16-71096285-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71096285
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 71096285
    reference: chr 16
allele count: 0
allele frequency: 0.0e0
allele num: 37432
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000394826
  ensembl transcript: ENST00000448691
  gene symbol: HYDIN
  hgvsc: ENST00000448691.1:c.2212-49T>C
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463767
  ensembl transcript: ENST00000393552
  gene symbol: HYDIN
  hgvsc: ENST00000393552.2:c.1066-49T>C
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000444970
  ensembl transcript: ENST00000538248
  gene symbol: HYDIN
  hgvsc: ENST00000538248.1:c.2293-49T>C
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000398544
  ensembl transcript: ENST00000448089
  gene symbol: HYDIN
  hgvsc: ENST00000448089.2:c.2212-49T>C
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463093
  ensembl transcript: ENST00000539447
  gene symbol: HYDIN
  hgvsc: ENST00000539447.1:c.*1460-49T>C
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463422
  ensembl transcript: ENST00000545230
  gene symbol: HYDIN
  hgvsc: ENST00000545230.1:c.*185-49T>C
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157423
  ensembl transcript: ENST00000540892
  gene symbol: HYDIN
  hgvsc: ENST00000540892.1:n.651T>C
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000437341
  ensembl transcript: ENST00000541601
  gene symbol: HYDIN
  hgvsc: ENST00000541601.1:c.2263-49T>C
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000377197
  ensembl transcript: ENST00000393567
  gene symbol: HYDIN
  hgvsc: ENST00000393567.2:c.2212-49T>C
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000314736
  ensembl transcript: ENST00000321489
  gene symbol: HYDIN
  hgvsc: ENST00000321489.5:c.2212-49T>C
  variant of: http://identifiers.org/hgnc/19368
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1155
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2587
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4301
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30974
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9914
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9724
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 914
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2646
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 129
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: A
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD

16-71096286-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71096286
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 71096286
    reference: chr 16
allele count: 0
allele frequency: 0.0e0
allele num: 36566
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463767
  ensembl transcript: ENST00000393552
  gene symbol: HYDIN
  hgvsc: ENST00000393552.2:c.1066-50A>G
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000394826
  ensembl transcript: ENST00000448691
  gene symbol: HYDIN
  hgvsc: ENST00000448691.1:c.2212-50A>G
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000377197
  ensembl transcript: ENST00000393567
  gene symbol: HYDIN
  hgvsc: ENST00000393567.2:c.2212-50A>G
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000398544
  ensembl transcript: ENST00000448089
  gene symbol: HYDIN
  hgvsc: ENST00000448089.2:c.2212-50A>G
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000444970
  ensembl transcript: ENST00000538248
  gene symbol: HYDIN
  hgvsc: ENST00000538248.1:c.2293-50A>G
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157423
  ensembl transcript: ENST00000540892
  gene symbol: HYDIN
  hgvsc: ENST00000540892.1:n.650A>G
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463422
  ensembl transcript: ENST00000545230
  gene symbol: HYDIN
  hgvsc: ENST00000545230.1:c.*185-50A>G
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000314736
  ensembl transcript: ENST00000321489
  gene symbol: HYDIN
  hgvsc: ENST00000321489.5:c.2212-50A>G
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000437341
  ensembl transcript: ENST00000541601
  gene symbol: HYDIN
  hgvsc: ENST00000541601.1:c.2263-50A>G
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463093
  ensembl transcript: ENST00000539447
  gene symbol: HYDIN
  hgvsc: ENST00000539447.1:c.*1460-50A>G
  variant of: http://identifiers.org/hgnc/19368
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4287
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2548
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1181
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9887
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30990
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9740
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11764
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 608
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1307
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: T
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

16-71098560-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71098560
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 71098560
    reference: chr 16
allele count: 1
allele frequency: 2.703579539310046e-5
allele num: 36988
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000377197
  ensembl transcript: ENST00000393567
  gene symbol: HYDIN
  hgvsc: ENST00000393567.2:c.2211+48T>C
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000437341
  ensembl transcript: ENST00000541601
  gene symbol: HYDIN
  hgvsc: ENST00000541601.1:c.2262+48T>C
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000314736
  ensembl transcript: ENST00000321489
  gene symbol: HYDIN
  hgvsc: ENST00000321489.5:c.2211+48T>C
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000398544
  ensembl transcript: ENST00000448089
  gene symbol: HYDIN
  hgvsc: ENST00000448089.2:c.2211+48T>C
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463767
  ensembl transcript: ENST00000393552
  gene symbol: HYDIN
  hgvsc: ENST00000393552.2:c.1065+48T>C
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463422
  ensembl transcript: ENST00000545230
  gene symbol: HYDIN
  hgvsc: ENST00000545230.1:c.*184+48T>C
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000444970
  ensembl transcript: ENST00000538248
  gene symbol: HYDIN
  hgvsc: ENST00000538248.1:c.2292+48T>C
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463093
  ensembl transcript: ENST00000539447
  gene symbol: HYDIN
  hgvsc: ENST00000539447.1:c.*1459+48T>C
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000394826
  ensembl transcript: ENST00000448691
  gene symbol: HYDIN
  hgvsc: ENST00000448691.1:c.2211+48T>C
  variant of: http://identifiers.org/hgnc/19368
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 28940
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1210
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12760
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3015
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12733
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1051
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2950
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9400
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16586
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD

16-71098562-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71098562
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 71098562
    reference: chr 16
allele count: 0
allele frequency: 0.0e0
allele num: 37056
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000377197
  ensembl transcript: ENST00000393567
  gene symbol: HYDIN
  hgvsc: ENST00000393567.2:c.2211+46G>A
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463093
  ensembl transcript: ENST00000539447
  gene symbol: HYDIN
  hgvsc: ENST00000539447.1:c.*1459+46G>A
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463767
  ensembl transcript: ENST00000393552
  gene symbol: HYDIN
  hgvsc: ENST00000393552.2:c.1065+46G>A
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000314736
  ensembl transcript: ENST00000321489
  gene symbol: HYDIN
  hgvsc: ENST00000321489.5:c.2211+46G>A
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000444970
  ensembl transcript: ENST00000538248
  gene symbol: HYDIN
  hgvsc: ENST00000538248.1:c.2292+46G>A
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000437341
  ensembl transcript: ENST00000541601
  gene symbol: HYDIN
  hgvsc: ENST00000541601.1:c.2262+46G>A
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000394826
  ensembl transcript: ENST00000448691
  gene symbol: HYDIN
  hgvsc: ENST00000448691.1:c.2211+46G>A
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463422
  ensembl transcript: ENST00000545230
  gene symbol: HYDIN
  hgvsc: ENST00000545230.1:c.*184+46G>A
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000398544
  ensembl transcript: ENST00000448089
  gene symbol: HYDIN
  hgvsc: ENST00000448089.2:c.2211+46G>A
  variant of: http://identifiers.org/hgnc/19368
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2840
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12775
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1391
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12678
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28975
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2937
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5925
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7705
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1309
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP

16-71098565-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71098565
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 71098565
    reference: chr 16
allele count: 0
allele frequency: 0.0e0
allele num: 37178
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000444970
  ensembl transcript: ENST00000538248
  gene symbol: HYDIN
  hgvsc: ENST00000538248.1:c.2292+43T>A
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000394826
  ensembl transcript: ENST00000448691
  gene symbol: HYDIN
  hgvsc: ENST00000448691.1:c.2211+43T>A
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000314736
  ensembl transcript: ENST00000321489
  gene symbol: HYDIN
  hgvsc: ENST00000321489.5:c.2211+43T>A
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000377197
  ensembl transcript: ENST00000393567
  gene symbol: HYDIN
  hgvsc: ENST00000393567.2:c.2211+43T>A
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463422
  ensembl transcript: ENST00000545230
  gene symbol: HYDIN
  hgvsc: ENST00000545230.1:c.*184+43T>A
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000437341
  ensembl transcript: ENST00000541601
  gene symbol: HYDIN
  hgvsc: ENST00000541601.1:c.2262+43T>A
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463093
  ensembl transcript: ENST00000539447
  gene symbol: HYDIN
  hgvsc: ENST00000539447.1:c.*1459+43T>A
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463767
  ensembl transcript: ENST00000393552
  gene symbol: HYDIN
  hgvsc: ENST00000393552.2:c.1065+43T>A
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000398544
  ensembl transcript: ENST00000448089
  gene symbol: HYDIN
  hgvsc: ENST00000448089.2:c.2211+43T>A
  variant of: http://identifiers.org/hgnc/19368
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12759
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29145
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12465
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1720
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2556
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7026
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5465
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 777
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: East Asian
population: Other
reference allele: A
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum

16-71098567-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71098567
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 71098567
    reference: chr 16
allele count: 5
allele frequency: 1.337613697164259e-4
allele num: 37380
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000314736
  ensembl transcript: ENST00000321489
  gene symbol: HYDIN
  hgvsc: ENST00000321489.5:c.2211+41A>G
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463093
  ensembl transcript: ENST00000539447
  gene symbol: HYDIN
  hgvsc: ENST00000539447.1:c.*1459+41A>G
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000394826
  ensembl transcript: ENST00000448691
  gene symbol: HYDIN
  hgvsc: ENST00000448691.1:c.2211+41A>G
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000377197
  ensembl transcript: ENST00000393567
  gene symbol: HYDIN
  hgvsc: ENST00000393567.2:c.2211+41A>G
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463767
  ensembl transcript: ENST00000393552
  gene symbol: HYDIN
  hgvsc: ENST00000393552.2:c.1065+41A>G
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463422
  ensembl transcript: ENST00000545230
  gene symbol: HYDIN
  hgvsc: ENST00000545230.1:c.*184+41A>G
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000437341
  ensembl transcript: ENST00000541601
  gene symbol: HYDIN
  hgvsc: ENST00000541601.1:c.2262+41A>G
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000398544
  ensembl transcript: ENST00000448089
  gene symbol: HYDIN
  hgvsc: ENST00000448089.2:c.2211+41A>G
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000444970
  ensembl transcript: ENST00000538248
  gene symbol: HYDIN
  hgvsc: ENST00000538248.1:c.2292+41A>G
  variant of: http://identifiers.org/hgnc/19368
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12734
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1954
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2401
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29319
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12241
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 777
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 102
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20424
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 123
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4475
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
population: South Asian
reference allele: T
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: FS

http://identifiers.org/exac.variant/16-71098574-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71098574
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 71098574
    reference: chr 16
allele count: 2
allele frequency: 5.18887505188875e-5
allele num: 38544
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463093
  ensembl transcript: ENST00000539447
  gene symbol: HYDIN
  hgvsc: ENST00000539447.1:c.*1459+34T>G
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463422
  ensembl transcript: ENST00000545230
  gene symbol: HYDIN
  hgvsc: ENST00000545230.1:c.*184+34T>G
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000377197
  ensembl transcript: ENST00000393567
  gene symbol: HYDIN
  hgvsc: ENST00000393567.2:c.2211+34T>G
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000437341
  ensembl transcript: ENST00000541601
  gene symbol: HYDIN
  hgvsc: ENST00000541601.1:c.2262+34T>G
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000314736
  ensembl transcript: ENST00000321489
  gene symbol: HYDIN
  hgvsc: ENST00000321489.5:c.2211+34T>G
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000394826
  ensembl transcript: ENST00000448691
  gene symbol: HYDIN
  hgvsc: ENST00000448691.1:c.2211+34T>G
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000398544
  ensembl transcript: ENST00000448089
  gene symbol: HYDIN
  hgvsc: ENST00000448089.2:c.2211+34T>G
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463767
  ensembl transcript: ENST00000393552
  gene symbol: HYDIN
  hgvsc: ENST00000393552.2:c.1065+34T>G
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000444970
  ensembl transcript: ENST00000538248
  gene symbol: HYDIN
  hgvsc: ENST00000538248.1:c.2292+34T>G
  variant of: http://identifiers.org/hgnc/19368
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30308
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1951
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10693
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12731
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2929
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 349
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8922
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 136
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4108
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: A
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD

16-71098576-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71098576
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 71098576
    reference: chr 16
allele count: 11
allele frequency: 2.782555904077709e-4
allele num: 39532
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000314736
  ensembl transcript: ENST00000321489
  gene symbol: HYDIN
  hgvsc: ENST00000321489.5:c.2211+32T>C
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000377197
  ensembl transcript: ENST00000393567
  gene symbol: HYDIN
  hgvsc: ENST00000393567.2:c.2211+32T>C
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000394826
  ensembl transcript: ENST00000448691
  gene symbol: HYDIN
  hgvsc: ENST00000448691.1:c.2211+32T>C
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463422
  ensembl transcript: ENST00000545230
  gene symbol: HYDIN
  hgvsc: ENST00000545230.1:c.*184+32T>C
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463767
  ensembl transcript: ENST00000393552
  gene symbol: HYDIN
  hgvsc: ENST00000393552.2:c.1065+32T>C
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000437341
  ensembl transcript: ENST00000541601
  gene symbol: HYDIN
  hgvsc: ENST00000541601.1:c.2262+32T>C
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000398544
  ensembl transcript: ENST00000448089
  gene symbol: HYDIN
  hgvsc: ENST00000448089.2:c.2211+32T>C
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463093
  ensembl transcript: ENST00000539447
  gene symbol: HYDIN
  hgvsc: ENST00000539447.1:c.*1459+32T>C
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000444970
  ensembl transcript: ENST00000538248
  gene symbol: HYDIN
  hgvsc: ENST00000538248.1:c.2292+32T>C
  variant of: http://identifiers.org/hgnc/19368
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 9082
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 684
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1565
  bin: 1.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 12600
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31514
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3877
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 329
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3842
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7961
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 398
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
reference allele: A
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP

http://identifiers.org/exac.variant/16-71098581-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71098581
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 71098581
    reference: chr 16
allele count: 5
allele frequency: 1.160900859066636e-4
allele num: 43070
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000314736
  ensembl transcript: ENST00000321489
  gene symbol: HYDIN
  hgvsc: ENST00000321489.5:c.2211+27T>G
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000377197
  ensembl transcript: ENST00000393567
  gene symbol: HYDIN
  hgvsc: ENST00000393567.2:c.2211+27T>G
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000437341
  ensembl transcript: ENST00000541601
  gene symbol: HYDIN
  hgvsc: ENST00000541601.1:c.2262+27T>G
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000398544
  ensembl transcript: ENST00000448089
  gene symbol: HYDIN
  hgvsc: ENST00000448089.2:c.2211+27T>G
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463767
  ensembl transcript: ENST00000393552
  gene symbol: HYDIN
  hgvsc: ENST00000393552.2:c.1065+27T>G
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000444970
  ensembl transcript: ENST00000538248
  gene symbol: HYDIN
  hgvsc: ENST00000538248.1:c.2292+27T>G
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000394826
  ensembl transcript: ENST00000448691
  gene symbol: HYDIN
  hgvsc: ENST00000448691.1:c.2211+27T>G
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463422
  ensembl transcript: ENST00000545230
  gene symbol: HYDIN
  hgvsc: ENST00000545230.1:c.*184+27T>G
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463093
  ensembl transcript: ENST00000539447
  gene symbol: HYDIN
  hgvsc: ENST00000539447.1:c.*1459+27T>G
  variant of: http://identifiers.org/hgnc/19368
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 5060
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10617
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33872
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8068
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 919
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 877
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 275
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 138
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 800
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4310
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
population: Other
reference allele: A
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD

16-71098582-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71098582
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 71098582
    reference: chr 16
allele count: 1
allele frequency: 2.256114069127335e-5
allele num: 44324
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000437341
  ensembl transcript: ENST00000541601
  gene symbol: HYDIN
  hgvsc: ENST00000541601.1:c.2262+26A>G
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000394826
  ensembl transcript: ENST00000448691
  gene symbol: HYDIN
  hgvsc: ENST00000448691.1:c.2211+26A>G
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463093
  ensembl transcript: ENST00000539447
  gene symbol: HYDIN
  hgvsc: ENST00000539447.1:c.*1459+26A>G
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000377197
  ensembl transcript: ENST00000393567
  gene symbol: HYDIN
  hgvsc: ENST00000393567.2:c.2211+26A>G
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463767
  ensembl transcript: ENST00000393552
  gene symbol: HYDIN
  hgvsc: ENST00000393552.2:c.1065+26A>G
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000398544
  ensembl transcript: ENST00000448089
  gene symbol: HYDIN
  hgvsc: ENST00000448089.2:c.2211+26A>G
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000314736
  ensembl transcript: ENST00000321489
  gene symbol: HYDIN
  hgvsc: ENST00000321489.5:c.2211+26A>G
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000444970
  ensembl transcript: ENST00000538248
  gene symbol: HYDIN
  hgvsc: ENST00000538248.1:c.2292+26A>G
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463422
  ensembl transcript: ENST00000545230
  gene symbol: HYDIN
  hgvsc: ENST00000545230.1:c.*184+26A>G
  variant of: http://identifiers.org/hgnc/19368
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 975
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9826
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9535
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34011
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4320
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 138
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1249
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 247
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
population: Other
reference allele: T
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum

16-71098594-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71098594
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 71098594
    reference: chr 16
allele count: 1
allele frequency: 1.296109080540218e-5
allele num: 77154
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000437341
  ensembl transcript: ENST00000541601
  gene symbol: HYDIN
  hgvsc: ENST00000541601.1:c.2262+14T>C
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000444970
  ensembl transcript: ENST00000538248
  gene symbol: HYDIN
  hgvsc: ENST00000538248.1:c.2292+14T>C
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463093
  ensembl transcript: ENST00000539447
  gene symbol: HYDIN
  hgvsc: ENST00000539447.1:c.*1459+14T>C
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000394826
  ensembl transcript: ENST00000448691
  gene symbol: HYDIN
  hgvsc: ENST00000448691.1:c.2211+14T>C
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463422
  ensembl transcript: ENST00000545230
  gene symbol: HYDIN
  hgvsc: ENST00000545230.1:c.*184+14T>C
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000314736
  ensembl transcript: ENST00000321489
  gene symbol: HYDIN
  hgvsc: ENST00000321489.5:c.2211+14T>C
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463767
  ensembl transcript: ENST00000393552
  gene symbol: HYDIN
  hgvsc: ENST00000393552.2:c.1065+14T>C
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000377197
  ensembl transcript: ENST00000393567
  gene symbol: HYDIN
  hgvsc: ENST00000393567.2:c.2211+14T>C
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000398544
  ensembl transcript: ENST00000448089
  gene symbol: HYDIN
  hgvsc: ENST00000448089.2:c.2211+14T>C
  variant of: http://identifiers.org/hgnc/19368
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2402
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3572
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30596
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 809
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21342
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 327
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 201
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: East Asian
reference allele: A
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum

16-71098605-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71098605
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 71098605
    reference: chr 16
allele count: 29
allele frequency: 2.849786757335744e-4
allele num: 101762
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000398544
  ensembl transcript: ENST00000448089
  gene symbol: HYDIN
  hgvsc: ENST00000448089.2:c.2211+3G>A
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463422
  ensembl transcript: ENST00000545230
  gene symbol: HYDIN
  hgvsc: ENST00000545230.1:c.*184+3G>A
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000314736
  ensembl transcript: ENST00000321489
  gene symbol: HYDIN
  hgvsc: ENST00000321489.5:c.2211+3G>A
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000437341
  ensembl transcript: ENST00000541601
  gene symbol: HYDIN
  hgvsc: ENST00000541601.1:c.2262+3G>A
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000394826
  ensembl transcript: ENST00000448691
  gene symbol: HYDIN
  hgvsc: ENST00000448691.1:c.2211+3G>A
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463767
  ensembl transcript: ENST00000393552
  gene symbol: HYDIN
  hgvsc: ENST00000393552.2:c.1065+3G>A
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463093
  ensembl transcript: ENST00000539447
  gene symbol: HYDIN
  hgvsc: ENST00000539447.1:c.*1459+3G>A
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000377197
  ensembl transcript: ENST00000393567
  gene symbol: HYDIN
  hgvsc: ENST00000393567.2:c.2211+3G>A
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000444970
  ensembl transcript: ENST00000538248
  gene symbol: HYDIN
  hgvsc: ENST00000538248.1:c.2292+3G>A
  variant of: http://identifiers.org/hgnc/19368
canonical: true
consequence: splice region
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 4.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 43045
  bin: 2.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 9599
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 4285
  bin: 2.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 436
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 817
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1423
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 44314
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 239
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 1.75e1
  variant carriers: 0
hgvs: c.2211+3G>A
num of homozygotes: 0
population: East Asian
population: Other
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ

16-71098612-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71098612
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 71098612
    reference: chr 16
allele count: 1
allele frequency: 9.059612248595761e-6
allele num: 110380
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000398544
  ensembl transcript: ENST00000448089
  gene symbol: HYDIN
  hgvsc: ENST00000448089.2:c.2207C>T
  hgvsp: ENSP00000398544.2:p.Pro736Leu
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463767
  ensembl transcript: ENST00000393552
  gene symbol: HYDIN
  hgvsc: ENST00000393552.2:c.1061C>T
  hgvsp: ENSP00000463767.1:p.Pro354Leu
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463093
  ensembl transcript: ENST00000539447
  gene symbol: HYDIN
  hgvsc: ENST00000539447.1:c.*1455C>T
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000394826
  ensembl transcript: ENST00000448691
  gene symbol: HYDIN
  hgvsc: ENST00000448691.1:c.2207C>T
  hgvsp: ENSP00000394826.1:p.Pro736Leu
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000314736
  ensembl transcript: ENST00000321489
  gene symbol: HYDIN
  hgvsc: ENST00000321489.5:c.2207C>T
  hgvsp: ENSP00000314736.5:p.Pro736Leu
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463422
  ensembl transcript: ENST00000545230
  gene symbol: HYDIN
  hgvsc: ENST00000545230.1:c.*180C>T
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000377197
  ensembl transcript: ENST00000393567
  gene symbol: HYDIN
  hgvsc: ENST00000393567.2:c.2207C>T
  hgvsp: ENSP00000377197.2:p.Pro736Leu
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000437341
  ensembl transcript: ENST00000541601
  gene symbol: HYDIN
  hgvsc: ENST00000541601.1:c.2258C>T
  hgvsp: ENSP00000437341.1:p.Pro753Leu
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000444970
  ensembl transcript: ENST00000538248
  gene symbol: HYDIN
  hgvsc: ENST00000538248.1:c.2288C>T
  hgvsp: ENSP00000444970.1:p.Pro763Leu
  variant of: http://identifiers.org/hgnc/19368
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5420
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46876
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5432
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 976
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 188
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Pro736Leu
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: Latino
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff

16-71098613-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71098613
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 71098613
    reference: chr 16
allele count: 1
allele frequency: 8.991673710144407e-6
allele num: 111214
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000437341
  ensembl transcript: ENST00000541601
  gene symbol: HYDIN
  hgvsc: ENST00000541601.1:c.2257C>T
  hgvsp: ENSP00000437341.1:p.Pro753Ser
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000314736
  ensembl transcript: ENST00000321489
  gene symbol: HYDIN
  hgvsc: ENST00000321489.5:c.2206C>T
  hgvsp: ENSP00000314736.5:p.Pro736Ser
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000398544
  ensembl transcript: ENST00000448089
  gene symbol: HYDIN
  hgvsc: ENST00000448089.2:c.2206C>T
  hgvsp: ENSP00000398544.2:p.Pro736Ser
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463093
  ensembl transcript: ENST00000539447
  gene symbol: HYDIN
  hgvsc: ENST00000539447.1:c.*1454C>T
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463422
  ensembl transcript: ENST00000545230
  gene symbol: HYDIN
  hgvsc: ENST00000545230.1:c.*179C>T
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000394826
  ensembl transcript: ENST00000448691
  gene symbol: HYDIN
  hgvsc: ENST00000448691.1:c.2206C>T
  hgvsp: ENSP00000394826.1:p.Pro736Ser
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000444970
  ensembl transcript: ENST00000538248
  gene symbol: HYDIN
  hgvsc: ENST00000538248.1:c.2287C>T
  hgvsp: ENSP00000444970.1:p.Pro763Ser
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463767
  ensembl transcript: ENST00000393552
  gene symbol: HYDIN
  hgvsc: ENST00000393552.2:c.1060C>T
  hgvsp: ENSP00000463767.1:p.Pro354Ser
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000377197
  ensembl transcript: ENST00000393567
  gene symbol: HYDIN
  hgvsc: ENST00000393567.2:c.2206C>T
  hgvsp: ENSP00000377197.2:p.Pro736Ser
  variant of: http://identifiers.org/hgnc/19368
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5573
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1016
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5001
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 47172
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5089
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 239
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 219
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Pro736Ser
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Other
population: African
population: South Asian
population: Latino
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: MQ

16-71098618-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71098618
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 71098618
    reference: chr 16
allele count: 1
allele frequency: 8.738508860847985e-6
allele num: 114436
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463093
  ensembl transcript: ENST00000539447
  gene symbol: HYDIN
  hgvsc: ENST00000539447.1:c.*1449T>C
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463767
  ensembl transcript: ENST00000393552
  gene symbol: HYDIN
  hgvsc: ENST00000393552.2:c.1055T>C
  hgvsp: ENSP00000463767.1:p.Val352Ala
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000444970
  ensembl transcript: ENST00000538248
  gene symbol: HYDIN
  hgvsc: ENST00000538248.1:c.2282T>C
  hgvsp: ENSP00000444970.1:p.Val761Ala
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463422
  ensembl transcript: ENST00000545230
  gene symbol: HYDIN
  hgvsc: ENST00000545230.1:c.*174T>C
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000314736
  ensembl transcript: ENST00000321489
  gene symbol: HYDIN
  hgvsc: ENST00000321489.5:c.2201T>C
  hgvsp: ENSP00000314736.5:p.Val734Ala
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000437341
  ensembl transcript: ENST00000541601
  gene symbol: HYDIN
  hgvsc: ENST00000541601.1:c.2252T>C
  hgvsp: ENSP00000437341.1:p.Val751Ala
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000398544
  ensembl transcript: ENST00000448089
  gene symbol: HYDIN
  hgvsc: ENST00000448089.2:c.2201T>C
  hgvsp: ENSP00000398544.2:p.Val734Ala
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000377197
  ensembl transcript: ENST00000393567
  gene symbol: HYDIN
  hgvsc: ENST00000393567.2:c.2201T>C
  hgvsp: ENSP00000377197.2:p.Val734Ala
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000394826
  ensembl transcript: ENST00000448691
  gene symbol: HYDIN
  hgvsc: ENST00000448691.1:c.2201T>C
  hgvsp: ENSP00000394826.1:p.Val734Ala
  variant of: http://identifiers.org/hgnc/19368
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6149
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48330
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1085
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3425
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 146
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 173
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Val734Ala
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Other
reference allele: A
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/16-71098628-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71098628
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 71098628
    reference: chr 16
allele count: 1
allele frequency: 8.514406375587495e-6
allele num: 117448
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000394826
  ensembl transcript: ENST00000448691
  gene symbol: HYDIN
  hgvsc: ENST00000448691.1:c.2191T>G
  hgvsp: ENSP00000394826.1:p.Phe731Val
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000377197
  ensembl transcript: ENST00000393567
  gene symbol: HYDIN
  hgvsc: ENST00000393567.2:c.2191T>G
  hgvsp: ENSP00000377197.2:p.Phe731Val
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000437341
  ensembl transcript: ENST00000541601
  gene symbol: HYDIN
  hgvsc: ENST00000541601.1:c.2242T>G
  hgvsp: ENSP00000437341.1:p.Phe748Val
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463767
  ensembl transcript: ENST00000393552
  gene symbol: HYDIN
  hgvsc: ENST00000393552.2:c.1045T>G
  hgvsp: ENSP00000463767.1:p.Phe349Val
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000444970
  ensembl transcript: ENST00000538248
  gene symbol: HYDIN
  hgvsc: ENST00000538248.1:c.2272T>G
  hgvsp: ENSP00000444970.1:p.Phe758Val
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463093
  ensembl transcript: ENST00000539447
  gene symbol: HYDIN
  hgvsc: ENST00000539447.1:c.*1439T>G
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000398544
  ensembl transcript: ENST00000448089
  gene symbol: HYDIN
  hgvsc: ENST00000448089.2:c.2191T>G
  hgvsp: ENSP00000398544.2:p.Phe731Val
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463422
  ensembl transcript: ENST00000545230
  gene symbol: HYDIN
  hgvsc: ENST00000545230.1:c.*164T>G
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000314736
  ensembl transcript: ENST00000321489
  gene symbol: HYDIN
  hgvsc: ENST00000321489.5:c.2191T>G
  hgvsp: ENSP00000314736.5:p.Phe731Val
  variant of: http://identifiers.org/hgnc/19368
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 49391
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1161
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1954
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6794
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 99
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 91
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Phe731Val
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
population: Other
reference allele: A
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff

16-71098628-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71098628
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 71098628
    reference: chr 16
allele count: 2
allele frequency: 1.702881275117499e-5
allele num: 117448
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463422
  ensembl transcript: ENST00000545230
  gene symbol: HYDIN
  hgvsc: ENST00000545230.1:c.*164T>C
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000437341
  ensembl transcript: ENST00000541601
  gene symbol: HYDIN
  hgvsc: ENST00000541601.1:c.2242T>C
  hgvsp: ENSP00000437341.1:p.Phe748Leu
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000377197
  ensembl transcript: ENST00000393567
  gene symbol: HYDIN
  hgvsc: ENST00000393567.2:c.2191T>C
  hgvsp: ENSP00000377197.2:p.Phe731Leu
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463093
  ensembl transcript: ENST00000539447
  gene symbol: HYDIN
  hgvsc: ENST00000539447.1:c.*1439T>C
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000314736
  ensembl transcript: ENST00000321489
  gene symbol: HYDIN
  hgvsc: ENST00000321489.5:c.2191T>C
  hgvsp: ENSP00000314736.5:p.Phe731Leu
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000398544
  ensembl transcript: ENST00000448089
  gene symbol: HYDIN
  hgvsc: ENST00000448089.2:c.2191T>C
  hgvsp: ENSP00000398544.2:p.Phe731Leu
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000394826
  ensembl transcript: ENST00000448691
  gene symbol: HYDIN
  hgvsc: ENST00000448691.1:c.2191T>C
  hgvsp: ENSP00000394826.1:p.Phe731Leu
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000444970
  ensembl transcript: ENST00000538248
  gene symbol: HYDIN
  hgvsc: ENST00000538248.1:c.2272T>C
  hgvsp: ENSP00000444970.1:p.Phe758Leu
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463767
  ensembl transcript: ENST00000393552
  gene symbol: HYDIN
  hgvsc: ENST00000393552.2:c.1045T>C
  hgvsp: ENSP00000463767.1:p.Phe349Leu
  variant of: http://identifiers.org/hgnc/19368
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 1161
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 49391
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6794
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1954
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 91
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2008
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Phe731Leu
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
population: Other
reference allele: A
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum

http://identifiers.org/exac.variant/16-71098630-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71098630
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 71098630
    reference: chr 16
allele count: 1
allele frequency: 8.492424757116652e-6
allele num: 117752
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000437341
  ensembl transcript: ENST00000541601
  gene symbol: HYDIN
  hgvsc: ENST00000541601.1:c.2240G>T
  hgvsp: ENSP00000437341.1:p.Gly747Val
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463767
  ensembl transcript: ENST00000393552
  gene symbol: HYDIN
  hgvsc: ENST00000393552.2:c.1043G>T
  hgvsp: ENSP00000463767.1:p.Gly348Val
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000314736
  ensembl transcript: ENST00000321489
  gene symbol: HYDIN
  hgvsc: ENST00000321489.5:c.2189G>T
  hgvsp: ENSP00000314736.5:p.Gly730Val
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000394826
  ensembl transcript: ENST00000448691
  gene symbol: HYDIN
  hgvsc: ENST00000448691.1:c.2189G>T
  hgvsp: ENSP00000394826.1:p.Gly730Val
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463422
  ensembl transcript: ENST00000545230
  gene symbol: HYDIN
  hgvsc: ENST00000545230.1:c.*162G>T
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000444970
  ensembl transcript: ENST00000538248
  gene symbol: HYDIN
  hgvsc: ENST00000538248.1:c.2270G>T
  hgvsp: ENSP00000444970.1:p.Gly757Val
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000398544
  ensembl transcript: ENST00000448089
  gene symbol: HYDIN
  hgvsc: ENST00000448089.2:c.2189G>T
  hgvsp: ENSP00000398544.2:p.Gly730Val
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000377197
  ensembl transcript: ENST00000393567
  gene symbol: HYDIN
  hgvsc: ENST00000393567.2:c.2189G>T
  hgvsp: ENSP00000377197.2:p.Gly730Val
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463093
  ensembl transcript: ENST00000539447
  gene symbol: HYDIN
  hgvsc: ENST00000539447.1:c.*1437G>T
  variant of: http://identifiers.org/hgnc/19368
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1179
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49471
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6880
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1800
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Gly730Val
num of homozygotes: 0
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
reference allele: C
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum

16-71098631-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71098631
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 71098631
    reference: chr 16
allele count: 1
allele frequency: 8.481764206955047e-6
allele num: 117900
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000398544
  ensembl transcript: ENST00000448089
  gene symbol: HYDIN
  hgvsc: ENST00000448089.2:c.2188G>A
  hgvsp: ENSP00000398544.2:p.Gly730Arg
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000314736
  ensembl transcript: ENST00000321489
  gene symbol: HYDIN
  hgvsc: ENST00000321489.5:c.2188G>A
  hgvsp: ENSP00000314736.5:p.Gly730Arg
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463093
  ensembl transcript: ENST00000539447
  gene symbol: HYDIN
  hgvsc: ENST00000539447.1:c.*1436G>A
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000377197
  ensembl transcript: ENST00000393567
  gene symbol: HYDIN
  hgvsc: ENST00000393567.2:c.2188G>A
  hgvsp: ENSP00000377197.2:p.Gly730Arg
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000394826
  ensembl transcript: ENST00000448691
  gene symbol: HYDIN
  hgvsc: ENST00000448691.1:c.2188G>A
  hgvsp: ENSP00000394826.1:p.Gly730Arg
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000444970
  ensembl transcript: ENST00000538248
  gene symbol: HYDIN
  hgvsc: ENST00000538248.1:c.2269G>A
  hgvsp: ENSP00000444970.1:p.Gly757Arg
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463422
  ensembl transcript: ENST00000545230
  gene symbol: HYDIN
  hgvsc: ENST00000545230.1:c.*161G>A
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463767
  ensembl transcript: ENST00000393552
  gene symbol: HYDIN
  hgvsc: ENST00000393552.2:c.1042G>A
  hgvsp: ENSP00000463767.1:p.Gly348Arg
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000437341
  ensembl transcript: ENST00000541601
  gene symbol: HYDIN
  hgvsc: ENST00000541601.1:c.2239G>A
  hgvsp: ENSP00000437341.1:p.Gly747Arg
  variant of: http://identifiers.org/hgnc/19368
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1722
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49499
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1201
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6935
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 118
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53436
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Gly730Arg
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: African
population: South Asian
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum

16-71098632-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71098632
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 71098632
    reference: chr 16
allele count: 1
allele frequency: 8.465966813410092e-6
allele num: 118120
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000437341
  ensembl transcript: ENST00000541601
  gene symbol: HYDIN
  hgvsc: ENST00000541601.1:c.2238A>G
  hgvsp: ENST00000541601.1:c.2238A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000314736
  ensembl transcript: ENST00000321489
  gene symbol: HYDIN
  hgvsc: ENST00000321489.5:c.2187A>G
  hgvsp: ENST00000321489.5:c.2187A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000444970
  ensembl transcript: ENST00000538248
  gene symbol: HYDIN
  hgvsc: ENST00000538248.1:c.2268A>G
  hgvsp: ENST00000538248.1:c.2268A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463767
  ensembl transcript: ENST00000393552
  gene symbol: HYDIN
  hgvsc: ENST00000393552.2:c.1041A>G
  hgvsp: ENST00000393552.2:c.1041A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463422
  ensembl transcript: ENST00000545230
  gene symbol: HYDIN
  hgvsc: ENST00000545230.1:c.*160A>G
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463093
  ensembl transcript: ENST00000539447
  gene symbol: HYDIN
  hgvsc: ENST00000539447.1:c.*1435A>G
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000394826
  ensembl transcript: ENST00000448691
  gene symbol: HYDIN
  hgvsc: ENST00000448691.1:c.2187A>G
  hgvsp: ENST00000448691.1:c.2187A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000398544
  ensembl transcript: ENST00000448089
  gene symbol: HYDIN
  hgvsc: ENST00000448089.2:c.2187A>G
  hgvsp: ENST00000448089.2:c.2187A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000377197
  ensembl transcript: ENST00000393567
  gene symbol: HYDIN
  hgvsc: ENST00000393567.2:c.2187A>G
  hgvsp: ENST00000393567.2:c.2187A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/19368
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1614
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49583
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1196
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6983
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 203
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 440
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53573
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Pro729Pro
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
population: Latino
reference allele: T
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP

16-71098642-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71098642
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 71098642
    reference: chr 16
allele count: 328
allele frequency: 2.748219522413071e-3
allele num: 119350
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463767
  ensembl transcript: ENST00000393552
  gene symbol: HYDIN
  hgvsc: ENST00000393552.2:c.1031A>G
  hgvsp: ENSP00000463767.1:p.Asp344Gly
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463093
  ensembl transcript: ENST00000539447
  gene symbol: HYDIN
  hgvsc: ENST00000539447.1:c.*1425A>G
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463422
  ensembl transcript: ENST00000545230
  gene symbol: HYDIN
  hgvsc: ENST00000545230.1:c.*150A>G
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000314736
  ensembl transcript: ENST00000321489
  gene symbol: HYDIN
  hgvsc: ENST00000321489.5:c.2177A>G
  hgvsp: ENSP00000314736.5:p.Asp726Gly
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000398544
  ensembl transcript: ENST00000448089
  gene symbol: HYDIN
  hgvsc: ENST00000448089.2:c.2177A>G
  hgvsp: ENSP00000398544.2:p.Asp726Gly
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000437341
  ensembl transcript: ENST00000541601
  gene symbol: HYDIN
  hgvsc: ENST00000541601.1:c.2228A>G
  hgvsp: ENSP00000437341.1:p.Asp743Gly
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000394826
  ensembl transcript: ENST00000448691
  gene symbol: HYDIN
  hgvsc: ENST00000448691.1:c.2177A>G
  hgvsp: ENSP00000394826.1:p.Asp726Gly
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000444970
  ensembl transcript: ENST00000538248
  gene symbol: HYDIN
  hgvsc: ENST00000538248.1:c.2258A>G
  hgvsp: ENSP00000444970.1:p.Asp753Gly
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000377197
  ensembl transcript: ENST00000393567
  gene symbol: HYDIN
  hgvsc: ENST00000393567.2:c.2177A>G
  hgvsp: ENSP00000377197.2:p.Asp726Gly
  variant of: http://identifiers.org/hgnc/19368
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1240
  bin: 3.25e1
  variant carriers: 32
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 6.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 1014
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7385
  bin: 2.75e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 49560
  bin: 2.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 5.75e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 1.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 3.75e1
  variant carriers: 50
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 4.75e1
  variant carriers: 46
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 5.25e1
  variant carriers: 48
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 4.25e1
  variant carriers: 45
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 6.25e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.25e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Asp726Gly
num of homozygotes: 1
population: Other
population: African
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum

16-71098643-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71098643
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 71098643
    reference: chr 16
allele count: 3
allele frequency: 2.512689079853259e-5
allele num: 119394
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463767
  ensembl transcript: ENST00000393552
  gene symbol: HYDIN
  hgvsc: ENST00000393552.2:c.1030G>C
  hgvsp: ENSP00000463767.1:p.Asp344His
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463093
  ensembl transcript: ENST00000539447
  gene symbol: HYDIN
  hgvsc: ENST00000539447.1:c.*1424G>C
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000398544
  ensembl transcript: ENST00000448089
  gene symbol: HYDIN
  hgvsc: ENST00000448089.2:c.2176G>C
  hgvsp: ENSP00000398544.2:p.Asp726His
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000444970
  ensembl transcript: ENST00000538248
  gene symbol: HYDIN
  hgvsc: ENST00000538248.1:c.2257G>C
  hgvsp: ENSP00000444970.1:p.Asp753His
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463422
  ensembl transcript: ENST00000545230
  gene symbol: HYDIN
  hgvsc: ENST00000545230.1:c.*149G>C
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000377197
  ensembl transcript: ENST00000393567
  gene symbol: HYDIN
  hgvsc: ENST00000393567.2:c.2176G>C
  hgvsp: ENSP00000377197.2:p.Asp726His
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000394826
  ensembl transcript: ENST00000448691
  gene symbol: HYDIN
  hgvsc: ENST00000448691.1:c.2176G>C
  hgvsp: ENSP00000394826.1:p.Asp726His
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000314736
  ensembl transcript: ENST00000321489
  gene symbol: HYDIN
  hgvsc: ENST00000321489.5:c.2176G>C
  hgvsp: ENSP00000314736.5:p.Asp726His
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000437341
  ensembl transcript: ENST00000541601
  gene symbol: HYDIN
  hgvsc: ENST00000541601.1:c.2227G>C
  hgvsp: ENSP00000437341.1:p.Asp743His
  variant of: http://identifiers.org/hgnc/19368
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 988
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7585
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49568
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1283
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 357
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 103
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Asp726His
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD

16-71098644-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71098644
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 71098644
    reference: chr 16
allele count: 4
allele frequency: 3.348961821835231e-5
allele num: 119440
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000437341
  ensembl transcript: ENST00000541601
  gene symbol: HYDIN
  hgvsc: ENST00000541601.1:c.2226A>G
  hgvsp: ENST00000541601.1:c.2226A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000444970
  ensembl transcript: ENST00000538248
  gene symbol: HYDIN
  hgvsc: ENST00000538248.1:c.2256A>G
  hgvsp: ENST00000538248.1:c.2256A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000314736
  ensembl transcript: ENST00000321489
  gene symbol: HYDIN
  hgvsc: ENST00000321489.5:c.2175A>G
  hgvsp: ENST00000321489.5:c.2175A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000398544
  ensembl transcript: ENST00000448089
  gene symbol: HYDIN
  hgvsc: ENST00000448089.2:c.2175A>G
  hgvsp: ENST00000448089.2:c.2175A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000394826
  ensembl transcript: ENST00000448691
  gene symbol: HYDIN
  hgvsc: ENST00000448691.1:c.2175A>G
  hgvsp: ENST00000448691.1:c.2175A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463093
  ensembl transcript: ENST00000539447
  gene symbol: HYDIN
  hgvsc: ENST00000539447.1:c.*1423A>G
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000377197
  ensembl transcript: ENST00000393567
  gene symbol: HYDIN
  hgvsc: ENST00000393567.2:c.2175A>G
  hgvsp: ENST00000393567.2:c.2175A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463767
  ensembl transcript: ENST00000393552
  gene symbol: HYDIN
  hgvsc: ENST00000393552.2:c.1029A>G
  hgvsp: ENST00000393552.2:c.1029A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463422
  ensembl transcript: ENST00000545230
  gene symbol: HYDIN
  hgvsc: ENST00000545230.1:c.*148A>G
  variant of: http://identifiers.org/hgnc/19368
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1266
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 970
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7623
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49556
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1092
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Gln725Gln
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: East Asian
population: South Asian
population: Latino
population: African
reference allele: T
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD

16-71098650-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71098650
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 71098650
    reference: chr 16
allele count: 1
allele frequency: 8.378437253883405e-6
allele num: 119354
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000444970
  ensembl transcript: ENST00000538248
  gene symbol: HYDIN
  hgvsc: ENST00000538248.1:c.2250C>T
  hgvsp: ENST00000538248.1:c.2250C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000398544
  ensembl transcript: ENST00000448089
  gene symbol: HYDIN
  hgvsc: ENST00000448089.2:c.2169C>T
  hgvsp: ENST00000448089.2:c.2169C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463422
  ensembl transcript: ENST00000545230
  gene symbol: HYDIN
  hgvsc: ENST00000545230.1:c.*142C>T
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000377197
  ensembl transcript: ENST00000393567
  gene symbol: HYDIN
  hgvsc: ENST00000393567.2:c.2169C>T
  hgvsp: ENST00000393567.2:c.2169C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463767
  ensembl transcript: ENST00000393552
  gene symbol: HYDIN
  hgvsc: ENST00000393552.2:c.1023C>T
  hgvsp: ENST00000393552.2:c.1023C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000437341
  ensembl transcript: ENST00000541601
  gene symbol: HYDIN
  hgvsc: ENST00000541601.1:c.2220C>T
  hgvsp: ENST00000541601.1:c.2220C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000394826
  ensembl transcript: ENST00000448691
  gene symbol: HYDIN
  hgvsc: ENST00000448691.1:c.2169C>T
  hgvsp: ENST00000448691.1:c.2169C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000314736
  ensembl transcript: ENST00000321489
  gene symbol: HYDIN
  hgvsc: ENST00000321489.5:c.2169C>T
  hgvsp: ENST00000321489.5:c.2169C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463093
  ensembl transcript: ENST00000539447
  gene symbol: HYDIN
  hgvsc: ENST00000539447.1:c.*1417C>T
  variant of: http://identifiers.org/hgnc/19368
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 1005
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1288
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49037
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7746
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53932
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Ala723Ala
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD

16-71098659-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71098659
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 71098659
    reference: chr 16
allele count: 1
allele frequency: 8.425025696328374e-6
allele num: 118694
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000377197
  ensembl transcript: ENST00000393567
  gene symbol: HYDIN
  hgvsc: ENST00000393567.2:c.2160C>G
  hgvsp: ENST00000393567.2:c.2160C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000444970
  ensembl transcript: ENST00000538248
  gene symbol: HYDIN
  hgvsc: ENST00000538248.1:c.2241C>G
  hgvsp: ENST00000538248.1:c.2241C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000314736
  ensembl transcript: ENST00000321489
  gene symbol: HYDIN
  hgvsc: ENST00000321489.5:c.2160C>G
  hgvsp: ENST00000321489.5:c.2160C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000398544
  ensembl transcript: ENST00000448089
  gene symbol: HYDIN
  hgvsc: ENST00000448089.2:c.2160C>G
  hgvsp: ENST00000448089.2:c.2160C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463422
  ensembl transcript: ENST00000545230
  gene symbol: HYDIN
  hgvsc: ENST00000545230.1:c.*133C>G
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463767
  ensembl transcript: ENST00000393552
  gene symbol: HYDIN
  hgvsc: ENST00000393552.2:c.1014C>G
  hgvsp: ENST00000393552.2:c.1014C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000437341
  ensembl transcript: ENST00000541601
  gene symbol: HYDIN
  hgvsc: ENST00000541601.1:c.2211C>G
  hgvsp: ENST00000541601.1:c.2211C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463093
  ensembl transcript: ENST00000539447
  gene symbol: HYDIN
  hgvsc: ENST00000539447.1:c.*1408C>G
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000394826
  ensembl transcript: ENST00000448691
  gene symbol: HYDIN
  hgvsc: ENST00000448691.1:c.2160C>G
  hgvsp: ENST00000448691.1:c.2160C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/19368
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1281
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1317
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1201
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7864
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47653
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2854
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Leu720Leu
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: QD

16-71098662-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71098662
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 71098662
    reference: chr 16
allele count: 1
allele frequency: 8.457374830852504e-6
allele num: 118240
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000444970
  ensembl transcript: ENST00000538248
  gene symbol: HYDIN
  hgvsc: ENST00000538248.1:c.2238A>C
  hgvsp: ENST00000538248.1:c.2238A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000394826
  ensembl transcript: ENST00000448691
  gene symbol: HYDIN
  hgvsc: ENST00000448691.1:c.2157A>C
  hgvsp: ENST00000448691.1:c.2157A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463767
  ensembl transcript: ENST00000393552
  gene symbol: HYDIN
  hgvsc: ENST00000393552.2:c.1011A>C
  hgvsp: ENST00000393552.2:c.1011A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000314736
  ensembl transcript: ENST00000321489
  gene symbol: HYDIN
  hgvsc: ENST00000321489.5:c.2157A>C
  hgvsp: ENST00000321489.5:c.2157A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000377197
  ensembl transcript: ENST00000393567
  gene symbol: HYDIN
  hgvsc: ENST00000393567.2:c.2157A>C
  hgvsp: ENST00000393567.2:c.2157A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000437341
  ensembl transcript: ENST00000541601
  gene symbol: HYDIN
  hgvsc: ENST00000541601.1:c.2208A>C
  hgvsp: ENST00000541601.1:c.2208A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463422
  ensembl transcript: ENST00000545230
  gene symbol: HYDIN
  hgvsc: ENST00000545230.1:c.*130A>C
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000398544
  ensembl transcript: ENST00000448089
  gene symbol: HYDIN
  hgvsc: ENST00000448089.2:c.2157A>C
  hgvsp: ENST00000448089.2:c.2157A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463093
  ensembl transcript: ENST00000539447
  gene symbol: HYDIN
  hgvsc: ENST00000539447.1:c.*1405A>C
  variant of: http://identifiers.org/hgnc/19368
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 1529
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46726
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1777
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1269
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7806
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 237
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 162
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 95
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Thr719Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: Other
population: South Asian
reference allele: T
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: BaseQRankSum

16-71098670-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71098670
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 71098670
    reference: chr 16
allele count: 1
allele frequency: 8.545401719334827e-6
allele num: 117022
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000314736
  ensembl transcript: ENST00000321489
  gene symbol: HYDIN
  hgvsc: ENST00000321489.5:c.2149G>A
  hgvsp: ENSP00000314736.5:p.Glu717Lys
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463093
  ensembl transcript: ENST00000539447
  gene symbol: HYDIN
  hgvsc: ENST00000539447.1:c.*1397G>A
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463767
  ensembl transcript: ENST00000393552
  gene symbol: HYDIN
  hgvsc: ENST00000393552.2:c.1003G>A
  hgvsp: ENSP00000463767.1:p.Glu335Lys
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000398544
  ensembl transcript: ENST00000448089
  gene symbol: HYDIN
  hgvsc: ENST00000448089.2:c.2149G>A
  hgvsp: ENSP00000398544.2:p.Glu717Lys
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000377197
  ensembl transcript: ENST00000393567
  gene symbol: HYDIN
  hgvsc: ENST00000393567.2:c.2149G>A
  hgvsp: ENSP00000377197.2:p.Glu717Lys
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000444970
  ensembl transcript: ENST00000538248
  gene symbol: HYDIN
  hgvsc: ENST00000538248.1:c.2230G>A
  hgvsp: ENSP00000444970.1:p.Glu744Lys
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000394826
  ensembl transcript: ENST00000448691
  gene symbol: HYDIN
  hgvsc: ENST00000448691.1:c.2149G>A
  hgvsp: ENSP00000394826.1:p.Glu717Lys
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463422
  ensembl transcript: ENST00000545230
  gene symbol: HYDIN
  hgvsc: ENST00000545230.1:c.*122G>A
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000437341
  ensembl transcript: ENST00000541601
  gene symbol: HYDIN
  hgvsc: ENST00000541601.1:c.2200G>A
  hgvsp: ENSP00000437341.1:p.Glu734Lys
  variant of: http://identifiers.org/hgnc/19368
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1274
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2096
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44078
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7686
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1041
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3467
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 484
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4146
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Glu717Lys
num of homozygotes: 0
population: Other
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: C
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum

16-71098674-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71098674
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 71098674
    reference: chr 16
allele count: 5
allele frequency: 4.293835769369493e-5
allele num: 116446
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000437341
  ensembl transcript: ENST00000541601
  gene symbol: HYDIN
  hgvsc: ENST00000541601.1:c.2196G>A
  hgvsp: ENST00000541601.1:c.2196G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463422
  ensembl transcript: ENST00000545230
  gene symbol: HYDIN
  hgvsc: ENST00000545230.1:c.*118G>A
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000444970
  ensembl transcript: ENST00000538248
  gene symbol: HYDIN
  hgvsc: ENST00000538248.1:c.2226G>A
  hgvsp: ENST00000538248.1:c.2226G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000394826
  ensembl transcript: ENST00000448691
  gene symbol: HYDIN
  hgvsc: ENST00000448691.1:c.2145G>A
  hgvsp: ENST00000448691.1:c.2145G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000314736
  ensembl transcript: ENST00000321489
  gene symbol: HYDIN
  hgvsc: ENST00000321489.5:c.2145G>A
  hgvsp: ENST00000321489.5:c.2145G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463767
  ensembl transcript: ENST00000393552
  gene symbol: HYDIN
  hgvsc: ENST00000393552.2:c.999G>A
  hgvsp: ENST00000393552.2:c.999G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000398544
  ensembl transcript: ENST00000448089
  gene symbol: HYDIN
  hgvsc: ENST00000448089.2:c.2145G>A
  hgvsp: ENST00000448089.2:c.2145G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000377197
  ensembl transcript: ENST00000393567
  gene symbol: HYDIN
  hgvsc: ENST00000393567.2:c.2145G>A
  hgvsp: ENST00000393567.2:c.2145G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463093
  ensembl transcript: ENST00000539447
  gene symbol: HYDIN
  hgvsc: ENST00000539447.1:c.*1393G>A
  variant of: http://identifiers.org/hgnc/19368
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4324
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1333
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1259
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7578
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42790
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2344
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 286
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 278
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47242
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Pro715Pro
num of homozygotes: 0
population: Latino
population: African
population: Other
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP

16-71098675-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71098675
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 71098675
    reference: chr 16
allele count: 2
allele frequency: 1.724613686534216e-5
allele num: 115968
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000398544
  ensembl transcript: ENST00000448089
  gene symbol: HYDIN
  hgvsc: ENST00000448089.2:c.2144C>T
  hgvsp: ENSP00000398544.2:p.Pro715Leu
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463767
  ensembl transcript: ENST00000393552
  gene symbol: HYDIN
  hgvsc: ENST00000393552.2:c.998C>T
  hgvsp: ENSP00000463767.1:p.Pro333Leu
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000314736
  ensembl transcript: ENST00000321489
  gene symbol: HYDIN
  hgvsc: ENST00000321489.5:c.2144C>T
  hgvsp: ENSP00000314736.5:p.Pro715Leu
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000437341
  ensembl transcript: ENST00000541601
  gene symbol: HYDIN
  hgvsc: ENST00000541601.1:c.2195C>T
  hgvsp: ENSP00000437341.1:p.Pro732Leu
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463422
  ensembl transcript: ENST00000545230
  gene symbol: HYDIN
  hgvsc: ENST00000545230.1:c.*117C>T
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000394826
  ensembl transcript: ENST00000448691
  gene symbol: HYDIN
  hgvsc: ENST00000448691.1:c.2144C>T
  hgvsp: ENSP00000394826.1:p.Pro715Leu
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000444970
  ensembl transcript: ENST00000538248
  gene symbol: HYDIN
  hgvsc: ENST00000538248.1:c.2225C>T
  hgvsp: ENSP00000444970.1:p.Pro742Leu
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463093
  ensembl transcript: ENST00000539447
  gene symbol: HYDIN
  hgvsc: ENST00000539447.1:c.*1392C>T
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000377197
  ensembl transcript: ENST00000393567
  gene symbol: HYDIN
  hgvsc: ENST00000393567.2:c.2144C>T
  hgvsp: ENSP00000377197.2:p.Pro715Leu
  variant of: http://identifiers.org/hgnc/19368
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7441
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2582
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41386
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5362
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1544
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1291
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1344
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 282
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Pro715Leu
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD

16-71098679-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71098679
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 71098679
    reference: chr 16
allele count: 4
allele frequency: 3.460447089763998e-5
allele num: 115592
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463767
  ensembl transcript: ENST00000393552
  gene symbol: HYDIN
  hgvsc: ENST00000393552.2:c.994T>C
  hgvsp: ENSP00000463767.1:p.Tyr332His
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000314736
  ensembl transcript: ENST00000321489
  gene symbol: HYDIN
  hgvsc: ENST00000321489.5:c.2140T>C
  hgvsp: ENSP00000314736.5:p.Tyr714His
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463093
  ensembl transcript: ENST00000539447
  gene symbol: HYDIN
  hgvsc: ENST00000539447.1:c.*1388T>C
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463422
  ensembl transcript: ENST00000545230
  gene symbol: HYDIN
  hgvsc: ENST00000545230.1:c.*113T>C
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000437341
  ensembl transcript: ENST00000541601
  gene symbol: HYDIN
  hgvsc: ENST00000541601.1:c.2191T>C
  hgvsp: ENSP00000437341.1:p.Tyr731His
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000444970
  ensembl transcript: ENST00000538248
  gene symbol: HYDIN
  hgvsc: ENST00000538248.1:c.2221T>C
  hgvsp: ENSP00000444970.1:p.Tyr741His
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000394826
  ensembl transcript: ENST00000448691
  gene symbol: HYDIN
  hgvsc: ENST00000448691.1:c.2140T>C
  hgvsp: ENSP00000394826.1:p.Tyr714His
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000398544
  ensembl transcript: ENST00000448089
  gene symbol: HYDIN
  hgvsc: ENST00000448089.2:c.2140T>C
  hgvsp: ENSP00000398544.2:p.Tyr714His
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000377197
  ensembl transcript: ENST00000393567
  gene symbol: HYDIN
  hgvsc: ENST00000393567.2:c.2140T>C
  hgvsp: ENSP00000377197.2:p.Tyr714His
  variant of: http://identifiers.org/hgnc/19368
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 7390
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2797
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40379
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1735
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1176
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6156
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 352
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 44670
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Tyr714His
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP

16-71098694-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71098694
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 71098694
    reference: chr 16
allele count: 1
allele frequency: 8.897747090436701e-6
allele num: 112388
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000377197
  ensembl transcript: ENST00000393567
  gene symbol: HYDIN
  hgvsc: ENST00000393567.2:c.2125C>T
  hgvsp: ENSP00000377197.2:p.His709Tyr
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463093
  ensembl transcript: ENST00000539447
  gene symbol: HYDIN
  hgvsc: ENST00000539447.1:c.*1373C>T
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000444970
  ensembl transcript: ENST00000538248
  gene symbol: HYDIN
  hgvsc: ENST00000538248.1:c.2206C>T
  hgvsp: ENSP00000444970.1:p.His736Tyr
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000398544
  ensembl transcript: ENST00000448089
  gene symbol: HYDIN
  hgvsc: ENST00000448089.2:c.2125C>T
  hgvsp: ENSP00000398544.2:p.His709Tyr
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463767
  ensembl transcript: ENST00000393552
  gene symbol: HYDIN
  hgvsc: ENST00000393552.2:c.979C>T
  hgvsp: ENSP00000463767.1:p.His327Tyr
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463422
  ensembl transcript: ENST00000545230
  gene symbol: HYDIN
  hgvsc: ENST00000545230.1:c.*98C>T
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000437341
  ensembl transcript: ENST00000541601
  gene symbol: HYDIN
  hgvsc: ENST00000541601.1:c.2176C>T
  hgvsp: ENSP00000437341.1:p.His726Tyr
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000394826
  ensembl transcript: ENST00000448691
  gene symbol: HYDIN
  hgvsc: ENST00000448691.1:c.2125C>T
  hgvsp: ENSP00000394826.1:p.His709Tyr
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000314736
  ensembl transcript: ENST00000321489
  gene symbol: HYDIN
  hgvsc: ENST00000321489.5:c.2125C>T
  hgvsp: ENSP00000314736.5:p.His709Tyr
  variant of: http://identifiers.org/hgnc/19368
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 4700
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1113
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4133
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6223
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30427
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12874
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1940
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 799
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 837
  bin: 5.25e1
  variant carriers: 0
hgvs: p.His709Tyr
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: Latino
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: DP

16-71098695-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71098695
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 71098695
    reference: chr 16
allele count: 2
allele frequency: 1.782626521917393e-5
allele num: 112194
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000398544
  ensembl transcript: ENST00000448089
  gene symbol: HYDIN
  hgvsc: ENST00000448089.2:c.2124G>A
  hgvsp: ENST00000448089.2:c.2124G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000314736
  ensembl transcript: ENST00000321489
  gene symbol: HYDIN
  hgvsc: ENST00000321489.5:c.2124G>A
  hgvsp: ENST00000321489.5:c.2124G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463422
  ensembl transcript: ENST00000545230
  gene symbol: HYDIN
  hgvsc: ENST00000545230.1:c.*97G>A
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000394826
  ensembl transcript: ENST00000448691
  gene symbol: HYDIN
  hgvsc: ENST00000448691.1:c.2124G>A
  hgvsp: ENST00000448691.1:c.2124G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000377197
  ensembl transcript: ENST00000393567
  gene symbol: HYDIN
  hgvsc: ENST00000393567.2:c.2124G>A
  hgvsp: ENST00000393567.2:c.2124G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463767
  ensembl transcript: ENST00000393552
  gene symbol: HYDIN
  hgvsc: ENST00000393552.2:c.978G>A
  hgvsp: ENST00000393552.2:c.978G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000437341
  ensembl transcript: ENST00000541601
  gene symbol: HYDIN
  hgvsc: ENST00000541601.1:c.2175G>A
  hgvsp: ENST00000541601.1:c.2175G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000444970
  ensembl transcript: ENST00000538248
  gene symbol: HYDIN
  hgvsc: ENST00000538248.1:c.2205G>A
  hgvsp: ENST00000538248.1:c.2205G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463093
  ensembl transcript: ENST00000539447
  gene symbol: HYDIN
  hgvsc: ENST00000539447.1:c.*1372G>A
  variant of: http://identifiers.org/hgnc/19368
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6166
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13291
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4202
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29781
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4954
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1076
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4557
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 117
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Gly708Gly
num of homozygotes: 0
population: East Asian
population: Latino
population: Other
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: QD

16-71098698-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71098698
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 71098698
    reference: chr 16
allele count: 2
allele frequency: 1.790157712894506e-5
allele num: 111722
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463767
  ensembl transcript: ENST00000393552
  gene symbol: HYDIN
  hgvsc: ENST00000393552.2:c.975T>C
  hgvsp: ENST00000393552.2:c.975T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000398544
  ensembl transcript: ENST00000448089
  gene symbol: HYDIN
  hgvsc: ENST00000448089.2:c.2121T>C
  hgvsp: ENST00000448089.2:c.2121T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000437341
  ensembl transcript: ENST00000541601
  gene symbol: HYDIN
  hgvsc: ENST00000541601.1:c.2172T>C
  hgvsp: ENST00000541601.1:c.2172T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000394826
  ensembl transcript: ENST00000448691
  gene symbol: HYDIN
  hgvsc: ENST00000448691.1:c.2121T>C
  hgvsp: ENST00000448691.1:c.2121T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000314736
  ensembl transcript: ENST00000321489
  gene symbol: HYDIN
  hgvsc: ENST00000321489.5:c.2121T>C
  hgvsp: ENST00000321489.5:c.2121T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463422
  ensembl transcript: ENST00000545230
  gene symbol: HYDIN
  hgvsc: ENST00000545230.1:c.*94T>C
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000444970
  ensembl transcript: ENST00000538248
  gene symbol: HYDIN
  hgvsc: ENST00000538248.1:c.2202T>C
  hgvsp: ENST00000538248.1:c.2202T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463093
  ensembl transcript: ENST00000539447
  gene symbol: HYDIN
  hgvsc: ENST00000539447.1:c.*1369T>C
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000377197
  ensembl transcript: ENST00000393567
  gene symbol: HYDIN
  hgvsc: ENST00000393567.2:c.2121T>C
  hgvsp: ENST00000393567.2:c.2121T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/19368
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5843
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1017
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6112
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27477
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14531
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4449
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 144
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1770
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10943
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Phe707Phe
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
population: European (Finnish)
population: African
population: South Asian
reference allele: A
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP

16-71098709-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71098709
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 71098709
    reference: chr 16
allele count: 2
allele frequency: 1.847029053767016e-5
allele num: 108282
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463767
  ensembl transcript: ENST00000393552
  gene symbol: HYDIN
  hgvsc: ENST00000393552.2:c.964G>A
  hgvsp: ENSP00000463767.1:p.Glu322Lys
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000314736
  ensembl transcript: ENST00000321489
  gene symbol: HYDIN
  hgvsc: ENST00000321489.5:c.2110G>A
  hgvsp: ENSP00000314736.5:p.Glu704Lys
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000437341
  ensembl transcript: ENST00000541601
  gene symbol: HYDIN
  hgvsc: ENST00000541601.1:c.2161G>A
  hgvsp: ENSP00000437341.1:p.Glu721Lys
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463093
  ensembl transcript: ENST00000539447
  gene symbol: HYDIN
  hgvsc: ENST00000539447.1:c.*1358G>A
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000444970
  ensembl transcript: ENST00000538248
  gene symbol: HYDIN
  hgvsc: ENST00000538248.1:c.2191G>A
  hgvsp: ENSP00000444970.1:p.Glu731Lys
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000394826
  ensembl transcript: ENST00000448691
  gene symbol: HYDIN
  hgvsc: ENST00000448691.1:c.2110G>A
  hgvsp: ENSP00000394826.1:p.Glu704Lys
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000398544
  ensembl transcript: ENST00000448089
  gene symbol: HYDIN
  hgvsc: ENST00000448089.2:c.2110G>A
  hgvsp: ENSP00000398544.2:p.Glu704Lys
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463422
  ensembl transcript: ENST00000545230
  gene symbol: HYDIN
  hgvsc: ENST00000545230.1:c.*83G>A
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000377197
  ensembl transcript: ENST00000393567
  gene symbol: HYDIN
  hgvsc: ENST00000393567.2:c.2110G>A
  hgvsp: ENSP00000377197.2:p.Glu704Lys
  variant of: http://identifiers.org/hgnc/19368
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 17981
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4139
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12730
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 916
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5600
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17718
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 828
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1354
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 867
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Glu704Lys
num of homozygotes: 0
population: East Asian
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
reference allele: C
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: MQ

16-71098712-TA-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71098712
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 71098711
    reference: chr 16
allele count: 1
allele frequency: 9.303537204845282e-6
allele num: 107486
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000377197
  ensembl transcript: ENST00000393567
  gene symbol: HYDIN
  hgvsc: ENST00000393567.2:c.2106delT
  hgvsp: ENSP00000377197.2:p.Asn702LysfsTer11
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000394826
  ensembl transcript: ENST00000448691
  gene symbol: HYDIN
  hgvsc: ENST00000448691.1:c.2106delT
  hgvsp: ENSP00000394826.1:p.Asn702LysfsTer11
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000444970
  ensembl transcript: ENST00000538248
  gene symbol: HYDIN
  hgvsc: ENST00000538248.1:c.2187delT
  hgvsp: ENSP00000444970.1:p.Asn729LysfsTer11
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463093
  ensembl transcript: ENST00000539447
  gene symbol: HYDIN
  hgvsc: ENST00000539447.1:c.*1354delT
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000398544
  ensembl transcript: ENST00000448089
  gene symbol: HYDIN
  hgvsc: ENST00000448089.2:c.2106delT
  hgvsp: ENSP00000398544.2:p.Asn702LysfsTer11
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463767
  ensembl transcript: ENST00000393552
  gene symbol: HYDIN
  hgvsc: ENST00000393552.2:c.960delT
  hgvsp: ENSP00000463767.1:p.Asn320LysfsTer11
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463422
  ensembl transcript: ENST00000545230
  gene symbol: HYDIN
  hgvsc: ENST00000545230.1:c.*79delT
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000437341
  ensembl transcript: ENST00000541601
  gene symbol: HYDIN
  hgvsc: ENST00000541601.1:c.2157delT
  hgvsp: ENSP00000437341.1:p.Asn719LysfsTer11
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000314736
  ensembl transcript: ENST00000321489
  gene symbol: HYDIN
  hgvsc: ENST00000321489.5:c.2106delT
  hgvsp: ENSP00000314736.5:p.Asn702LysfsTer11
  variant of: http://identifiers.org/hgnc/19368
canonical: true
consequence: frameshift
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3821
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18261
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6006
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13996
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 817
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16119
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 235
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5334
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Asn702LysfsTer11
num of homozygotes: 0
population: African
population: Other
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: TA
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum

16-71098724-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71098724
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 71098724
    reference: chr 16
allele count: 1
allele frequency: 9.6324266009093e-6
allele num: 103816
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000394826
  ensembl transcript: ENST00000448691
  gene symbol: HYDIN
  hgvsc: ENST00000448691.1:c.2095C>T
  hgvsp: ENSP00000394826.1:p.His699Tyr
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000398544
  ensembl transcript: ENST00000448089
  gene symbol: HYDIN
  hgvsc: ENST00000448089.2:c.2095C>T
  hgvsp: ENSP00000398544.2:p.His699Tyr
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000444970
  ensembl transcript: ENST00000538248
  gene symbol: HYDIN
  hgvsc: ENST00000538248.1:c.2176C>T
  hgvsp: ENSP00000444970.1:p.His726Tyr
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000314736
  ensembl transcript: ENST00000321489
  gene symbol: HYDIN
  hgvsc: ENST00000321489.5:c.2095C>T
  hgvsp: ENSP00000314736.5:p.His699Tyr
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463093
  ensembl transcript: ENST00000539447
  gene symbol: HYDIN
  hgvsc: ENST00000539447.1:c.*1343C>T
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000437341
  ensembl transcript: ENST00000541601
  gene symbol: HYDIN
  hgvsc: ENST00000541601.1:c.2146C>T
  hgvsp: ENSP00000437341.1:p.His716Tyr
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463767
  ensembl transcript: ENST00000393552
  gene symbol: HYDIN
  hgvsc: ENST00000393552.2:c.949C>T
  hgvsp: ENSP00000463767.1:p.His317Tyr
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463422
  ensembl transcript: ENST00000545230
  gene symbol: HYDIN
  hgvsc: ENST00000545230.1:c.*68C>T
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000377197
  ensembl transcript: ENST00000393567
  gene symbol: HYDIN
  hgvsc: ENST00000393567.2:c.2095C>T
  hgvsp: ENSP00000377197.2:p.His699Tyr
  variant of: http://identifiers.org/hgnc/19368
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 7620
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2653
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15574
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 753
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14660
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17957
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 265
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 895
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 222
  bin: 7.75e1
  variant carriers: 0
hgvs: p.His699Tyr
num of homozygotes: 0
population: Other
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD

16-71098728-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71098728
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 71098728
    reference: chr 16
allele count: 2
allele frequency: 1.918575649437857e-5
allele num: 104244
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000377197
  ensembl transcript: ENST00000393567
  gene symbol: HYDIN
  hgvsc: ENST00000393567.2:c.2091C>T
  hgvsp: ENST00000393567.2:c.2091C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000314736
  ensembl transcript: ENST00000321489
  gene symbol: HYDIN
  hgvsc: ENST00000321489.5:c.2091C>T
  hgvsp: ENST00000321489.5:c.2091C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000444970
  ensembl transcript: ENST00000538248
  gene symbol: HYDIN
  hgvsc: ENST00000538248.1:c.2172C>T
  hgvsp: ENST00000538248.1:c.2172C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463422
  ensembl transcript: ENST00000545230
  gene symbol: HYDIN
  hgvsc: ENST00000545230.1:c.*64C>T
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000394826
  ensembl transcript: ENST00000448691
  gene symbol: HYDIN
  hgvsc: ENST00000448691.1:c.2091C>T
  hgvsp: ENST00000448691.1:c.2091C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000437341
  ensembl transcript: ENST00000541601
  gene symbol: HYDIN
  hgvsc: ENST00000541601.1:c.2142C>T
  hgvsp: ENST00000541601.1:c.2142C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000398544
  ensembl transcript: ENST00000448089
  gene symbol: HYDIN
  hgvsc: ENST00000448089.2:c.2091C>T
  hgvsp: ENST00000448089.2:c.2091C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463767
  ensembl transcript: ENST00000393552
  gene symbol: HYDIN
  hgvsc: ENST00000393552.2:c.945C>T
  hgvsp: ENST00000393552.2:c.945C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463093
  ensembl transcript: ENST00000539447
  gene symbol: HYDIN
  hgvsc: ENST00000539447.1:c.*1339C>T
  variant of: http://identifiers.org/hgnc/19368
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 16809
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17978
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7569
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 558
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12928
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3193
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 619
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2769
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Ala697Ala
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: G
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: MQ

16-71098745-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71098745
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 71098745
    reference: chr 16
allele count: 1
allele frequency: 9.48622599984822e-6
allele num: 105416
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000444970
  ensembl transcript: ENST00000538248
  gene symbol: HYDIN
  hgvsc: ENST00000538248.1:c.2157-2A>G
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463422
  ensembl transcript: ENST00000545230
  gene symbol: HYDIN
  hgvsc: ENST00000545230.1:c.*49-2A>G
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000437341
  ensembl transcript: ENST00000541601
  gene symbol: HYDIN
  hgvsc: ENST00000541601.1:c.2127-2A>G
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: true
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000377197
  ensembl transcript: ENST00000393567
  gene symbol: HYDIN
  hgvsc: ENST00000393567.2:c.2076-2A>G
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463767
  ensembl transcript: ENST00000393552
  gene symbol: HYDIN
  hgvsc: ENST00000393552.2:c.930-2A>G
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000314736
  ensembl transcript: ENST00000321489
  gene symbol: HYDIN
  hgvsc: ENST00000321489.5:c.2076-2A>G
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463093
  ensembl transcript: ENST00000539447
  gene symbol: HYDIN
  hgvsc: ENST00000539447.1:c.*1324-2A>G
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000398544
  ensembl transcript: ENST00000448089
  gene symbol: HYDIN
  hgvsc: ENST00000448089.2:c.2076-2A>G
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000394826
  ensembl transcript: ENST00000448691
  gene symbol: HYDIN
  hgvsc: ENST00000448691.1:c.2076-2A>G
  variant of: http://identifiers.org/hgnc/19368
canonical: true
consequence: splice acceptor
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 7440
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 716
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24577
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4422
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15093
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7062
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 489
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 417
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12570
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 655
  bin: 5.75e1
  variant carriers: 0
hgvs: c.2076-2A>G
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: Other
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP

16-71098746-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71098746
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 71098746
    reference: chr 16
allele count: 1
allele frequency: 9.497578117580016e-6
allele num: 105290
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463093
  ensembl transcript: ENST00000539447
  gene symbol: HYDIN
  hgvsc: ENST00000539447.1:c.*1324-3C>T
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463767
  ensembl transcript: ENST00000393552
  gene symbol: HYDIN
  hgvsc: ENST00000393552.2:c.930-3C>T
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463422
  ensembl transcript: ENST00000545230
  gene symbol: HYDIN
  hgvsc: ENST00000545230.1:c.*49-3C>T
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000394826
  ensembl transcript: ENST00000448691
  gene symbol: HYDIN
  hgvsc: ENST00000448691.1:c.2076-3C>T
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000314736
  ensembl transcript: ENST00000321489
  gene symbol: HYDIN
  hgvsc: ENST00000321489.5:c.2076-3C>T
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000377197
  ensembl transcript: ENST00000393567
  gene symbol: HYDIN
  hgvsc: ENST00000393567.2:c.2076-3C>T
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000398544
  ensembl transcript: ENST00000448089
  gene symbol: HYDIN
  hgvsc: ENST00000448089.2:c.2076-3C>T
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000437341
  ensembl transcript: ENST00000541601
  gene symbol: HYDIN
  hgvsc: ENST00000541601.1:c.2127-3C>T
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000444970
  ensembl transcript: ENST00000538248
  gene symbol: HYDIN
  hgvsc: ENST00000538248.1:c.2157-3C>T
  variant of: http://identifiers.org/hgnc/19368
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 728
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7171
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4430
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7426
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24625
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14937
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 503
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 420
  bin: 7.75e1
  variant carriers: 0
hgvs: c.2076-3C>T
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
population: Other
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: QD
site quality: MQ

16-71098749-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71098749
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 71098749
    reference: chr 16
allele count: 1
allele frequency: 9.505703422053232e-6
allele num: 105200
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000444970
  ensembl transcript: ENST00000538248
  gene symbol: HYDIN
  hgvsc: ENST00000538248.1:c.2157-6G>A
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000398544
  ensembl transcript: ENST00000448089
  gene symbol: HYDIN
  hgvsc: ENST00000448089.2:c.2076-6G>A
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463422
  ensembl transcript: ENST00000545230
  gene symbol: HYDIN
  hgvsc: ENST00000545230.1:c.*49-6G>A
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000437341
  ensembl transcript: ENST00000541601
  gene symbol: HYDIN
  hgvsc: ENST00000541601.1:c.2127-6G>A
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463767
  ensembl transcript: ENST00000393552
  gene symbol: HYDIN
  hgvsc: ENST00000393552.2:c.930-6G>A
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000377197
  ensembl transcript: ENST00000393567
  gene symbol: HYDIN
  hgvsc: ENST00000393567.2:c.2076-6G>A
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000394826
  ensembl transcript: ENST00000448691
  gene symbol: HYDIN
  hgvsc: ENST00000448691.1:c.2076-6G>A
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000314736
  ensembl transcript: ENST00000321489
  gene symbol: HYDIN
  hgvsc: ENST00000321489.5:c.2076-6G>A
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463093
  ensembl transcript: ENST00000539447
  gene symbol: HYDIN
  hgvsc: ENST00000539447.1:c.*1324-6G>A
  variant of: http://identifiers.org/hgnc/19368
canonical: true
consequence: splice region
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6996
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25280
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14428
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7357
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 776
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4503
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 484
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3556
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12197
  bin: 2.25e1
  variant carriers: 0
hgvs: c.2076-6G>A
num of homozygotes: 0
population: East Asian
population: Other
population: Latino
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ

16-71098750-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71098750
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 71098750
    reference: chr 16
allele count: 1
allele frequency: 9.483527113404017e-6
allele num: 105446
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000444970
  ensembl transcript: ENST00000538248
  gene symbol: HYDIN
  hgvsc: ENST00000538248.1:c.2157-7C>T
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463767
  ensembl transcript: ENST00000393552
  gene symbol: HYDIN
  hgvsc: ENST00000393552.2:c.930-7C>T
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000314736
  ensembl transcript: ENST00000321489
  gene symbol: HYDIN
  hgvsc: ENST00000321489.5:c.2076-7C>T
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000394826
  ensembl transcript: ENST00000448691
  gene symbol: HYDIN
  hgvsc: ENST00000448691.1:c.2076-7C>T
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463093
  ensembl transcript: ENST00000539447
  gene symbol: HYDIN
  hgvsc: ENST00000539447.1:c.*1324-7C>T
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000398544
  ensembl transcript: ENST00000448089
  gene symbol: HYDIN
  hgvsc: ENST00000448089.2:c.2076-7C>T
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463422
  ensembl transcript: ENST00000545230
  gene symbol: HYDIN
  hgvsc: ENST00000545230.1:c.*49-7C>T
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000437341
  ensembl transcript: ENST00000541601
  gene symbol: HYDIN
  hgvsc: ENST00000541601.1:c.2127-7C>T
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000377197
  ensembl transcript: ENST00000393567
  gene symbol: HYDIN
  hgvsc: ENST00000393567.2:c.2076-7C>T
  variant of: http://identifiers.org/hgnc/19368
canonical: true
consequence: splice region
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 4576
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25605
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7318
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6842
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14227
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 783
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 862
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 95
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5735
  bin: 3.25e1
  variant carriers: 0
hgvs: c.2076-7C>T
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
population: East Asian
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum

16-71098754-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71098754
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 71098754
    reference: chr 16
allele count: 3
allele frequency: 2.827041595205337e-5
allele num: 106118
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463422
  ensembl transcript: ENST00000545230
  gene symbol: HYDIN
  hgvsc: ENST00000545230.1:c.*49-11C>T
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000394826
  ensembl transcript: ENST00000448691
  gene symbol: HYDIN
  hgvsc: ENST00000448691.1:c.2076-11C>T
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463093
  ensembl transcript: ENST00000539447
  gene symbol: HYDIN
  hgvsc: ENST00000539447.1:c.*1324-11C>T
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000314736
  ensembl transcript: ENST00000321489
  gene symbol: HYDIN
  hgvsc: ENST00000321489.5:c.2076-11C>T
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000444970
  ensembl transcript: ENST00000538248
  gene symbol: HYDIN
  hgvsc: ENST00000538248.1:c.2157-11C>T
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000398544
  ensembl transcript: ENST00000448089
  gene symbol: HYDIN
  hgvsc: ENST00000448089.2:c.2076-11C>T
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000377197
  ensembl transcript: ENST00000393567
  gene symbol: HYDIN
  hgvsc: ENST00000393567.2:c.2076-11C>T
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463767
  ensembl transcript: ENST00000393552
  gene symbol: HYDIN
  hgvsc: ENST00000393552.2:c.930-11C>T
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000437341
  ensembl transcript: ENST00000541601
  gene symbol: HYDIN
  hgvsc: ENST00000541601.1:c.2127-11C>T
  variant of: http://identifiers.org/hgnc/19368
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 7176
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26719
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6377
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 879
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13413
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4809
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 167
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 985
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 582
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 292
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Other
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD

16-71098759-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71098759
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 71098759
    reference: chr 16
allele count: 1
allele frequency: 9.386674676629058e-6
allele num: 106534
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463767
  ensembl transcript: ENST00000393552
  gene symbol: HYDIN
  hgvsc: ENST00000393552.2:c.930-16G>C
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000398544
  ensembl transcript: ENST00000448089
  gene symbol: HYDIN
  hgvsc: ENST00000448089.2:c.2076-16G>C
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463422
  ensembl transcript: ENST00000545230
  gene symbol: HYDIN
  hgvsc: ENST00000545230.1:c.*49-16G>C
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000314736
  ensembl transcript: ENST00000321489
  gene symbol: HYDIN
  hgvsc: ENST00000321489.5:c.2076-16G>C
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000394826
  ensembl transcript: ENST00000448691
  gene symbol: HYDIN
  hgvsc: ENST00000448691.1:c.2076-16G>C
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000437341
  ensembl transcript: ENST00000541601
  gene symbol: HYDIN
  hgvsc: ENST00000541601.1:c.2127-16G>C
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463093
  ensembl transcript: ENST00000539447
  gene symbol: HYDIN
  hgvsc: ENST00000539447.1:c.*1324-16G>C
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000377197
  ensembl transcript: ENST00000393567
  gene symbol: HYDIN
  hgvsc: ENST00000393567.2:c.2076-16G>C
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000444970
  ensembl transcript: ENST00000538248
  gene symbol: HYDIN
  hgvsc: ENST00000538248.1:c.2157-16G>C
  variant of: http://identifiers.org/hgnc/19368
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6110
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 991
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5295
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6903
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27634
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12458
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11292
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 363
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 571
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4937
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 183
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP

16-71098768-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71098768
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 71098768
    reference: chr 16
allele count: 1
allele frequency: 9.294544102611768e-6
allele num: 107590
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000377197
  ensembl transcript: ENST00000393567
  gene symbol: HYDIN
  hgvsc: ENST00000393567.2:c.2076-25T>C
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000394826
  ensembl transcript: ENST00000448691
  gene symbol: HYDIN
  hgvsc: ENST00000448691.1:c.2076-25T>C
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000444970
  ensembl transcript: ENST00000538248
  gene symbol: HYDIN
  hgvsc: ENST00000538248.1:c.2157-25T>C
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463767
  ensembl transcript: ENST00000393552
  gene symbol: HYDIN
  hgvsc: ENST00000393552.2:c.930-25T>C
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000314736
  ensembl transcript: ENST00000321489
  gene symbol: HYDIN
  hgvsc: ENST00000321489.5:c.2076-25T>C
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463093
  ensembl transcript: ENST00000539447
  gene symbol: HYDIN
  hgvsc: ENST00000539447.1:c.*1324-25T>C
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463422
  ensembl transcript: ENST00000545230
  gene symbol: HYDIN
  hgvsc: ENST00000545230.1:c.*49-25T>C
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000398544
  ensembl transcript: ENST00000448089
  gene symbol: HYDIN
  hgvsc: ENST00000448089.2:c.2076-25T>C
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000437341
  ensembl transcript: ENST00000541601
  gene symbol: HYDIN
  hgvsc: ENST00000541601.1:c.2127-25T>C
  variant of: http://identifiers.org/hgnc/19368
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5777
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1088
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28805
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11255
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6573
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5945
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 312
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1241
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 189
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 400
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 877
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum

16-71098776-CAG-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71098776
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 71098774
    reference: chr 16
allele count: 1
allele frequency: 9.249495902473315e-6
allele num: 108114
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463093
  ensembl transcript: ENST00000539447
  gene symbol: HYDIN
  hgvsc: ENST00000539447.1:c.*1324-35_*1324-34delCT
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000377197
  ensembl transcript: ENST00000393567
  gene symbol: HYDIN
  hgvsc: ENST00000393567.2:c.2076-35_2076-34delCT
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000314736
  ensembl transcript: ENST00000321489
  gene symbol: HYDIN
  hgvsc: ENST00000321489.5:c.2076-35_2076-34delCT
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000394826
  ensembl transcript: ENST00000448691
  gene symbol: HYDIN
  hgvsc: ENST00000448691.1:c.2076-35_2076-34delCT
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000437341
  ensembl transcript: ENST00000541601
  gene symbol: HYDIN
  hgvsc: ENST00000541601.1:c.2127-35_2127-34delCT
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463767
  ensembl transcript: ENST00000393552
  gene symbol: HYDIN
  hgvsc: ENST00000393552.2:c.930-35_930-34delCT
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000398544
  ensembl transcript: ENST00000448089
  gene symbol: HYDIN
  hgvsc: ENST00000448089.2:c.2076-35_2076-34delCT
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463422
  ensembl transcript: ENST00000545230
  gene symbol: HYDIN
  hgvsc: ENST00000545230.1:c.*49-35_*49-34delCT
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000444970
  ensembl transcript: ENST00000538248
  gene symbol: HYDIN
  hgvsc: ENST00000538248.1:c.2157-35_2157-34delCT
  variant of: http://identifiers.org/hgnc/19368
canonical: true
consequence: intron
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 6281
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29194
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10296
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6044
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1218
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6435
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3334
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 719
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 167
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1112
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Other
population: East Asian
population: Latino
population: European (Finnish)
population: African
reference allele: CAG
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum

16-71098788-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71098788
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 71098788
    reference: chr 16
allele count: 1
allele frequency: 9.164558818138496e-6
allele num: 109116
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000444970
  ensembl transcript: ENST00000538248
  gene symbol: HYDIN
  hgvsc: ENST00000538248.1:c.2157-45A>G
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000394826
  ensembl transcript: ENST00000448691
  gene symbol: HYDIN
  hgvsc: ENST00000448691.1:c.2076-45A>G
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463767
  ensembl transcript: ENST00000393552
  gene symbol: HYDIN
  hgvsc: ENST00000393552.2:c.930-45A>G
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463422
  ensembl transcript: ENST00000545230
  gene symbol: HYDIN
  hgvsc: ENST00000545230.1:c.*49-45A>G
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463093
  ensembl transcript: ENST00000539447
  gene symbol: HYDIN
  hgvsc: ENST00000539447.1:c.*1324-45A>G
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000377197
  ensembl transcript: ENST00000393567
  gene symbol: HYDIN
  hgvsc: ENST00000393567.2:c.2076-45A>G
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000314736
  ensembl transcript: ENST00000321489
  gene symbol: HYDIN
  hgvsc: ENST00000321489.5:c.2076-45A>G
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000437341
  ensembl transcript: ENST00000541601
  gene symbol: HYDIN
  hgvsc: ENST00000541601.1:c.2127-45A>G
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000398544
  ensembl transcript: ENST00000448089
  gene symbol: HYDIN
  hgvsc: ENST00000448089.2:c.2076-45A>G
  variant of: http://identifiers.org/hgnc/19368
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6895
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9432
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5872
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29349
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1355
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6588
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 112
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 360
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3185
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 793
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4156
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: Latino
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD

16-71098795-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71098795
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 71098795
    reference: chr 16
allele count: 234
allele frequency: 2.1465920557747e-3
allele num: 109010
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463767
  ensembl transcript: ENST00000393552
  gene symbol: HYDIN
  hgvsc: ENST00000393552.2:c.930-52G>A
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000437341
  ensembl transcript: ENST00000541601
  gene symbol: HYDIN
  hgvsc: ENST00000541601.1:c.2127-52G>A
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000314736
  ensembl transcript: ENST00000321489
  gene symbol: HYDIN
  hgvsc: ENST00000321489.5:c.2076-52G>A
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463422
  ensembl transcript: ENST00000545230
  gene symbol: HYDIN
  hgvsc: ENST00000545230.1:c.*49-52G>A
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000377197
  ensembl transcript: ENST00000393567
  gene symbol: HYDIN
  hgvsc: ENST00000393567.2:c.2076-52G>A
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463093
  ensembl transcript: ENST00000539447
  gene symbol: HYDIN
  hgvsc: ENST00000539447.1:c.*1324-52G>A
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000394826
  ensembl transcript: ENST00000448691
  gene symbol: HYDIN
  hgvsc: ENST00000448691.1:c.2076-52G>A
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000444970
  ensembl transcript: ENST00000538248
  gene symbol: HYDIN
  hgvsc: ENST00000538248.1:c.2157-52G>A
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000398544
  ensembl transcript: ENST00000448089
  gene symbol: HYDIN
  hgvsc: ENST00000448089.2:c.2076-52G>A
  variant of: http://identifiers.org/hgnc/19368
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9675
  bin: 2.75e1
  variant carriers: 28
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5501
  bin: 7.5e0
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 1840
  bin: 3.25e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 9314
  bin: 1.25e1
  variant carriers: 29
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 5.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 4.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 6840
  bin: 1.75e1
  variant carriers: 50
genotype depth: GenotypeDepth
  all individuals: 26287
  bin: 2.25e1
  variant carriers: 55
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 3.75e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 258
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8169
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 2.5e0
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 2292
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 218
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 6
population: Other
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum

16-71100712-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71100712
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 71100712
    reference: chr 16
allele count: 42
allele frequency: 6.381039197812215e-3
allele num: 6582
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463767
  ensembl transcript: ENST00000393552
  gene symbol: HYDIN
  hgvsc: ENST00000393552.2:c.929+481C>T
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000444970
  ensembl transcript: ENST00000538248
  gene symbol: HYDIN
  hgvsc: ENST00000538248.1:c.2156+481C>T
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000398544
  ensembl transcript: ENST00000448089
  gene symbol: HYDIN
  hgvsc: ENST00000448089.2:c.2075+481C>T
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000437341
  ensembl transcript: ENST00000541601
  gene symbol: HYDIN
  hgvsc: ENST00000541601.1:c.2126+481C>T
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000377197
  ensembl transcript: ENST00000393567
  gene symbol: HYDIN
  hgvsc: ENST00000393567.2:c.2075+481C>T
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000394826
  ensembl transcript: ENST00000448691
  gene symbol: HYDIN
  hgvsc: ENST00000448691.1:c.2075+481C>T
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463422
  ensembl transcript: ENST00000545230
  gene symbol: HYDIN
  hgvsc: ENST00000545230.1:c.*22C>T
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463093
  ensembl transcript: ENST00000539447
  gene symbol: HYDIN
  hgvsc: ENST00000539447.1:c.*1323+481C>T
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000446122
  ensembl transcript: ENST00000542890
  gene symbol: HYDIN
  hgvsc: ENST00000542890.1:c.*22C>T
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000288168
  ensembl transcript: ENST00000288168
  gene symbol: HYDIN
  hgvsc: ENST00000288168.10:c.*429C>T
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000314736
  ensembl transcript: ENST00000321489
  gene symbol: HYDIN
  hgvsc: ENST00000321489.5:c.2075+481C>T
  variant of: http://identifiers.org/hgnc/19368
canonical: false
consequence: 3' UTR
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 979
  bin: 2.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1569
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3235
  bin: 7.5e0
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1701
  bin: 1.25e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 1.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 177
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Other
population: European (Finnish)
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff

16-71100726-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71100726
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 71100726
    reference: chr 16
allele count: 2
allele frequency: 2.648305084745763e-4
allele num: 7552
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000314736
  ensembl transcript: ENST00000321489
  gene symbol: HYDIN
  hgvsc: ENST00000321489.5:c.2075+467G>A
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000446122
  ensembl transcript: ENST00000542890
  gene symbol: HYDIN
  hgvsc: ENST00000542890.1:c.*8G>A
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000377197
  ensembl transcript: ENST00000393567
  gene symbol: HYDIN
  hgvsc: ENST00000393567.2:c.2075+467G>A
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463767
  ensembl transcript: ENST00000393552
  gene symbol: HYDIN
  hgvsc: ENST00000393552.2:c.929+467G>A
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000394826
  ensembl transcript: ENST00000448691
  gene symbol: HYDIN
  hgvsc: ENST00000448691.1:c.2075+467G>A
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000444970
  ensembl transcript: ENST00000538248
  gene symbol: HYDIN
  hgvsc: ENST00000538248.1:c.2156+467G>A
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463093
  ensembl transcript: ENST00000539447
  gene symbol: HYDIN
  hgvsc: ENST00000539447.1:c.*1323+467G>A
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000398544
  ensembl transcript: ENST00000448089
  gene symbol: HYDIN
  hgvsc: ENST00000448089.2:c.2075+467G>A
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000288168
  ensembl transcript: ENST00000288168
  gene symbol: HYDIN
  hgvsc: ENST00000288168.10:c.*415G>A
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463422
  ensembl transcript: ENST00000545230
  gene symbol: HYDIN
  hgvsc: ENST00000545230.1:c.*8G>A
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000437341
  ensembl transcript: ENST00000541601
  gene symbol: HYDIN
  hgvsc: ENST00000541601.1:c.2126+467G>A
  variant of: http://identifiers.org/hgnc/19368
canonical: false
consequence: 3' UTR
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 1521
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1455
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1379
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2995
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 544
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum

16-71100755-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71100755
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 71100755
    reference: chr 16
allele count: 2
allele frequency: 1.893222264293828e-4
allele num: 10564
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000377197
  ensembl transcript: ENST00000393567
  gene symbol: HYDIN
  hgvsc: ENST00000393567.2:c.2075+438G>A
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000437341
  ensembl transcript: ENST00000541601
  gene symbol: HYDIN
  hgvsc: ENST00000541601.1:c.2126+438G>A
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000377181
  ensembl transcript: ENST00000393550
  gene symbol: HYDIN
  hgvsc: ENST00000393550.2:c.2202G>A
  hgvsp: ENST00000393550.2:c.2202G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000394826
  ensembl transcript: ENST00000448691
  gene symbol: HYDIN
  hgvsc: ENST00000448691.1:c.2075+438G>A
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000444970
  ensembl transcript: ENST00000538248
  gene symbol: HYDIN
  hgvsc: ENST00000538248.1:c.2156+438G>A
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000288168
  ensembl transcript: ENST00000288168
  gene symbol: HYDIN
  hgvsc: ENST00000288168.10:c.*386G>A
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000314736
  ensembl transcript: ENST00000321489
  gene symbol: HYDIN
  hgvsc: ENST00000321489.5:c.2075+438G>A
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463093
  ensembl transcript: ENST00000539447
  gene symbol: HYDIN
  hgvsc: ENST00000539447.1:c.*1323+438G>A
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000446122
  ensembl transcript: ENST00000542890
  gene symbol: HYDIN
  hgvsc: ENST00000542890.1:c.362G>A
  hgvsp: ENST00000542890.1:c.362G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463422
  ensembl transcript: ENST00000545230
  gene symbol: HYDIN
  hgvsc: ENST00000545230.1:c.1566G>A
  hgvsp: ENST00000545230.1:c.1566G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463767
  ensembl transcript: ENST00000393552
  gene symbol: HYDIN
  hgvsc: ENST00000393552.2:c.929+438G>A
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000398544
  ensembl transcript: ENST00000448089
  gene symbol: HYDIN
  hgvsc: ENST00000448089.2:c.2075+438G>A
  variant of: http://identifiers.org/hgnc/19368
canonical: false
consequence: synonymous
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1491
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 791
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1902
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3175
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 809
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg734Arg
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: C
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ

16-71100756-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71100756
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 71100756
    reference: chr 16
allele count: 13
allele frequency: 1.177109742846795e-3
allele num: 11044
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000444970
  ensembl transcript: ENST00000538248
  gene symbol: HYDIN
  hgvsc: ENST00000538248.1:c.2156+437G>A
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000314736
  ensembl transcript: ENST00000321489
  gene symbol: HYDIN
  hgvsc: ENST00000321489.5:c.2075+437G>A
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000437341
  ensembl transcript: ENST00000541601
  gene symbol: HYDIN
  hgvsc: ENST00000541601.1:c.2126+437G>A
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000446122
  ensembl transcript: ENST00000542890
  gene symbol: HYDIN
  hgvsc: ENST00000542890.1:c.361G>A
  hgvsp: ENSP00000446122.1:p.Arg121Gln
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000288168
  ensembl transcript: ENST00000288168
  gene symbol: HYDIN
  hgvsc: ENST00000288168.10:c.*385G>A
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000377181
  ensembl transcript: ENST00000393550
  gene symbol: HYDIN
  hgvsc: ENST00000393550.2:c.2201G>A
  hgvsp: ENSP00000377181.2:p.Arg734Gln
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000398544
  ensembl transcript: ENST00000448089
  gene symbol: HYDIN
  hgvsc: ENST00000448089.2:c.2075+437G>A
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463767
  ensembl transcript: ENST00000393552
  gene symbol: HYDIN
  hgvsc: ENST00000393552.2:c.929+437G>A
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000377197
  ensembl transcript: ENST00000393567
  gene symbol: HYDIN
  hgvsc: ENST00000393567.2:c.2075+437G>A
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463422
  ensembl transcript: ENST00000545230
  gene symbol: HYDIN
  hgvsc: ENST00000545230.1:c.1565G>A
  hgvsp: ENSP00000463422.1:p.Arg522Gln
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000394826
  ensembl transcript: ENST00000448691
  gene symbol: HYDIN
  hgvsc: ENST00000448691.1:c.2075+437G>A
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463093
  ensembl transcript: ENST00000539447
  gene symbol: HYDIN
  hgvsc: ENST00000539447.1:c.*1323+437G>A
  variant of: http://identifiers.org/hgnc/19368
canonical: false
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1499
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 970
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1665
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Arg734Gln
num of homozygotes: 0
population: Other
population: Latino
population: South Asian
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: DP

16-71100757-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71100757
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 71100757
    reference: chr 16
allele count: 13
allele frequency: 1.099086912411228e-3
allele num: 11828
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000437341
  ensembl transcript: ENST00000541601
  gene symbol: HYDIN
  hgvsc: ENST00000541601.1:c.2126+436C>T
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000444970
  ensembl transcript: ENST00000538248
  gene symbol: HYDIN
  hgvsc: ENST00000538248.1:c.2156+436C>T
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000446122
  ensembl transcript: ENST00000542890
  gene symbol: HYDIN
  hgvsc: ENST00000542890.1:c.360C>T
  hgvsp: ENSP00000446122.1:p.Arg121Trp
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463767
  ensembl transcript: ENST00000393552
  gene symbol: HYDIN
  hgvsc: ENST00000393552.2:c.929+436C>T
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000314736
  ensembl transcript: ENST00000321489
  gene symbol: HYDIN
  hgvsc: ENST00000321489.5:c.2075+436C>T
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463422
  ensembl transcript: ENST00000545230
  gene symbol: HYDIN
  hgvsc: ENST00000545230.1:c.1564C>T
  hgvsp: ENSP00000463422.1:p.Arg522Trp
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000377181
  ensembl transcript: ENST00000393550
  gene symbol: HYDIN
  hgvsc: ENST00000393550.2:c.2200C>T
  hgvsp: ENSP00000377181.2:p.Arg734Trp
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000398544
  ensembl transcript: ENST00000448089
  gene symbol: HYDIN
  hgvsc: ENST00000448089.2:c.2075+436C>T
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463093
  ensembl transcript: ENST00000539447
  gene symbol: HYDIN
  hgvsc: ENST00000539447.1:c.*1323+436C>T
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000288168
  ensembl transcript: ENST00000288168
  gene symbol: HYDIN
  hgvsc: ENST00000288168.10:c.*384C>T
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000377197
  ensembl transcript: ENST00000393567
  gene symbol: HYDIN
  hgvsc: ENST00000393567.2:c.2075+436C>T
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000394826
  ensembl transcript: ENST00000448691
  gene symbol: HYDIN
  hgvsc: ENST00000448691.1:c.2075+436C>T
  variant of: http://identifiers.org/hgnc/19368
canonical: false
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1544
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1199
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1338
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3791
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg734Trp
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum

http://identifiers.org/exac.variant/16-71100794-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71100794
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 71100794
    reference: chr 16
allele count: 1
allele frequency: 6.870019236053861e-5
allele num: 14556
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000377181
  ensembl transcript: ENST00000393550
  gene symbol: HYDIN
  hgvsc: ENST00000393550.2:c.2163G>T
  hgvsp: ENST00000393550.2:c.2163G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000288168
  ensembl transcript: ENST00000288168
  gene symbol: HYDIN
  hgvsc: ENST00000288168.10:c.*347G>T
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000377197
  ensembl transcript: ENST00000393567
  gene symbol: HYDIN
  hgvsc: ENST00000393567.2:c.2075+399G>T
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000314736
  ensembl transcript: ENST00000321489
  gene symbol: HYDIN
  hgvsc: ENST00000321489.5:c.2075+399G>T
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463093
  ensembl transcript: ENST00000539447
  gene symbol: HYDIN
  hgvsc: ENST00000539447.1:c.*1323+399G>T
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463767
  ensembl transcript: ENST00000393552
  gene symbol: HYDIN
  hgvsc: ENST00000393552.2:c.929+399G>T
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000437341
  ensembl transcript: ENST00000541601
  gene symbol: HYDIN
  hgvsc: ENST00000541601.1:c.2126+399G>T
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000446122
  ensembl transcript: ENST00000542890
  gene symbol: HYDIN
  hgvsc: ENST00000542890.1:c.323G>T
  hgvsp: ENST00000542890.1:c.323G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000394826
  ensembl transcript: ENST00000448691
  gene symbol: HYDIN
  hgvsc: ENST00000448691.1:c.2075+399G>T
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463422
  ensembl transcript: ENST00000545230
  gene symbol: HYDIN
  hgvsc: ENST00000545230.1:c.1527G>T
  hgvsp: ENST00000545230.1:c.1527G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000398544
  ensembl transcript: ENST00000448089
  gene symbol: HYDIN
  hgvsc: ENST00000448089.2:c.2075+399G>T
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000444970
  ensembl transcript: ENST00000538248
  gene symbol: HYDIN
  hgvsc: ENST00000538248.1:c.2156+399G>T
  variant of: http://identifiers.org/hgnc/19368
canonical: false
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 5182
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1503
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 846
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1998
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu721Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
population: Latino
population: African
population: South Asian
reference allele: C
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff

16-71100801-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71100801
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 71100801
    reference: chr 16
allele count: 1
allele frequency: 6.77323218639935e-5
allele num: 14764
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000288168
  ensembl transcript: ENST00000288168
  gene symbol: HYDIN
  hgvsc: ENST00000288168.10:c.*340C>G
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000314736
  ensembl transcript: ENST00000321489
  gene symbol: HYDIN
  hgvsc: ENST00000321489.5:c.2075+392C>G
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463767
  ensembl transcript: ENST00000393552
  gene symbol: HYDIN
  hgvsc: ENST00000393552.2:c.929+392C>G
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000394826
  ensembl transcript: ENST00000448691
  gene symbol: HYDIN
  hgvsc: ENST00000448691.1:c.2075+392C>G
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000446122
  ensembl transcript: ENST00000542890
  gene symbol: HYDIN
  hgvsc: ENST00000542890.1:c.316C>G
  hgvsp: ENSP00000446122.1:p.Ser106Ter
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463093
  ensembl transcript: ENST00000539447
  gene symbol: HYDIN
  hgvsc: ENST00000539447.1:c.*1323+392C>G
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000444970
  ensembl transcript: ENST00000538248
  gene symbol: HYDIN
  hgvsc: ENST00000538248.1:c.2156+392C>G
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463422
  ensembl transcript: ENST00000545230
  gene symbol: HYDIN
  hgvsc: ENST00000545230.1:c.1520C>G
  hgvsp: ENSP00000463422.1:p.Ser507Ter
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000377181
  ensembl transcript: ENST00000393550
  gene symbol: HYDIN
  hgvsc: ENST00000393550.2:c.2156C>G
  hgvsp: ENSP00000377181.2:p.Ser719Ter
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000377197
  ensembl transcript: ENST00000393567
  gene symbol: HYDIN
  hgvsc: ENST00000393567.2:c.2075+392C>G
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000437341
  ensembl transcript: ENST00000541601
  gene symbol: HYDIN
  hgvsc: ENST00000541601.1:c.2126+392C>G
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000398544
  ensembl transcript: ENST00000448089
  gene symbol: HYDIN
  hgvsc: ENST00000448089.2:c.2075+392C>G
  variant of: http://identifiers.org/hgnc/19368
canonical: false
consequence: stop gained
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5267
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1522
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2141
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 827
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Ser719Ter
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP

http://identifiers.org/exac.variant/16-71100802-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71100802
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 71100802
    reference: chr 16
allele count: 1
allele frequency: 6.760411032990806e-5
allele num: 14792
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463422
  ensembl transcript: ENST00000545230
  gene symbol: HYDIN
  hgvsc: ENST00000545230.1:c.1519T>G
  hgvsp: ENSP00000463422.1:p.Ser507Ala
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000377197
  ensembl transcript: ENST00000393567
  gene symbol: HYDIN
  hgvsc: ENST00000393567.2:c.2075+391T>G
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000288168
  ensembl transcript: ENST00000288168
  gene symbol: HYDIN
  hgvsc: ENST00000288168.10:c.*339T>G
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000377181
  ensembl transcript: ENST00000393550
  gene symbol: HYDIN
  hgvsc: ENST00000393550.2:c.2155T>G
  hgvsp: ENSP00000377181.2:p.Ser719Ala
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000446122
  ensembl transcript: ENST00000542890
  gene symbol: HYDIN
  hgvsc: ENST00000542890.1:c.315T>G
  hgvsp: ENSP00000446122.1:p.Ser106Ala
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000444970
  ensembl transcript: ENST00000538248
  gene symbol: HYDIN
  hgvsc: ENST00000538248.1:c.2156+391T>G
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000314736
  ensembl transcript: ENST00000321489
  gene symbol: HYDIN
  hgvsc: ENST00000321489.5:c.2075+391T>G
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463093
  ensembl transcript: ENST00000539447
  gene symbol: HYDIN
  hgvsc: ENST00000539447.1:c.*1323+391T>G
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000394826
  ensembl transcript: ENST00000448691
  gene symbol: HYDIN
  hgvsc: ENST00000448691.1:c.2075+391T>G
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000437341
  ensembl transcript: ENST00000541601
  gene symbol: HYDIN
  hgvsc: ENST00000541601.1:c.2126+391T>G
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463767
  ensembl transcript: ENST00000393552
  gene symbol: HYDIN
  hgvsc: ENST00000393552.2:c.929+391T>G
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000398544
  ensembl transcript: ENST00000448089
  gene symbol: HYDIN
  hgvsc: ENST00000448089.2:c.2075+391T>G
  variant of: http://identifiers.org/hgnc/19368
canonical: false
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 2151
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5275
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 827
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1523
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser719Ala
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
population: European (Finnish)
population: South Asian
reference allele: A
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: DP

16-71100811-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71100811
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 71100811
    reference: chr 16
allele count: 1
allele frequency: 6.674676278200507e-5
allele num: 14982
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463767
  ensembl transcript: ENST00000393552
  gene symbol: HYDIN
  hgvsc: ENST00000393552.2:c.929+382G>A
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000314736
  ensembl transcript: ENST00000321489
  gene symbol: HYDIN
  hgvsc: ENST00000321489.5:c.2075+382G>A
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000444970
  ensembl transcript: ENST00000538248
  gene symbol: HYDIN
  hgvsc: ENST00000538248.1:c.2156+382G>A
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000377197
  ensembl transcript: ENST00000393567
  gene symbol: HYDIN
  hgvsc: ENST00000393567.2:c.2075+382G>A
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463093
  ensembl transcript: ENST00000539447
  gene symbol: HYDIN
  hgvsc: ENST00000539447.1:c.*1323+382G>A
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000288168
  ensembl transcript: ENST00000288168
  gene symbol: HYDIN
  hgvsc: ENST00000288168.10:c.*330G>A
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463422
  ensembl transcript: ENST00000545230
  gene symbol: HYDIN
  hgvsc: ENST00000545230.1:c.1510G>A
  hgvsp: ENSP00000463422.1:p.Val504Met
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000394826
  ensembl transcript: ENST00000448691
  gene symbol: HYDIN
  hgvsc: ENST00000448691.1:c.2075+382G>A
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000446122
  ensembl transcript: ENST00000542890
  gene symbol: HYDIN
  hgvsc: ENST00000542890.1:c.306G>A
  hgvsp: ENSP00000446122.1:p.Val103Met
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000398544
  ensembl transcript: ENST00000448089
  gene symbol: HYDIN
  hgvsc: ENST00000448089.2:c.2075+382G>A
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000377181
  ensembl transcript: ENST00000393550
  gene symbol: HYDIN
  hgvsc: ENST00000393550.2:c.2146G>A
  hgvsp: ENSP00000377181.2:p.Val716Met
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000437341
  ensembl transcript: ENST00000541601
  gene symbol: HYDIN
  hgvsc: ENST00000541601.1:c.2126+382G>A
  variant of: http://identifiers.org/hgnc/19368
canonical: false
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5342
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 811
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1545
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2344
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val716Met
num of homozygotes: 0
population: South Asian
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Latino
reference allele: C
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ

16-71100823-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71100823
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 71100823
    reference: chr 16
allele count: 1
allele frequency: 6.573757559821194e-5
allele num: 15212
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463767
  ensembl transcript: ENST00000393552
  gene symbol: HYDIN
  hgvsc: ENST00000393552.2:c.929+370T>C
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000398544
  ensembl transcript: ENST00000448089
  gene symbol: HYDIN
  hgvsc: ENST00000448089.2:c.2075+370T>C
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463422
  ensembl transcript: ENST00000545230
  gene symbol: HYDIN
  hgvsc: ENST00000545230.1:c.1498T>C
  hgvsp: ENSP00000463422.1:p.Cys500Arg
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000437341
  ensembl transcript: ENST00000541601
  gene symbol: HYDIN
  hgvsc: ENST00000541601.1:c.2126+370T>C
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000377181
  ensembl transcript: ENST00000393550
  gene symbol: HYDIN
  hgvsc: ENST00000393550.2:c.2134T>C
  hgvsp: ENSP00000377181.2:p.Cys712Arg
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000446122
  ensembl transcript: ENST00000542890
  gene symbol: HYDIN
  hgvsc: ENST00000542890.1:c.294T>C
  hgvsp: ENSP00000446122.1:p.Cys99Arg
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000288168
  ensembl transcript: ENST00000288168
  gene symbol: HYDIN
  hgvsc: ENST00000288168.10:c.*318T>C
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000314736
  ensembl transcript: ENST00000321489
  gene symbol: HYDIN
  hgvsc: ENST00000321489.5:c.2075+370T>C
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000377197
  ensembl transcript: ENST00000393567
  gene symbol: HYDIN
  hgvsc: ENST00000393567.2:c.2075+370T>C
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000394826
  ensembl transcript: ENST00000448691
  gene symbol: HYDIN
  hgvsc: ENST00000448691.1:c.2075+370T>C
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463093
  ensembl transcript: ENST00000539447
  gene symbol: HYDIN
  hgvsc: ENST00000539447.1:c.*1323+370T>C
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000444970
  ensembl transcript: ENST00000538248
  gene symbol: HYDIN
  hgvsc: ENST00000538248.1:c.2156+370T>C
  variant of: http://identifiers.org/hgnc/19368
canonical: false
consequence: missense
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5403
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1562
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 792
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2462
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Cys712Arg
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP

16-71100826-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71100826
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 71100826
    reference: chr 16
allele count: 1
allele frequency: 6.563402467839328e-5
allele num: 15236
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000288168
  ensembl transcript: ENST00000288168
  gene symbol: HYDIN
  hgvsc: ENST00000288168.10:c.*315T>C
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000398544
  ensembl transcript: ENST00000448089
  gene symbol: HYDIN
  hgvsc: ENST00000448089.2:c.2075+367T>C
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000394826
  ensembl transcript: ENST00000448691
  gene symbol: HYDIN
  hgvsc: ENST00000448691.1:c.2075+367T>C
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463767
  ensembl transcript: ENST00000393552
  gene symbol: HYDIN
  hgvsc: ENST00000393552.2:c.929+367T>C
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000446122
  ensembl transcript: ENST00000542890
  gene symbol: HYDIN
  hgvsc: ENST00000542890.1:c.291T>C
  hgvsp: ENST00000542890.1:c.291T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000444970
  ensembl transcript: ENST00000538248
  gene symbol: HYDIN
  hgvsc: ENST00000538248.1:c.2156+367T>C
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000314736
  ensembl transcript: ENST00000321489
  gene symbol: HYDIN
  hgvsc: ENST00000321489.5:c.2075+367T>C
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463422
  ensembl transcript: ENST00000545230
  gene symbol: HYDIN
  hgvsc: ENST00000545230.1:c.1495T>C
  hgvsp: ENST00000545230.1:c.1495T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000377181
  ensembl transcript: ENST00000393550
  gene symbol: HYDIN
  hgvsc: ENST00000393550.2:c.2131T>C
  hgvsp: ENST00000393550.2:c.2131T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000377197
  ensembl transcript: ENST00000393567
  gene symbol: HYDIN
  hgvsc: ENST00000393567.2:c.2075+367T>C
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463093
  ensembl transcript: ENST00000539447
  gene symbol: HYDIN
  hgvsc: ENST00000539447.1:c.*1323+367T>C
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000437341
  ensembl transcript: ENST00000541601
  gene symbol: HYDIN
  hgvsc: ENST00000541601.1:c.2126+367T>C
  variant of: http://identifiers.org/hgnc/19368
canonical: false
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5395
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 789
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1563
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2424
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu711Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: East Asian
population: African
population: Latino
population: South Asian
reference allele: A
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: DP

16-71100827-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71100827
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 71100827
    reference: chr 16
allele count: 1
allele frequency: 6.556517178075007e-5
allele num: 15252
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463093
  ensembl transcript: ENST00000539447
  gene symbol: HYDIN
  hgvsc: ENST00000539447.1:c.*1323+366G>A
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463767
  ensembl transcript: ENST00000393552
  gene symbol: HYDIN
  hgvsc: ENST00000393552.2:c.929+366G>A
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000444970
  ensembl transcript: ENST00000538248
  gene symbol: HYDIN
  hgvsc: ENST00000538248.1:c.2156+366G>A
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000446122
  ensembl transcript: ENST00000542890
  gene symbol: HYDIN
  hgvsc: ENST00000542890.1:c.290G>A
  hgvsp: ENST00000542890.1:c.290G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000437341
  ensembl transcript: ENST00000541601
  gene symbol: HYDIN
  hgvsc: ENST00000541601.1:c.2126+366G>A
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000377181
  ensembl transcript: ENST00000393550
  gene symbol: HYDIN
  hgvsc: ENST00000393550.2:c.2130G>A
  hgvsp: ENST00000393550.2:c.2130G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000398544
  ensembl transcript: ENST00000448089
  gene symbol: HYDIN
  hgvsc: ENST00000448089.2:c.2075+366G>A
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463422
  ensembl transcript: ENST00000545230
  gene symbol: HYDIN
  hgvsc: ENST00000545230.1:c.1494G>A
  hgvsp: ENST00000545230.1:c.1494G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000314736
  ensembl transcript: ENST00000321489
  gene symbol: HYDIN
  hgvsc: ENST00000321489.5:c.2075+366G>A
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000377197
  ensembl transcript: ENST00000393567
  gene symbol: HYDIN
  hgvsc: ENST00000393567.2:c.2075+366G>A
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000288168
  ensembl transcript: ENST00000288168
  gene symbol: HYDIN
  hgvsc: ENST00000288168.10:c.*314G>A
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000394826
  ensembl transcript: ENST00000448691
  gene symbol: HYDIN
  hgvsc: ENST00000448691.1:c.2075+366G>A
  variant of: http://identifiers.org/hgnc/19368
canonical: false
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 1562
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2456
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5403
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 783
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu710Glu
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: Other
population: East Asian
reference allele: C
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: FS

16-71100833-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71100833
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 71100833
    reference: chr 16
allele count: 9
allele frequency: 5.889281507656066e-4
allele num: 15282
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463422
  ensembl transcript: ENST00000545230
  gene symbol: HYDIN
  hgvsc: ENST00000545230.1:c.1488T>C
  hgvsp: ENST00000545230.1:c.1488T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000446122
  ensembl transcript: ENST00000542890
  gene symbol: HYDIN
  hgvsc: ENST00000542890.1:c.284T>C
  hgvsp: ENST00000542890.1:c.284T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000437341
  ensembl transcript: ENST00000541601
  gene symbol: HYDIN
  hgvsc: ENST00000541601.1:c.2126+360T>C
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000288168
  ensembl transcript: ENST00000288168
  gene symbol: HYDIN
  hgvsc: ENST00000288168.10:c.*308T>C
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000444970
  ensembl transcript: ENST00000538248
  gene symbol: HYDIN
  hgvsc: ENST00000538248.1:c.2156+360T>C
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000314736
  ensembl transcript: ENST00000321489
  gene symbol: HYDIN
  hgvsc: ENST00000321489.5:c.2075+360T>C
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000377197
  ensembl transcript: ENST00000393567
  gene symbol: HYDIN
  hgvsc: ENST00000393567.2:c.2075+360T>C
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000377181
  ensembl transcript: ENST00000393550
  gene symbol: HYDIN
  hgvsc: ENST00000393550.2:c.2124T>C
  hgvsp: ENST00000393550.2:c.2124T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000394826
  ensembl transcript: ENST00000448691
  gene symbol: HYDIN
  hgvsc: ENST00000448691.1:c.2075+360T>C
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463767
  ensembl transcript: ENST00000393552
  gene symbol: HYDIN
  hgvsc: ENST00000393552.2:c.929+360T>C
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000398544
  ensembl transcript: ENST00000448089
  gene symbol: HYDIN
  hgvsc: ENST00000448089.2:c.2075+360T>C
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463093
  ensembl transcript: ENST00000539447
  gene symbol: HYDIN
  hgvsc: ENST00000539447.1:c.*1323+360T>C
  variant of: http://identifiers.org/hgnc/19368
canonical: false
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2408
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5363
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1579
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 777
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala708Ala
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: African
reference allele: A
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD

16-71100838-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71100838
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 71100838
    reference: chr 16
allele count: 5277
allele frequency: 3.366292421536106e-1
allele num: 15676
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000288168
  ensembl transcript: ENST00000288168
  gene symbol: HYDIN
  hgvsc: ENST00000288168.10:c.*303A>G
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000314736
  ensembl transcript: ENST00000321489
  gene symbol: HYDIN
  hgvsc: ENST00000321489.5:c.2075+355A>G
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000398544
  ensembl transcript: ENST00000448089
  gene symbol: HYDIN
  hgvsc: ENST00000448089.2:c.2075+355A>G
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000446122
  ensembl transcript: ENST00000542890
  gene symbol: HYDIN
  hgvsc: ENST00000542890.1:c.281-2A>G
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463422
  ensembl transcript: ENST00000545230
  gene symbol: HYDIN
  hgvsc: ENST00000545230.1:c.1485-2A>G
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000437341
  ensembl transcript: ENST00000541601
  gene symbol: HYDIN
  hgvsc: ENST00000541601.1:c.2126+355A>G
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000377181
  ensembl transcript: ENST00000393550
  gene symbol: HYDIN
  hgvsc: ENST00000393550.2:c.2121-2A>G
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463767
  ensembl transcript: ENST00000393552
  gene symbol: HYDIN
  hgvsc: ENST00000393552.2:c.929+355A>G
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000377197
  ensembl transcript: ENST00000393567
  gene symbol: HYDIN
  hgvsc: ENST00000393567.2:c.2075+355A>G
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463093
  ensembl transcript: ENST00000539447
  gene symbol: HYDIN
  hgvsc: ENST00000539447.1:c.*1323+355A>G
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000394826
  ensembl transcript: ENST00000448691
  gene symbol: HYDIN
  hgvsc: ENST00000448691.1:c.2075+355A>G
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000444970
  ensembl transcript: ENST00000538248
  gene symbol: HYDIN
  hgvsc: ENST00000538248.1:c.2156+355A>G
  variant of: http://identifiers.org/hgnc/19368
canonical: false
consequence: splice acceptor
filter: InbreedingCoeff_Filter
genotype depth: GenotypeDepth
  all individuals: 1683
  bin: 2.5e0
  variant carriers: 144
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 7.5e0
  variant carriers: 235
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 5.75e1
  variant carriers: 273
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 6.75e1
  variant carriers: 273
genotype depth: GenotypeDepth
  all individuals: 2204
  bin: 2.25e1
  variant carriers: 179
genotype depth: GenotypeDepth
  all individuals: 1225
  bin: 9.75e1
  variant carriers: 1224
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 4.75e1
  variant carriers: 242
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 1.75e1
  variant carriers: 210
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 7.75e1
  variant carriers: 271
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 6.25e1
  variant carriers: 264
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 4.25e1
  variant carriers: 211
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 3.75e1
  variant carriers: 205
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 1.25e1
  variant carriers: 177
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 8.75e1
  variant carriers: 174
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 3.25e1
  variant carriers: 188
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 9.25e1
  variant carriers: 184
genotype depth: GenotypeDepth
  all individuals: 804
  bin: 2.75e1
  variant carriers: 188
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 5.25e1
  variant carriers: 258
genotype quality: GenotypeQuality
hgvs: c.2121-2A>G
num of homozygotes: 312
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
population: Latino
reference allele: T
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ

16-71100847-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71100847
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 71100847
    reference: chr 16
allele count: 2
allele frequency: 1.312680493567866e-4
allele num: 15236
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463767
  ensembl transcript: ENST00000393552
  gene symbol: HYDIN
  hgvsc: ENST00000393552.2:c.929+346T>C
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000377181
  ensembl transcript: ENST00000393550
  gene symbol: HYDIN
  hgvsc: ENST00000393550.2:c.2121-11T>C
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000377197
  ensembl transcript: ENST00000393567
  gene symbol: HYDIN
  hgvsc: ENST00000393567.2:c.2075+346T>C
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000394826
  ensembl transcript: ENST00000448691
  gene symbol: HYDIN
  hgvsc: ENST00000448691.1:c.2075+346T>C
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000288168
  ensembl transcript: ENST00000288168
  gene symbol: HYDIN
  hgvsc: ENST00000288168.10:c.*294T>C
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463093
  ensembl transcript: ENST00000539447
  gene symbol: HYDIN
  hgvsc: ENST00000539447.1:c.*1323+346T>C
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000398544
  ensembl transcript: ENST00000448089
  gene symbol: HYDIN
  hgvsc: ENST00000448089.2:c.2075+346T>C
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000437341
  ensembl transcript: ENST00000541601
  gene symbol: HYDIN
  hgvsc: ENST00000541601.1:c.2126+346T>C
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000446122
  ensembl transcript: ENST00000542890
  gene symbol: HYDIN
  hgvsc: ENST00000542890.1:c.281-11T>C
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463422
  ensembl transcript: ENST00000545230
  gene symbol: HYDIN
  hgvsc: ENST00000545230.1:c.1485-11T>C
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000444970
  ensembl transcript: ENST00000538248
  gene symbol: HYDIN
  hgvsc: ENST00000538248.1:c.2156+346T>C
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000314736
  ensembl transcript: ENST00000321489
  gene symbol: HYDIN
  hgvsc: ENST00000321489.5:c.2075+346T>C
  variant of: http://identifiers.org/hgnc/19368
canonical: false
consequence: 3' UTR
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1945
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2188
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2318
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 659
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 577
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1558
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
population: Other
reference allele: A
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ

16-71100850-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71100850
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 71100850
    reference: chr 16
allele count: 2
allele frequency: 1.316309069369488e-4
allele num: 15194
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463767
  ensembl transcript: ENST00000393552
  gene symbol: HYDIN
  hgvsc: ENST00000393552.2:c.929+343A>G
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000288168
  ensembl transcript: ENST00000288168
  gene symbol: HYDIN
  hgvsc: ENST00000288168.10:c.*291A>G
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000398544
  ensembl transcript: ENST00000448089
  gene symbol: HYDIN
  hgvsc: ENST00000448089.2:c.2075+343A>G
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463422
  ensembl transcript: ENST00000545230
  gene symbol: HYDIN
  hgvsc: ENST00000545230.1:c.1485-14A>G
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000444970
  ensembl transcript: ENST00000538248
  gene symbol: HYDIN
  hgvsc: ENST00000538248.1:c.2156+343A>G
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463093
  ensembl transcript: ENST00000539447
  gene symbol: HYDIN
  hgvsc: ENST00000539447.1:c.*1323+343A>G
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000314736
  ensembl transcript: ENST00000321489
  gene symbol: HYDIN
  hgvsc: ENST00000321489.5:c.2075+343A>G
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000394826
  ensembl transcript: ENST00000448691
  gene symbol: HYDIN
  hgvsc: ENST00000448691.1:c.2075+343A>G
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000437341
  ensembl transcript: ENST00000541601
  gene symbol: HYDIN
  hgvsc: ENST00000541601.1:c.2126+343A>G
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000377197
  ensembl transcript: ENST00000393567
  gene symbol: HYDIN
  hgvsc: ENST00000393567.2:c.2075+343A>G
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000377181
  ensembl transcript: ENST00000393550
  gene symbol: HYDIN
  hgvsc: ENST00000393550.2:c.2121-14A>G
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000446122
  ensembl transcript: ENST00000542890
  gene symbol: HYDIN
  hgvsc: ENST00000542890.1:c.281-14A>G
  variant of: http://identifiers.org/hgnc/19368
canonical: false
consequence: 3' UTR
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 575
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 667
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1545
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2154
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2356
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1926
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
population: South Asian
population: Latino
reference allele: T
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD

http://identifiers.org/exac.variant/16-71100867-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71100867
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 71100867
    reference: chr 16
allele count: 1
allele frequency: 6.817562039814562e-5
allele num: 14668
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000288168
  ensembl transcript: ENST00000288168
  gene symbol: HYDIN
  hgvsc: ENST00000288168.10:c.*274T>G
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000394826
  ensembl transcript: ENST00000448691
  gene symbol: HYDIN
  hgvsc: ENST00000448691.1:c.2075+326T>G
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000377197
  ensembl transcript: ENST00000393567
  gene symbol: HYDIN
  hgvsc: ENST00000393567.2:c.2075+326T>G
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000314736
  ensembl transcript: ENST00000321489
  gene symbol: HYDIN
  hgvsc: ENST00000321489.5:c.2075+326T>G
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463093
  ensembl transcript: ENST00000539447
  gene symbol: HYDIN
  hgvsc: ENST00000539447.1:c.*1323+326T>G
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000398544
  ensembl transcript: ENST00000448089
  gene symbol: HYDIN
  hgvsc: ENST00000448089.2:c.2075+326T>G
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000446122
  ensembl transcript: ENST00000542890
  gene symbol: HYDIN
  hgvsc: ENST00000542890.1:c.281-31T>G
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463767
  ensembl transcript: ENST00000393552
  gene symbol: HYDIN
  hgvsc: ENST00000393552.2:c.929+326T>G
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000377181
  ensembl transcript: ENST00000393550
  gene symbol: HYDIN
  hgvsc: ENST00000393550.2:c.2121-31T>G
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000437341
  ensembl transcript: ENST00000541601
  gene symbol: HYDIN
  hgvsc: ENST00000541601.1:c.2126+326T>G
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000444970
  ensembl transcript: ENST00000538248
  gene symbol: HYDIN
  hgvsc: ENST00000538248.1:c.2156+326T>G
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463422
  ensembl transcript: ENST00000545230
  gene symbol: HYDIN
  hgvsc: ENST00000545230.1:c.1485-31T>G
  variant of: http://identifiers.org/hgnc/19368
canonical: false
consequence: 3' UTR
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 1649
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2487
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1458
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 901
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1004
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 742
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1284
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
population: African
reference allele: A
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum

16-71100868-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71100868
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 71100868
    reference: chr 16
allele count: 1
allele frequency: 6.835269993164729e-5
allele num: 14630
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000394826
  ensembl transcript: ENST00000448691
  gene symbol: HYDIN
  hgvsc: ENST00000448691.1:c.2075+325C>A
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000288168
  ensembl transcript: ENST00000288168
  gene symbol: HYDIN
  hgvsc: ENST00000288168.10:c.*273C>A
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000446122
  ensembl transcript: ENST00000542890
  gene symbol: HYDIN
  hgvsc: ENST00000542890.1:c.281-32C>A
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000437341
  ensembl transcript: ENST00000541601
  gene symbol: HYDIN
  hgvsc: ENST00000541601.1:c.2126+325C>A
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463093
  ensembl transcript: ENST00000539447
  gene symbol: HYDIN
  hgvsc: ENST00000539447.1:c.*1323+325C>A
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000398544
  ensembl transcript: ENST00000448089
  gene symbol: HYDIN
  hgvsc: ENST00000448089.2:c.2075+325C>A
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463767
  ensembl transcript: ENST00000393552
  gene symbol: HYDIN
  hgvsc: ENST00000393552.2:c.929+325C>A
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463422
  ensembl transcript: ENST00000545230
  gene symbol: HYDIN
  hgvsc: ENST00000545230.1:c.1485-32C>A
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000314736
  ensembl transcript: ENST00000321489
  gene symbol: HYDIN
  hgvsc: ENST00000321489.5:c.2075+325C>A
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000377181
  ensembl transcript: ENST00000393550
  gene symbol: HYDIN
  hgvsc: ENST00000393550.2:c.2121-32C>A
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000444970
  ensembl transcript: ENST00000538248
  gene symbol: HYDIN
  hgvsc: ENST00000538248.1:c.2156+325C>A
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000377197
  ensembl transcript: ENST00000393567
  gene symbol: HYDIN
  hgvsc: ENST00000393567.2:c.2075+325C>A
  variant of: http://identifiers.org/hgnc/19368
canonical: false
consequence: 3' UTR
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1427
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1225
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1003
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 956
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1677
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 754
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2501
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum

16-71100869-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71100869
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 71100869
    reference: chr 16
allele count: 7
allele frequency: 4.900588070568468e-4
allele num: 14284
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000444970
  ensembl transcript: ENST00000538248
  gene symbol: HYDIN
  hgvsc: ENST00000538248.1:c.2156+324G>C
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463093
  ensembl transcript: ENST00000539447
  gene symbol: HYDIN
  hgvsc: ENST00000539447.1:c.*1323+324G>C
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000377181
  ensembl transcript: ENST00000393550
  gene symbol: HYDIN
  hgvsc: ENST00000393550.2:c.2121-33G>C
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000446122
  ensembl transcript: ENST00000542890
  gene symbol: HYDIN
  hgvsc: ENST00000542890.1:c.281-33G>C
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000394826
  ensembl transcript: ENST00000448691
  gene symbol: HYDIN
  hgvsc: ENST00000448691.1:c.2075+324G>C
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000288168
  ensembl transcript: ENST00000288168
  gene symbol: HYDIN
  hgvsc: ENST00000288168.10:c.*272G>C
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000398544
  ensembl transcript: ENST00000448089
  gene symbol: HYDIN
  hgvsc: ENST00000448089.2:c.2075+324G>C
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000377197
  ensembl transcript: ENST00000393567
  gene symbol: HYDIN
  hgvsc: ENST00000393567.2:c.2075+324G>C
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000437341
  ensembl transcript: ENST00000541601
  gene symbol: HYDIN
  hgvsc: ENST00000541601.1:c.2126+324G>C
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463422
  ensembl transcript: ENST00000545230
  gene symbol: HYDIN
  hgvsc: ENST00000545230.1:c.1485-33G>C
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463767
  ensembl transcript: ENST00000393552
  gene symbol: HYDIN
  hgvsc: ENST00000393552.2:c.929+324G>C
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000314736
  ensembl transcript: ENST00000321489
  gene symbol: HYDIN
  hgvsc: ENST00000321489.5:c.2075+324G>C
  variant of: http://identifiers.org/hgnc/19368
canonical: false
consequence: 3' UTR
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 989
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2500
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1205
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1625
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1720
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 737
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 837
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
population: Latino
reference allele: C
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum

http://identifiers.org/exac.variant/16-71100877-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71100877
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 71100877
    reference: chr 16
allele count: 1
allele frequency: 7.265329845975008e-5
allele num: 13764
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000288168
  ensembl transcript: ENST00000288168
  gene symbol: HYDIN
  hgvsc: ENST00000288168.10:c.*264G>T
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000446122
  ensembl transcript: ENST00000542890
  gene symbol: HYDIN
  hgvsc: ENST00000542890.1:c.281-41G>T
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000314736
  ensembl transcript: ENST00000321489
  gene symbol: HYDIN
  hgvsc: ENST00000321489.5:c.2075+316G>T
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463093
  ensembl transcript: ENST00000539447
  gene symbol: HYDIN
  hgvsc: ENST00000539447.1:c.*1323+316G>T
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463767
  ensembl transcript: ENST00000393552
  gene symbol: HYDIN
  hgvsc: ENST00000393552.2:c.929+316G>T
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463422
  ensembl transcript: ENST00000545230
  gene symbol: HYDIN
  hgvsc: ENST00000545230.1:c.1485-41G>T
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000398544
  ensembl transcript: ENST00000448089
  gene symbol: HYDIN
  hgvsc: ENST00000448089.2:c.2075+316G>T
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000377197
  ensembl transcript: ENST00000393567
  gene symbol: HYDIN
  hgvsc: ENST00000393567.2:c.2075+316G>T
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000377181
  ensembl transcript: ENST00000393550
  gene symbol: HYDIN
  hgvsc: ENST00000393550.2:c.2121-41G>T
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000437341
  ensembl transcript: ENST00000541601
  gene symbol: HYDIN
  hgvsc: ENST00000541601.1:c.2126+316G>T
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000444970
  ensembl transcript: ENST00000538248
  gene symbol: HYDIN
  hgvsc: ENST00000538248.1:c.2156+316G>T
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000394826
  ensembl transcript: ENST00000448691
  gene symbol: HYDIN
  hgvsc: ENST00000448691.1:c.2075+316G>T
  variant of: http://identifiers.org/hgnc/19368
canonical: false
consequence: 3' UTR
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 2616
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1935
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1620
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1045
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1458
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD

16-71101111-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71101111
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 71101111
    reference: chr 16
allele count: 0
allele frequency: 0.0e0
allele num: 4910
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000446122
  ensembl transcript: ENST00000542890
  gene symbol: HYDIN
  hgvsc: ENST00000542890.1:c.280+82G>A
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000288168
  ensembl transcript: ENST00000288168
  gene symbol: HYDIN
  hgvsc: ENST00000288168.10:c.*30G>A
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463422
  ensembl transcript: ENST00000545230
  gene symbol: HYDIN
  hgvsc: ENST00000545230.1:c.1484+82G>A
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000377181
  ensembl transcript: ENST00000393550
  gene symbol: HYDIN
  hgvsc: ENST00000393550.2:c.2120+82G>A
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463767
  ensembl transcript: ENST00000393552
  gene symbol: HYDIN
  hgvsc: ENST00000393552.2:c.929+82G>A
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000398544
  ensembl transcript: ENST00000448089
  gene symbol: HYDIN
  hgvsc: ENST00000448089.2:c.2075+82G>A
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463093
  ensembl transcript: ENST00000539447
  gene symbol: HYDIN
  hgvsc: ENST00000539447.1:c.*1323+82G>A
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000437341
  ensembl transcript: ENST00000541601
  gene symbol: HYDIN
  hgvsc: ENST00000541601.1:c.2126+82G>A
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000377197
  ensembl transcript: ENST00000393567
  gene symbol: HYDIN
  hgvsc: ENST00000393567.2:c.2075+82G>A
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000394826
  ensembl transcript: ENST00000448691
  gene symbol: HYDIN
  hgvsc: ENST00000448691.1:c.2075+82G>A
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000314736
  ensembl transcript: ENST00000321489
  gene symbol: HYDIN
  hgvsc: ENST00000321489.5:c.2075+82G>A
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000444970
  ensembl transcript: ENST00000538248
  gene symbol: HYDIN
  hgvsc: ENST00000538248.1:c.2156+82G>A
  variant of: http://identifiers.org/hgnc/19368
canonical: false
consequence: 3' UTR
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 40733
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 745
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10788
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1025
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Latino
reference allele: C
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: VQSLOD

16-71101118-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71101118
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 71101118
    reference: chr 16
allele count: 1
allele frequency: 1.984126984126984e-4
allele num: 5040
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000398544
  ensembl transcript: ENST00000448089
  gene symbol: HYDIN
  hgvsc: ENST00000448089.2:c.2075+75C>T
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463093
  ensembl transcript: ENST00000539447
  gene symbol: HYDIN
  hgvsc: ENST00000539447.1:c.*1323+75C>T
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463422
  ensembl transcript: ENST00000545230
  gene symbol: HYDIN
  hgvsc: ENST00000545230.1:c.1484+75C>T
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000288168
  ensembl transcript: ENST00000288168
  gene symbol: HYDIN
  hgvsc: ENST00000288168.10:c.*23C>T
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000437341
  ensembl transcript: ENST00000541601
  gene symbol: HYDIN
  hgvsc: ENST00000541601.1:c.2126+75C>T
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000377197
  ensembl transcript: ENST00000393567
  gene symbol: HYDIN
  hgvsc: ENST00000393567.2:c.2075+75C>T
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000377181
  ensembl transcript: ENST00000393550
  gene symbol: HYDIN
  hgvsc: ENST00000393550.2:c.2120+75C>T
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000314736
  ensembl transcript: ENST00000321489
  gene symbol: HYDIN
  hgvsc: ENST00000321489.5:c.2075+75C>T
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000394826
  ensembl transcript: ENST00000448691
  gene symbol: HYDIN
  hgvsc: ENST00000448691.1:c.2075+75C>T
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000444970
  ensembl transcript: ENST00000538248
  gene symbol: HYDIN
  hgvsc: ENST00000538248.1:c.2156+75C>T
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000463767
  ensembl transcript: ENST00000393552
  gene symbol: HYDIN
  hgvsc: ENST00000393552.2:c.929+75C>T
  variant of: http://identifiers.org/hgnc/19368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157423
  ensembl protein: ENSP00000446122
  ensembl transcript: ENST00000542890
  gene symbol: HYDIN
  hgvsc: ENST00000542890.1:c.280+75C>T
  variant of: http://identifiers.org/hgnc/19368
canonical: false
consequence: 3' UTR
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 12999
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39785
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1009
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
reference allele: G

GenotypeQuality
all individuals: 56
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17189
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11933
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 100
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1485
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 502
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1065
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1209
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3251
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7012
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 763
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 116
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 177
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 380
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9179
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1970
bin: 3.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2764
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4488
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1338
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 300
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 18632
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2054
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7856
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.73e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.73e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.48e-1

QD
type: SiteQuality
SIO_000300: 3.57e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.59e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 6.07775e5

BaseQRankSum
type: SiteQuality
SIO_000300: 2.05e0

MQ
type: SiteQuality
SIO_000300: 3.528e1

VQSLOD
type: SiteQuality
SIO_000300: -3.461e0

GenotypeQuality
all individuals: 144
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15857
bin: 2.25e1
variant carriers: 1

GenotypeQuality
all individuals: 370
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7069
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 130
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10391
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1093
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2629
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3246
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1462
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 764
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 179
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1966
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 913
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 116
bin: 8.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 292
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2674
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4404
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1292
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 18232
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1990
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7682
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 7.31e-1

DP
type: SiteQuality
SIO_000300: 6.07943e5

VQSLOD
type: SiteQuality
SIO_000300: -4.147e0

MQ
type: SiteQuality
SIO_000300: 3.466e1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.322e1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.31e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.31e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.66e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.31e-1

GenotypeQuality
all individuals: 102
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4498
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 116
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 886
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6025
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9269
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 501
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1022
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 255
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 92
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 849
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 71
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1043
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5436
bin: 3.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2368
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2788
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2236
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3360
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4104
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 4.578754578754579e-5
allele num: 21840
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 292
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 5.3033e5

BaseQRankSum
type: SiteQuality
SIO_000300: 3.65e-1

QD
type: SiteQuality
SIO_000300: 4.52e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.09e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.8e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.53e-1

FS
type: SiteQuality
SIO_000300: 2.551e0

MQ
type: SiteQuality
SIO_000300: 3.735e1

MQRankSum
type: SiteQuality
SIO_000300: 1.45e0

VQSLOD
type: SiteQuality
SIO_000300: -3.958e0

GenotypeQuality
all individuals: 9526
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 99
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4497
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 115
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 270
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 92
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 360
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18210
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 981
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5437
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 69
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 848
bin: 9.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3352
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4112
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2244
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 292
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2370
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 21894
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2792
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 2.456e1

MQRankSum
type: SiteQuality
SIO_000300: 1.16e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.76e-1

QD
type: SiteQuality
SIO_000300: 6.66e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.61e-1

VQSLOD
type: SiteQuality
SIO_000300: -6.038e0

BaseQRankSum
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.1e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 5.33686e5

GenotypeQuality
all individuals: 1589
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5717
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 93
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 849
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19175
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 845
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2942
bin: 3.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4472
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 824
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9585
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 257
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 283
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 99
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 74
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 120
bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 21962
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2796
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2360
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4134
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2252
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3380
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 294
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -5.978e0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 6.33e0

MQ
type: SiteQuality
SIO_000300: 2.574e1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.2e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.38e0

BaseQRankSum
type: SiteQuality
SIO_000300: 7.2e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.03e-2

DP
type: SiteQuality
SIO_000300: 5.3927e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
all individuals: 5478
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 781
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 190
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6058
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1882
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9608
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 658
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 98
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 299
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 853
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 5468
bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 2360
num of homozygotes: 0

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

East Asian
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allele frequency: 1.469723691945914e-3
allele num: 3402
num of homozygotes: 0

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

South Asian
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allele frequency: 0.0e0
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DP
type: SiteQuality
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BaseQRankSum
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MQ
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InbreedingCoeff
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ReadPosRankSum
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VQSLOD
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MQRankSum
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QD
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ClippingRankSum
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SIO_000300: 5.79e-1

FS
type: SiteQuality
SIO_000300: 3.941e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 frequency: 0.0e0
allele num: 4240
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
allele num: 2406
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 2
allele frequency: 8.797395970792646e-5
allele num: 22734
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

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

MQ
type: SiteQuality
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FS
type: SiteQuality
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InbreedingCoeff
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DP
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VQSLOD
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BaseQRankSum
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MQRankSum
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ClippingRankSum
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ReadPosRankSum
type: SiteQuality
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 23316
num of homozygotes: 0

Latino
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allele frequency: 6.587615283267457e-4
allele num: 3036
num of homozygotes: 0

African
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allele count: 9
allele frequency: 2.088167053364269e-3
allele num: 4310
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East Asian
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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South Asian
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Other
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ReadPosRankSum
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FS
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MQRankSum
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VQSLOD
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ClippingRankSum
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MQ
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QD
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InbreedingCoeff
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SIO_000300: -1.6e-2

BaseQRankSum
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 2670
num of homozygotes: 0

Latino
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allele count: 4
allele frequency: 1.182732111176819e-3
allele num: 3382
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 3.954444795950648e-5
allele num: 25288
num of homozygotes: 0

African
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allele frequency: 0.0e0
allele num: 4698
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East Asian
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allele count: 0
allele frequency: 0.0e0
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South Asian
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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
allele num: 318
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.12e-1

VQSLOD
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SIO_000300: -4.546e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
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MQRankSum
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DP
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SIO_000300: 6.62139e5

MQ
type: SiteQuality
SIO_000300: 2.927e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.4e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 1.37e0

QD
type: SiteQuality
SIO_000300: 1.11e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele count: 0
allele frequency: 0.0e0
allele num: 4790
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 3006
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 2718
num of homozygotes: 0

East Asian
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allele frequency: 2.529084471421346e-4
allele num: 3954
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Latino
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

Other
type: Population
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allele frequency: 0.0e0
allele num: 328
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MQ
type: SiteQuality
SIO_000300: 2.811e1

QD
type: SiteQuality
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VQSLOD
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ClippingRankSum
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InbreedingCoeff
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ReadPosRankSum
type: SiteQuality
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FS
type: SiteQuality
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BaseQRankSum
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SIO_000300: 1.68e0

DP
type: SiteQuality
SIO_000300: 6.83305e5

MQRankSum
type: SiteQuality
SIO_000300: -3.4e-1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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num of homozygotes: 0

African
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allele frequency: 0.0e0
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Latino
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European (Non-Finnish)
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allele num: 44294
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European (Finnish)
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Other
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East Asian
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ClippingRankSum
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BaseQRankSum
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MQRankSum
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FS
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DP
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InbreedingCoeff
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MQ
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VQSLOD
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QD
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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Other
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European (Finnish)
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Latino
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African
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European (Non-Finnish)
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allele num: 57368
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South Asian
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InbreedingCoeff
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FS
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BaseQRankSum
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QD
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DP
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ReadPosRankSum
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MQRankSum
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ClippingRankSum
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VQSLOD
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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African
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South Asian
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European (Non-Finnish)
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European (Finnish)
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Other
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Latino
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ClippingRankSum
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FS
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DP
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MQ
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MQRankSum
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BaseQRankSum
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ReadPosRankSum
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VQSLOD
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QD
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InbreedingCoeff
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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European (Non-Finnish)
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Other
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African
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South Asian
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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 count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -3.628e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.5e-1

QD
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BaseQRankSum
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ReadPosRankSum
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SIO_000300: 1.79e0

InbreedingCoeff
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SIO_000300: -7.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 3.03e-1

FS
type: SiteQuality
SIO_000300: 5.783e0

DP
type: SiteQuality
SIO_000300: 1.287088e6

MQ
type: SiteQuality
SIO_000300: 3.669e1

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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bin: 1.75e1
variant carriers: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 10864
num of homozygotes: 0

African
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allele frequency: 0.0e0
allele num: 9766
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.568676664365941e-5
allele num: 63748
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6324
num of homozygotes: 0

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: 4.19e0

MQ
type: SiteQuality
SIO_000300: 3.074e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
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QD
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VQSLOD
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ClippingRankSum
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DP
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ReadPosRankSum
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SIO_000300: 1.8e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

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

African
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allele frequency: 0.0e0
allele num: 10042
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65166
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
allele num: 8422
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6470
num of homozygotes: 0

South Asian
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allele frequency: 6.518055012384304e-5
allele num: 15342
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11136
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: -2.683e0

ClippingRankSum
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FS
type: SiteQuality
SIO_000300: 2.108e0

QD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.342892e6

MQRankSum
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SIO_000300: 8.49e-1

MQ
type: SiteQuality
SIO_000300: 3.507e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.37e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.8e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6470
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11136
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65166
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8422
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 1.991635132443736e-4
allele num: 10042
num of homozygotes: 0

South Asian
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
allele num: 870
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 3.507e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.37e-1

FS
type: SiteQuality
SIO_000300: 2.108e0

MQRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.342892e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 8.9e-2

VQSLOD
type: SiteQuality
SIO_000300: -2.683e0

QD
type: SiteQuality
SIO_000300: 1.077e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.8e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8434
num of homozygotes: 0

South Asian
type: Population
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allele frequency: 6.485084306095979e-5
allele num: 15420
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65308
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
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European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6472
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11174
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 3.791e1

FS
type: SiteQuality
SIO_000300: 4.603e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.974e0

VQSLOD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -3.59e-1

DP
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QD
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ReadPosRankSum
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InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -1.585e0

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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Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11184
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.529753709652746e-5
allele num: 65370
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6486
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African
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allele count: 0
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South Asian
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allele count: 0
allele frequency: 0.0e0
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Other
type: Population
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BaseQRankSum
type: SiteQuality
SIO_000300: -2.12e-1

QD
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FS
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DP
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VQSLOD
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MQRankSum
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InbreedingCoeff
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ClippingRankSum
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MQ
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SIO_000300: 3.221e1

ReadPosRankSum
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SIO_000300: 6.96e-1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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European (Finnish)
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65454
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African
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Other
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South Asian
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allele frequency: 6.439979392065946e-5
allele num: 15528
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Latino
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ReadPosRankSum
type: SiteQuality
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VQSLOD
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MQ
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MQRankSum
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QD
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ClippingRankSum
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BaseQRankSum
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InbreedingCoeff
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FS
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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African
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South Asian
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East Asian
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Latino
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allele frequency: 9.701887458105486e-4
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European (Non-Finnish)
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allele frequency: 4.077240208560689e-3
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European (Finnish)
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allele frequency: 5.805071799572258e-3
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VQSLOD
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QD
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DP
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MQRankSum
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InbreedingCoeff
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FS
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MQ
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BaseQRankSum
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ReadPosRankSum
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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East Asian
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allele frequency: 0.0e0
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European (Finnish)
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African
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South Asian
type: Population
allele count: 1
allele frequency: 6.286145335680161e-5
allele num: 15908
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.030027573250917e-5
allele num: 66006
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 3.369e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.58e-1

DP
type: SiteQuality
SIO_000300: 1.364305e6

QD
type: SiteQuality
SIO_000300: 8.81e0

MQRankSum
type: SiteQuality
SIO_000300: -5.17e-1

FS
type: SiteQuality
SIO_000300: 1.129e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.06e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.7e-2

VQSLOD
type: SiteQuality
SIO_000300: -2.657e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 4

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.057118628668343e-5
allele num: 66038
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6544
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15916
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10210
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.08e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

DP
type: SiteQuality
SIO_000300: 1.364487e6

ReadPosRankSum
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SIO_000300: -9.55e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 3.405e1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.92e-1

MQRankSum
type: SiteQuality
SIO_000300: -9.379999999999999e-1

QD
type: SiteQuality
SIO_000300: 1.056e1

GenotypeQuality
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variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10206
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6534
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11330
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.293266205160478e-5
allele num: 15890
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66000
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.362713e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 7.39e-1

MQ
type: SiteQuality
SIO_000300: 3.801e1

VQSLOD
type: SiteQuality
SIO_000300: -3.229e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 7.24e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.9e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.731e0

QD
type: SiteQuality
SIO_000300: 1.118e1

GenotypeQuality
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variant carriers: 0

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

African
type: Population
allele count: 1
allele frequency: 9.850275807722617e-5
allele num: 10152
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11280
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15746
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8462
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6492
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65686
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 876
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ClippingRankSum
type: SiteQuality
SIO_000300: -1.008e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.6e0

BaseQRankSum
type: SiteQuality
SIO_000300: 7.71e-1

DP
type: SiteQuality
SIO_000300: 1.351579e6

MQRankSum
type: SiteQuality
SIO_000300: 1.38e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.031e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.2e-3

FS
type: SiteQuality
SIO_000300: 1.4e0

MQ
type: SiteQuality
SIO_000300: 3.858e1

QD
type: SiteQuality
SIO_000300: 9.34e0

GenotypeQuality
all individuals: 419
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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65470
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11238
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.889240506329114e-5
allele num: 10112
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8436
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6450
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15664
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -4.867e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.03e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.32e-1

FS
type: SiteQuality
SIO_000300: 1.674e0

MQ
type: SiteQuality
SIO_000300: 2.809e1

MQRankSum
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SIO_000300: -1.903e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-3

DP
type: SiteQuality
SIO_000300: 1.342261e6

QD
type: SiteQuality
SIO_000300: 5.69e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.61e0

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

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10010
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.54206760424377e-5
allele num: 64848
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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South Asian
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MQ
type: SiteQuality
SIO_000300: 3.65e1

MQRankSum
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DP
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VQSLOD
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QD
type: SiteQuality
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InbreedingCoeff
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FS
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ClippingRankSum
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SIO_000300: -3.24e-1

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

East Asian
type: Population
allele count: 4
allele frequency: 4.799616030717543e-4
allele num: 8334
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.548562933597621e-5
allele num: 64576
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ClippingRankSum
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InbreedingCoeff
type: SiteQuality
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MQRankSum
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QD
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FS
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MQ
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VQSLOD
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BaseQRankSum
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ReadPosRankSum
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

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 frequency: 0.0e0
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European (Non-Finnish)
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allele num: 64304
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Latino
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allele frequency: 9.048136083966703e-5
allele num: 11052
num of homozygotes: 0

East Asian
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Other
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South Asian
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VQSLOD
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ReadPosRankSum
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FS
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InbreedingCoeff
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DP
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MQ
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ClippingRankSum
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MQRankSum
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BaseQRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
type: Population
allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

Latino
type: Population
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allele frequency: 9.066183136899366e-5
allele num: 11030
num of homozygotes: 0

East Asian
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South Asian
type: Population
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allele frequency: 6.541077969649399e-5
allele num: 15288
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European (Finnish)
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allele frequency: 0.0e0
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Other
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allele count: 0
allele frequency: 0.0e0
allele num: 838
num of homozygotes: 0

European (Non-Finnish)
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allele count: 2
allele frequency: 3.120124804992199e-5
allele num: 64100
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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MQ
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FS
type: SiteQuality
SIO_000300: 6.693e0

QD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8098
num of homozygotes: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9550
num of homozygotes: 0

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

Other
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allele frequency: 0.0e0
allele num: 828
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.601075923020269e-5
allele num: 62458
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
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BaseQRankSum
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ReadPosRankSum
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FS
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VQSLOD
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MQ
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ClippingRankSum
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MQRankSum
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QD
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele frequency: 0.0e0
allele num: 8092
num of homozygotes: 0

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

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9524
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European (Non-Finnish)
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allele count: 2
allele frequency: 3.207595586348473e-5
allele num: 62352
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

VQSLOD
type: SiteQuality
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MQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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DP
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InbreedingCoeff
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BaseQRankSum
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MQ
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.23e-1

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 62090
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8052
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10656
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5810
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9500
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South Asian
type: Population
allele count: 2
allele frequency: 1.352265043948614e-4
allele num: 14790
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.6e-3

FS
type: SiteQuality
SIO_000300: 5.901e0

MQ
type: SiteQuality
SIO_000300: 3.908e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.42e-1

ClippingRankSum
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QD
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MQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: 1.63e0

DP
type: SiteQuality
SIO_000300: 1.143427e6

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 7842
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 796
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14118
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.653767281868095e-5
allele num: 60468
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5554
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African
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allele count: 1
allele frequency: 1.095050372317127e-4
allele num: 9132
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ClippingRankSum
type: SiteQuality
SIO_000300: 4.15e-1

BaseQRankSum
type: SiteQuality
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QD
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MQRankSum
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VQSLOD
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FS
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InbreedingCoeff
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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DP
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 3.573e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele count: 1
allele frequency: 1.104972375690608e-4
allele num: 9050
num of homozygotes: 0

Other
type: Population
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South Asian
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Latino
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allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
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European (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 frequency: 0.0e0
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QD
type: SiteQuality
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FS
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ReadPosRankSum
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ClippingRankSum
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DP
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InbreedingCoeff
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MQRankSum
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VQSLOD
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MQ
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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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Other
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African
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Latino
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South Asian
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European (Finnish)
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East Asian
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European (Non-Finnish)
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allele frequency: 1.71638460746284e-5
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MQ
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ReadPosRankSum
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FS
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MQRankSum
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QD
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InbreedingCoeff
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ClippingRankSum
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DP
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BaseQRankSum
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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European (Non-Finnish)
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South Asian
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Other
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African
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East Asian
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European (Finnish)
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ReadPosRankSum
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MQRankSum
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ClippingRankSum
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QD
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DP
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VQSLOD
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InbreedingCoeff
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FS
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BaseQRankSum
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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African
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Latino
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Other
type: Population
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European (Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
allele num: 13462
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.6933653943848e-5
allele num: 59054
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.05e0

MQRankSum
type: SiteQuality
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QD
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MQ
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InbreedingCoeff
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VQSLOD
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ClippingRankSum
type: SiteQuality
SIO_000300: -3.42e-1

FS
type: SiteQuality
SIO_000300: 1.09e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.18e0

DP
type: SiteQuality
SIO_000300: 1.082436e6

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 7748
num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 1.69485780143046e-5
allele num: 59002
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 10260
num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
allele num: 13436
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 778
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5332
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.75e-1

VQSLOD
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MQRankSum
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ReadPosRankSum
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BaseQRankSum
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InbreedingCoeff
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FS
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DP
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SIO_000300: 1.083679e6

QD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 4.411e1

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

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

Latino
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allele count: 1
allele frequency: 9.746588693957115e-5
allele num: 10260
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5326
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8734
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 58988
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.08e-1

QD
type: SiteQuality
SIO_000300: 5.42e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.7e-3

FS
type: SiteQuality
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DP
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VQSLOD
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ClippingRankSum
type: SiteQuality
SIO_000300: 5.93e-1

MQRankSum
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SIO_000300: 3.81e-1

BaseQRankSum
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SIO_000300: 6.63e-1

MQ
type: SiteQuality
SIO_000300: 3.319e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 10286
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.691303318337111e-5
allele num: 59126
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 8742
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 776
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7740
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

ClippingRankSum
type: SiteQuality
SIO_000300: -5.3e-2

QD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 3.515e1

VQSLOD
type: SiteQuality
SIO_000300: -3.116e0

FS
type: SiteQuality
SIO_000300: 3.017e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.01e0

MQRankSum
type: SiteQuality
SIO_000300: 4.89e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.5e-3

DP
type: SiteQuality
SIO_000300: 1.096039e6

BaseQRankSum
type: SiteQuality
SIO_000300: 2.53e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 8822
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.681916038751345e-5
allele num: 59456
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 784
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Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 10334
num of homozygotes: 0

East Asian
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allele count: 1
allele frequency: 1.284686536485098e-4
allele num: 7784
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5398
num of homozygotes: 0

South Asian
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allele count: 1
allele frequency: 7.385524372230428e-5
allele num: 13540
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MQRankSum
type: SiteQuality
SIO_000300: 7.69e-1

DP
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 9.26e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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BaseQRankSum
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MQ
type: SiteQuality
SIO_000300: 3.828e1

VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele frequency: 0.0e0
allele num: 10384
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African
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South Asian
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European (Finnish)
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allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.674536990522121e-5
allele num: 59718
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Other
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QD
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InbreedingCoeff
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MQRankSum
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ReadPosRankSum
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MQ
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FS
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BaseQRankSum
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ClippingRankSum
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VQSLOD
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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num of homozygotes: 0

Latino
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allele frequency: 9.584052137243626e-5
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East Asian
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Other
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African
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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ReadPosRankSum
type: SiteQuality
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DP
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FS
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BaseQRankSum
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MQ
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QD
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VQSLOD
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ClippingRankSum
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InbreedingCoeff
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MQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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num of homozygotes: 0

European (Non-Finnish)
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Other
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East Asian
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Latino
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European (Finnish)
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African
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DP
type: SiteQuality
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ReadPosRankSum
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MQRankSum
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MQ
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FS
type: SiteQuality
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InbreedingCoeff
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QD
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BaseQRankSum
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VQSLOD
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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East Asian
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African
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Latino
type: Population
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Other
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European (Non-Finnish)
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European (Finnish)
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FS
type: SiteQuality
SIO_000300: 9.031000000000001e0

InbreedingCoeff
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BaseQRankSum
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DP
type: SiteQuality
SIO_000300: 1.183697e6

MQRankSum
type: SiteQuality
SIO_000300: 3.56e-1

MQ
type: SiteQuality
SIO_000300: 4.829e1

VQSLOD
type: SiteQuality
SIO_000300: -1.755e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.3e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.43e-1

QD
type: SiteQuality
SIO_000300: 1.892e1

GenotypeQuality
all individuals: 3778
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6327
bin: 5.25e1
variant carriers: 3

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 16746
bin: 6.25e1
variant carriers: 2

GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
all individuals: 1080
bin: 9.75e1
variant carriers: 214

GenotypeQuality
all individuals: 3044
bin: 2.75e1
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GenotypeQuality
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GenotypeQuality
all individuals: 839
bin: 7.25e1
variant carriers: 2

GenotypeQuality
all individuals: 5300
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 121
bin: 9.25e1
variant carriers: 3

GenotypeQuality
all individuals: 3004
bin: 6.75e1
variant carriers: 2

GenotypeQuality
all individuals: 365
bin: 8.25e1
variant carriers: 2

GenotypeQuality
all individuals: 137
bin: 8.75e1
variant carriers: 1

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 800
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7870
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5590
num of homozygotes: 0

Latino
type: Population
allele count: 8
allele frequency: 7.593014426727411e-4
allele num: 10536
num of homozygotes: 0

African
type: Population
allele count: 225
allele frequency: 2.454723979925813e-2
allele num: 9166
num of homozygotes: 6

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.641012176310348e-5
allele num: 60938
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14110
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.26e-1

MQ
type: SiteQuality
SIO_000300: 4.16e1

DP
type: SiteQuality
SIO_000300: 1.216425e6

MQRankSum
type: SiteQuality
SIO_000300: 3.58e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.8e-1

QD
type: SiteQuality
SIO_000300: 1.214e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -1.086e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.02e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -2.67e0

GenotypeQuality
all individuals: 603
bin: 2.75e1
variant carriers: 1

GenotypeQuality
all individuals: 703
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 5.75e1
variant carriers: 5

GenotypeQuality
all individuals: 329
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variant carriers: 4

GenotypeQuality
all individuals: 3082
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variant carriers: 1

GenotypeQuality
all individuals: 130
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variant carriers: 3

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 14
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 16

GenotypeQuality
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variant carriers: 3

GenotypeQuality
all individuals: 55
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variant carriers: 2

GenotypeQuality
all individuals: 105
bin: 4.25e1
variant carriers: 5

East Asian
type: Population
allele count: 11
allele frequency: 8.333333333333333e-2
allele num: 132
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 8.620689655172414e-3
allele num: 116
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 6.821282401091405e-4
allele num: 1466
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 80
num of homozygotes: 0

African
type: Population
allele count: 14
allele frequency: 4.964539007092199e-2
allele num: 282
num of homozygotes: 0

South Asian
type: Population
allele count: 9
allele frequency: 3.084304318026045e-3
allele num: 2918
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 3.778337531486146e-3
allele num: 1588
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 8.3905e4

FS
type: SiteQuality
SIO_000300: 1.2165e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.93e-1

QD
type: SiteQuality
SIO_000300: 3.61e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.849e0

MQ
type: SiteQuality
SIO_000300: 2.2e1

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -6.453e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.89e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.35e-2

GenotypeQuality
all individuals: 136
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2927
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variant carriers: 0

GenotypeQuality
all individuals: 65
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variant carriers: 0

GenotypeQuality
all individuals: 41
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variant carriers: 0

GenotypeQuality
all individuals: 124
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variant carriers: 0

GenotypeQuality
all individuals: 620
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variant carriers: 1

GenotypeQuality
all individuals: 183
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variant carriers: 0

GenotypeQuality
all individuals: 271
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 15
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 9.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3608
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 126
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 6.666666666666667e-3
allele num: 300
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 138
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1486
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1810
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 84
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.68e0

DP
type: SiteQuality
SIO_000300: 9.57e4

ClippingRankSum
type: SiteQuality
SIO_000300: -4.23e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.17e-1

VQSLOD
type: SiteQuality
SIO_000300: -7.425e0

FS
type: SiteQuality
SIO_000300: 1.4785e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.8e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.29e-1

MQ
type: SiteQuality
SIO_000300: 2.2e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.237e0

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

GenotypeDepth
all individuals: 0
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variant carriers: 0

GenotypeQuality
all individuals: 120
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variant carriers: 0

GenotypeQuality
all individuals: 122
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 350
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variant carriers: 0

GenotypeQuality
all individuals: 469
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variant carriers: 0

GenotypeQuality
all individuals: 78
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variant carriers: 0

GenotypeQuality
all individuals: 81
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GenotypeQuality
all individuals: 3051
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variant carriers: 0

GenotypeQuality
all individuals: 169
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variant carriers: 0

GenotypeQuality
all individuals: 32
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variant carriers: 0

GenotypeQuality
all individuals: 218
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variant carriers: 0

GenotypeQuality
all individuals: 1333
bin: 7.5e0
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GenotypeQuality
all individuals: 1941
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variant carriers: 0

GenotypeQuality
all individuals: 26
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variant carriers: 0

GenotypeQuality
all individuals: 293
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GenotypeQuality
all individuals: 44
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variant carriers: 0

GenotypeQuality
all individuals: 47
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variant carriers: 0

GenotypeQuality
all individuals: 121
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GenotypeQuality
all individuals: 126
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variant carriers: 0

GenotypeQuality
all individuals: 54
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variant carriers: 1

GenotypeQuality
all individuals: 20
bin: 9.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 160
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 114
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1512
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 386
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2642
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 3.572704537334762e-4
allele num: 5598
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 152
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -2.11e-1

DP
type: SiteQuality
SIO_000300: 1.30076e5

VQSLOD
type: SiteQuality
SIO_000300: -5.181e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.24e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.87e-2

QD
type: SiteQuality
SIO_000300: 2.3e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.3e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 9.61e-1

MQ
type: SiteQuality
SIO_000300: 2.752e1

GenotypeDepth
all individuals: 0
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3448
bin: 2.25e1
variant carriers: 3

GenotypeQuality
all individuals: 1348
bin: 7.5e0
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GenotypeQuality
all individuals: 276
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variant carriers: 0

GenotypeQuality
all individuals: 131
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GenotypeQuality
all individuals: 69
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variant carriers: 10

GenotypeQuality
all individuals: 87
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variant carriers: 0

GenotypeQuality
all individuals: 77
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variant carriers: 0

GenotypeQuality
all individuals: 38
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variant carriers: 0

GenotypeQuality
all individuals: 1705
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variant carriers: 0

GenotypeQuality
all individuals: 45
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variant carriers: 0

GenotypeQuality
all individuals: 182
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 170
bin: 3.75e1
variant carriers: 2

GenotypeQuality
all individuals: 143
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variant carriers: 1

GenotypeQuality
all individuals: 3405
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 85
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variant carriers: 0

GenotypeQuality
all individuals: 31
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GenotypeQuality
all individuals: 234
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 1.75e1
variant carriers: 1

GenotypeQuality
all individuals: 23
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variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 587
bin: 6.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 154
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 118
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 5.072708826513358e-4
allele num: 5914
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 162
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 398
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 5
allele frequency: 3.272251308900524e-3
allele num: 1528
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 1.805054151624549e-3
allele num: 2770
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -2.83e-1

FS
type: SiteQuality
SIO_000300: 1.367e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.96e-1

MQ
type: SiteQuality
SIO_000300: 2.498e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.82e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 3.7e-2

VQSLOD
type: SiteQuality
SIO_000300: -4.837e0

QD
type: SiteQuality
SIO_000300: 6.25e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.75e-1

DP
type: SiteQuality
SIO_000300: 1.37496e5

GenotypeDepth
all individuals: 0
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variant carriers: 0

GenotypeDepth
all individuals: 12
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 48
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variant carriers: 1

GenotypeQuality
all individuals: 25
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1368
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GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 29
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GenotypeQuality
all individuals: 79
bin: 9.75e1
variant carriers: 7

GenotypeQuality
all individuals: 43
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GenotypeQuality
all individuals: 763
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variant carriers: 0

GenotypeQuality
all individuals: 3839
bin: 6.25e1
variant carriers: 1

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 166
num of homozygotes: 0

African
type: Population
allele count: 12
allele frequency: 2.941176470588235e-2
allele num: 408
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1534
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 162
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 124
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2988
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.551349674216568e-4
allele num: 6446
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -4.384e0

DP
type: SiteQuality
SIO_000300: 1.47345e5

FS
type: SiteQuality
SIO_000300: 7.01e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.97e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 1.54e0

MQ
type: SiteQuality
SIO_000300: 2.716e1

MQRankSum
type: SiteQuality
SIO_000300: -4.17e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.06e-1

QD
type: SiteQuality
SIO_000300: 3.33e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.04e-1

GenotypeDepth
all individuals: 4
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 8
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 17
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GenotypeQuality
all individuals: 58
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GenotypeQuality
all individuals: 34
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GenotypeQuality
all individuals: 44
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GenotypeQuality
all individuals: 13
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variant carriers: 0

GenotypeQuality
all individuals: 815
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 94
bin: 9.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4198
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1604
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 184
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 184
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 170
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.628664495114007e-3
allele num: 614
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7602
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.80638e5

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.77e0

QD
type: SiteQuality
SIO_000300: 1.38e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.28e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.449e0

VQSLOD
type: SiteQuality
SIO_000300: -3.897e0

MQRankSum
type: SiteQuality
SIO_000300: 1.22e0

MQ
type: SiteQuality
SIO_000300: 3.473e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.23e-2

GenotypeDepth
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variant carriers: 0

GenotypeDepth
all individuals: 4
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variant carriers: 0

GenotypeQuality
all individuals: 10
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GenotypeQuality
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GenotypeQuality
all individuals: 59
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GenotypeQuality
all individuals: 169
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GenotypeQuality
all individuals: 41
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GenotypeQuality
all individuals: 68
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GenotypeQuality
all individuals: 5386
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GenotypeQuality
all individuals: 9
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 1616
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 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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South Asian
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allele frequency: 1.315097317201473e-4
allele num: 7604
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4336
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

MQRankSum
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SIO_000300: 4.28e-1

ClippingRankSum
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FS
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QD
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MQ
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SIO_000300: 3.116e1

BaseQRankSum
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SIO_000300: 5.629999999999999e-1

ReadPosRankSum
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SIO_000300: 1.8e0

VQSLOD
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InbreedingCoeff
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DP
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SIO_000300: 1.83364e5

GenotypeDepth
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variant carriers: 0

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: 178
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 2.295684113865932e-4
allele num: 4356
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
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num of homozygotes: 0

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

European (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: 2.74e0

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

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

South Asian
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allele frequency: 1.313715186547556e-4
allele num: 7612
num of homozygotes: 0

Other
type: Population
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num of homozygotes: 0

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

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

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

Latino
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num of homozygotes: 0

VQSLOD
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FS
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InbreedingCoeff
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BaseQRankSum
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DP
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ReadPosRankSum
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QD
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MQRankSum
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ClippingRankSum
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MQ
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GenotypeDepth
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 750
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 194
num of homozygotes: 0

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 192
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

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

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

South Asian
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allele num: 7614
num of homozygotes: 0

VQSLOD
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FS
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MQ
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ClippingRankSum
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QD
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ReadPosRankSum
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BaseQRankSum
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InbreedingCoeff
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SIO_000300: -2.59e-2

MQRankSum
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DP
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4650
num of homozygotes: 0

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

Other
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num of homozygotes: 0

East Asian
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African
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allele frequency: 0.0e0
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Latino
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South Asian
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allele num: 7614
num of homozygotes: 0

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

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

South Asian
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allele frequency: 0.0e0
allele num: 7614
num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 0.0e0
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European (Finnish)
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allele num: 1646
num of homozygotes: 0

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

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: 8

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

Latino
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South Asian
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num of homozygotes: 0

European (Non-Finnish)
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European (Finnish)
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Other
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African
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InbreedingCoeff
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DP
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MQ
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ClippingRankSum
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BaseQRankSum
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MQRankSum
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FS
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ReadPosRankSum
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VQSLOD
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QD
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GenotypeDepth
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variant carriers: 223

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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bin: 4.75e1
variant carriers: 26

GenotypeQuality
all individuals: 50
bin: 8.25e1
variant carriers: 37

GenotypeQuality
all individuals: 4677
bin: 9.75e1
variant carriers: 4661

GenotypeQuality
all individuals: 34
bin: 8.75e1
variant carriers: 29

GenotypeQuality
all individuals: 39
bin: 9.25e1
variant carriers: 35

GenotypeQuality
all individuals: 2454
bin: 6.25e1
variant carriers: 32

African
type: Population
allele count: 171
allele frequency: 2.159090909090909e-1
allele num: 792
num of homozygotes: 4

South Asian
type: Population
allele count: 2086
allele frequency: 2.742571653957402e-1
allele num: 7606
num of homozygotes: 91

European (Finnish)
type: Population
allele count: 709
allele frequency: 4.175500588928151e-1
allele num: 1698
num of homozygotes: 33

East Asian
type: Population
allele count: 36
allele frequency: 1.855670103092784e-1
allele num: 194
num of homozygotes: 1

European (Non-Finnish)
type: Population
allele count: 2136
allele frequency: 4.292604501607717e-1
allele num: 4976
num of homozygotes: 178

Other
type: Population
allele count: 72
allele frequency: 3.711340206185567e-1
allele num: 194
num of homozygotes: 3

Latino
type: Population
allele count: 67
allele frequency: 3.101851851851852e-1
allele num: 216
num of homozygotes: 2

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.333e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.88e-1

QD
type: SiteQuality
SIO_000300: 1.001e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.04e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.14e-1

FS
type: SiteQuality
SIO_000300: 1.201e0

DP
type: SiteQuality
SIO_000300: 4.3429e5

MQRankSum
type: SiteQuality
SIO_000300: 4.3e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.225e1

MQ
type: SiteQuality
SIO_000300: 3.217e1

GenotypeDepth
all individuals: 19
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 19
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 90
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 954
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 203
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 80
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 74
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 945
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
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variant carriers: 0

GenotypeQuality
all individuals: 48
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variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27
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variant carriers: 0

GenotypeQuality
all individuals: 69
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variant carriers: 0

GenotypeQuality
all individuals: 205
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variant carriers: 0

GenotypeQuality
all individuals: 194
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variant carriers: 0

GenotypeQuality
all individuals: 444
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 122
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variant carriers: 0

GenotypeQuality
all individuals: 2105
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variant carriers: 0

GenotypeQuality
all individuals: 4842
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 2
allele frequency: 2.617801047120419e-3
allele num: 764
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4672
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 194
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 202
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7570
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1644
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 190
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.378e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.4e-2

QD
type: SiteQuality
SIO_000300: 2.32e0

VQSLOD
type: SiteQuality
SIO_000300: -4.302e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.14e-2

DP
type: SiteQuality
SIO_000300: 2.26784e5

MQRankSum
type: SiteQuality
SIO_000300: -1.911e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.9e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.78e-1

MQ
type: SiteQuality
SIO_000300: 3.344e1

GenotypeDepth
all individuals: 576
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 28
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 67
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 84
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variant carriers: 0

GenotypeQuality
all individuals: 27
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variant carriers: 0

GenotypeQuality
all individuals: 58
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variant carriers: 0

GenotypeQuality
all individuals: 54
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variant carriers: 0

GenotypeQuality
all individuals: 938
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variant carriers: 0

GenotypeQuality
all individuals: 92
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variant carriers: 0

GenotypeQuality
all individuals: 193
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variant carriers: 0

GenotypeQuality
all individuals: 2124
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GenotypeQuality
all individuals: 993
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variant carriers: 0

GenotypeQuality
all individuals: 30
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variant carriers: 0

GenotypeQuality
all individuals: 222
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GenotypeQuality
all individuals: 442
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variant carriers: 2

GenotypeQuality
all individuals: 13
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GenotypeQuality
all individuals: 41
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variant carriers: 0

GenotypeQuality
all individuals: 32
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variant carriers: 0

GenotypeQuality
all individuals: 122
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variant carriers: 0

GenotypeQuality
all individuals: 4807
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variant carriers: 0

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

GenotypeQuality
all individuals: 201
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 760
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4642
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 194
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1646
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 190
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 2.645502645502646e-4
allele num: 7560
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 202
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.562e0

DP
type: SiteQuality
SIO_000300: 2.25713e5

VQSLOD
type: SiteQuality
SIO_000300: -4.218e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.12e-2

FS
type: SiteQuality
SIO_000300: 5.315e0

MQ
type: SiteQuality
SIO_000300: 3.227e1

MQRankSum
type: SiteQuality
SIO_000300: 4.4e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.75e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.34e-1

QD
type: SiteQuality
SIO_000300: 2.98e0

GenotypeDepth
all individuals: 10
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 27
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 679
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 115
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variant carriers: 0

GenotypeQuality
all individuals: 36
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variant carriers: 0

GenotypeQuality
all individuals: 67
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variant carriers: 0

GenotypeQuality
all individuals: 431
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variant carriers: 0

GenotypeQuality
all individuals: 89
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variant carriers: 0

GenotypeQuality
all individuals: 447
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2113
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variant carriers: 0

GenotypeQuality
all individuals: 450
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variant carriers: 0

GenotypeQuality
all individuals: 3004
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variant carriers: 0

GenotypeQuality
all individuals: 42
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variant carriers: 0

GenotypeQuality
all individuals: 63
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GenotypeQuality
all individuals: 440
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GenotypeQuality
all individuals: 1798
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 147
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variant carriers: 0

GenotypeQuality
all individuals: 190
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 158
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variant carriers: 0

GenotypeQuality
all individuals: 223
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29
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GenotypeQuality
all individuals: 50
bin: 4.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 186
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 194
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1620
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.35795763172189e-4
allele num: 7364
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 188
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4394
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 722
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.95016e5

MQRankSum
type: SiteQuality
SIO_000300: 5.56e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.5e-2

QD
type: SiteQuality
SIO_000300: 1.52e0

MQ
type: SiteQuality
SIO_000300: 3.298e1

VQSLOD
type: SiteQuality
SIO_000300: -3.825e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.66e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.62e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.463e0

GenotypeDepth
all individuals: 116
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 14
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variant carriers: 0

GenotypeQuality
all individuals: 459
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variant carriers: 0

GenotypeQuality
all individuals: 13
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variant carriers: 0

GenotypeQuality
all individuals: 98
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variant carriers: 0

GenotypeQuality
all individuals: 159
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variant carriers: 0

GenotypeQuality
all individuals: 114
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GenotypeQuality
all individuals: 31
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GenotypeQuality
all individuals: 2130
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GenotypeQuality
all individuals: 65
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variant carriers: 0

GenotypeQuality
all individuals: 2879
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variant carriers: 0

GenotypeQuality
all individuals: 245
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variant carriers: 0

GenotypeQuality
all individuals: 57
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variant carriers: 0

GenotypeQuality
all individuals: 151
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GenotypeQuality
all individuals: 479
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GenotypeQuality
all individuals: 676
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variant carriers: 0

GenotypeQuality
all individuals: 1819
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42
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variant carriers: 0

GenotypeQuality
all individuals: 67
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variant carriers: 0

GenotypeQuality
all individuals: 190
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variant carriers: 0

GenotypeQuality
all individuals: 440
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 469
bin: 3.25e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.360544217687075e-4
allele num: 7350
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 194
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 188
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 720
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4372
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 186
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1620
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.58e-2

QD
type: SiteQuality
SIO_000300: 2.18e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.5e-2

MQ
type: SiteQuality
SIO_000300: 3.116e1

VQSLOD
type: SiteQuality
SIO_000300: -4.381e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.93125e5

MQRankSum
type: SiteQuality
SIO_000300: -8.92e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.982e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.83e-1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
all individuals: 96
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GenotypeQuality
all individuals: 614
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GenotypeQuality
all individuals: 445
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GenotypeQuality
all individuals: 146
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GenotypeQuality
all individuals: 2031
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GenotypeQuality
all individuals: 600
bin: 2.75e1
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GenotypeQuality
all individuals: 66
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GenotypeQuality
all individuals: 99
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GenotypeQuality
all individuals: 91
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GenotypeQuality
all individuals: 103
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GenotypeQuality
all individuals: 183
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 442
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GenotypeQuality
all individuals: 2221
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GenotypeQuality
all individuals: 1852
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GenotypeQuality
all individuals: 209
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GenotypeQuality
all individuals: 41
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GenotypeQuality
all individuals: 104
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GenotypeQuality
all individuals: 73
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GenotypeQuality
all individuals: 707
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 416
bin: 3.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 682
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4216
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1612
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 190
num of homozygotes: 0

South Asian
type: Population
allele count: 7
allele frequency: 9.706045479755962e-4
allele num: 7212
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 184
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 188
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.33e-1

VQSLOD
type: SiteQuality
SIO_000300: -4.761e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.92e-1

MQ
type: SiteQuality
SIO_000300: 2.963e1

DP
type: SiteQuality
SIO_000300: 1.82196e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.71e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -2.628e0

QD
type: SiteQuality
SIO_000300: 6.05e0

MQRankSum
type: SiteQuality
SIO_000300: -4.62e-1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
all individuals: 648
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variant carriers: 0

GenotypeQuality
all individuals: 60
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GenotypeQuality
all individuals: 1318
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GenotypeQuality
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GenotypeQuality
all individuals: 439
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 222
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GenotypeQuality
all individuals: 141
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GenotypeQuality
all individuals: 677
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GenotypeQuality
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GenotypeQuality
all individuals: 87
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GenotypeQuality
all individuals: 67
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GenotypeQuality
all individuals: 102
bin: 8.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 182
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 666
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4018
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 184
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 186
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 1610
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.445504481063891e-4
allele num: 6918
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.291e0

DP
type: SiteQuality
SIO_000300: 1.72768e5

FS
type: SiteQuality
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QD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -2.99e-2

BaseQRankSum
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MQ
type: SiteQuality
SIO_000300: 3.007e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.44e0

MQRankSum
type: SiteQuality
SIO_000300: 4.3e-1

VQSLOD
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SIO_000300: -5.79e0

GenotypeDepth
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variant carriers: 0

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
all individuals: 4620
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GenotypeQuality
all individuals: 353
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GenotypeQuality
all individuals: 66
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GenotypeQuality
all individuals: 43
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GenotypeQuality
all individuals: 87
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GenotypeQuality
all individuals: 35
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GenotypeQuality
all individuals: 39
bin: 9.75e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 248
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 846
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2872
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 380
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 260
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 254
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 2.2e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.27e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.31e-1

QD
type: SiteQuality
SIO_000300: 3.383e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.43e-2

MQRankSum
type: SiteQuality
SIO_000300: 7.31e-1

DP
type: SiteQuality
SIO_000300: 2.21045e5

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -5.986e0

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

GenotypeDepth
all individuals: 882
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 34528
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 190
bin: 3.75e1
variant carriers: 0