENST00000574940
  gene symbol: ZSCAN32
  hgvsc: ENST00000574940.1:c.1135G>A
  hgvsp: ENSP00000459772.1:p.Gly379Ser
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000302502
  ensembl transcript: ENST00000304926
  gene symbol: ZSCAN32
  hgvsc: ENST00000304926.3:c.499G>A
  hgvsp: ENSP00000302502.3:p.Gly167Ser
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000407312
  ensembl transcript: ENST00000422427
  gene symbol: ZSCAN32
  hgvsc: ENST00000422427.2:c.499G>A
  hgvsp: ENSP00000407312.2:p.Gly167Ser
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000262621
  ensembl transcript: ENST00000576906
  gene symbol: NAA60
  hgvsc: ENST00000576906.1:n.633C>T
  variant of: http://identifiers.org/hgnc/25875
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000380057
  ensembl transcript: ENST00000396846
  gene symbol: ZSCAN32
  hgvsc: ENST00000396846.3:c.1135G>A
  hgvsp: ENSP00000380057.3:p.Gly379Ser
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140987
  ensembl transcript: ENST00000574084
  gene symbol: ZSCAN32
  hgvsc: ENST00000574084.1:n.584G>A
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000380061
  ensembl transcript: ENST00000396852
  gene symbol: ZSCAN32
  hgvsc: ENST00000396852.4:c.1135G>A
  hgvsp: ENSP00000380061.4:p.Gly379Ser
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262621
  ensembl protein: ENSP00000477472
  ensembl transcript: ENST00000575785
  gene symbol: NAA60
  hgvsc: ENST00000575785.1:c.-13+19376C>T
  variant of: http://identifiers.org/hgnc/25875
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000458899
  ensembl transcript: ENST00000575350
  gene symbol: ZSCAN32
  hgvsc: ENST00000575350.1:c.499G>A
  hgvsp: ENSP00000458899.1:p.Gly167Ser
  variant of: http://identifiers.org/hgnc/20812
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8229
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8150
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1977
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 796
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1194
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3196
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1512
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7802
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7451
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly167Ser
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
population: East Asian
reference allele: C
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum

http://identifiers.org/exac.variant/16-3434567-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3434567
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3434567
    reference: chr 16
allele count: 1
allele frequency: 8.236689509752241e-6
allele num: 121408
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000407312
  ensembl transcript: ENST00000422427
  gene symbol: ZSCAN32
  hgvsc: ENST00000422427.2:c.490G>T
  hgvsp: ENSP00000407312.2:p.Val164Leu
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000460487
  ensembl transcript: ENST00000573327
  gene symbol: ZSCAN32
  hgvsc: ENST00000573327.1:c.1126G>T
  hgvsp: ENSP00000460487.1:p.Val376Leu
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000380061
  ensembl transcript: ENST00000396852
  gene symbol: ZSCAN32
  hgvsc: ENST00000396852.4:c.1126G>T
  hgvsp: ENSP00000380061.4:p.Val376Leu
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000458899
  ensembl transcript: ENST00000575350
  gene symbol: ZSCAN32
  hgvsc: ENST00000575350.1:c.490G>T
  hgvsp: ENSP00000458899.1:p.Val164Leu
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000459069
  ensembl transcript: ENST00000576500
  gene symbol: ZSCAN32
  hgvsc: ENST00000576500.1:c.*180G>T
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000459960
  ensembl transcript: ENST00000573830
  gene symbol: ZSCAN32
  hgvsc: ENST00000573830.1:c.259G>T
  hgvsp: ENSP00000459960.1:p.Val87Leu
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262621
  ensembl protein: ENSP00000477472
  ensembl transcript: ENST00000575785
  gene symbol: NAA60
  hgvsc: ENST00000575785.1:c.-13+19385C>A
  variant of: http://identifiers.org/hgnc/25875
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000380057
  ensembl transcript: ENST00000396846
  gene symbol: ZSCAN32
  hgvsc: ENST00000396846.3:c.1126G>T
  hgvsp: ENSP00000380057.3:p.Val376Leu
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000459772
  ensembl transcript: ENST00000574940
  gene symbol: ZSCAN32
  hgvsc: ENST00000574940.1:c.1126G>T
  hgvsp: ENSP00000459772.1:p.Val376Leu
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000302502
  ensembl transcript: ENST00000304926
  gene symbol: ZSCAN32
  hgvsc: ENST00000304926.3:c.490G>T
  hgvsp: ENSP00000302502.3:p.Val164Leu
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000262621
  ensembl transcript: ENST00000576906
  gene symbol: NAA60
  hgvsc: ENST00000576906.1:n.642C>A
  variant of: http://identifiers.org/hgnc/25875
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000391787
  ensembl transcript: ENST00000439568
  gene symbol: ZSCAN32
  hgvsc: ENST00000439568.2:c.259G>T
  hgvsp: ENSP00000391787.2:p.Val87Leu
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140987
  ensembl transcript: ENST00000574084
  gene symbol: ZSCAN32
  hgvsc: ENST00000574084.1:n.575G>T
  variant of: http://identifiers.org/hgnc/20812
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7221
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4788
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8150
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8228
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7440
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1194
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1976
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6606
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val164Leu
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum

16-3434567-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3434567
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3434567
    reference: chr 16
allele count: 1
allele frequency: 8.236689509752241e-6
allele num: 121408
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000459772
  ensembl transcript: ENST00000574940
  gene symbol: ZSCAN32
  hgvsc: ENST00000574940.1:c.1126G>A
  hgvsp: ENSP00000459772.1:p.Val376Ile
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000262621
  ensembl transcript: ENST00000576906
  gene symbol: NAA60
  hgvsc: ENST00000576906.1:n.642C>T
  variant of: http://identifiers.org/hgnc/25875
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000380061
  ensembl transcript: ENST00000396852
  gene symbol: ZSCAN32
  hgvsc: ENST00000396852.4:c.1126G>A
  hgvsp: ENSP00000380061.4:p.Val376Ile
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000302502
  ensembl transcript: ENST00000304926
  gene symbol: ZSCAN32
  hgvsc: ENST00000304926.3:c.490G>A
  hgvsp: ENSP00000302502.3:p.Val164Ile
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000459069
  ensembl transcript: ENST00000576500
  gene symbol: ZSCAN32
  hgvsc: ENST00000576500.1:c.*180G>A
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140987
  ensembl transcript: ENST00000574084
  gene symbol: ZSCAN32
  hgvsc: ENST00000574084.1:n.575G>A
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262621
  ensembl protein: ENSP00000477472
  ensembl transcript: ENST00000575785
  gene symbol: NAA60
  hgvsc: ENST00000575785.1:c.-13+19385C>T
  variant of: http://identifiers.org/hgnc/25875
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000460487
  ensembl transcript: ENST00000573327
  gene symbol: ZSCAN32
  hgvsc: ENST00000573327.1:c.1126G>A
  hgvsp: ENSP00000460487.1:p.Val376Ile
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000380057
  ensembl transcript: ENST00000396846
  gene symbol: ZSCAN32
  hgvsc: ENST00000396846.3:c.1126G>A
  hgvsp: ENSP00000380057.3:p.Val376Ile
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000458899
  ensembl transcript: ENST00000575350
  gene symbol: ZSCAN32
  hgvsc: ENST00000575350.1:c.490G>A
  hgvsp: ENSP00000458899.1:p.Val164Ile
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000391787
  ensembl transcript: ENST00000439568
  gene symbol: ZSCAN32
  hgvsc: ENST00000439568.2:c.259G>A
  hgvsp: ENSP00000391787.2:p.Val87Ile
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000407312
  ensembl transcript: ENST00000422427
  gene symbol: ZSCAN32
  hgvsc: ENST00000422427.2:c.490G>A
  hgvsp: ENSP00000407312.2:p.Val164Ile
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000459960
  ensembl transcript: ENST00000573830
  gene symbol: ZSCAN32
  hgvsc: ENST00000573830.1:c.259G>A
  hgvsp: ENSP00000459960.1:p.Val87Ile
  variant of: http://identifiers.org/hgnc/20812
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7803
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3196
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8228
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1976
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6606
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7221
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1514
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7440
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val164Ile
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum

16-3434568-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3434568
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3434568
    reference: chr 16
allele count: 2
allele frequency: 1.647337901950448e-5
allele num: 121408
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000459772
  ensembl transcript: ENST00000574940
  gene symbol: ZSCAN32
  hgvsc: ENST00000574940.1:c.1125G>A
  hgvsp: ENST00000574940.1:c.1125G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140987
  ensembl transcript: ENST00000574084
  gene symbol: ZSCAN32
  hgvsc: ENST00000574084.1:n.574G>A
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000407312
  ensembl transcript: ENST00000422427
  gene symbol: ZSCAN32
  hgvsc: ENST00000422427.2:c.489G>A
  hgvsp: ENST00000422427.2:c.489G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000391787
  ensembl transcript: ENST00000439568
  gene symbol: ZSCAN32
  hgvsc: ENST00000439568.2:c.258G>A
  hgvsp: ENST00000439568.2:c.258G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000459960
  ensembl transcript: ENST00000573830
  gene symbol: ZSCAN32
  hgvsc: ENST00000573830.1:c.258G>A
  hgvsp: ENST00000573830.1:c.258G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000380057
  ensembl transcript: ENST00000396846
  gene symbol: ZSCAN32
  hgvsc: ENST00000396846.3:c.1125G>A
  hgvsp: ENST00000396846.3:c.1125G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000380061
  ensembl transcript: ENST00000396852
  gene symbol: ZSCAN32
  hgvsc: ENST00000396852.4:c.1125G>A
  hgvsp: ENST00000396852.4:c.1125G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000458899
  ensembl transcript: ENST00000575350
  gene symbol: ZSCAN32
  hgvsc: ENST00000575350.1:c.489G>A
  hgvsp: ENST00000575350.1:c.489G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000460487
  ensembl transcript: ENST00000573327
  gene symbol: ZSCAN32
  hgvsc: ENST00000573327.1:c.1125G>A
  hgvsp: ENST00000573327.1:c.1125G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000302502
  ensembl transcript: ENST00000304926
  gene symbol: ZSCAN32
  hgvsc: ENST00000304926.3:c.489G>A
  hgvsp: ENST00000304926.3:c.489G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000459069
  ensembl transcript: ENST00000576500
  gene symbol: ZSCAN32
  hgvsc: ENST00000576500.1:c.*179G>A
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000262621
  ensembl transcript: ENST00000576906
  gene symbol: NAA60
  hgvsc: ENST00000576906.1:n.643C>T
  variant of: http://identifiers.org/hgnc/25875
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262621
  ensembl protein: ENSP00000477472
  ensembl transcript: ENST00000575785
  gene symbol: NAA60
  hgvsc: ENST00000575785.1:c.-13+19386C>T
  variant of: http://identifiers.org/hgnc/25875
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1515
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7803
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1194
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7439
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1976
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7222
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8150
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6606
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu163Glu
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Other
population: Latino
population: African
population: East Asian
reference allele: C
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD

http://identifiers.org/exac.variant/16-3434571-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3434571
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3434571
    reference: chr 16
allele count: 1
allele frequency: 8.236825198095647e-6
allele num: 121406
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000407312
  ensembl transcript: ENST00000422427
  gene symbol: ZSCAN32
  hgvsc: ENST00000422427.2:c.486G>T
  hgvsp: ENST00000422427.2:c.486G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000380061
  ensembl transcript: ENST00000396852
  gene symbol: ZSCAN32
  hgvsc: ENST00000396852.4:c.1122G>T
  hgvsp: ENST00000396852.4:c.1122G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000459772
  ensembl transcript: ENST00000574940
  gene symbol: ZSCAN32
  hgvsc: ENST00000574940.1:c.1122G>T
  hgvsp: ENST00000574940.1:c.1122G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000380057
  ensembl transcript: ENST00000396846
  gene symbol: ZSCAN32
  hgvsc: ENST00000396846.3:c.1122G>T
  hgvsp: ENST00000396846.3:c.1122G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140987
  ensembl transcript: ENST00000574084
  gene symbol: ZSCAN32
  hgvsc: ENST00000574084.1:n.571G>T
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262621
  ensembl protein: ENSP00000477472
  ensembl transcript: ENST00000575785
  gene symbol: NAA60
  hgvsc: ENST00000575785.1:c.-13+19389C>A
  variant of: http://identifiers.org/hgnc/25875
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000459069
  ensembl transcript: ENST00000576500
  gene symbol: ZSCAN32
  hgvsc: ENST00000576500.1:c.*176G>T
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000459960
  ensembl transcript: ENST00000573830
  gene symbol: ZSCAN32
  hgvsc: ENST00000573830.1:c.255G>T
  hgvsp: ENST00000573830.1:c.255G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000302502
  ensembl transcript: ENST00000304926
  gene symbol: ZSCAN32
  hgvsc: ENST00000304926.3:c.486G>T
  hgvsp: ENST00000304926.3:c.486G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000391787
  ensembl transcript: ENST00000439568
  gene symbol: ZSCAN32
  hgvsc: ENST00000439568.2:c.255G>T
  hgvsp: ENST00000439568.2:c.255G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000460487
  ensembl transcript: ENST00000573327
  gene symbol: ZSCAN32
  hgvsc: ENST00000573327.1:c.1122G>T
  hgvsp: ENST00000573327.1:c.1122G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000262621
  ensembl transcript: ENST00000576906
  gene symbol: NAA60
  hgvsc: ENST00000576906.1:n.646C>A
  variant of: http://identifiers.org/hgnc/25875
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000458899
  ensembl transcript: ENST00000575350
  gene symbol: ZSCAN32
  hgvsc: ENST00000575350.1:c.486G>T
  hgvsp: ENST00000575350.1:c.486G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20812
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4787
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6606
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7803
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3195
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1976
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1519
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7436
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 795
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1194
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr162Thr
num of homozygotes: 0
population: Other
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum

16-3434571-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3434571
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3434571
    reference: chr 16
allele count: 5
allele frequency: 4.118412599047823e-5
allele num: 121406
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000380057
  ensembl transcript: ENST00000396846
  gene symbol: ZSCAN32
  hgvsc: ENST00000396846.3:c.1122G>A
  hgvsp: ENST00000396846.3:c.1122G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000458899
  ensembl transcript: ENST00000575350
  gene symbol: ZSCAN32
  hgvsc: ENST00000575350.1:c.486G>A
  hgvsp: ENST00000575350.1:c.486G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000262621
  ensembl transcript: ENST00000576906
  gene symbol: NAA60
  hgvsc: ENST00000576906.1:n.646C>T
  variant of: http://identifiers.org/hgnc/25875
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000380061
  ensembl transcript: ENST00000396852
  gene symbol: ZSCAN32
  hgvsc: ENST00000396852.4:c.1122G>A
  hgvsp: ENST00000396852.4:c.1122G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000460487
  ensembl transcript: ENST00000573327
  gene symbol: ZSCAN32
  hgvsc: ENST00000573327.1:c.1122G>A
  hgvsp: ENST00000573327.1:c.1122G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140987
  ensembl transcript: ENST00000574084
  gene symbol: ZSCAN32
  hgvsc: ENST00000574084.1:n.571G>A
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000302502
  ensembl transcript: ENST00000304926
  gene symbol: ZSCAN32
  hgvsc: ENST00000304926.3:c.486G>A
  hgvsp: ENST00000304926.3:c.486G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000459960
  ensembl transcript: ENST00000573830
  gene symbol: ZSCAN32
  hgvsc: ENST00000573830.1:c.255G>A
  hgvsp: ENST00000573830.1:c.255G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000391787
  ensembl transcript: ENST00000439568
  gene symbol: ZSCAN32
  hgvsc: ENST00000439568.2:c.255G>A
  hgvsp: ENST00000439568.2:c.255G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000459772
  ensembl transcript: ENST00000574940
  gene symbol: ZSCAN32
  hgvsc: ENST00000574940.1:c.1122G>A
  hgvsp: ENST00000574940.1:c.1122G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000407312
  ensembl transcript: ENST00000422427
  gene symbol: ZSCAN32
  hgvsc: ENST00000422427.2:c.486G>A
  hgvsp: ENST00000422427.2:c.486G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262621
  ensembl protein: ENSP00000477472
  ensembl transcript: ENST00000575785
  gene symbol: NAA60
  hgvsc: ENST00000575785.1:c.-13+19389C>T
  variant of: http://identifiers.org/hgnc/25875
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000459069
  ensembl transcript: ENST00000576500
  gene symbol: ZSCAN32
  hgvsc: ENST00000576500.1:c.*176G>A
  variant of: http://identifiers.org/hgnc/20812
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6606
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1194
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7803
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7221
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7436
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4787
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1976
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8224
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr162Thr
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD

16-3434572-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3434572
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3434572
    reference: chr 16
allele count: 2
allele frequency: 1.647337901950448e-5
allele num: 121408
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000459960
  ensembl transcript: ENST00000573830
  gene symbol: ZSCAN32
  hgvsc: ENST00000573830.1:c.254C>T
  hgvsp: ENSP00000459960.1:p.Thr85Met
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000302502
  ensembl transcript: ENST00000304926
  gene symbol: ZSCAN32
  hgvsc: ENST00000304926.3:c.485C>T
  hgvsp: ENSP00000302502.3:p.Thr162Met
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000460487
  ensembl transcript: ENST00000573327
  gene symbol: ZSCAN32
  hgvsc: ENST00000573327.1:c.1121C>T
  hgvsp: ENSP00000460487.1:p.Thr374Met
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000391787
  ensembl transcript: ENST00000439568
  gene symbol: ZSCAN32
  hgvsc: ENST00000439568.2:c.254C>T
  hgvsp: ENSP00000391787.2:p.Thr85Met
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140987
  ensembl transcript: ENST00000574084
  gene symbol: ZSCAN32
  hgvsc: ENST00000574084.1:n.570C>T
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000459772
  ensembl transcript: ENST00000574940
  gene symbol: ZSCAN32
  hgvsc: ENST00000574940.1:c.1121C>T
  hgvsp: ENSP00000459772.1:p.Thr374Met
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000380061
  ensembl transcript: ENST00000396852
  gene symbol: ZSCAN32
  hgvsc: ENST00000396852.4:c.1121C>T
  hgvsp: ENSP00000380061.4:p.Thr374Met
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000407312
  ensembl transcript: ENST00000422427
  gene symbol: ZSCAN32
  hgvsc: ENST00000422427.2:c.485C>T
  hgvsp: ENSP00000407312.2:p.Thr162Met
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000459069
  ensembl transcript: ENST00000576500
  gene symbol: ZSCAN32
  hgvsc: ENST00000576500.1:c.*175C>T
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000380057
  ensembl transcript: ENST00000396846
  gene symbol: ZSCAN32
  hgvsc: ENST00000396846.3:c.1121C>T
  hgvsp: ENSP00000380057.3:p.Thr374Met
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000458899
  ensembl transcript: ENST00000575350
  gene symbol: ZSCAN32
  hgvsc: ENST00000575350.1:c.485C>T
  hgvsp: ENSP00000458899.1:p.Thr162Met
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262621
  ensembl protein: ENSP00000477472
  ensembl transcript: ENST00000575785
  gene symbol: NAA60
  hgvsc: ENST00000575785.1:c.-13+19390G>A
  variant of: http://identifiers.org/hgnc/25875
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000262621
  ensembl transcript: ENST00000576906
  gene symbol: NAA60
  hgvsc: ENST00000576906.1:n.647G>A
  variant of: http://identifiers.org/hgnc/25875
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8150
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7436
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6608
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7218
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1976
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3196
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4786
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7805
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr162Met
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: East Asian
population: South Asian
reference allele: G
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: QD

16-3434574-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3434574
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3434574
    reference: chr 16
allele count: 1
allele frequency: 8.238318064983852e-6
allele num: 121384
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000380057
  ensembl transcript: ENST00000396846
  gene symbol: ZSCAN32
  hgvsc: ENST00000396846.3:c.1119C>T
  hgvsp: ENST00000396846.3:c.1119C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000391787
  ensembl transcript: ENST00000439568
  gene symbol: ZSCAN32
  hgvsc: ENST00000439568.2:c.252C>T
  hgvsp: ENST00000439568.2:c.252C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000262621
  ensembl transcript: ENST00000576906
  gene symbol: NAA60
  hgvsc: ENST00000576906.1:n.649G>A
  variant of: http://identifiers.org/hgnc/25875
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000459069
  ensembl transcript: ENST00000576500
  gene symbol: ZSCAN32
  hgvsc: ENST00000576500.1:c.*173C>T
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000407312
  ensembl transcript: ENST00000422427
  gene symbol: ZSCAN32
  hgvsc: ENST00000422427.2:c.483C>T
  hgvsp: ENST00000422427.2:c.483C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000459772
  ensembl transcript: ENST00000574940
  gene symbol: ZSCAN32
  hgvsc: ENST00000574940.1:c.1119C>T
  hgvsp: ENST00000574940.1:c.1119C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000460487
  ensembl transcript: ENST00000573327
  gene symbol: ZSCAN32
  hgvsc: ENST00000573327.1:c.1119C>T
  hgvsp: ENST00000573327.1:c.1119C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000380061
  ensembl transcript: ENST00000396852
  gene symbol: ZSCAN32
  hgvsc: ENST00000396852.4:c.1119C>T
  hgvsp: ENST00000396852.4:c.1119C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000302502
  ensembl transcript: ENST00000304926
  gene symbol: ZSCAN32
  hgvsc: ENST00000304926.3:c.483C>T
  hgvsp: ENST00000304926.3:c.483C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000459960
  ensembl transcript: ENST00000573830
  gene symbol: ZSCAN32
  hgvsc: ENST00000573830.1:c.252C>T
  hgvsp: ENST00000573830.1:c.252C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140987
  ensembl transcript: ENST00000574084
  gene symbol: ZSCAN32
  hgvsc: ENST00000574084.1:n.568C>T
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262621
  ensembl protein: ENSP00000477472
  ensembl transcript: ENST00000575785
  gene symbol: NAA60
  hgvsc: ENST00000575785.1:c.-13+19392G>A
  variant of: http://identifiers.org/hgnc/25875
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000458899
  ensembl transcript: ENST00000575350
  gene symbol: ZSCAN32
  hgvsc: ENST00000575350.1:c.483C>T
  hgvsp: ENST00000575350.1:c.483C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20812
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6607
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4786
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8148
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1193
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8220
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3194
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1531
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 796
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro161Pro
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ

16-3434577-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3434577
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3434577
    reference: chr 16
allele count: 1
allele frequency: 8.236689509752241e-6
allele num: 121408
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000459069
  ensembl transcript: ENST00000576500
  gene symbol: ZSCAN32
  hgvsc: ENST00000576500.1:c.*170A>T
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000262621
  ensembl transcript: ENST00000576906
  gene symbol: NAA60
  hgvsc: ENST00000576906.1:n.652T>A
  variant of: http://identifiers.org/hgnc/25875
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000460487
  ensembl transcript: ENST00000573327
  gene symbol: ZSCAN32
  hgvsc: ENST00000573327.1:c.1116A>T
  hgvsp: ENSP00000460487.1:p.Glu372Asp
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262621
  ensembl protein: ENSP00000477472
  ensembl transcript: ENST00000575785
  gene symbol: NAA60
  hgvsc: ENST00000575785.1:c.-13+19395T>A
  variant of: http://identifiers.org/hgnc/25875
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000380061
  ensembl transcript: ENST00000396852
  gene symbol: ZSCAN32
  hgvsc: ENST00000396852.4:c.1116A>T
  hgvsp: ENSP00000380061.4:p.Glu372Asp
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000459960
  ensembl transcript: ENST00000573830
  gene symbol: ZSCAN32
  hgvsc: ENST00000573830.1:c.249A>T
  hgvsp: ENSP00000459960.1:p.Glu83Asp
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000302502
  ensembl transcript: ENST00000304926
  gene symbol: ZSCAN32
  hgvsc: ENST00000304926.3:c.480A>T
  hgvsp: ENSP00000302502.3:p.Glu160Asp
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000391787
  ensembl transcript: ENST00000439568
  gene symbol: ZSCAN32
  hgvsc: ENST00000439568.2:c.249A>T
  hgvsp: ENSP00000391787.2:p.Glu83Asp
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000380057
  ensembl transcript: ENST00000396846
  gene symbol: ZSCAN32
  hgvsc: ENST00000396846.3:c.1116A>T
  hgvsp: ENSP00000380057.3:p.Glu372Asp
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140987
  ensembl transcript: ENST00000574084
  gene symbol: ZSCAN32
  hgvsc: ENST00000574084.1:n.565A>T
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000459772
  ensembl transcript: ENST00000574940
  gene symbol: ZSCAN32
  hgvsc: ENST00000574940.1:c.1116A>T
  hgvsp: ENSP00000459772.1:p.Glu372Asp
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000458899
  ensembl transcript: ENST00000575350
  gene symbol: ZSCAN32
  hgvsc: ENST00000575350.1:c.480A>T
  hgvsp: ENSP00000458899.1:p.Glu160Asp
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000407312
  ensembl transcript: ENST00000422427
  gene symbol: ZSCAN32
  hgvsc: ENST00000422427.2:c.480A>T
  hgvsp: ENSP00000407312.2:p.Glu160Asp
  variant of: http://identifiers.org/hgnc/20812
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 795
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8222
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4785
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7799
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7433
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7220
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1194
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1523
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu160Asp
num of homozygotes: 0
population: South Asian
population: African
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ

16-3434578-T-TC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3434578
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3434579
    reference: chr 16
allele count: 2
allele frequency: 1.647337901950448e-5
allele num: 121408
alternate allele: TC
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000407312
  ensembl transcript: ENST00000422427
  gene symbol: ZSCAN32
  hgvsc: ENST00000422427.2:c.478dupG
  hgvsp: ENSP00000407312.2:p.Glu160GlyfsTer17
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000380061
  ensembl transcript: ENST00000396852
  gene symbol: ZSCAN32
  hgvsc: ENST00000396852.4:c.1114dupG
  hgvsp: ENSP00000380061.4:p.Glu372GlyfsTer17
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000459772
  ensembl transcript: ENST00000574940
  gene symbol: ZSCAN32
  hgvsc: ENST00000574940.1:c.1114dupG
  hgvsp: ENSP00000459772.1:p.Glu372GlyfsTer17
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000460487
  ensembl transcript: ENST00000573327
  gene symbol: ZSCAN32
  hgvsc: ENST00000573327.1:c.1114dupG
  hgvsp: ENSP00000460487.1:p.Glu372GlyfsTer17
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000458899
  ensembl transcript: ENST00000575350
  gene symbol: ZSCAN32
  hgvsc: ENST00000575350.1:c.478dupG
  hgvsp: ENSP00000458899.1:p.Glu160GlyfsTer17
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000302502
  ensembl transcript: ENST00000304926
  gene symbol: ZSCAN32
  hgvsc: ENST00000304926.3:c.478dupG
  hgvsp: ENSP00000302502.3:p.Glu160GlyfsTer17
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000459960
  ensembl transcript: ENST00000573830
  gene symbol: ZSCAN32
  hgvsc: ENST00000573830.1:c.247dupG
  hgvsp: ENSP00000459960.1:p.Glu83GlyfsTer17
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000380057
  ensembl transcript: ENST00000396846
  gene symbol: ZSCAN32
  hgvsc: ENST00000396846.3:c.1114dupG
  hgvsp: ENSP00000380057.3:p.Glu372GlyfsTer17
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000262621
  ensembl transcript: ENST00000576906
  gene symbol: NAA60
  hgvsc: ENST00000576906.1:n.657dupC
  variant of: http://identifiers.org/hgnc/25875
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000459069
  ensembl transcript: ENST00000576500
  gene symbol: ZSCAN32
  hgvsc: ENST00000576500.1:c.*168dupG
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000391787
  ensembl transcript: ENST00000439568
  gene symbol: ZSCAN32
  hgvsc: ENST00000439568.2:c.247dupG
  hgvsp: ENSP00000391787.2:p.Glu83GlyfsTer17
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262621
  ensembl protein: ENSP00000477472
  ensembl transcript: ENST00000575785
  gene symbol: NAA60
  hgvsc: ENST00000575785.1:c.-13+19400dupC
  variant of: http://identifiers.org/hgnc/25875
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140987
  ensembl transcript: ENST00000574084
  gene symbol: ZSCAN32
  hgvsc: ENST00000574084.1:n.563dupG
  variant of: http://identifiers.org/hgnc/20812
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8148
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 795
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7433
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7218
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6606
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1976
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1194
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8221
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4786
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7801
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu160GlyfsTer17
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
reference allele: T
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: DP

16-3434586-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3434586
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3434586
    reference: chr 16
allele count: 1
allele frequency: 8.236960890909689e-6
allele num: 121404
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000459772
  ensembl transcript: ENST00000574940
  gene symbol: ZSCAN32
  hgvsc: ENST00000574940.1:c.1107G>C
  hgvsp: ENSP00000459772.1:p.Gln369His
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000460487
  ensembl transcript: ENST00000573327
  gene symbol: ZSCAN32
  hgvsc: ENST00000573327.1:c.1107G>C
  hgvsp: ENSP00000460487.1:p.Gln369His
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000391787
  ensembl transcript: ENST00000439568
  gene symbol: ZSCAN32
  hgvsc: ENST00000439568.2:c.240G>C
  hgvsp: ENSP00000391787.2:p.Gln80His
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000380061
  ensembl transcript: ENST00000396852
  gene symbol: ZSCAN32
  hgvsc: ENST00000396852.4:c.1107G>C
  hgvsp: ENSP00000380061.4:p.Gln369His
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000262621
  ensembl transcript: ENST00000576906
  gene symbol: NAA60
  hgvsc: ENST00000576906.1:n.661C>G
  variant of: http://identifiers.org/hgnc/25875
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000380057
  ensembl transcript: ENST00000396846
  gene symbol: ZSCAN32
  hgvsc: ENST00000396846.3:c.1107G>C
  hgvsp: ENSP00000380057.3:p.Gln369His
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000459960
  ensembl transcript: ENST00000573830
  gene symbol: ZSCAN32
  hgvsc: ENST00000573830.1:c.240G>C
  hgvsp: ENSP00000459960.1:p.Gln80His
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000407312
  ensembl transcript: ENST00000422427
  gene symbol: ZSCAN32
  hgvsc: ENST00000422427.2:c.471G>C
  hgvsp: ENSP00000407312.2:p.Gln157His
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000459069
  ensembl transcript: ENST00000576500
  gene symbol: ZSCAN32
  hgvsc: ENST00000576500.1:c.*161G>C
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000458899
  ensembl transcript: ENST00000575350
  gene symbol: ZSCAN32
  hgvsc: ENST00000575350.1:c.471G>C
  hgvsp: ENSP00000458899.1:p.Gln157His
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262621
  ensembl protein: ENSP00000477472
  ensembl transcript: ENST00000575785
  gene symbol: NAA60
  hgvsc: ENST00000575785.1:c.-13+19404C>G
  variant of: http://identifiers.org/hgnc/25875
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000302502
  ensembl transcript: ENST00000304926
  gene symbol: ZSCAN32
  hgvsc: ENST00000304926.3:c.471G>C
  hgvsp: ENSP00000302502.3:p.Gln157His
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140987
  ensembl transcript: ENST00000574084
  gene symbol: ZSCAN32
  hgvsc: ENST00000574084.1:n.556G>C
  variant of: http://identifiers.org/hgnc/20812
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4786
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6606
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7225
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7416
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 795
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3195
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1193
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8150
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8222
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln157His
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: South Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

16-3434591-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3434591
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3434591
    reference: chr 16
allele count: 1
allele frequency: 8.236960890909689e-6
allele num: 121404
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000380057
  ensembl transcript: ENST00000396846
  gene symbol: ZSCAN32
  hgvsc: ENST00000396846.3:c.1102C>T
  hgvsp: ENSP00000380057.3:p.His368Tyr
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000407312
  ensembl transcript: ENST00000422427
  gene symbol: ZSCAN32
  hgvsc: ENST00000422427.2:c.466C>T
  hgvsp: ENSP00000407312.2:p.His156Tyr
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000391787
  ensembl transcript: ENST00000439568
  gene symbol: ZSCAN32
  hgvsc: ENST00000439568.2:c.235C>T
  hgvsp: ENSP00000391787.2:p.His79Tyr
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140987
  ensembl transcript: ENST00000574084
  gene symbol: ZSCAN32
  hgvsc: ENST00000574084.1:n.551C>T
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000459772
  ensembl transcript: ENST00000574940
  gene symbol: ZSCAN32
  hgvsc: ENST00000574940.1:c.1102C>T
  hgvsp: ENSP00000459772.1:p.His368Tyr
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000458899
  ensembl transcript: ENST00000575350
  gene symbol: ZSCAN32
  hgvsc: ENST00000575350.1:c.466C>T
  hgvsp: ENSP00000458899.1:p.His156Tyr
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000460487
  ensembl transcript: ENST00000573327
  gene symbol: ZSCAN32
  hgvsc: ENST00000573327.1:c.1102C>T
  hgvsp: ENSP00000460487.1:p.His368Tyr
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000380061
  ensembl transcript: ENST00000396852
  gene symbol: ZSCAN32
  hgvsc: ENST00000396852.4:c.1102C>T
  hgvsp: ENSP00000380061.4:p.His368Tyr
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000459960
  ensembl transcript: ENST00000573830
  gene symbol: ZSCAN32
  hgvsc: ENST00000573830.1:c.235C>T
  hgvsp: ENSP00000459960.1:p.His79Tyr
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000302502
  ensembl transcript: ENST00000304926
  gene symbol: ZSCAN32
  hgvsc: ENST00000304926.3:c.466C>T
  hgvsp: ENSP00000302502.3:p.His156Tyr
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000262621
  ensembl transcript: ENST00000576906
  gene symbol: NAA60
  hgvsc: ENST00000576906.1:n.666G>A
  variant of: http://identifiers.org/hgnc/25875
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000459069
  ensembl transcript: ENST00000576500
  gene symbol: ZSCAN32
  hgvsc: ENST00000576500.1:c.*156C>T
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262621
  ensembl protein: ENSP00000477472
  ensembl transcript: ENST00000575785
  gene symbol: NAA60
  hgvsc: ENST00000575785.1:c.-13+19409G>A
  variant of: http://identifiers.org/hgnc/25875
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8149
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7410
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1524
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8222
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1193
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7803
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 795
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3194
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His156Tyr
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
population: African
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP

16-3434592-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3434592
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3434592
    reference: chr 16
allele count: 2
allele frequency: 1.647392178181938e-5
allele num: 121404
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000460487
  ensembl transcript: ENST00000573327
  gene symbol: ZSCAN32
  hgvsc: ENST00000573327.1:c.1101T>C
  hgvsp: ENST00000573327.1:c.1101T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000380057
  ensembl transcript: ENST00000396846
  gene symbol: ZSCAN32
  hgvsc: ENST00000396846.3:c.1101T>C
  hgvsp: ENST00000396846.3:c.1101T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000262621
  ensembl transcript: ENST00000576906
  gene symbol: NAA60
  hgvsc: ENST00000576906.1:n.667A>G
  variant of: http://identifiers.org/hgnc/25875
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000380061
  ensembl transcript: ENST00000396852
  gene symbol: ZSCAN32
  hgvsc: ENST00000396852.4:c.1101T>C
  hgvsp: ENST00000396852.4:c.1101T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000459960
  ensembl transcript: ENST00000573830
  gene symbol: ZSCAN32
  hgvsc: ENST00000573830.1:c.234T>C
  hgvsp: ENST00000573830.1:c.234T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000302502
  ensembl transcript: ENST00000304926
  gene symbol: ZSCAN32
  hgvsc: ENST00000304926.3:c.465T>C
  hgvsp: ENST00000304926.3:c.465T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000459069
  ensembl transcript: ENST00000576500
  gene symbol: ZSCAN32
  hgvsc: ENST00000576500.1:c.*155T>C
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000407312
  ensembl transcript: ENST00000422427
  gene symbol: ZSCAN32
  hgvsc: ENST00000422427.2:c.465T>C
  hgvsp: ENST00000422427.2:c.465T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140987
  ensembl transcript: ENST00000574084
  gene symbol: ZSCAN32
  hgvsc: ENST00000574084.1:n.550T>C
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000459772
  ensembl transcript: ENST00000574940
  gene symbol: ZSCAN32
  hgvsc: ENST00000574940.1:c.1101T>C
  hgvsp: ENST00000574940.1:c.1101T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000458899
  ensembl transcript: ENST00000575350
  gene symbol: ZSCAN32
  hgvsc: ENST00000575350.1:c.465T>C
  hgvsp: ENST00000575350.1:c.465T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262621
  ensembl protein: ENSP00000477472
  ensembl transcript: ENST00000575785
  gene symbol: NAA60
  hgvsc: ENST00000575785.1:c.-13+19410A>G
  variant of: http://identifiers.org/hgnc/25875
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000391787
  ensembl transcript: ENST00000439568
  gene symbol: ZSCAN32
  hgvsc: ENST00000439568.2:c.234T>C
  hgvsp: ENST00000439568.2:c.234T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20812
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7408
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4786
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 795
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8223
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3194
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1193
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7802
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1977
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7228
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn155Asn
num of homozygotes: 0
population: East Asian
population: Other
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
population: European (Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum

16-3434594-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3434594
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3434594
    reference: chr 16
allele count: 1
allele frequency: 8.237096588194593e-6
allele num: 121402
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000380057
  ensembl transcript: ENST00000396846
  gene symbol: ZSCAN32
  hgvsc: ENST00000396846.3:c.1099A>G
  hgvsp: ENSP00000380057.3:p.Asn367Asp
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000459960
  ensembl transcript: ENST00000573830
  gene symbol: ZSCAN32
  hgvsc: ENST00000573830.1:c.232A>G
  hgvsp: ENSP00000459960.1:p.Asn78Asp
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000407312
  ensembl transcript: ENST00000422427
  gene symbol: ZSCAN32
  hgvsc: ENST00000422427.2:c.463A>G
  hgvsp: ENSP00000407312.2:p.Asn155Asp
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000459069
  ensembl transcript: ENST00000576500
  gene symbol: ZSCAN32
  hgvsc: ENST00000576500.1:c.*153A>G
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000380061
  ensembl transcript: ENST00000396852
  gene symbol: ZSCAN32
  hgvsc: ENST00000396852.4:c.1099A>G
  hgvsp: ENSP00000380061.4:p.Asn367Asp
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000460487
  ensembl transcript: ENST00000573327
  gene symbol: ZSCAN32
  hgvsc: ENST00000573327.1:c.1099A>G
  hgvsp: ENSP00000460487.1:p.Asn367Asp
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000391787
  ensembl transcript: ENST00000439568
  gene symbol: ZSCAN32
  hgvsc: ENST00000439568.2:c.232A>G
  hgvsp: ENSP00000391787.2:p.Asn78Asp
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140987
  ensembl transcript: ENST00000574084
  gene symbol: ZSCAN32
  hgvsc: ENST00000574084.1:n.548A>G
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000458899
  ensembl transcript: ENST00000575350
  gene symbol: ZSCAN32
  hgvsc: ENST00000575350.1:c.463A>G
  hgvsp: ENSP00000458899.1:p.Asn155Asp
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000459772
  ensembl transcript: ENST00000574940
  gene symbol: ZSCAN32
  hgvsc: ENST00000574940.1:c.1099A>G
  hgvsp: ENSP00000459772.1:p.Asn367Asp
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000302502
  ensembl transcript: ENST00000304926
  gene symbol: ZSCAN32
  hgvsc: ENST00000304926.3:c.463A>G
  hgvsp: ENSP00000302502.3:p.Asn155Asp
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000262621
  ensembl transcript: ENST00000576906
  gene symbol: NAA60
  hgvsc: ENST00000576906.1:n.669T>C
  variant of: http://identifiers.org/hgnc/25875
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262621
  ensembl protein: ENSP00000477472
  ensembl transcript: ENST00000575785
  gene symbol: NAA60
  hgvsc: ENST00000575785.1:c.-13+19412T>C
  variant of: http://identifiers.org/hgnc/25875
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7225
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1977
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4787
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1524
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6605
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8149
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8220
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3194
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7803
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn155Asp
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum

16-3434603-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3434603
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3434603
    reference: chr 16
allele count: 1
allele frequency: 8.237096588194593e-6
allele num: 121402
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000460487
  ensembl transcript: ENST00000573327
  gene symbol: ZSCAN32
  hgvsc: ENST00000573327.1:c.1090G>A
  hgvsp: ENSP00000460487.1:p.Gly364Arg
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000391787
  ensembl transcript: ENST00000439568
  gene symbol: ZSCAN32
  hgvsc: ENST00000439568.2:c.223G>A
  hgvsp: ENSP00000391787.2:p.Gly75Arg
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140987
  ensembl transcript: ENST00000574084
  gene symbol: ZSCAN32
  hgvsc: ENST00000574084.1:n.539G>A
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000302502
  ensembl transcript: ENST00000304926
  gene symbol: ZSCAN32
  hgvsc: ENST00000304926.3:c.454G>A
  hgvsp: ENSP00000302502.3:p.Gly152Arg
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000407312
  ensembl transcript: ENST00000422427
  gene symbol: ZSCAN32
  hgvsc: ENST00000422427.2:c.454G>A
  hgvsp: ENSP00000407312.2:p.Gly152Arg
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000459960
  ensembl transcript: ENST00000573830
  gene symbol: ZSCAN32
  hgvsc: ENST00000573830.1:c.223G>A
  hgvsp: ENSP00000459960.1:p.Gly75Arg
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000459772
  ensembl transcript: ENST00000574940
  gene symbol: ZSCAN32
  hgvsc: ENST00000574940.1:c.1090G>A
  hgvsp: ENSP00000459772.1:p.Gly364Arg
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000380061
  ensembl transcript: ENST00000396852
  gene symbol: ZSCAN32
  hgvsc: ENST00000396852.4:c.1090G>A
  hgvsp: ENSP00000380061.4:p.Gly364Arg
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000380057
  ensembl transcript: ENST00000396846
  gene symbol: ZSCAN32
  hgvsc: ENST00000396846.3:c.1090G>A
  hgvsp: ENSP00000380057.3:p.Gly364Arg
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000262621
  ensembl transcript: ENST00000576906
  gene symbol: NAA60
  hgvsc: ENST00000576906.1:n.678C>T
  variant of: http://identifiers.org/hgnc/25875
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262621
  ensembl protein: ENSP00000477472
  ensembl transcript: ENST00000575785
  gene symbol: NAA60
  hgvsc: ENST00000575785.1:c.-13+19421C>T
  variant of: http://identifiers.org/hgnc/25875
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000458899
  ensembl transcript: ENST00000575350
  gene symbol: ZSCAN32
  hgvsc: ENST00000575350.1:c.454G>A
  hgvsp: ENSP00000458899.1:p.Gly152Arg
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000459069
  ensembl transcript: ENST00000576500
  gene symbol: ZSCAN32
  hgvsc: ENST00000576500.1:c.*144G>A
  variant of: http://identifiers.org/hgnc/20812
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7221
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 796
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1525
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1977
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7396
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3195
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6605
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1193
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7813
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly152Arg
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD

16-3434607-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3434607
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3434607
    reference: chr 16
allele count: 1
allele frequency: 8.237639422047218e-6
allele num: 121394
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000407312
  ensembl transcript: ENST00000422427
  gene symbol: ZSCAN32
  hgvsc: ENST00000422427.2:c.450G>A
  hgvsp: ENST00000422427.2:c.450G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262621
  ensembl protein: ENSP00000477472
  ensembl transcript: ENST00000575785
  gene symbol: NAA60
  hgvsc: ENST00000575785.1:c.-13+19425C>T
  variant of: http://identifiers.org/hgnc/25875
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000459960
  ensembl transcript: ENST00000573830
  gene symbol: ZSCAN32
  hgvsc: ENST00000573830.1:c.219G>A
  hgvsp: ENST00000573830.1:c.219G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000460487
  ensembl transcript: ENST00000573327
  gene symbol: ZSCAN32
  hgvsc: ENST00000573327.1:c.1086G>A
  hgvsp: ENST00000573327.1:c.1086G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000391787
  ensembl transcript: ENST00000439568
  gene symbol: ZSCAN32
  hgvsc: ENST00000439568.2:c.219G>A
  hgvsp: ENST00000439568.2:c.219G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000459069
  ensembl transcript: ENST00000576500
  gene symbol: ZSCAN32
  hgvsc: ENST00000576500.1:c.*140G>A
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000380061
  ensembl transcript: ENST00000396852
  gene symbol: ZSCAN32
  hgvsc: ENST00000396852.4:c.1086G>A
  hgvsp: ENST00000396852.4:c.1086G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000459772
  ensembl transcript: ENST00000574940
  gene symbol: ZSCAN32
  hgvsc: ENST00000574940.1:c.1086G>A
  hgvsp: ENST00000574940.1:c.1086G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000458899
  ensembl transcript: ENST00000575350
  gene symbol: ZSCAN32
  hgvsc: ENST00000575350.1:c.450G>A
  hgvsp: ENST00000575350.1:c.450G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000302502
  ensembl transcript: ENST00000304926
  gene symbol: ZSCAN32
  hgvsc: ENST00000304926.3:c.450G>A
  hgvsp: ENST00000304926.3:c.450G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000380057
  ensembl transcript: ENST00000396846
  gene symbol: ZSCAN32
  hgvsc: ENST00000396846.3:c.1086G>A
  hgvsp: ENST00000396846.3:c.1086G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000262621
  ensembl transcript: ENST00000576906
  gene symbol: NAA60
  hgvsc: ENST00000576906.1:n.682C>T
  variant of: http://identifiers.org/hgnc/25875
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140987
  ensembl transcript: ENST00000574084
  gene symbol: ZSCAN32
  hgvsc: ENST00000574084.1:n.535G>A
  variant of: http://identifiers.org/hgnc/20812
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8149
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7819
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1526
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 796
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7225
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3195
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8224
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6606
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu150Glu
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Other
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: C
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD

16-3434611-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3434611
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3434611
    reference: chr 16
allele count: 3
allele frequency: 2.471169686985173e-5
allele num: 121400
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000458899
  ensembl transcript: ENST00000575350
  gene symbol: ZSCAN32
  hgvsc: ENST00000575350.1:c.446T>C
  hgvsp: ENSP00000458899.1:p.Ile149Thr
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000459772
  ensembl transcript: ENST00000574940
  gene symbol: ZSCAN32
  hgvsc: ENST00000574940.1:c.1082T>C
  hgvsp: ENSP00000459772.1:p.Ile361Thr
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000459960
  ensembl transcript: ENST00000573830
  gene symbol: ZSCAN32
  hgvsc: ENST00000573830.1:c.215T>C
  hgvsp: ENSP00000459960.1:p.Ile72Thr
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140987
  ensembl transcript: ENST00000574084
  gene symbol: ZSCAN32
  hgvsc: ENST00000574084.1:n.531T>C
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000459069
  ensembl transcript: ENST00000576500
  gene symbol: ZSCAN32
  hgvsc: ENST00000576500.1:c.*136T>C
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000391787
  ensembl transcript: ENST00000439568
  gene symbol: ZSCAN32
  hgvsc: ENST00000439568.2:c.215T>C
  hgvsp: ENSP00000391787.2:p.Ile72Thr
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000302502
  ensembl transcript: ENST00000304926
  gene symbol: ZSCAN32
  hgvsc: ENST00000304926.3:c.446T>C
  hgvsp: ENSP00000302502.3:p.Ile149Thr
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000460487
  ensembl transcript: ENST00000573327
  gene symbol: ZSCAN32
  hgvsc: ENST00000573327.1:c.1082T>C
  hgvsp: ENSP00000460487.1:p.Ile361Thr
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000380061
  ensembl transcript: ENST00000396852
  gene symbol: ZSCAN32
  hgvsc: ENST00000396852.4:c.1082T>C
  hgvsp: ENSP00000380061.4:p.Ile361Thr
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000380057
  ensembl transcript: ENST00000396846
  gene symbol: ZSCAN32
  hgvsc: ENST00000396846.3:c.1082T>C
  hgvsp: ENSP00000380057.3:p.Ile361Thr
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000407312
  ensembl transcript: ENST00000422427
  gene symbol: ZSCAN32
  hgvsc: ENST00000422427.2:c.446T>C
  hgvsp: ENSP00000407312.2:p.Ile149Thr
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262621
  ensembl protein: ENSP00000477472
  ensembl transcript: ENST00000575785
  gene symbol: NAA60
  hgvsc: ENST00000575785.1:c.-13+19429A>G
  variant of: http://identifiers.org/hgnc/25875
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000262621
  ensembl transcript: ENST00000576906
  gene symbol: NAA60
  hgvsc: ENST00000576906.1:n.686A>G
  variant of: http://identifiers.org/hgnc/25875
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1977
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4787
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3194
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7226
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8228
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7375
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6605
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1193
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8150
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile149Thr
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
population: Other
population: East Asian
population: South Asian
reference allele: A
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP

16-3434612-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3434612
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3434612
    reference: chr 16
allele count: 7
allele frequency: 5.766157597324503e-5
allele num: 121398
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000391787
  ensembl transcript: ENST00000439568
  gene symbol: ZSCAN32
  hgvsc: ENST00000439568.2:c.214A>G
  hgvsp: ENSP00000391787.2:p.Ile72Val
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140987
  ensembl transcript: ENST00000574084
  gene symbol: ZSCAN32
  hgvsc: ENST00000574084.1:n.530A>G
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262621
  ensembl protein: ENSP00000477472
  ensembl transcript: ENST00000575785
  gene symbol: NAA60
  hgvsc: ENST00000575785.1:c.-13+19430T>C
  variant of: http://identifiers.org/hgnc/25875
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000407312
  ensembl transcript: ENST00000422427
  gene symbol: ZSCAN32
  hgvsc: ENST00000422427.2:c.445A>G
  hgvsp: ENSP00000407312.2:p.Ile149Val
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000459069
  ensembl transcript: ENST00000576500
  gene symbol: ZSCAN32
  hgvsc: ENST00000576500.1:c.*135A>G
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000302502
  ensembl transcript: ENST00000304926
  gene symbol: ZSCAN32
  hgvsc: ENST00000304926.3:c.445A>G
  hgvsp: ENSP00000302502.3:p.Ile149Val
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000380061
  ensembl transcript: ENST00000396852
  gene symbol: ZSCAN32
  hgvsc: ENST00000396852.4:c.1081A>G
  hgvsp: ENSP00000380061.4:p.Ile361Val
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000380057
  ensembl transcript: ENST00000396846
  gene symbol: ZSCAN32
  hgvsc: ENST00000396846.3:c.1081A>G
  hgvsp: ENSP00000380057.3:p.Ile361Val
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000458899
  ensembl transcript: ENST00000575350
  gene symbol: ZSCAN32
  hgvsc: ENST00000575350.1:c.445A>G
  hgvsp: ENSP00000458899.1:p.Ile149Val
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000262621
  ensembl transcript: ENST00000576906
  gene symbol: NAA60
  hgvsc: ENST00000576906.1:n.687T>C
  variant of: http://identifiers.org/hgnc/25875
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000460487
  ensembl transcript: ENST00000573327
  gene symbol: ZSCAN32
  hgvsc: ENST00000573327.1:c.1081A>G
  hgvsp: ENSP00000460487.1:p.Ile361Val
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000459960
  ensembl transcript: ENST00000573830
  gene symbol: ZSCAN32
  hgvsc: ENST00000573830.1:c.214A>G
  hgvsp: ENSP00000459960.1:p.Ile72Val
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000459772
  ensembl transcript: ENST00000574940
  gene symbol: ZSCAN32
  hgvsc: ENST00000574940.1:c.1081A>G
  hgvsp: ENSP00000459772.1:p.Ile361Val
  variant of: http://identifiers.org/hgnc/20812
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7374
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1977
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8228
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7819
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8149
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1193
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7226
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4787
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile149Val
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
population: Other
population: Latino
reference allele: T
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ

16-3434613-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3434613
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3434613
    reference: chr 16
allele count: 11
allele frequency: 9.061254077564335e-5
allele num: 121396
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000380057
  ensembl transcript: ENST00000396846
  gene symbol: ZSCAN32
  hgvsc: ENST00000396846.3:c.1080T>C
  hgvsp: ENST00000396846.3:c.1080T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000407312
  ensembl transcript: ENST00000422427
  gene symbol: ZSCAN32
  hgvsc: ENST00000422427.2:c.444T>C
  hgvsp: ENST00000422427.2:c.444T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000459069
  ensembl transcript: ENST00000576500
  gene symbol: ZSCAN32
  hgvsc: ENST00000576500.1:c.*134T>C
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262621
  ensembl protein: ENSP00000477472
  ensembl transcript: ENST00000575785
  gene symbol: NAA60
  hgvsc: ENST00000575785.1:c.-13+19431A>G
  variant of: http://identifiers.org/hgnc/25875
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000460487
  ensembl transcript: ENST00000573327
  gene symbol: ZSCAN32
  hgvsc: ENST00000573327.1:c.1080T>C
  hgvsp: ENST00000573327.1:c.1080T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000459960
  ensembl transcript: ENST00000573830
  gene symbol: ZSCAN32
  hgvsc: ENST00000573830.1:c.213T>C
  hgvsp: ENST00000573830.1:c.213T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000459772
  ensembl transcript: ENST00000574940
  gene symbol: ZSCAN32
  hgvsc: ENST00000574940.1:c.1080T>C
  hgvsp: ENST00000574940.1:c.1080T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140987
  ensembl transcript: ENST00000574084
  gene symbol: ZSCAN32
  hgvsc: ENST00000574084.1:n.529T>C
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000262621
  ensembl transcript: ENST00000576906
  gene symbol: NAA60
  hgvsc: ENST00000576906.1:n.688A>G
  variant of: http://identifiers.org/hgnc/25875
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000380061
  ensembl transcript: ENST00000396852
  gene symbol: ZSCAN32
  hgvsc: ENST00000396852.4:c.1080T>C
  hgvsp: ENST00000396852.4:c.1080T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000302502
  ensembl transcript: ENST00000304926
  gene symbol: ZSCAN32
  hgvsc: ENST00000304926.3:c.444T>C
  hgvsp: ENST00000304926.3:c.444T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000458899
  ensembl transcript: ENST00000575350
  gene symbol: ZSCAN32
  hgvsc: ENST00000575350.1:c.444T>C
  hgvsp: ENST00000575350.1:c.444T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20812
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140987
  ensembl protein: ENSP00000391787
  ensembl transcript: ENST00000439568
  gene symbol: ZSCAN32
  hgvsc: ENST00000439568.2:c.213T>C
  hgvsp: ENST00000439568.2:c.213T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20812
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8149
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1193
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 796
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8227
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6599
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7225
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1976
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3193
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4786
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp148Asp
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS

GenotypeQuality
all individuals: 8
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8596
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3235
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2718
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3814
bin: 7.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 1378
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1769
bin: 9.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66688
num of homozygotes: 0

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

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

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

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

South Asian
type: Population
allele count: 3
allele frequency: 1.817520901490367e-4
allele num: 16506
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 3.498e0

VQSLOD
type: SiteQuality
SIO_000300: 1.12e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.81e-1

MQ
type: SiteQuality
SIO_000300: 5.969e1

MQRankSum
type: SiteQuality
SIO_000300: 1.04e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.379999999999999e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

QD
type: SiteQuality
SIO_000300: 8.43e0

DP
type: SiteQuality
SIO_000300: 2.036005e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.831e0

GenotypeQuality
all individuals: 1
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8585
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3234
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 15
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31713
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3813
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2716
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7316
bin: 9.75e1
variant carriers: 1

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

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

African
type: Population
allele count: 1
allele frequency: 9.63020030816641e-5
allele num: 10384
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66664
num of homozygotes: 0

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

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

DP
type: SiteQuality
SIO_000300: 2.034772e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.4e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.1e-1

QD
type: SiteQuality
SIO_000300: 1.263e1

MQRankSum
type: SiteQuality
SIO_000300: 9.54e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.15e0

VQSLOD
type: SiteQuality
SIO_000300: 6.38e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

FS
type: SiteQuality
SIO_000300: 5.752e0

MQ
type: SiteQuality
SIO_000300: 5.908e1

GenotypeQuality
all individuals: 165
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1770
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 1379
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3810
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3232
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 4.25e1
variant carriers: 0

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

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

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.001921229586936e-5
allele num: 66624
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.29e-1

FS
type: SiteQuality
SIO_000300: 5.355e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 7.66e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.29e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.33e-1

DP
type: SiteQuality
SIO_000300: 2.03391e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.952e0

MQ
type: SiteQuality
SIO_000300: 5.959e1

QD
type: SiteQuality
SIO_000300: 1.055e1

GenotypeQuality
all individuals: 1
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31555
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 254
bin: 2.25e1
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GenotypeQuality
all individuals: 1375
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7346
bin: 9.75e1
variant carriers: 50

GenotypeQuality
all individuals: 2710
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3805
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 3.75e1
variant carriers: 0

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

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

South Asian
type: Population
allele count: 18
allele frequency: 1.090776875530239e-3
allele num: 16502
num of homozygotes: 1

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

European (Non-Finnish)
type: Population
allele count: 26
allele frequency: 3.904607436775395e-4
allele num: 66588
num of homozygotes: 0

Latino
type: Population
allele count: 6
allele frequency: 5.192107995846313e-4
allele num: 11556
num of homozygotes: 0

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: 3.85e0

MQRankSum
type: SiteQuality
SIO_000300: 3.11e-1

MQ
type: SiteQuality
SIO_000300: 5.964e1

VQSLOD
type: SiteQuality
SIO_000300: 5.86e0

DP
type: SiteQuality
SIO_000300: 2.034377e6

ClippingRankSum
type: SiteQuality
SIO_000300: -2.09e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.2e-1

QD
type: SiteQuality
SIO_000300: 1.414e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.42e-2

GenotypeQuality
all individuals: 77
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3206
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1767
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8436
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 49
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2703
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 89
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1369
bin: 8.75e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11532
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66384
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: 8588
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16488
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.697439875872769e-5
allele num: 10312
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.06e0

FS
type: SiteQuality
SIO_000300: 5.88e-1

DP
type: SiteQuality
SIO_000300: 2.023517e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.3e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.923e0

QD
type: SiteQuality
SIO_000300: 1.45e1

VQSLOD
type: SiteQuality
SIO_000300: 2.0e0

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.3e-3

GenotypeQuality
all individuals: 70
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2703
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 89
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8436
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
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variant carriers: 0

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

GenotypeQuality
all individuals: 3206
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1369
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3784
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1767
bin: 9.25e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66384
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16488
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.697439875872769e-5
allele num: 10312
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11532
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -3.923e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.06e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.3e-1

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.023517e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.3e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 2.0e0

FS
type: SiteQuality
SIO_000300: 5.88e-1

QD
type: SiteQuality
SIO_000300: 1.45e1

GenotypeQuality
all individuals: 2701
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8434
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1768
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 41
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 79
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variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 91
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3205
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31116
bin: 6.25e1
variant carriers: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16488
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: 8580
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.506795648374167e-5
allele num: 66366
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10310
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.12e0

QD
type: SiteQuality
SIO_000300: 1.484e1

VQSLOD
type: SiteQuality
SIO_000300: 5.4e-1

FS
type: SiteQuality
SIO_000300: 4.814e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.81e0

MQRankSum
type: SiteQuality
SIO_000300: 9.85e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.9e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.58e0

DP
type: SiteQuality
SIO_000300: 2.022608e6

GenotypeQuality
all individuals: 79
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1368
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3779
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 91
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 7297
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3205
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1768
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8434
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2701
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.506795648374167e-5
allele num: 66366
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16488
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10310
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 1.58e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.81e0

QD
type: SiteQuality
SIO_000300: 1.484e1

MQRankSum
type: SiteQuality
SIO_000300: 9.85e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 5.4e-1

FS
type: SiteQuality
SIO_000300: 4.814e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.9e-3

DP
type: SiteQuality
SIO_000300: 2.022608e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.12e0

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

GenotypeQuality
all individuals: 3
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 637
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3775
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29
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variant carriers: 0

GenotypeQuality
all individuals: 8427
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1764
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31098
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2698
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3196
bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 35
allele frequency: 3.396739130434783e-3
allele num: 10304
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8574
num of homozygotes: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.668515950069348e-5
allele num: 11536
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66358
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16486
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 6.04e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 2.24e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.0e-2

DP
type: SiteQuality
SIO_000300: 2.022705e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.77e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.773e0

QD
type: SiteQuality
SIO_000300: 1.801e1

MQ
type: SiteQuality
SIO_000300: 5.57e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.67e-1

GenotypeQuality
all individuals: 1183
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 167
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 223
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 132
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7291
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 10
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8261
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30172
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3744
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1762
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1364
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 66
bin: 4.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6600
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10252
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.514325519413653e-5
allele num: 66036
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8498
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.738223535546671e-4
allele num: 11506
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.999e1

VQSLOD
type: SiteQuality
SIO_000300: -4.153e-1

QD
type: SiteQuality
SIO_000300: 1.674e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.4e-3

FS
type: SiteQuality
SIO_000300: 1.208e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.68e0

MQRankSum
type: SiteQuality
SIO_000300: 1.43e0

DP
type: SiteQuality
SIO_000300: 2.006072e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.93e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.24e-1

GenotypeQuality
all individuals: 448
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 2.5e0
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GenotypeQuality
all individuals: 660
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1748
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22913
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2582
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 518
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 497
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 107
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1853
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 765
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3524
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7267
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1417
bin: 3.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.546551190844417e-5
allele num: 64660
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11368
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8272
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9882
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16342
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.172e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.03e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.59e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

FS
type: SiteQuality
SIO_000300: 5.87e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.32e-1

DP
type: SiteQuality
SIO_000300: 1.888753e6

MQRankSum
type: SiteQuality
SIO_000300: 1.03e0

VQSLOD
type: SiteQuality
SIO_000300: 3.18e-1

MQ
type: SiteQuality
SIO_000300: 5.969e1

GenotypeQuality
all individuals: 1368
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 643
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3523
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 93
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7268
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 659
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1404
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 23288
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 517
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2848
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4133
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6578
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2581
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1748
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 262
bin: 5.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.546742560168286e-5
allele num: 64652
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16340
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9884
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8270
num of homozygotes: 0

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

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

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

FS
type: SiteQuality
SIO_000300: 1.419e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.73e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.31e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.77e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.11e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 2.93e-1

DP
type: SiteQuality
SIO_000300: 1.888435e6

MQ
type: SiteQuality
SIO_000300: 6.036e1

QD
type: SiteQuality
SIO_000300: 1.552e1

GenotypeQuality
all individuals: 1736
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 89
bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7267
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 437
bin: 5.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8246
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11356
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9816
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.130456105934282e-5
allele num: 16312
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64506
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.792e0

VQSLOD
type: SiteQuality
SIO_000300: -2.525e0

MQ
type: SiteQuality
SIO_000300: 5.931e1

MQRankSum
type: SiteQuality
SIO_000300: 7.47e-1

QD
type: SiteQuality
SIO_000300: 3.17e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.08e0

DP
type: SiteQuality
SIO_000300: 1.873154e6

ClippingRankSum
type: SiteQuality
SIO_000300: 8.3e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.4e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -1.356e0

GenotypeQuality
all individuals: 755
bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
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: 2.5e0
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GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7265
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4576
bin: 2.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9784
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.551782998665467e-5
allele num: 64442
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6552
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8226
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -2.9e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.6e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.29e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.17e-1

MQ
type: SiteQuality
SIO_000300: 5.968e1

QD
type: SiteQuality
SIO_000300: 1.799e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.09e0

VQSLOD
type: SiteQuality
SIO_000300: -4.968e-1

DP
type: SiteQuality
SIO_000300: 1.864044e6

GenotypeQuality
all individuals: 4674
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 102
bin: 1.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 5

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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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: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2121
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2529
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19712
bin: 6.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11346
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64296
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.141751627564181e-5
allele num: 16282
num of homozygotes: 0

East Asian
type: Population
allele count: 4
allele frequency: 4.873294346978557e-4
allele num: 8208
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.743e1

MQRankSum
type: SiteQuality
SIO_000300: 1.02e-1

DP
type: SiteQuality
SIO_000300: 1.856727e6

VQSLOD
type: SiteQuality
SIO_000300: 1.5e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.11e-1

FS
type: SiteQuality
SIO_000300: 2.52e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -1.065e0

MQ
type: SiteQuality
SIO_000300: 5.961e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.82e-1

GenotypeQuality
all individuals: 2552
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4708
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 138
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20276
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3442
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7260
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 861
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 65
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GenotypeQuality
all individuals: 105
bin: 1.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2757
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 429
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1344
bin: 8.75e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.140243153628883e-5
allele num: 16286
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11336
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6546
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.668534080298786e-5
allele num: 64260
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8200
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9726
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.44e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.379999999999999e-1

QD
type: SiteQuality
SIO_000300: 1.353e1

DP
type: SiteQuality
SIO_000300: 1.855754e6

ClippingRankSum
type: SiteQuality
SIO_000300: -2.29e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.11e-1

FS
type: SiteQuality
SIO_000300: 2.859e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.2e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

GenotypeQuality
all individuals: 2681
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18279
bin: 6.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 7260
bin: 9.75e1
variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 3428
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
all individuals: 2035
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variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 421
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 639
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variant carriers: 0

GenotypeQuality
all individuals: 174
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1088
bin: 4.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11320
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64098
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.165988407941794e-5
allele num: 16218
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9644
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8194
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6542
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 3.399e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.85e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 8.61e-1

QD
type: SiteQuality
SIO_000300: 1.118e1

MQRankSum
type: SiteQuality
SIO_000300: -4.36e-1

DP
type: SiteQuality
SIO_000300: 1.836177e6

ClippingRankSum
type: SiteQuality
SIO_000300: -8.94e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.04e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.8e-3

GenotypeQuality
all individuals: 4527
bin: 7.5e0
variant carriers: 672

GenotypeQuality
all individuals: 5724
bin: 2.25e1
variant carriers: 795

GenotypeQuality
all individuals: 2040
bin: 4.25e1
variant carriers: 575

GenotypeQuality
all individuals: 1901
bin: 9.75e1
variant carriers: 431

GenotypeQuality
all individuals: 19007
bin: 2.5e0
variant carriers: 597

GenotypeQuality
all individuals: 3126
bin: 3.25e1
variant carriers: 708

GenotypeQuality
all individuals: 1161
bin: 5.75e1
variant carriers: 367

GenotypeQuality
all individuals: 3043
bin: 6.25e1
variant carriers: 321

GenotypeQuality
all individuals: 598
bin: 7.75e1
variant carriers: 174

GenotypeQuality
all individuals: 3784
bin: 1.25e1
variant carriers: 758

GenotypeQuality
all individuals: 1226
bin: 6.75e1
variant carriers: 225

GenotypeQuality
all individuals: 1794
bin: 4.75e1
variant carriers: 502

GenotypeQuality
all individuals: 3585
bin: 2.75e1
variant carriers: 786

GenotypeQuality
all individuals: 323
bin: 8.75e1
variant carriers: 92

GenotypeQuality
all individuals: 3257
bin: 1.75e1
variant carriers: 789

GenotypeQuality
all individuals: 730
bin: 7.25e1
variant carriers: 184

GenotypeQuality
all individuals: 281
bin: 9.25e1
variant carriers: 84

GenotypeQuality
all individuals: 452
bin: 8.25e1
variant carriers: 139

South Asian
type: Population
allele count: 1353
allele frequency: 1.842320261437909e-1
allele num: 7344
num of homozygotes: 0

Latino
type: Population
allele count: 628
allele frequency: 1.184905660377358e-1
allele num: 5300
num of homozygotes: 0

East Asian
type: Population
allele count: 451
allele frequency: 1.081534772182254e-1
allele num: 4170
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3109
allele frequency: 9.94689019708216e-2
allele num: 31256
num of homozygotes: 0

African
type: Population
allele count: 498
allele frequency: 9.677419354838709e-2
allele num: 5146
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 163
allele frequency: 4.175204918032787e-2
allele num: 3904
num of homozygotes: 0

Other
type: Population
allele count: 44
allele frequency: 9.482758620689655e-2
allele num: 464
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.59e0

MQ
type: SiteQuality
SIO_000300: 5.996e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.15e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.65e-1

QD
type: SiteQuality
SIO_000300: 1.21e0

DP
type: SiteQuality
SIO_000300: 1.755226e6

MQRankSum
type: SiteQuality
SIO_000300: 2.17e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.102e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.43e-1

GenotypeQuality
all individuals: 3585
bin: 2.75e1
variant carriers: 9

GenotypeQuality
all individuals: 1226
bin: 6.75e1
variant carriers: 7

GenotypeQuality
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bin: 4.75e1
variant carriers: 7

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
all individuals: 281
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variant carriers: 5

GenotypeQuality
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variant carriers: 7

GenotypeQuality
all individuals: 3126
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1161
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GenotypeQuality
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bin: 6.25e1
variant carriers: 11

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1901
bin: 9.75e1
variant carriers: 229

GenotypeQuality
all individuals: 452
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variant carriers: 3

GenotypeQuality
all individuals: 3784
bin: 1.25e1
variant carriers: 5

GenotypeQuality
all individuals: 323
bin: 8.75e1
variant carriers: 10

East Asian
type: Population
allele count: 1
allele frequency: 2.398081534772182e-4
allele num: 4170
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 2.561475409836066e-4
allele num: 3904
num of homozygotes: 0

South Asian
type: Population
allele count: 11
allele frequency: 1.497821350762527e-3
allele num: 7344
num of homozygotes: 0

Latino
type: Population
allele count: 19
allele frequency: 3.584905660377358e-3
allele num: 5300
num of homozygotes: 0

African
type: Population
allele count: 236
allele frequency: 4.586086280606296e-2
allele num: 5146
num of homozygotes: 1

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 464
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 29
allele frequency: 9.27821858203225e-4
allele num: 31256
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.996e1

QD
type: SiteQuality
SIO_000300: 1.21e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.43e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.59e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.755226e6

MQRankSum
type: SiteQuality
SIO_000300: 2.17e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.15e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.65e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.102e-1

GenotypeQuality
all individuals: 1794
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1490
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 2040
bin: 4.25e1
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GenotypeQuality
all individuals: 3043
bin: 6.25e1
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GenotypeQuality
all individuals: 3257
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1161
bin: 5.75e1
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GenotypeQuality
all individuals: 452
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variant carriers: 2

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
all individuals: 19007
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 3585
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GenotypeQuality
all individuals: 1226
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GenotypeQuality
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GenotypeQuality
all individuals: 730
bin: 7.25e1
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GenotypeQuality
all individuals: 1901
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variant carriers: 4

GenotypeQuality
all individuals: 598
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 281
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5300
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4170
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3904
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 464
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7344
num of homozygotes: 0

African
type: Population
allele count: 7
allele frequency: 1.360279828993393e-3
allele num: 5146
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 31256
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.65e-1

QD
type: SiteQuality
SIO_000300: 1.21e0

MQRankSum
type: SiteQuality
SIO_000300: 2.17e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.43e-1

MQ
type: SiteQuality
SIO_000300: 5.996e1

DP
type: SiteQuality
SIO_000300: 1.755226e6

VQSLOD
type: SiteQuality
SIO_000300: 2.59e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.15e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.102e-1

GenotypeQuality
all individuals: 2450
bin: 3.75e1
variant carriers: 341

GenotypeQuality
all individuals: 3043
bin: 6.25e1
variant carriers: 151

GenotypeQuality
all individuals: 730
bin: 7.25e1
variant carriers: 122

GenotypeQuality
all individuals: 2040
bin: 4.25e1
variant carriers: 294

GenotypeQuality
all individuals: 19007
bin: 2.5e0
variant carriers: 382

GenotypeQuality
all individuals: 3257
bin: 1.75e1
variant carriers: 415

GenotypeQuality
all individuals: 598
bin: 7.75e1
variant carriers: 82

GenotypeQuality
all individuals: 3126
bin: 3.25e1
variant carriers: 414

GenotypeQuality
all individuals: 3784
bin: 1.25e1
variant carriers: 465

GenotypeQuality
all individuals: 4527
bin: 7.5e0
variant carriers: 516

GenotypeQuality
all individuals: 3585
bin: 2.75e1
variant carriers: 445

GenotypeQuality
all individuals: 5724
bin: 2.25e1
variant carriers: 443

GenotypeQuality
all individuals: 281
bin: 9.25e1
variant carriers: 45

GenotypeQuality
all individuals: 323
bin: 8.75e1
variant carriers: 59

GenotypeQuality
all individuals: 1490
bin: 5.25e1
variant carriers: 219

GenotypeQuality
all individuals: 1901
bin: 9.75e1
variant carriers: 614

GenotypeQuality
all individuals: 1794
bin: 4.75e1
variant carriers: 265

GenotypeQuality
all individuals: 1161
bin: 5.75e1
variant carriers: 198

East Asian
type: Population
allele count: 245
allele frequency: 5.875299760191847e-2
allele num: 4170
num of homozygotes: 0

African
type: Population
allele count: 298
allele frequency: 5.79090555771473e-2
allele num: 5146
num of homozygotes: 0

Latino
type: Population
allele count: 353
allele frequency: 6.660377358490566e-2
allele num: 5300
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 129
allele frequency: 3.304303278688524e-2
allele num: 3904
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2294
allele frequency: 7.339390836959304e-2
allele num: 31256
num of homozygotes: 0

Other
type: Population
allele count: 33
allele frequency: 7.112068965517242e-2
allele num: 464
num of homozygotes: 0

South Asian
type: Population
allele count: 493
allele frequency: 6.712962962962964e-2
allele num: 7344
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.996e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.15e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.102e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 2.17e-1

QD
type: SiteQuality
SIO_000300: 1.21e0

VQSLOD
type: SiteQuality
SIO_000300: 2.59e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.43e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.65e-1

DP
type: SiteQuality
SIO_000300: 1.755226e6

African
type: Population
allele count: 1
allele frequency: 1.94325689856199e-4
allele num: 5146
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5300
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 464
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.43e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.59e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.102e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.65e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.15e-1

MQ
type: SiteQuality
SIO_000300: 5.996e1

MQRankSum
type: SiteQuality
SIO_000300: 2.17e-1

QD
type: SiteQuality
SIO_000300: 1.21e0

DP
type: SiteQuality
SIO_000300: 1.755226e6

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4170
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 464
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3904
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.59e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.65e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.15e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.102e-1

MQ
type: SiteQuality
SIO_000300: 5.996e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.43e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.17e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.21e0

DP
type: SiteQuality
SIO_000300: 1.755226e6

GenotypeQuality
all individuals: 2964
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 323
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 207
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10029
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 480
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6386
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variant carriers: 0

GenotypeQuality
all individuals: 568
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variant carriers: 0

GenotypeQuality
all individuals: 96
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3020
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1181
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2218
bin: 7.25e1
variant carriers: 1

GenotypeQuality
all individuals: 2310
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 649
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2973
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1433
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21978
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 690
bin: 5.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 60470
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6482
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 2.303086135421465e-4
allele num: 8684
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11080
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7940
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.8e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.84e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.06e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.041e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -2.787e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.41e0

DP
type: SiteQuality
SIO_000300: 1.482442e6

QD
type: SiteQuality
SIO_000300: 1.84e1

GenotypeQuality
all individuals: 906
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 369
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10079
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1360
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1332
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1923
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 510
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 711
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3020
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3167
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 759
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2068
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 636
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2156
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 506
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 742
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20499
bin: 6.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 824
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.679825298168991e-5
allele num: 59530
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13970
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8514
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10982
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6446
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7862
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.02e0

DP
type: SiteQuality
SIO_000300: 1.468657e6

ClippingRankSum
type: SiteQuality
SIO_000300: -2.96e-1

QD
type: SiteQuality
SIO_000300: 6.93e0

MQRankSum
type: SiteQuality
SIO_000300: 3.22e-1

MQ
type: SiteQuality
SIO_000300: 5.916e1

FS
type: SiteQuality
SIO_000300: 6.4e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.38e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.67e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.07e0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10982
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6446
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 5.039475894506971e-5
allele num: 59530
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.916e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.07e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.67e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.38e-2

QD
type: SiteQuality
SIO_000300: 6.93e0

FS
type: SiteQuality
SIO_000300: 6.4e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.22e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.96e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.02e0

DP
type: SiteQuality
SIO_000300: 1.468657e6

GenotypeQuality
all individuals: 506
bin: 1.75e1
variant carriers: 4

GenotypeQuality
all individuals: 636
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 742
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2156
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1923
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3167
bin: 3.25e1
variant carriers: 2

GenotypeQuality
all individuals: 1332
bin: 7.5e0
variant carriers: 5

GenotypeQuality
all individuals: 510
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 10079
bin: 2.25e1
variant carriers: 1

GenotypeQuality
all individuals: 3124
bin: 2.75e1
variant carriers: 5

GenotypeQuality
all individuals: 20499
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1360
bin: 8.25e1
variant carriers: 2

GenotypeQuality
all individuals: 759
bin: 4.25e1
variant carriers: 2

GenotypeQuality
all individuals: 727
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2068
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 906
bin: 5.25e1
variant carriers: 5

GenotypeQuality
all individuals: 711
bin: 5.75e1
variant carriers: 1

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10982
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 824
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.679825298168991e-5
allele num: 59530
num of homozygotes: 0

African
type: Population
allele count: 13
allele frequency: 1.526896875734085e-3
allele num: 8514
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6446
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7862
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13970
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.96e-1

MQ
type: SiteQuality
SIO_000300: 5.916e1

FS
type: SiteQuality
SIO_000300: 6.4e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.38e-2

DP
type: SiteQuality
SIO_000300: 1.468657e6

MQRankSum
type: SiteQuality
SIO_000300: 3.22e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.02e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.07e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.67e-1

QD
type: SiteQuality
SIO_000300: 6.93e0

GenotypeQuality
all individuals: 718
bin: 5.75e1
variant carriers: 4

GenotypeQuality
all individuals: 789
bin: 4.25e1
variant carriers: 4

GenotypeQuality
all individuals: 898
bin: 5.25e1
variant carriers: 6

GenotypeQuality
all individuals: 3004
bin: 2.75e1
variant carriers: 2

GenotypeQuality
all individuals: 576
bin: 1.25e1
variant carriers: 4

GenotypeQuality
all individuals: 5417
bin: 6.75e1
variant carriers: 4

GenotypeQuality
all individuals: 1753
bin: 3.75e1
variant carriers: 4

GenotypeQuality
all individuals: 573
bin: 8.75e1
variant carriers: 6

GenotypeQuality
all individuals: 1219
bin: 8.25e1
variant carriers: 6

GenotypeQuality
all individuals: 1485
bin: 7.5e0
variant carriers: 2

GenotypeQuality
all individuals: 1880
bin: 7.25e1
variant carriers: 7

GenotypeQuality
all individuals: 3001
bin: 3.25e1
variant carriers: 1

GenotypeQuality
all individuals: 674
bin: 9.25e1
variant carriers: 9

GenotypeQuality
all individuals: 20702
bin: 6.25e1
variant carriers: 7

GenotypeQuality
all individuals: 1954
bin: 7.75e1
variant carriers: 5

GenotypeQuality
all individuals: 3053
bin: 9.75e1
variant carriers: 258

GenotypeQuality
all individuals: 653
bin: 1.75e1
variant carriers: 5

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

Latino
type: Population
allele count: 11
allele frequency: 1.013264554163596e-3
allele num: 10856
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.243781094527363e-3
allele num: 804
num of homozygotes: 0

East Asian
type: Population
allele count: 3
allele frequency: 3.849114703618168e-4
allele num: 7794
num of homozygotes: 0

African
type: Population
allele count: 266
allele frequency: 3.182579564489112e-2
allele num: 8358
num of homozygotes: 5

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6400
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 29
allele frequency: 4.984188092946514e-4
allele num: 58184
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -7.299e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.2e-3

FS
type: SiteQuality
SIO_000300: 8.194000000000001e0

MQ
type: SiteQuality
SIO_000300: 5.915e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.21e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.88e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.98e-1

DP
type: SiteQuality
SIO_000300: 1.459946e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.156e0

QD
type: SiteQuality
SIO_000300: 6.95e0

GenotypeQuality
all individuals: 797
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1454
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 651
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5350
bin: 3.25e1
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GenotypeQuality
all individuals: 1120
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variant carriers: 0

GenotypeQuality
all individuals: 239
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variant carriers: 0

GenotypeQuality
all individuals: 506
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GenotypeQuality
all individuals: 296
bin: 5.75e1
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GenotypeQuality
all individuals: 4090
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2352
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variant carriers: 0

GenotypeQuality
all individuals: 1703
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 543
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2756
bin: 9.75e1
variant carriers: 10

GenotypeQuality
all individuals: 4199
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4535
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11261
bin: 2.25e1
variant carriers: 1

GenotypeQuality
all individuals: 14728
bin: 6.25e1
variant carriers: 0

East Asian
type: Population
allele count: 10
allele frequency: 1.286670097786927e-3
allele num: 7772
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 57614
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10884
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8148
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 790
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12196
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.4e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 1.72e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.48e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.66e-1

QD
type: SiteQuality
SIO_000300: 1.322e1

DP
type: SiteQuality
SIO_000300: 1.31022e6

BaseQRankSum
type: SiteQuality
SIO_000300: 2.08e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.71e-1

GenotypeQuality
all individuals: 5569
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1784
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variant carriers: 0

GenotypeQuality
all individuals: 1921
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 296
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1105
bin: 8.25e1
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GenotypeQuality
all individuals: 294
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GenotypeQuality
all individuals: 4722
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GenotypeQuality
all individuals: 847
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variant carriers: 0

GenotypeQuality
all individuals: 2464
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 13021
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4155
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 540
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10928
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1575
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4415
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 596
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2817
bin: 9.75e1
variant carriers: 79

European (Non-Finnish)
type: Population
allele count: 57
allele frequency: 9.937238493723849e-4
allele num: 57360
num of homozygotes: 0

Latino
type: Population
allele count: 12
allele frequency: 1.104768919167741e-3
allele num: 10862
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 4
allele frequency: 6.232471174820816e-4
allele num: 6418
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.231223836493475e-4
allele num: 8122
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7754
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 8.337502084375521e-5
allele num: 11994
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.72e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.36e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.72e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.95e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.35e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.297382e6

QD
type: SiteQuality
SIO_000300: 1.394e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.9e-3

GenotypeDepth
all individuals: 5426
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1174
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 465
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 695
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 248
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3258
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 494
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2081
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1735
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1653
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 733
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 243
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2702
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2483
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1163
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 467
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3214
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33924
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2962
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 558
bin: 4.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 808
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9864
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11472
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8552
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.560305819940709e-5
allele num: 64090
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -3.98e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.3e-3

MQ
type: SiteQuality
SIO_000300: 5.88e1

QD
type: SiteQuality
SIO_000300: 1.265e1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.95e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.4e-1

DP
type: SiteQuality
SIO_000300: 2.441344e6

VQSLOD
type: SiteQuality
SIO_000300: -3.582e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.63e-1

GenotypeDepth
all individuals: 499
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 722
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 34046
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 438
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3349
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 48
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variant carriers: 0

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

GenotypeQuality
all individuals: 3322
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variant carriers: 0

GenotypeQuality
all individuals: 417
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variant carriers: 0

GenotypeQuality
all individuals: 81
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variant carriers: 0

GenotypeQuality
all individuals: 2726
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variant carriers: 0

GenotypeQuality
all individuals: 65
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variant carriers: 0

GenotypeQuality
all individuals: 208
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 105
bin: 2.5e0
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GenotypeQuality
all individuals: 4992
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variant carriers: 0

GenotypeQuality
all individuals: 2165
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 203
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1773
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2622
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3092
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 74
bin: 4.25e1
variant carriers: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10426
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8576
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.228501228501228e-3
allele num: 814
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64314
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 4.47e-1

DP
type: SiteQuality
SIO_000300: 2.467695e6

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 6.24e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

QD
type: SiteQuality
SIO_000300: 1.503e1

VQSLOD
type: SiteQuality
SIO_000300: 2.13e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.06e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.909999999999999e-1

GenotypeDepth
all individuals: 8148
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1976
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2892
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34057
bin: 9.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1799
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6582
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2171
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 104
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variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 5.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 286
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 297
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3335
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 44
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 188
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2753
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2739
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3118
bin: 8.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12508
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65058
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10302
num of homozygotes: 0

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

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

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

DP
type: SiteQuality
SIO_000300: 2.498607e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.754e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.0e-3

MQ
type: SiteQuality
SIO_000300: 5.373e1

QD
type: SiteQuality
SIO_000300: 8.5e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.754e0

VQSLOD
type: SiteQuality
SIO_000300: -2.633e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.3e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -5.5e-1

GenotypeDepth
all individuals: 6582
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1224
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 286
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6682
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2826
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3334
bin: 9.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 292
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1800
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variant carriers: 0

GenotypeQuality
all individuals: 197
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 96
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3118
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34057
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2747
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2755
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2171
bin: 8.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12644
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 858
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: 10308
num of homozygotes: 0

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.07e-2

MQRankSum
type: SiteQuality
SIO_000300: 8.93e-1

FS
type: SiteQuality
SIO_000300: 9.26e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.55e0

VQSLOD
type: SiteQuality
SIO_000300: 5.39e-1

QD
type: SiteQuality
SIO_000300: 1.173e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.107e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.945e0

DP
type: SiteQuality
SIO_000300: 2.499876e6

GenotypeDepth
all individuals: 355
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 499
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 82
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variant carriers: 0

GenotypeQuality
all individuals: 7670
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variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 7.5e0
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GenotypeQuality
all individuals: 85
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variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 1955
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variant carriers: 0

GenotypeQuality
all individuals: 202
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34059
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3126
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 2.5e0
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GenotypeQuality
all individuals: 1828
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2831
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 160
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2783
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2177
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3338
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11550
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10350
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 872
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.525087692542321e-5
allele num: 65570
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13924
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.066e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.37e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.94e-1

MQ
type: SiteQuality
SIO_000300: 5.906e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.800000000000001e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -3.042e0

VQSLOD
type: SiteQuality
SIO_000300: -6.69e-1

FS
type: SiteQuality
SIO_000300: 1.2188e1

DP
type: SiteQuality
SIO_000300: 2.51681e6

ClippingRankSum
type: SiteQuality
SIO_000300: -5.06e-1

GenotypeDepth
all individuals: 3197
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1170
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variant carriers: 0

GenotypeQuality
all individuals: 1304
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variant carriers: 0

GenotypeQuality
all individuals: 10
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GenotypeQuality
all individuals: 2181
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GenotypeQuality
all individuals: 2885
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variant carriers: 0

GenotypeQuality
all individuals: 36
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variant carriers: 0

GenotypeQuality
all individuals: 126
bin: 2.75e1
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GenotypeQuality
all individuals: 13
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
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variant carriers: 0

GenotypeQuality
all individuals: 117
bin: 3.75e1
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GenotypeQuality
all individuals: 34063
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variant carriers: 1

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

GenotypeQuality
all individuals: 99
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25
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GenotypeQuality
all individuals: 1843
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variant carriers: 0

GenotypeQuality
all individuals: 154
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8430
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3134
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2801
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3340
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 8.655011251514626e-5
allele num: 11554
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65902
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14860
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10380
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -4.31e-1

QD
type: SiteQuality
SIO_000300: 1.347e1

DP
type: SiteQuality
SIO_000300: 2.529552e6

ClippingRankSum
type: SiteQuality
SIO_000300: -3.85e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.02e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.7e-1

FS
type: SiteQuality
SIO_000300: 1.008e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-4

MQ
type: SiteQuality
SIO_000300: 5.942e1

VQSLOD
type: SiteQuality
SIO_000300: 6.55e-1

GenotypeDepth
all individuals: 499
bin: 8.25e1
variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 134
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GenotypeQuality
all individuals: 102
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GenotypeQuality
all individuals: 3345
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GenotypeQuality
all individuals: 3136
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GenotypeQuality
all individuals: 8
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GenotypeQuality
all individuals: 13
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GenotypeQuality
all individuals: 106
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variant carriers: 0

GenotypeQuality
all individuals: 92
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GenotypeQuality
all individuals: 1854
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2185
bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

European (Non-Finnish)
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allele count: 1
allele frequency: 1.51290508033526e-5
allele num: 66098
num of homozygotes: 0

Other
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num of homozygotes: 0

Latino
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allele frequency: 8.646031471554557e-5
allele num: 11566
num of homozygotes: 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
allele num: 10392
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

South Asian
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allele frequency: 0.0e0
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BaseQRankSum
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SIO_000300: -4.03e0

InbreedingCoeff
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VQSLOD
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MQRankSum
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SIO_000300: 1.38e0

ReadPosRankSum
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QD
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MQ
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FS
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DP
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ClippingRankSum
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SIO_000300: 6.7e-1

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

East Asian
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allele count: 1
allele frequency: 1.155802126675913e-4
allele num: 8652
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

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

African
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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

Latino
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num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 3.964e0

MQ
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MQRankSum
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DP
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ClippingRankSum
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ReadPosRankSum
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BaseQRankSum
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VQSLOD
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SIO_000300: -9.88e-1

InbreedingCoeff
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SIO_000300: 8.0e-4

QD
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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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

South Asian
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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

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 num: 66386
num of homozygotes: 0

East Asian
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Other
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BaseQRankSum
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InbreedingCoeff
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SIO_000300: -1.0e-4

MQ
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SIO_000300: 5.954e1

FS
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VQSLOD
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QD
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MQRankSum
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ReadPosRankSum
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

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

South Asian
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allele frequency: 1.243008079552517e-4
allele num: 16090
num of homozygotes: 0

East Asian
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allele count: 0
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
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ReadPosRankSum
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SIO_000300: -3.37e-1

BaseQRankSum
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SIO_000300: 6.52e0

InbreedingCoeff
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SIO_000300: 0.0e0

MQRankSum
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QD
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MQ
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SIO_000300: 5.988e1

ClippingRankSum
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SIO_000300: 8.2e-1

FS
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SIO_000300: 0.0e0

VQSLOD
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SIO_000300: -2.97e-1

DP
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SIO_000300: 2.550253e6

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: 1
allele frequency: 1.511944360447536e-4
allele num: 6614
num of homozygotes: 0

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

Latino
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num of homozygotes: 0

African
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num of homozygotes: 0

South Asian
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Other
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num of homozygotes: 0

East Asian
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MQ
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SIO_000300: 5.942e1

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

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

South Asian
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East Asian
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Latino
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num of homozygotes: 0

Other
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QD
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MQ
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VQSLOD
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MQRankSum
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InbreedingCoeff
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ReadPosRankSum
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DP
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FS
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ClippingRankSum
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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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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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Other
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East Asian
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European (Non-Finnish)
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South Asian
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InbreedingCoeff
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QD
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MQ
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ReadPosRankSum
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FS
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DP
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BaseQRankSum
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ClippingRankSum
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MQRankSum
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 2.25e1
variant carriers: 7

GenotypeQuality
all individuals: 2150
bin: 8.75e1
variant carriers: 7

GenotypeQuality
all individuals: 1803
bin: 7.25e1
variant carriers: 8

GenotypeQuality
all individuals: 134
bin: 4.75e1
variant carriers: 4

GenotypeQuality
all individuals: 2883
bin: 6.75e1
variant carriers: 9

GenotypeQuality
all individuals: 132
bin: 3.25e1
variant carriers: 5

GenotypeQuality
all individuals: 9232
bin: 6.25e1
variant carriers: 4

African
type: Population
allele count: 49
allele frequency: 4.931561996779388e-3
allele num: 9936
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.213444970270598e-4
allele num: 16482
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 140
allele frequency: 2.14322892746701e-3
allele num: 65322
num of homozygotes: 0

Latino
type: Population
allele count: 4
allele frequency: 3.472222222222222e-4
allele num: 11520
num of homozygotes: 0

East Asian
type: Population
allele count: 8
allele frequency: 9.328358208955224e-4
allele num: 8576
num of homozygotes: 0

Other
type: Population
allele count: 5
allele frequency: 5.617977528089887e-3
allele num: 890
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 22
allele frequency: 3.463476070528967e-3
allele num: 6352
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.42e0

MQRankSum
type: SiteQuality
SIO_000300: 7.000000000000001e-2

DP
type: SiteQuality
SIO_000300: 2.635074e6

BaseQRankSum
type: SiteQuality
SIO_000300: -5.521e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.299999999999999e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.607e0

QD
type: SiteQuality
SIO_000300: 1.27e0

FS
type: SiteQuality
SIO_000300: 2.71372e2

VQSLOD
type: SiteQuality
SIO_000300: -3.382e2

MQ
type: SiteQuality
SIO_000300: 5.939e1

GenotypeDepth
all individuals: 334
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1975
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variant carriers: 0

GenotypeDepth
all individuals: 1194
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variant carriers: 1

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 12
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variant carriers: 0

GenotypeQuality
all individuals: 1
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GenotypeQuality
all individuals: 34340
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variant carriers: 14

GenotypeQuality
all individuals: 2
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GenotypeQuality
all individuals: 3058
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 10
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GenotypeQuality
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GenotypeQuality
all individuals: 8
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GenotypeQuality
all individuals: 34
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variant carriers: 0

GenotypeQuality
all individuals: 6
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 18
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variant carriers: 0

GenotypeQuality
all individuals: 2177
bin: 8.75e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.51285930408472e-4
allele num: 6610
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.611687812379854e-5
allele num: 10404
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 12
allele frequency: 1.799154397433206e-4
allele num: 66698
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.0e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.96e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.0e-2

FS
type: SiteQuality
SIO_000300: 5.22e-1

MQ
type: SiteQuality
SIO_000300: 5.942e1

QD
type: SiteQuality
SIO_000300: 1.451e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

DP
type: SiteQuality
SIO_000300: 2.593418e6

VQSLOD
type: SiteQuality
SIO_000300: 2.58e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.93e0

GenotypeDepth
all individuals: 335
bin: 9.25e1
variant carriers: 2

GenotypeDepth
all individuals: 6604
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variant carriers: 0

GenotypeDepth
all individuals: 568
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GenotypeDepth
all individuals: 1974
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variant carriers: 0

GenotypeDepth
all individuals: 8225
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variant carriers: 0

GenotypeDepth
all individuals: 4
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GenotypeQuality
all individuals: 3125
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 0
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variant carriers: 0

GenotypeQuality
all individuals: 2
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GenotypeQuality
all individuals: 6
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variant carriers: 0

GenotypeQuality
all individuals: 4
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GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
all individuals: 6
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variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 3
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variant carriers: 0

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

GenotypeQuality
all individuals: 3326
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variant carriers: 0

GenotypeQuality
all individuals: 2175
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variant carriers: 0

GenotypeQuality
all individuals: 5
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variant carriers: 0

GenotypeQuality
all individuals: 34346
bin: 9.75e1
variant carriers: 12

GenotypeQuality
all individuals: 3
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variant carriers: 0

GenotypeQuality
all individuals: 1852
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variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2789
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 12
allele frequency: 1.153180857197771e-3
allele num: 10406
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66728
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 2.594542e6

MQ
type: SiteQuality
SIO_000300: 5.966e1

VQSLOD
type: SiteQuality
SIO_000300: 5.25e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.32e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.0e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 1.63e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

QD
type: SiteQuality
SIO_000300: 1.427e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.765e0

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

GenotypeDepth
all individuals: 6606
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variant carriers: 0

GenotypeDepth
all individuals: 795
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variant carriers: 0

GenotypeDepth
all individuals: 8152
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variant carriers: 0

GenotypeDepth
all individuals: 1974
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variant carriers: 0

GenotypeDepth
all individuals: 568
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variant carriers: 0

GenotypeQuality
all individuals: 3
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variant carriers: 0

GenotypeQuality
all individuals: 0
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variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 3128
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variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

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

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 10001
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variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 34342
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variant carriers: 1

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 2792
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GenotypeQuality
all individuals: 3069
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variant carriers: 0

GenotypeQuality
all individuals: 3
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variant carriers: 0

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
all individuals: 0
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variant carriers: 0

GenotypeQuality
all individuals: 3325
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variant carriers: 0

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
all individuals: 1859
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GenotypeQuality
all individuals: 2175
bin: 8.75e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66736
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.609840476648087e-5
allele num: 10406
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: -1.142e0

FS
type: SiteQuality
SIO_000300: 1.775e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

DP
type: SiteQuality
SIO_000300: 2.594e6

ClippingRankSum
type: SiteQuality
SIO_000300: 5.86e-1

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.268e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.965e0

MQ
type: SiteQuality
SIO_000300: 5.829e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.2e-2

GenotypeDepth
all individuals: 3198
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7210
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 796
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variant carriers: 0

GenotypeDepth
all individuals: 4789
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variant carriers: 0

GenotypeDepth
all individuals: 4
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variant carriers: 0

GenotypeDepth
all individuals: 373
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variant carriers: 0

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

GenotypeQuality
all individuals: 2175
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variant carriers: 0

GenotypeQuality
all individuals: 34342
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4
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variant carriers: 0

GenotypeQuality
all individuals: 2
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GenotypeQuality
all individuals: 0
bin: 7.5e0
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GenotypeQuality
all individuals: 3128
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GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 1858
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 3071
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GenotypeQuality
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GenotypeQuality
all individuals: 9999
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GenotypeQuality
all individuals: 3
bin: 5.25e1
variant carriers: 0

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

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

East Asian
type: Population
allele count: 1
allele frequency: 1.155535012710885e-4
allele num: 8654
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66738
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: 908
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.594023e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.25e-1

MQ
type: SiteQuality
SIO_000300: 5.986e1

BaseQRankSum
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SIO_000300: -6.063e0

FS
type: SiteQuality
SIO_000300: 2.303e0

QD
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SIO_000300: 1.186e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.44e-1

VQSLOD
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SIO_000300: 1.77e0

MQRankSum
type: SiteQuality
SIO_000300: -6.03e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

GenotypeDepth
all individuals: 3197
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variant carriers: 0

GenotypeDepth
all individuals: 1194
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variant carriers: 0

GenotypeDepth
all individuals: 6605
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GenotypeDepth
all individuals: 332
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GenotypeDepth
all individuals: 7800
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variant carriers: 0

GenotypeDepth
all individuals: 797
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variant carriers: 1

GenotypeQuality
all individuals: 3127
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 3

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 5.25e1
variant carriers: 0

South Asian
type: Population
allele count: 3
allele frequency: 1.816860465116279e-4
allele num: 16512
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66738
num of homozygotes: 0

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

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

VQSLOD
type: SiteQuality
SIO_000300: 6.25e-1

InbreedingCoeff
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 1.924e0

MQRankSum
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ReadPosRankSum
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ClippingRankSum
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SIO_000300: -1.051e0

DP
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 9.449999999999999e0

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
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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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variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.996793431028799e-5
allele num: 66738
num of homozygotes: 0

Other
type: Population
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

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

ClippingRankSum
type: SiteQuality
SIO_000300: 1.98e-1

FS
type: SiteQuality
SIO_000300: 2.395e0

ReadPosRankSum
type: SiteQuality
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InbreedingCoeff
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MQRankSum
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DP
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MQ
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VQSLOD
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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Other
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European (Finnish)
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Latino
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South Asian
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European (Non-Finnish)
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MQRankSum
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QD
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DP
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FS
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ClippingRankSum
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MQ
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VQSLOD
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InbreedingCoeff
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ReadPosRankSum
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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East Asian
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South Asian
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Other
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Latino
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European (Finnish)
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European (Non-Finnish)
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InbreedingCoeff
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VQSLOD
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MQ
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QD
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ReadPosRankSum
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FS
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MQRankSum
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DP
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BaseQRankSum
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ClippingRankSum
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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 (Finnish)
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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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African
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East Asian
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ClippingRankSum
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VQSLOD
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MQ
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ReadPosRankSum
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FS
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DP
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BaseQRankSum
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InbreedingCoeff
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MQRankSum
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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European (Non-Finnish)
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European (Finnish)
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East Asian
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African
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South Asian
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VQSLOD
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ClippingRankSum
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FS
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MQ
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DP
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BaseQRankSum
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ReadPosRankSum
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QD
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InbreedingCoeff
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MQRankSum
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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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African
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Latino
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European (Non-Finnish)
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MQ
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FS
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QD
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DP
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MQRankSum
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InbreedingCoeff
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ReadPosRankSum
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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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GenotypeQuality
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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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South Asian
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DP
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VQSLOD
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MQ
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MQRankSum
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InbreedingCoeff
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BaseQRankSum
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ReadPosRankSum
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ClippingRankSum
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FS
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QD
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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East Asian
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African
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European (Finnish)
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Latino
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South Asian
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ReadPosRankSum
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FS
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MQRankSum
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QD
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DP
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InbreedingCoeff
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VQSLOD
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MQ
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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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African
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Latino
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East Asian
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European (Non-Finnish)
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European (Finnish)
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DP
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VQSLOD
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FS
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QD
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InbreedingCoeff
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ReadPosRankSum
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MQ
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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 (Finnish)
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South Asian
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Latino
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African
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Other
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European (Non-Finnish)
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East Asian
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MQ
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InbreedingCoeff
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ReadPosRankSum
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ClippingRankSum
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VQSLOD
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FS
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MQRankSum
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QD
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DP
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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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Latino
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European (Non-Finnish)
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European (Finnish)
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VQSLOD
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MQ
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DP
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QD
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ClippingRankSum
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FS
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MQRankSum
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InbreedingCoeff
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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East Asian
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VQSLOD
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FS
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MQRankSum
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MQ
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DP
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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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MQ
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DP
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VQSLOD
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Latino
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African
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European (Finnish)
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South Asian
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European (Non-Finnish)
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FS
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DP
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VQSLOD
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ClippingRankSum
type: SiteQuality
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InbreedingCoeff
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MQRankSum
type: SiteQuality
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QD
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ReadPosRankSum
type: SiteQuality
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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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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 11578
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

African
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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: 6.056935190793458e-5
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num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 0.0e0
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Other
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FS
type: SiteQuality
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QD
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MQRankSum
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ReadPosRankSum
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InbreedingCoeff
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ClippingRankSum
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BaseQRankSum
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SIO_000300: -5.783e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 2.596064e6

VQSLOD
type: SiteQuality
SIO_000300: 6.42e-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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66724
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

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

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

South Asian
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FS
type: SiteQuality
SIO_000300: 2.212e0

BaseQRankSum
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SIO_000300: -2.455e0

QD
type: SiteQuality
SIO_000300: 1.475e1

DP
type: SiteQuality
SIO_000300: 2.596259e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.62e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.88e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.7e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.08e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.502e-1

GenotypeDepth
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variant carriers: 3

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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variant carriers: 0

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66728
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 num: 10406
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Other
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East Asian
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South Asian
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QD
type: SiteQuality
SIO_000300: 1.358e1

FS
type: SiteQuality
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MQRankSum
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MQ
type: SiteQuality
SIO_000300: 5.966e1

InbreedingCoeff
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SIO_000300: 1.4e-2

BaseQRankSum
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ReadPosRankSum
type: SiteQuality
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ClippingRankSum
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SIO_000300: 5.24e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.39e-1

DP
type: SiteQuality
SIO_000300: 2.596702e6

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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 count: 0
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num of homozygotes: 0

European (Non-Finnish)
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East Asian
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African
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European (Finnish)
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allele num: 6614
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Other
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Latino
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FS
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ReadPosRankSum
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ClippingRankSum
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BaseQRankSum
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QD
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VQSLOD
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MQRankSum
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InbreedingCoeff
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DP
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SIO_000300: 2.597574e6

MQ
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SIO_000300: 5.957e1

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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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 9

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 11

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

East Asian
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allele count: 0
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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

South Asian
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European (Finnish)
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allele num: 6614
num of homozygotes: 0

African
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European (Non-Finnish)
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Other
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DP
type: SiteQuality
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ClippingRankSum
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BaseQRankSum
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FS
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