16-31765930-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31765930
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 31765930
    reference: chr 16
allele count: 10
allele frequency: 7.011639321273314e-4
allele num: 14262
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000542684
  gene symbol: ZNF720
  hgvsc: ENST00000542684.1:n.284+709T>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000431546
  ensembl transcript: ENST00000534369
  gene symbol: ZNF720
  hgvsc: ENST00000534369.1:c.4-38021T>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000544044
  gene symbol: ZNF720
  hgvsc: ENST00000544044.1:n.278+709T>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000319222
  ensembl transcript: ENST00000316491
  gene symbol: ZNF720
  hgvsc: ENST00000316491.9:c.361+709T>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000441893
  ensembl transcript: ENST00000539915
  gene symbol: ZNF720
  hgvsc: ENST00000539915.1:c.151+709T>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000533488
  gene symbol: ZNF720
  hgvsc: ENST00000533488.2:n.453T>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000531864
  gene symbol: ZNF720
  hgvsc: ENST00000531864.2:n.324+709T>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000434091
  ensembl transcript: ENST00000534277
  gene symbol: ZNF720
  hgvsc: ENST00000534277.1:c.*370T>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000443758
  ensembl transcript: ENST00000398696
  gene symbol: ZNF720
  hgvsc: ENST00000398696.3:c.*323T>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000381694
  ensembl transcript: ENST00000398707
  gene symbol: ZNF720
  hgvsc: ENST00000398707.3:c.*384T>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000440701
  ensembl transcript: ENST00000399681
  gene symbol: ZNF720
  hgvsc: ENST00000399681.3:c.318T>G
  hgvsp: ENSP00000440701.1:p.Phe106Leu
  variant of: http://identifiers.org/hgnc/26987
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3147
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5111
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1708
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 335
  bin: 2.25e1
  variant carriers: 1
hgvs: p.Phe106Leu
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
reference allele: T
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD

16-31765960-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31765960
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 31765960
    reference: chr 16
allele count: 1
allele frequency: 6.952169076751947e-5
allele num: 14384
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000443758
  ensembl transcript: ENST00000398696
  gene symbol: ZNF720
  hgvsc: ENST00000398696.3:c.*353G>A
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000431546
  ensembl transcript: ENST00000534369
  gene symbol: ZNF720
  hgvsc: ENST00000534369.1:c.4-37991G>A
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000381694
  ensembl transcript: ENST00000398707
  gene symbol: ZNF720
  hgvsc: ENST00000398707.3:c.*414G>A
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000319222
  ensembl transcript: ENST00000316491
  gene symbol: ZNF720
  hgvsc: ENST00000316491.9:c.361+739G>A
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000440701
  ensembl transcript: ENST00000399681
  gene symbol: ZNF720
  hgvsc: ENST00000399681.3:c.348G>A
  hgvsp: ENST00000399681.3:c.348G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000542684
  gene symbol: ZNF720
  hgvsc: ENST00000542684.1:n.284+739G>A
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000533488
  gene symbol: ZNF720
  hgvsc: ENST00000533488.2:n.483G>A
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000544044
  gene symbol: ZNF720
  hgvsc: ENST00000544044.1:n.278+739G>A
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000434091
  ensembl transcript: ENST00000534277
  gene symbol: ZNF720
  hgvsc: ENST00000534277.1:c.*400G>A
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000441893
  ensembl transcript: ENST00000539915
  gene symbol: ZNF720
  hgvsc: ENST00000539915.1:c.151+739G>A
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000531864
  gene symbol: ZNF720
  hgvsc: ENST00000531864.2:n.324+739G>A
  variant of: http://identifiers.org/hgnc/26987
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1722
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5136
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4045
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 3.25e1
  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: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Lys116Lys
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
population: Other
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: MQ

16-31765978-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31765978
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 31765978
    reference: chr 16
allele count: 1
allele frequency: 6.90035881865857e-5
allele num: 14492
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000542684
  gene symbol: ZNF720
  hgvsc: ENST00000542684.1:n.284+757C>T
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000544044
  gene symbol: ZNF720
  hgvsc: ENST00000544044.1:n.278+757C>T
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000434091
  ensembl transcript: ENST00000534277
  gene symbol: ZNF720
  hgvsc: ENST00000534277.1:c.*418C>T
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000440701
  ensembl transcript: ENST00000399681
  gene symbol: ZNF720
  hgvsc: ENST00000399681.3:c.366C>T
  hgvsp: ENST00000399681.3:c.366C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000319222
  ensembl transcript: ENST00000316491
  gene symbol: ZNF720
  hgvsc: ENST00000316491.9:c.361+757C>T
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000531864
  gene symbol: ZNF720
  hgvsc: ENST00000531864.2:n.324+757C>T
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000381694
  ensembl transcript: ENST00000398707
  gene symbol: ZNF720
  hgvsc: ENST00000398707.3:c.*432C>T
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000443758
  ensembl transcript: ENST00000398696
  gene symbol: ZNF720
  hgvsc: ENST00000398696.3:c.*371C>T
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000441893
  ensembl transcript: ENST00000539915
  gene symbol: ZNF720
  hgvsc: ENST00000539915.1:c.151+757C>T
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000533488
  gene symbol: ZNF720
  hgvsc: ENST00000533488.2:n.501C>T
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000431546
  ensembl transcript: ENST00000534369
  gene symbol: ZNF720
  hgvsc: ENST00000534369.1:c.4-37973C>T
  variant of: http://identifiers.org/hgnc/26987
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5163
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1729
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 909
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5160
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Ile122Ile
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
population: East Asian
population: African
reference allele: C
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff

16-31766028-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31766028
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 31766028
    reference: chr 16
allele count: 6
allele frequency: 3.951007506914263e-4
allele num: 15186
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000443758
  ensembl transcript: ENST00000398696
  gene symbol: ZNF720
  hgvsc: ENST00000398696.3:c.*421C>T
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000319222
  ensembl transcript: ENST00000316491
  gene symbol: ZNF720
  hgvsc: ENST00000316491.9:c.361+807C>T
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000542684
  gene symbol: ZNF720
  hgvsc: ENST00000542684.1:n.284+807C>T
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000431546
  ensembl transcript: ENST00000534369
  gene symbol: ZNF720
  hgvsc: ENST00000534369.1:c.4-37923C>T
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000381694
  ensembl transcript: ENST00000398707
  gene symbol: ZNF720
  hgvsc: ENST00000398707.3:c.*482C>T
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000441893
  ensembl transcript: ENST00000539915
  gene symbol: ZNF720
  hgvsc: ENST00000539915.1:c.151+807C>T
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000434091
  ensembl transcript: ENST00000534277
  gene symbol: ZNF720
  hgvsc: ENST00000534277.1:c.*468C>T
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000533488
  gene symbol: ZNF720
  hgvsc: ENST00000533488.2:n.551C>T
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000531864
  gene symbol: ZNF720
  hgvsc: ENST00000531864.2:n.324+807C>T
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000440701
  ensembl transcript: ENST00000399681
  gene symbol: ZNF720
  hgvsc: ENST00000399681.3:c.416C>T
  hgvsp: ENSP00000440701.1:p.Ser139Leu
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000544044
  gene symbol: ZNF720
  hgvsc: ENST00000544044.1:n.278+807C>T
  variant of: http://identifiers.org/hgnc/26987
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14150
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5338
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1332
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1753
  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: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 558
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Ser139Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: South Asian
population: Other
population: East Asian
reference allele: C
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD

16-31766044-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31766044
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 31766044
    reference: chr 16
allele count: 310
allele frequency: 1.985143442622951e-2
allele num: 15616
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000381694
  ensembl transcript: ENST00000398707
  gene symbol: ZNF720
  hgvsc: ENST00000398707.3:c.*498T>C
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000542684
  gene symbol: ZNF720
  hgvsc: ENST00000542684.1:n.284+823T>C
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000441893
  ensembl transcript: ENST00000539915
  gene symbol: ZNF720
  hgvsc: ENST00000539915.1:c.151+823T>C
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000434091
  ensembl transcript: ENST00000534277
  gene symbol: ZNF720
  hgvsc: ENST00000534277.1:c.*484T>C
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000440701
  ensembl transcript: ENST00000399681
  gene symbol: ZNF720
  hgvsc: ENST00000399681.3:c.432T>C
  hgvsp: ENST00000399681.3:c.432T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000431546
  ensembl transcript: ENST00000534369
  gene symbol: ZNF720
  hgvsc: ENST00000534369.1:c.4-37907T>C
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000544044
  gene symbol: ZNF720
  hgvsc: ENST00000544044.1:n.278+823T>C
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000531864
  gene symbol: ZNF720
  hgvsc: ENST00000531864.2:n.324+823T>C
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000319222
  ensembl transcript: ENST00000316491
  gene symbol: ZNF720
  hgvsc: ENST00000316491.9:c.361+823T>C
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000533488
  gene symbol: ZNF720
  hgvsc: ENST00000533488.2:n.567T>C
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000443758
  ensembl transcript: ENST00000398696
  gene symbol: ZNF720
  hgvsc: ENST00000398696.3:c.*437T>C
  variant of: http://identifiers.org/hgnc/26987
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 5.75e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 5295
  bin: 2.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 19051
  bin: 2.5e0
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 5.25e1
  variant carriers: 29
genotype depth: GenotypeDepth
  all individuals: 1740
  bin: 2.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 4.75e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 1.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 1594
  bin: 7.5e0
  variant carriers: 46
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 1.75e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 3.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 3.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 9.75e1
  variant carriers: 76
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.75e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 4.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 6447
  bin: 6.25e1
  variant carriers: 2
hgvs: p.Asn144Asn
num of homozygotes: 4
population: South Asian
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum

16-31766060-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31766060
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 31766060
    reference: chr 16
allele count: 1
allele frequency: 6.2375249500998e-5
allele num: 16032
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000319222
  ensembl transcript: ENST00000316491
  gene symbol: ZNF720
  hgvsc: ENST00000316491.9:c.361+839A>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000434091
  ensembl transcript: ENST00000534277
  gene symbol: ZNF720
  hgvsc: ENST00000534277.1:c.*500A>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000381694
  ensembl transcript: ENST00000398707
  gene symbol: ZNF720
  hgvsc: ENST00000398707.3:c.*514A>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000440701
  ensembl transcript: ENST00000399681
  gene symbol: ZNF720
  hgvsc: ENST00000399681.3:c.448A>G
  hgvsp: ENSP00000440701.1:p.Ser150Gly
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000542684
  gene symbol: ZNF720
  hgvsc: ENST00000542684.1:n.284+839A>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000533488
  gene symbol: ZNF720
  hgvsc: ENST00000533488.2:n.583A>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000544044
  gene symbol: ZNF720
  hgvsc: ENST00000544044.1:n.278+839A>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000441893
  ensembl transcript: ENST00000539915
  gene symbol: ZNF720
  hgvsc: ENST00000539915.1:c.151+839A>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000531864
  gene symbol: ZNF720
  hgvsc: ENST00000531864.2:n.324+839A>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000443758
  ensembl transcript: ENST00000398696
  gene symbol: ZNF720
  hgvsc: ENST00000398696.3:c.*453A>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000431546
  ensembl transcript: ENST00000534369
  gene symbol: ZNF720
  hgvsc: ENST00000534369.1:c.4-37891A>G
  variant of: http://identifiers.org/hgnc/26987
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2003
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5501
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24607
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1897
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 221
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Ser150Gly
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
reference allele: A
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD

16-31766074-TC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31766074
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 31766073
    reference: chr 16
allele count: 0
allele frequency: 0.0e0
allele num: 16312
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000443758
  ensembl transcript: ENST00000398696
  gene symbol: ZNF720
  hgvsc: ENST00000398696.3:c.*468delC
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000434091
  ensembl transcript: ENST00000534277
  gene symbol: ZNF720
  hgvsc: ENST00000534277.1:c.*515delC
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000431546
  ensembl transcript: ENST00000534369
  gene symbol: ZNF720
  hgvsc: ENST00000534369.1:c.4-37876delC
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000544044
  gene symbol: ZNF720
  hgvsc: ENST00000544044.1:n.278+854delC
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000542684
  gene symbol: ZNF720
  hgvsc: ENST00000542684.1:n.284+854delC
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000440701
  ensembl transcript: ENST00000399681
  gene symbol: ZNF720
  hgvsc: ENST00000399681.3:c.463delC
  hgvsp: ENSP00000440701.1:p.Leu155Ter
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000319222
  ensembl transcript: ENST00000316491
  gene symbol: ZNF720
  hgvsc: ENST00000316491.9:c.361+854delC
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000441893
  ensembl transcript: ENST00000539915
  gene symbol: ZNF720
  hgvsc: ENST00000539915.1:c.151+854delC
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000533488
  gene symbol: ZNF720
  hgvsc: ENST00000533488.2:n.598delC
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000381694
  ensembl transcript: ENST00000398707
  gene symbol: ZNF720
  hgvsc: ENST00000398707.3:c.*529delC
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000531864
  gene symbol: ZNF720
  hgvsc: ENST00000531864.2:n.324+854delC
  variant of: http://identifiers.org/hgnc/26987
canonical: false
consequence: frameshift
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29790
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5544
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3081
  bin: 7.5e0
  variant carriers: 1
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: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1913
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Leu155Ter
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Other
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
reference allele: TC
site quality: DP
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD

16-31766096-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31766096
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 31766096
    reference: chr 16
allele count: 1
allele frequency: 5.851375073142189e-5
allele num: 17090
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000434091
  ensembl transcript: ENST00000534277
  gene symbol: ZNF720
  hgvsc: ENST00000534277.1:c.*536C>T
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000381694
  ensembl transcript: ENST00000398707
  gene symbol: ZNF720
  hgvsc: ENST00000398707.3:c.*550C>T
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000533488
  gene symbol: ZNF720
  hgvsc: ENST00000533488.2:n.619C>T
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000431546
  ensembl transcript: ENST00000534369
  gene symbol: ZNF720
  hgvsc: ENST00000534369.1:c.4-37855C>T
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000440701
  ensembl transcript: ENST00000399681
  gene symbol: ZNF720
  hgvsc: ENST00000399681.3:c.484C>T
  hgvsp: ENSP00000440701.1:p.His162Tyr
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000441893
  ensembl transcript: ENST00000539915
  gene symbol: ZNF720
  hgvsc: ENST00000539915.1:c.151+875C>T
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000443758
  ensembl transcript: ENST00000398696
  gene symbol: ZNF720
  hgvsc: ENST00000398696.3:c.*489C>T
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000319222
  ensembl transcript: ENST00000316491
  gene symbol: ZNF720
  hgvsc: ENST00000316491.9:c.361+875C>T
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000542684
  gene symbol: ZNF720
  hgvsc: ENST00000542684.1:n.284+875C>T
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000544044
  gene symbol: ZNF720
  hgvsc: ENST00000544044.1:n.278+875C>T
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000531864
  gene symbol: ZNF720
  hgvsc: ENST00000531864.2:n.324+875C>T
  variant of: http://identifiers.org/hgnc/26987
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6731
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1904
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34424
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5615
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
hgvs: p.His162Tyr
num of homozygotes: 0
population: East Asian
population: Other
population: Latino
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: QD

16-31766097-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31766097
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 31766097
    reference: chr 16
allele count: 0
allele frequency: 0.0e0
allele num: 17176
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000544044
  gene symbol: ZNF720
  hgvsc: ENST00000544044.1:n.278+876A>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000443758
  ensembl transcript: ENST00000398696
  gene symbol: ZNF720
  hgvsc: ENST00000398696.3:c.*490A>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000440701
  ensembl transcript: ENST00000399681
  gene symbol: ZNF720
  hgvsc: ENST00000399681.3:c.485A>G
  hgvsp: ENSP00000440701.1:p.His162Arg
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000319222
  ensembl transcript: ENST00000316491
  gene symbol: ZNF720
  hgvsc: ENST00000316491.9:c.361+876A>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000381694
  ensembl transcript: ENST00000398707
  gene symbol: ZNF720
  hgvsc: ENST00000398707.3:c.*551A>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000441893
  ensembl transcript: ENST00000539915
  gene symbol: ZNF720
  hgvsc: ENST00000539915.1:c.151+876A>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000542684
  gene symbol: ZNF720
  hgvsc: ENST00000542684.1:n.284+876A>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000531864
  gene symbol: ZNF720
  hgvsc: ENST00000531864.2:n.324+876A>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000533488
  gene symbol: ZNF720
  hgvsc: ENST00000533488.2:n.620A>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000434091
  ensembl transcript: ENST00000534277
  gene symbol: ZNF720
  hgvsc: ENST00000534277.1:c.*537A>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000431546
  ensembl transcript: ENST00000534369
  gene symbol: ZNF720
  hgvsc: ENST00000534369.1:c.4-37854A>G
  variant of: http://identifiers.org/hgnc/26987
canonical: false
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6984
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1894
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34522
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5644
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 4.25e1
  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: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 714
  bin: 1.75e1
  variant carriers: 1
hgvs: p.His162Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
population: African
population: Other
population: European (Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum

16-31766098-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31766098
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 31766098
    reference: chr 16
allele count: 0
allele frequency: 0.0e0
allele num: 17202
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000431546
  ensembl transcript: ENST00000534369
  gene symbol: ZNF720
  hgvsc: ENST00000534369.1:c.4-37853T>C
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000440701
  ensembl transcript: ENST00000399681
  gene symbol: ZNF720
  hgvsc: ENST00000399681.3:c.486T>C
  hgvsp: ENST00000399681.3:c.486T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000381694
  ensembl transcript: ENST00000398707
  gene symbol: ZNF720
  hgvsc: ENST00000398707.3:c.*552T>C
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000443758
  ensembl transcript: ENST00000398696
  gene symbol: ZNF720
  hgvsc: ENST00000398696.3:c.*491T>C
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000533488
  gene symbol: ZNF720
  hgvsc: ENST00000533488.2:n.621T>C
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000434091
  ensembl transcript: ENST00000534277
  gene symbol: ZNF720
  hgvsc: ENST00000534277.1:c.*538T>C
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000531864
  gene symbol: ZNF720
  hgvsc: ENST00000531864.2:n.324+877T>C
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000542684
  gene symbol: ZNF720
  hgvsc: ENST00000542684.1:n.284+877T>C
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000319222
  ensembl transcript: ENST00000316491
  gene symbol: ZNF720
  hgvsc: ENST00000316491.9:c.361+877T>C
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000544044
  gene symbol: ZNF720
  hgvsc: ENST00000544044.1:n.278+877T>C
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000441893
  ensembl transcript: ENST00000539915
  gene symbol: ZNF720
  hgvsc: ENST00000539915.1:c.151+877T>C
  variant of: http://identifiers.org/hgnc/26987
canonical: false
consequence: synonymous
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 5658
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7244
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34604
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1888
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1599
  bin: 2.5e0
  variant carriers: 0
hgvs: p.His162His
num of homozygotes: 0
population: South Asian
population: Other
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ

16-31766104-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31766104
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 31766104
    reference: chr 16
allele count: 1
allele frequency: 5.716245569909683e-5
allele num: 17494
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000531864
  gene symbol: ZNF720
  hgvsc: ENST00000531864.2:n.324+883A>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000542684
  gene symbol: ZNF720
  hgvsc: ENST00000542684.1:n.284+883A>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000381694
  ensembl transcript: ENST00000398707
  gene symbol: ZNF720
  hgvsc: ENST00000398707.3:c.*558A>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000443758
  ensembl transcript: ENST00000398696
  gene symbol: ZNF720
  hgvsc: ENST00000398696.3:c.*497A>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000434091
  ensembl transcript: ENST00000534277
  gene symbol: ZNF720
  hgvsc: ENST00000534277.1:c.*544A>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000319222
  ensembl transcript: ENST00000316491
  gene symbol: ZNF720
  hgvsc: ENST00000316491.9:c.361+883A>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000440701
  ensembl transcript: ENST00000399681
  gene symbol: ZNF720
  hgvsc: ENST00000399681.3:c.492A>G
  hgvsp: ENST00000399681.3:c.492A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000533488
  gene symbol: ZNF720
  hgvsc: ENST00000533488.2:n.627A>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000441893
  ensembl transcript: ENST00000539915
  gene symbol: ZNF720
  hgvsc: ENST00000539915.1:c.151+883A>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000544044
  gene symbol: ZNF720
  hgvsc: ENST00000544044.1:n.278+883A>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000431546
  ensembl transcript: ENST00000534369
  gene symbol: ZNF720
  hgvsc: ENST00000534369.1:c.4-37847A>G
  variant of: http://identifiers.org/hgnc/26987
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 34646
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 606
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  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: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8783
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5746
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1860
  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: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 201
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Glu164Glu
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Other
population: African
population: Latino
population: European (Finnish)
population: East Asian
reference allele: A
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum

16-31766121-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31766121
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 31766121
    reference: chr 16
allele count: 0
allele frequency: 0.0e0
allele num: 18108
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000434091
  ensembl transcript: ENST00000534277
  gene symbol: ZNF720
  hgvsc: ENST00000534277.1:c.*561G>A
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000440701
  ensembl transcript: ENST00000399681
  gene symbol: ZNF720
  hgvsc: ENST00000399681.3:c.509G>A
  hgvsp: ENSP00000440701.1:p.Cys170Tyr
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000431546
  ensembl transcript: ENST00000534369
  gene symbol: ZNF720
  hgvsc: ENST00000534369.1:c.4-37830G>A
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000441893
  ensembl transcript: ENST00000539915
  gene symbol: ZNF720
  hgvsc: ENST00000539915.1:c.151+900G>A
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000531864
  gene symbol: ZNF720
  hgvsc: ENST00000531864.2:n.324+900G>A
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000319222
  ensembl transcript: ENST00000316491
  gene symbol: ZNF720
  hgvsc: ENST00000316491.9:c.361+900G>A
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000443758
  ensembl transcript: ENST00000398696
  gene symbol: ZNF720
  hgvsc: ENST00000398696.3:c.*514G>A
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000542684
  gene symbol: ZNF720
  hgvsc: ENST00000542684.1:n.284+900G>A
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000544044
  gene symbol: ZNF720
  hgvsc: ENST00000544044.1:n.278+900G>A
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000381694
  ensembl transcript: ENST00000398707
  gene symbol: ZNF720
  hgvsc: ENST00000398707.3:c.*575G>A
  variant of: http://identifiers.org/hgnc/26987
canonical: false
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13007
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 865
  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: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1839
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33186
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5731
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  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: 0
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1296
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1347
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Cys170Tyr
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
population: East Asian
population: African
population: Latino
reference allele: G
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: QD

16-31766133-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31766133
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 31766133
    reference: chr 16
allele count: 52
allele frequency: 2.805049088359046e-3
allele num: 18538
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000381694
  ensembl transcript: ENST00000398707
  gene symbol: ZNF720
  hgvsc: ENST00000398707.3:c.*587A>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000443758
  ensembl transcript: ENST00000398696
  gene symbol: ZNF720
  hgvsc: ENST00000398696.3:c.*526A>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000542684
  gene symbol: ZNF720
  hgvsc: ENST00000542684.1:n.284+912A>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000431546
  ensembl transcript: ENST00000534369
  gene symbol: ZNF720
  hgvsc: ENST00000534369.1:c.4-37818A>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000434091
  ensembl transcript: ENST00000534277
  gene symbol: ZNF720
  hgvsc: ENST00000534277.1:c.*573A>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000319222
  ensembl transcript: ENST00000316491
  gene symbol: ZNF720
  hgvsc: ENST00000316491.9:c.361+912A>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000440701
  ensembl transcript: ENST00000399681
  gene symbol: ZNF720
  hgvsc: ENST00000399681.3:c.521A>G
  hgvsp: ENSP00000440701.1:p.Asp174Gly
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000441893
  ensembl transcript: ENST00000539915
  gene symbol: ZNF720
  hgvsc: ENST00000539915.1:c.151+912A>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000531864
  gene symbol: ZNF720
  hgvsc: ENST00000531864.2:n.324+912A>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000544044
  gene symbol: ZNF720
  hgvsc: ENST00000544044.1:n.278+912A>G
  variant of: http://identifiers.org/hgnc/26987
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5657
  bin: 2.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15897
  bin: 7.5e0
  variant carriers: 45
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31293
  bin: 2.5e0
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1795
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1157
  bin: 1.25e1
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 4.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 436
  bin: 1.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1147
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14361
  bin: 2.25e1
  variant carriers: 2
hgvs: p.Asp174Gly
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
population: African
population: European (Finnish)
reference allele: A
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum

16-31766134-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31766134
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 31766134
    reference: chr 16
allele count: 0
allele frequency: 0.0e0
allele num: 18538
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000440701
  ensembl transcript: ENST00000399681
  gene symbol: ZNF720
  hgvsc: ENST00000399681.3:c.522C>G
  hgvsp: ENSP00000440701.1:p.Asp174Glu
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000443758
  ensembl transcript: ENST00000398696
  gene symbol: ZNF720
  hgvsc: ENST00000398696.3:c.*527C>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000381694
  ensembl transcript: ENST00000398707
  gene symbol: ZNF720
  hgvsc: ENST00000398707.3:c.*588C>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000431546
  ensembl transcript: ENST00000534369
  gene symbol: ZNF720
  hgvsc: ENST00000534369.1:c.4-37817C>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000542684
  gene symbol: ZNF720
  hgvsc: ENST00000542684.1:n.284+913C>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000441893
  ensembl transcript: ENST00000539915
  gene symbol: ZNF720
  hgvsc: ENST00000539915.1:c.151+913C>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000434091
  ensembl transcript: ENST00000534277
  gene symbol: ZNF720
  hgvsc: ENST00000534277.1:c.*574C>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000319222
  ensembl transcript: ENST00000316491
  gene symbol: ZNF720
  hgvsc: ENST00000316491.9:c.361+913C>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000544044
  gene symbol: ZNF720
  hgvsc: ENST00000544044.1:n.278+913C>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000531864
  gene symbol: ZNF720
  hgvsc: ENST00000531864.2:n.324+913C>G
  variant of: http://identifiers.org/hgnc/26987
canonical: false
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1780
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31198
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1176
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5627
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16089
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  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: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14657
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 184
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Asp174Glu
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: Other
population: South Asian
reference allele: C
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: MQ

16-31766141-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31766141
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 31766141
    reference: chr 16
allele count: 1
allele frequency: 5.414185165132648e-5
allele num: 18470
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000531864
  gene symbol: ZNF720
  hgvsc: ENST00000531864.2:n.324+920T>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000441893
  ensembl transcript: ENST00000539915
  gene symbol: ZNF720
  hgvsc: ENST00000539915.1:c.151+920T>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000431546
  ensembl transcript: ENST00000534369
  gene symbol: ZNF720
  hgvsc: ENST00000534369.1:c.4-37810T>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000319222
  ensembl transcript: ENST00000316491
  gene symbol: ZNF720
  hgvsc: ENST00000316491.9:c.361+920T>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000544044
  gene symbol: ZNF720
  hgvsc: ENST00000544044.1:n.278+920T>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000443758
  ensembl transcript: ENST00000398696
  gene symbol: ZNF720
  hgvsc: ENST00000398696.3:c.*534T>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000434091
  ensembl transcript: ENST00000534277
  gene symbol: ZNF720
  hgvsc: ENST00000534277.1:c.*581T>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000542684
  gene symbol: ZNF720
  hgvsc: ENST00000542684.1:n.284+920T>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000440701
  ensembl transcript: ENST00000399681
  gene symbol: ZNF720
  hgvsc: ENST00000399681.3:c.529T>G
  hgvsp: ENSP00000440701.1:p.Phe177Val
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000381694
  ensembl transcript: ENST00000398707
  gene symbol: ZNF720
  hgvsc: ENST00000398707.3:c.*595T>G
  variant of: http://identifiers.org/hgnc/26987
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1728
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5330
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31021
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1405
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16367
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 395
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 203
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1990
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Phe177Val
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
reference allele: T
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: QD

16-31766148-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31766148
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 31766148
    reference: chr 16
allele count: 0
allele frequency: 0.0e0
allele num: 18366
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000434091
  ensembl transcript: ENST00000534277
  gene symbol: ZNF720
  hgvsc: ENST00000534277.1:c.*588A>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000542684
  gene symbol: ZNF720
  hgvsc: ENST00000542684.1:n.284+927A>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000440701
  ensembl transcript: ENST00000399681
  gene symbol: ZNF720
  hgvsc: ENST00000399681.3:c.536A>G
  hgvsp: ENSP00000440701.1:p.His179Arg
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000441893
  ensembl transcript: ENST00000539915
  gene symbol: ZNF720
  hgvsc: ENST00000539915.1:c.151+927A>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000319222
  ensembl transcript: ENST00000316491
  gene symbol: ZNF720
  hgvsc: ENST00000316491.9:c.361+927A>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000381694
  ensembl transcript: ENST00000398707
  gene symbol: ZNF720
  hgvsc: ENST00000398707.3:c.*602A>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000443758
  ensembl transcript: ENST00000398696
  gene symbol: ZNF720
  hgvsc: ENST00000398696.3:c.*541A>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000431546
  ensembl transcript: ENST00000534369
  gene symbol: ZNF720
  hgvsc: ENST00000534369.1:c.4-37803A>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000544044
  gene symbol: ZNF720
  hgvsc: ENST00000544044.1:n.278+927A>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000531864
  gene symbol: ZNF720
  hgvsc: ENST00000531864.2:n.324+927A>G
  variant of: http://identifiers.org/hgnc/26987
canonical: false
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30719
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16711
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1628
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5164
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1611
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 371
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 170
  bin: 4.75e1
  variant carriers: 0
hgvs: p.His179Arg
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
population: Other
population: African
population: European (Non-Finnish)
reference allele: A
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff

16-31766150-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31766150
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 31766150
    reference: chr 16
allele count: 1
allele frequency: 5.496317467296911e-5
allele num: 18194
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000443758
  ensembl transcript: ENST00000398696
  gene symbol: ZNF720
  hgvsc: ENST00000398696.3:c.*543C>T
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000542684
  gene symbol: ZNF720
  hgvsc: ENST00000542684.1:n.284+929C>T
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000434091
  ensembl transcript: ENST00000534277
  gene symbol: ZNF720
  hgvsc: ENST00000534277.1:c.*590C>T
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000440701
  ensembl transcript: ENST00000399681
  gene symbol: ZNF720
  hgvsc: ENST00000399681.3:c.538C>T
  hgvsp: ENSP00000440701.1:p.Arg180Cys
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000431546
  ensembl transcript: ENST00000534369
  gene symbol: ZNF720
  hgvsc: ENST00000534369.1:c.4-37801C>T
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000531864
  gene symbol: ZNF720
  hgvsc: ENST00000531864.2:n.324+929C>T
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000381694
  ensembl transcript: ENST00000398707
  gene symbol: ZNF720
  hgvsc: ENST00000398707.3:c.*604C>T
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000319222
  ensembl transcript: ENST00000316491
  gene symbol: ZNF720
  hgvsc: ENST00000316491.9:c.361+929C>T
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000544044
  gene symbol: ZNF720
  hgvsc: ENST00000544044.1:n.278+929C>T
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000441893
  ensembl transcript: ENST00000539915
  gene symbol: ZNF720
  hgvsc: ENST00000539915.1:c.151+929C>T
  variant of: http://identifiers.org/hgnc/26987
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16837
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5102
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1678
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 3.25e1
  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: 30581
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1618
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 111
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 197
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 111
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Arg180Cys
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
reference allele: C
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum

16-31766151-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31766151
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 31766151
    reference: chr 16
allele count: 2
allele frequency: 1.095530236634531e-4
allele num: 18256
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000431546
  ensembl transcript: ENST00000534369
  gene symbol: ZNF720
  hgvsc: ENST00000534369.1:c.4-37800G>A
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000319222
  ensembl transcript: ENST00000316491
  gene symbol: ZNF720
  hgvsc: ENST00000316491.9:c.361+930G>A
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000544044
  gene symbol: ZNF720
  hgvsc: ENST00000544044.1:n.278+930G>A
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000542684
  gene symbol: ZNF720
  hgvsc: ENST00000542684.1:n.284+930G>A
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000441893
  ensembl transcript: ENST00000539915
  gene symbol: ZNF720
  hgvsc: ENST00000539915.1:c.151+930G>A
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000381694
  ensembl transcript: ENST00000398707
  gene symbol: ZNF720
  hgvsc: ENST00000398707.3:c.*605G>A
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000531864
  gene symbol: ZNF720
  hgvsc: ENST00000531864.2:n.324+930G>A
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000434091
  ensembl transcript: ENST00000534277
  gene symbol: ZNF720
  hgvsc: ENST00000534277.1:c.*591G>A
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000440701
  ensembl transcript: ENST00000399681
  gene symbol: ZNF720
  hgvsc: ENST00000399681.3:c.539G>A
  hgvsp: ENSP00000440701.1:p.Arg180His
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000443758
  ensembl transcript: ENST00000398696
  gene symbol: ZNF720
  hgvsc: ENST00000398696.3:c.*544G>A
  variant of: http://identifiers.org/hgnc/26987
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17049
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30417
  bin: 2.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1608
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1705
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5099
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 168
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 14373
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Arg180His
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: QD

http://identifiers.org/exac.variant/16-31766157-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31766157
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 31766157
    reference: chr 16
allele count: 0
allele frequency: 0.0e0
allele num: 18076
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000440701
  ensembl transcript: ENST00000399681
  gene symbol: ZNF720
  hgvsc: ENST00000399681.3:c.545A>C
  hgvsp: ENSP00000440701.1:p.His182Pro
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000381694
  ensembl transcript: ENST00000398707
  gene symbol: ZNF720
  hgvsc: ENST00000398707.3:c.*611A>C
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000544044
  gene symbol: ZNF720
  hgvsc: ENST00000544044.1:n.278+936A>C
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000542684
  gene symbol: ZNF720
  hgvsc: ENST00000542684.1:n.284+936A>C
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000431546
  ensembl transcript: ENST00000534369
  gene symbol: ZNF720
  hgvsc: ENST00000534369.1:c.4-37794A>C
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000531864
  gene symbol: ZNF720
  hgvsc: ENST00000531864.2:n.324+936A>C
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000434091
  ensembl transcript: ENST00000534277
  gene symbol: ZNF720
  hgvsc: ENST00000534277.1:c.*597A>C
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000443758
  ensembl transcript: ENST00000398696
  gene symbol: ZNF720
  hgvsc: ENST00000398696.3:c.*550A>C
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000441893
  ensembl transcript: ENST00000539915
  gene symbol: ZNF720
  hgvsc: ENST00000539915.1:c.151+936A>C
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000319222
  ensembl transcript: ENST00000316491
  gene symbol: ZNF720
  hgvsc: ENST00000316491.9:c.361+936A>C
  variant of: http://identifiers.org/hgnc/26987
canonical: false
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1511
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30213
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1930
  bin: 1.25e1
  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 depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17331
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.75e1
  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 depth: GenotypeDepth
  all individuals: 4867
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 466
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28656
  bin: 7.5e0
  variant carriers: 0
hgvs: p.His182Pro
num of homozygotes: 0
population: Other
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
population: African
reference allele: A
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: DP
site quality: VQSLOD

16-31766158-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31766158
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 31766158
    reference: chr 16
allele count: 0
allele frequency: 0.0e0
allele num: 18082
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000381694
  ensembl transcript: ENST00000398707
  gene symbol: ZNF720
  hgvsc: ENST00000398707.3:c.*612C>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000544044
  gene symbol: ZNF720
  hgvsc: ENST00000544044.1:n.278+937C>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000440701
  ensembl transcript: ENST00000399681
  gene symbol: ZNF720
  hgvsc: ENST00000399681.3:c.546C>G
  hgvsp: ENSP00000440701.1:p.His182Gln
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000531864
  gene symbol: ZNF720
  hgvsc: ENST00000531864.2:n.324+937C>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000443758
  ensembl transcript: ENST00000398696
  gene symbol: ZNF720
  hgvsc: ENST00000398696.3:c.*551C>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000542684
  gene symbol: ZNF720
  hgvsc: ENST00000542684.1:n.284+937C>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000431546
  ensembl transcript: ENST00000534369
  gene symbol: ZNF720
  hgvsc: ENST00000534369.1:c.4-37793C>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000441893
  ensembl transcript: ENST00000539915
  gene symbol: ZNF720
  hgvsc: ENST00000539915.1:c.151+937C>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000319222
  ensembl transcript: ENST00000316491
  gene symbol: ZNF720
  hgvsc: ENST00000316491.9:c.361+937C>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000434091
  ensembl transcript: ENST00000534277
  gene symbol: ZNF720
  hgvsc: ENST00000534277.1:c.*598C>G
  variant of: http://identifiers.org/hgnc/26987
canonical: false
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  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: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1511
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1930
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30097
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17506
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4878
  bin: 2.25e1
  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: 0
  bin: 6.25e1
  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 quality: GenotypeQuality
  all individuals: 489
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14904
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28684
  bin: 7.5e0
  variant carriers: 0
hgvs: p.His182Gln
num of homozygotes: 0
population: Other
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff

16-31766187-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31766187
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 31766187
    reference: chr 16
allele count: 1
allele frequency: 5.84932147870847e-5
allele num: 17096
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000531864
  gene symbol: ZNF720
  hgvsc: ENST00000531864.2:n.324+966G>T
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000544044
  gene symbol: ZNF720
  hgvsc: ENST00000544044.1:n.278+966G>T
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000431546
  ensembl transcript: ENST00000534369
  gene symbol: ZNF720
  hgvsc: ENST00000534369.1:c.4-37764G>T
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000381694
  ensembl transcript: ENST00000398707
  gene symbol: ZNF720
  hgvsc: ENST00000398707.3:c.*641G>T
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000542684
  gene symbol: ZNF720
  hgvsc: ENST00000542684.1:n.284+966G>T
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000434091
  ensembl transcript: ENST00000534277
  gene symbol: ZNF720
  hgvsc: ENST00000534277.1:c.*627G>T
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000443758
  ensembl transcript: ENST00000398696
  gene symbol: ZNF720
  hgvsc: ENST00000398696.3:c.*580G>T
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000440701
  ensembl transcript: ENST00000399681
  gene symbol: ZNF720
  hgvsc: ENST00000399681.3:c.575G>T
  hgvsp: ENSP00000440701.1:p.Gly192Val
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000441893
  ensembl transcript: ENST00000539915
  gene symbol: ZNF720
  hgvsc: ENST00000539915.1:c.151+966G>T
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000319222
  ensembl transcript: ENST00000316491
  gene symbol: ZNF720
  hgvsc: ENST00000316491.9:c.361+966G>T
  variant of: http://identifiers.org/hgnc/26987
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1128
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 745
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17235
  bin: 7.5e0
  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: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30810
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3648
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2955
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1665
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Gly192Val
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: DP

16-31766235-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31766235
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 31766235
    reference: chr 16
allele count: 1
allele frequency: 6.850253459377997e-5
allele num: 14598
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000531864
  gene symbol: ZNF720
  hgvsc: ENST00000531864.2:n.324+1014G>C
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000381694
  ensembl transcript: ENST00000398707
  gene symbol: ZNF720
  hgvsc: ENST00000398707.3:c.*689G>C
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000434091
  ensembl transcript: ENST00000534277
  gene symbol: ZNF720
  hgvsc: ENST00000534277.1:c.*675G>C
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000443758
  ensembl transcript: ENST00000398696
  gene symbol: ZNF720
  hgvsc: ENST00000398696.3:c.*628G>C
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000440701
  ensembl transcript: ENST00000399681
  gene symbol: ZNF720
  hgvsc: ENST00000399681.3:c.623G>C
  hgvsp: ENSP00000440701.1:p.Ser208Thr
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000319222
  ensembl transcript: ENST00000316491
  gene symbol: ZNF720
  hgvsc: ENST00000316491.9:c.361+1014G>C
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000431546
  ensembl transcript: ENST00000534369
  gene symbol: ZNF720
  hgvsc: ENST00000534369.1:c.4-37716G>C
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000441893
  ensembl transcript: ENST00000539915
  gene symbol: ZNF720
  hgvsc: ENST00000539915.1:c.151+1014G>C
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000544044
  gene symbol: ZNF720
  hgvsc: ENST00000544044.1:n.278+1014G>C
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000542684
  gene symbol: ZNF720
  hgvsc: ENST00000542684.1:n.284+1014G>C
  variant of: http://identifiers.org/hgnc/26987
canonical: false
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33495
  bin: 2.5e0
  variant carriers: 1
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: 9
  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: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 832
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 882
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14104
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3132
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2455
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Ser208Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: South Asian
population: East Asian
population: Other
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: QD

16-31766238-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31766238
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 31766238
    reference: chr 16
allele count: 1
allele frequency: 6.882312456985548e-5
allele num: 14530
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000381694
  ensembl transcript: ENST00000398707
  gene symbol: ZNF720
  hgvsc: ENST00000398707.3:c.*692C>T
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000544044
  gene symbol: ZNF720
  hgvsc: ENST00000544044.1:n.278+1017C>T
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000531864
  gene symbol: ZNF720
  hgvsc: ENST00000531864.2:n.324+1017C>T
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000431546
  ensembl transcript: ENST00000534369
  gene symbol: ZNF720
  hgvsc: ENST00000534369.1:c.4-37713C>T
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000443758
  ensembl transcript: ENST00000398696
  gene symbol: ZNF720
  hgvsc: ENST00000398696.3:c.*631C>T
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000434091
  ensembl transcript: ENST00000534277
  gene symbol: ZNF720
  hgvsc: ENST00000534277.1:c.*678C>T
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000319222
  ensembl transcript: ENST00000316491
  gene symbol: ZNF720
  hgvsc: ENST00000316491.9:c.361+1017C>T
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000542684
  gene symbol: ZNF720
  hgvsc: ENST00000542684.1:n.284+1017C>T
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000440701
  ensembl transcript: ENST00000399681
  gene symbol: ZNF720
  hgvsc: ENST00000399681.3:c.626C>T
  hgvsp: ENSP00000440701.1:p.Ser209Leu
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000441893
  ensembl transcript: ENST00000539915
  gene symbol: ZNF720
  hgvsc: ENST00000539915.1:c.151+1017C>T
  variant of: http://identifiers.org/hgnc/26987
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 893
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13928
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2438
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3105
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33583
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  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: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 104
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31528
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Ser209Leu
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
population: South Asian
reference allele: C
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum

16-31766247-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31766247
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 31766247
    reference: chr 16
allele count: 1
allele frequency: 7.006726457399103e-5
allele num: 14272
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000544044
  gene symbol: ZNF720
  hgvsc: ENST00000544044.1:n.278+1026C>T
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000531864
  gene symbol: ZNF720
  hgvsc: ENST00000531864.2:n.324+1026C>T
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000431546
  ensembl transcript: ENST00000534369
  gene symbol: ZNF720
  hgvsc: ENST00000534369.1:c.4-37704C>T
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000434091
  ensembl transcript: ENST00000534277
  gene symbol: ZNF720
  hgvsc: ENST00000534277.1:c.*687C>T
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000443758
  ensembl transcript: ENST00000398696
  gene symbol: ZNF720
  hgvsc: ENST00000398696.3:c.*640C>T
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000441893
  ensembl transcript: ENST00000539915
  gene symbol: ZNF720
  hgvsc: ENST00000539915.1:c.151+1026C>T
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000381694
  ensembl transcript: ENST00000398707
  gene symbol: ZNF720
  hgvsc: ENST00000398707.3:c.*701C>T
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000440701
  ensembl transcript: ENST00000399681
  gene symbol: ZNF720
  hgvsc: ENST00000399681.3:c.635C>T
  hgvsp: ENSP00000440701.1:p.Thr212Ile
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000319222
  ensembl transcript: ENST00000316491
  gene symbol: ZNF720
  hgvsc: ENST00000316491.9:c.361+1026C>T
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000542684
  gene symbol: ZNF720
  hgvsc: ENST00000542684.1:n.284+1026C>T
  variant of: http://identifiers.org/hgnc/26987
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13512
  bin: 7.5e0
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 3008
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 874
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2450
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33815
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 829
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2041
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 103
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Thr212Ile
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum

16-31766269-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31766269
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 31766269
    reference: chr 16
allele count: 0
allele frequency: 0.0e0
allele num: 14308
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000542684
  gene symbol: ZNF720
  hgvsc: ENST00000542684.1:n.284+1048T>C
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000381694
  ensembl transcript: ENST00000398707
  gene symbol: ZNF720
  hgvsc: ENST00000398707.3:c.*723T>C
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000431546
  ensembl transcript: ENST00000534369
  gene symbol: ZNF720
  hgvsc: ENST00000534369.1:c.4-37682T>C
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000440701
  ensembl transcript: ENST00000399681
  gene symbol: ZNF720
  hgvsc: ENST00000399681.3:c.657T>C
  hgvsp: ENST00000399681.3:c.657T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000531864
  gene symbol: ZNF720
  hgvsc: ENST00000531864.2:n.324+1048T>C
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000544044
  gene symbol: ZNF720
  hgvsc: ENST00000544044.1:n.278+1048T>C
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000434091
  ensembl transcript: ENST00000534277
  gene symbol: ZNF720
  hgvsc: ENST00000534277.1:c.*709T>C
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000441893
  ensembl transcript: ENST00000539915
  gene symbol: ZNF720
  hgvsc: ENST00000539915.1:c.151+1048T>C
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000319222
  ensembl transcript: ENST00000316491
  gene symbol: ZNF720
  hgvsc: ENST00000316491.9:c.361+1048T>C
  variant of: http://identifiers.org/hgnc/26987
canonical: false
consequence: synonymous
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 33970
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2560
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 832
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 862
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13464
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 4.25e1
  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: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2909
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 117
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Thr219Thr
num of homozygotes: 0
population: Other
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
population: Latino
reference allele: T
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: QD

16-31766291-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31766291
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 31766291
    reference: chr 16
allele count: 0
allele frequency: 0.0e0
allele num: 15148
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000319222
  ensembl transcript: ENST00000316491
  gene symbol: ZNF720
  hgvsc: ENST00000316491.9:c.361+1070A>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000440701
  ensembl transcript: ENST00000399681
  gene symbol: ZNF720
  hgvsc: ENST00000399681.3:c.679A>G
  hgvsp: ENSP00000440701.1:p.Lys227Glu
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000542684
  gene symbol: ZNF720
  hgvsc: ENST00000542684.1:n.284+1070A>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000434091
  ensembl transcript: ENST00000534277
  gene symbol: ZNF720
  hgvsc: ENST00000534277.1:c.*731A>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000531864
  gene symbol: ZNF720
  hgvsc: ENST00000531864.2:n.324+1070A>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000544044
  gene symbol: ZNF720
  hgvsc: ENST00000544044.1:n.278+1070A>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000441893
  ensembl transcript: ENST00000539915
  gene symbol: ZNF720
  hgvsc: ENST00000539915.1:c.151+1070A>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000381694
  ensembl transcript: ENST00000398707
  gene symbol: ZNF720
  hgvsc: ENST00000398707.3:c.*745A>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000431546
  ensembl transcript: ENST00000534369
  gene symbol: ZNF720
  hgvsc: ENST00000534369.1:c.4-37660A>G
  variant of: http://identifiers.org/hgnc/26987
canonical: false
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 2931
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2854
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33097
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14705
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 793
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  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: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 926
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3317
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2358
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31024
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Lys227Glu
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: Latino
population: African
population: South Asian
population: East Asian
reference allele: A
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: MQ

16-31766296-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31766296
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 31766296
    reference: chr 16
allele count: 0
allele frequency: 0.0e0
allele num: 15260
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000531864
  gene symbol: ZNF720
  hgvsc: ENST00000531864.2:n.324+1075G>A
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000431546
  ensembl transcript: ENST00000534369
  gene symbol: ZNF720
  hgvsc: ENST00000534369.1:c.4-37655G>A
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000440701
  ensembl transcript: ENST00000399681
  gene symbol: ZNF720
  hgvsc: ENST00000399681.3:c.684G>A
  hgvsp: ENST00000399681.3:c.684G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000319222
  ensembl transcript: ENST00000316491
  gene symbol: ZNF720
  hgvsc: ENST00000316491.9:c.361+1075G>A
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000434091
  ensembl transcript: ENST00000534277
  gene symbol: ZNF720
  hgvsc: ENST00000534277.1:c.*736G>A
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000381694
  ensembl transcript: ENST00000398707
  gene symbol: ZNF720
  hgvsc: ENST00000398707.3:c.*750G>A
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000441893
  ensembl transcript: ENST00000539915
  gene symbol: ZNF720
  hgvsc: ENST00000539915.1:c.151+1075G>A
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000542684
  gene symbol: ZNF720
  hgvsc: ENST00000542684.1:n.284+1075G>A
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000544044
  gene symbol: ZNF720
  hgvsc: ENST00000544044.1:n.278+1075G>A
  variant of: http://identifiers.org/hgnc/26987
canonical: false
consequence: synonymous
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 816
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2776
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  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: 8
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 952
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32741
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15209
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3138
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12366
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 718
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 778
  bin: 2.75e1
  variant carriers: 1
hgvs: p.Ala228Ala
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
population: European (Finnish)
population: Other
population: East Asian
reference allele: G
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD

16-31766304-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31766304
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 31766304
    reference: chr 16
allele count: 1
allele frequency: 6.266449429753102e-5
allele num: 15958
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000434091
  ensembl transcript: ENST00000534277
  gene symbol: ZNF720
  hgvsc: ENST00000534277.1:c.*744A>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000440701
  ensembl transcript: ENST00000399681
  gene symbol: ZNF720
  hgvsc: ENST00000399681.3:c.692A>G
  hgvsp: ENSP00000440701.1:p.Lys231Arg
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000381694
  ensembl transcript: ENST00000398707
  gene symbol: ZNF720
  hgvsc: ENST00000398707.3:c.*758A>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000542684
  gene symbol: ZNF720
  hgvsc: ENST00000542684.1:n.284+1083A>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000441893
  ensembl transcript: ENST00000539915
  gene symbol: ZNF720
  hgvsc: ENST00000539915.1:c.151+1083A>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000531864
  gene symbol: ZNF720
  hgvsc: ENST00000531864.2:n.324+1083A>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000431546
  ensembl transcript: ENST00000534369
  gene symbol: ZNF720
  hgvsc: ENST00000534369.1:c.4-37647A>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000544044
  gene symbol: ZNF720
  hgvsc: ENST00000544044.1:n.278+1083A>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000319222
  ensembl transcript: ENST00000316491
  gene symbol: ZNF720
  hgvsc: ENST00000316491.9:c.361+1083A>G
  variant of: http://identifiers.org/hgnc/26987
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32065
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16114
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2598
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3553
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 771
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 964
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3935
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30311
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 133
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 743
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Lys231Arg
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Other
population: East Asian
population: African
reference allele: A
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: MQ

16-31766316-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31766316
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 31766316
    reference: chr 16
allele count: 1
allele frequency: 5.98014591556034e-5
allele num: 16722
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000531864
  gene symbol: ZNF720
  hgvsc: ENST00000531864.2:n.324+1095A>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000542684
  gene symbol: ZNF720
  hgvsc: ENST00000542684.1:n.284+1095A>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000431546
  ensembl transcript: ENST00000534369
  gene symbol: ZNF720
  hgvsc: ENST00000534369.1:c.4-37635A>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000319222
  ensembl transcript: ENST00000316491
  gene symbol: ZNF720
  hgvsc: ENST00000316491.9:c.361+1095A>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000441893
  ensembl transcript: ENST00000539915
  gene symbol: ZNF720
  hgvsc: ENST00000539915.1:c.151+1095A>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000434091
  ensembl transcript: ENST00000534277
  gene symbol: ZNF720
  hgvsc: ENST00000534277.1:c.*756A>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000381694
  ensembl transcript: ENST00000398707
  gene symbol: ZNF720
  hgvsc: ENST00000398707.3:c.*770A>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000544044
  gene symbol: ZNF720
  hgvsc: ENST00000544044.1:n.278+1095A>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000440701
  ensembl transcript: ENST00000399681
  gene symbol: ZNF720
  hgvsc: ENST00000399681.3:c.704A>G
  hgvsp: ENSP00000440701.1:p.His235Arg
  variant of: http://identifiers.org/hgnc/26987
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17536
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1096
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30768
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2419
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 701
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4087
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2025
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 693
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1900
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 640
  bin: 3.25e1
  variant carriers: 0
hgvs: p.His235Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: East Asian
population: European (Finnish)
population: African
population: South Asian
population: Latino
reference allele: A
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ

16-31766325-ATCT-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31766325
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 31766322
    reference: chr 16
allele count: 1
allele frequency: 5.74184657785944e-5
allele num: 17416
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000431546
  ensembl transcript: ENST00000534369
  gene symbol: ZNF720
  hgvsc: ENST00000534369.1:c.4-37621_4-37619delCTT
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000544044
  gene symbol: ZNF720
  hgvsc: ENST00000544044.1:n.278+1109_278+1111delCTT
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000434091
  ensembl transcript: ENST00000534277
  gene symbol: ZNF720
  hgvsc: ENST00000534277.1:c.*770_*772delCTT
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000319222
  ensembl transcript: ENST00000316491
  gene symbol: ZNF720
  hgvsc: ENST00000316491.9:c.361+1109_361+1111delCTT
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000440701
  ensembl transcript: ENST00000399681
  gene symbol: ZNF720
  hgvsc: ENST00000399681.3:c.718_720delCTT
  hgvsp: ENSP00000440701.1:p.Leu240del
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000531864
  gene symbol: ZNF720
  hgvsc: ENST00000531864.2:n.324+1109_324+1111delCTT
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000381694
  ensembl transcript: ENST00000398707
  gene symbol: ZNF720
  hgvsc: ENST00000398707.3:c.*784_*786delCTT
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000441893
  ensembl transcript: ENST00000539915
  gene symbol: ZNF720
  hgvsc: ENST00000539915.1:c.151+1109_151+1111delCTT
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000542684
  gene symbol: ZNF720
  hgvsc: ENST00000542684.1:n.284+1109_284+1111delCTT
  variant of: http://identifiers.org/hgnc/26987
canonical: false
consequence: inframe deletion
filter: VQSRTrancheINDEL96.00to97.00
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  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: 6
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2220
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4551
  bin: 2.25e1
  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: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18827
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1205
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 657
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29548
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 168
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 589
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15699
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 97
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 411
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Leu240del
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
population: Other
reference allele: ATCT
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD

16-31766331-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31766331
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 31766331
    reference: chr 16
allele count: 2
allele frequency: 1.109754744201531e-4
allele num: 18022
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000531864
  gene symbol: ZNF720
  hgvsc: ENST00000531864.2:n.324+1110T>C
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000431546
  ensembl transcript: ENST00000534369
  gene symbol: ZNF720
  hgvsc: ENST00000534369.1:c.4-37620T>C
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000381694
  ensembl transcript: ENST00000398707
  gene symbol: ZNF720
  hgvsc: ENST00000398707.3:c.*785T>C
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000440701
  ensembl transcript: ENST00000399681
  gene symbol: ZNF720
  hgvsc: ENST00000399681.3:c.719T>C
  hgvsp: ENSP00000440701.1:p.Leu240Pro
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000441893
  ensembl transcript: ENST00000539915
  gene symbol: ZNF720
  hgvsc: ENST00000539915.1:c.151+1110T>C
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000542684
  gene symbol: ZNF720
  hgvsc: ENST00000542684.1:n.284+1110T>C
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000434091
  ensembl transcript: ENST00000534277
  gene symbol: ZNF720
  hgvsc: ENST00000534277.1:c.*771T>C
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000319222
  ensembl transcript: ENST00000316491
  gene symbol: ZNF720
  hgvsc: ENST00000316491.9:c.361+1110T>C
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000544044
  gene symbol: ZNF720
  hgvsc: ENST00000544044.1:n.278+1110T>C
  variant of: http://identifiers.org/hgnc/26987
canonical: false
consequence: missense
filter: PASS
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: 4986
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2071
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28527
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 614
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19775
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1282
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  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: 0
  bin: 7.75e1
  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 quality: GenotypeQuality
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2296
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 540
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 27122
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Leu240Pro
num of homozygotes: 1
population: African
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: T
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum

16-31766333-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31766333
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 31766333
    reference: chr 16
allele count: 1
allele frequency: 5.506001541680432e-5
allele num: 18162
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000441893
  ensembl transcript: ENST00000539915
  gene symbol: ZNF720
  hgvsc: ENST00000539915.1:c.151+1112G>A
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000544044
  gene symbol: ZNF720
  hgvsc: ENST00000544044.1:n.278+1112G>A
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000431546
  ensembl transcript: ENST00000534369
  gene symbol: ZNF720
  hgvsc: ENST00000534369.1:c.4-37618G>A
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000434091
  ensembl transcript: ENST00000534277
  gene symbol: ZNF720
  hgvsc: ENST00000534277.1:c.*773G>A
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000381694
  ensembl transcript: ENST00000398707
  gene symbol: ZNF720
  hgvsc: ENST00000398707.3:c.*787G>A
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000542684
  gene symbol: ZNF720
  hgvsc: ENST00000542684.1:n.284+1112G>A
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000440701
  ensembl transcript: ENST00000399681
  gene symbol: ZNF720
  hgvsc: ENST00000399681.3:c.721G>A
  hgvsp: ENSP00000440701.1:p.Val241Met
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000531864
  gene symbol: ZNF720
  hgvsc: ENST00000531864.2:n.324+1112G>A
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000319222
  ensembl transcript: ENST00000316491
  gene symbol: ZNF720
  hgvsc: ENST00000316491.9:c.361+1112G>A
  variant of: http://identifiers.org/hgnc/26987
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1311
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2007
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28173
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20070
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5150
  bin: 2.25e1
  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 depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 584
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 551
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1742
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5588
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2419
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Val241Met
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

16-31766335-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31766335
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 31766335
    reference: chr 16
allele count: 0
allele frequency: 0.0e0
allele num: 18254
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000434091
  ensembl transcript: ENST00000534277
  gene symbol: ZNF720
  hgvsc: ENST00000534277.1:c.*775G>T
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000542684
  gene symbol: ZNF720
  hgvsc: ENST00000542684.1:n.284+1114G>T
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000319222
  ensembl transcript: ENST00000316491
  gene symbol: ZNF720
  hgvsc: ENST00000316491.9:c.361+1114G>T
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000544044
  gene symbol: ZNF720
  hgvsc: ENST00000544044.1:n.278+1114G>T
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000440701
  ensembl transcript: ENST00000399681
  gene symbol: ZNF720
  hgvsc: ENST00000399681.3:c.723G>T
  hgvsp: ENST00000399681.3:c.723G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000431546
  ensembl transcript: ENST00000534369
  gene symbol: ZNF720
  hgvsc: ENST00000534369.1:c.4-37616G>T
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000441893
  ensembl transcript: ENST00000539915
  gene symbol: ZNF720
  hgvsc: ENST00000539915.1:c.151+1114G>T
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000531864
  gene symbol: ZNF720
  hgvsc: ENST00000531864.2:n.324+1114G>T
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000381694
  ensembl transcript: ENST00000398707
  gene symbol: ZNF720
  hgvsc: ENST00000398707.3:c.*789G>T
  variant of: http://identifiers.org/hgnc/26987
canonical: false
consequence: synonymous
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 27875
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1954
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5276
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20375
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1344
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 3.75e1
  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 depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 526
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 503
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17228
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Val241Val
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

16-31766345-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31766345
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 31766345
    reference: chr 16
allele count: 2
allele frequency: 1.02082482645978e-4
allele num: 19592
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000431546
  ensembl transcript: ENST00000534369
  gene symbol: ZNF720
  hgvsc: ENST00000534369.1:c.4-37606A>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000441893
  ensembl transcript: ENST00000539915
  gene symbol: ZNF720
  hgvsc: ENST00000539915.1:c.151+1124A>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000542684
  gene symbol: ZNF720
  hgvsc: ENST00000542684.1:n.284+1124A>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000440701
  ensembl transcript: ENST00000399681
  gene symbol: ZNF720
  hgvsc: ENST00000399681.3:c.733A>G
  hgvsp: ENSP00000440701.1:p.Ile245Val
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000319222
  ensembl transcript: ENST00000316491
  gene symbol: ZNF720
  hgvsc: ENST00000316491.9:c.361+1124A>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000381694
  ensembl transcript: ENST00000398707
  gene symbol: ZNF720
  hgvsc: ENST00000398707.3:c.*799A>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000531864
  gene symbol: ZNF720
  hgvsc: ENST00000531864.2:n.324+1124A>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000544044
  gene symbol: ZNF720
  hgvsc: ENST00000544044.1:n.278+1124A>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000434091
  ensembl transcript: ENST00000534277
  gene symbol: ZNF720
  hgvsc: ENST00000534277.1:c.*785A>G
  variant of: http://identifiers.org/hgnc/26987
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 21396
  bin: 7.5e0
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26648
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1560
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5877
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1762
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 217
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2319
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25418
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 118
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Ile245Val
num of homozygotes: 0
population: South Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
reference allele: A
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS

16-31766372-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31766372
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 31766372
    reference: chr 16
allele count: 2
allele frequency: 9.402030838661151e-5
allele num: 21272
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000441893
  ensembl transcript: ENST00000539915
  gene symbol: ZNF720
  hgvsc: ENST00000539915.1:c.151+1151T>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000431546
  ensembl transcript: ENST00000534369
  gene symbol: ZNF720
  hgvsc: ENST00000534369.1:c.4-37579T>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000544044
  gene symbol: ZNF720
  hgvsc: ENST00000544044.1:n.278+1151T>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000440701
  ensembl transcript: ENST00000399681
  gene symbol: ZNF720
  hgvsc: ENST00000399681.3:c.760T>G
  hgvsp: ENSP00000440701.1:p.Cys254Gly
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000531864
  gene symbol: ZNF720
  hgvsc: ENST00000531864.2:n.324+1151T>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000434091
  ensembl transcript: ENST00000534277
  gene symbol: ZNF720
  hgvsc: ENST00000534277.1:c.*812T>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000381694
  ensembl transcript: ENST00000398707
  gene symbol: ZNF720
  hgvsc: ENST00000398707.3:c.*826T>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000319222
  ensembl transcript: ENST00000316491
  gene symbol: ZNF720
  hgvsc: ENST00000316491.9:c.361+1151T>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000542684
  gene symbol: ZNF720
  hgvsc: ENST00000542684.1:n.284+1151T>G
  variant of: http://identifiers.org/hgnc/26987
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1879
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23100
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 24559
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1924
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6157
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  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: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 514
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 17496
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 5.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 23396
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Cys254Gly
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
population: African
population: Latino
population: European (Non-Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff

16-31766389-ATCATT-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31766389
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 31766384
    reference: chr 16
allele count: 0
allele frequency: 0.0e0
allele num: 22378
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000441893
  ensembl transcript: ENST00000539915
  gene symbol: ZNF720
  hgvsc: ENST00000539915.1:c.151+1170_151+1174delCATTT
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000440701
  ensembl transcript: ENST00000399681
  gene symbol: ZNF720
  hgvsc: ENST00000399681.3:c.779_783delCATTT
  hgvsp: ENSP00000440701.1:p.Ser260Ter
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000431546
  ensembl transcript: ENST00000534369
  gene symbol: ZNF720
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000381694
  ensembl transcript: ENST00000398707
  gene symbol: ZNF720
  hgvsc: ENST00000398707.3:c.*845_*849delCATTT
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000544044
  gene symbol: ZNF720
  hgvsc: ENST00000544044.1:n.278+1170_278+1174delCATTT
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000434091
  ensembl transcript: ENST00000534277
  gene symbol: ZNF720
  hgvsc: ENST00000534277.1:c.*831_*835delCATTT
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000319222
  ensembl transcript: ENST00000316491
  gene symbol: ZNF720
  hgvsc: ENST00000316491.9:c.361+1170_361+1174delCATTT
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000531864
  gene symbol: ZNF720
  hgvsc: ENST00000531864.2:n.324+1170_324+1174delCATTT
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000542684
  gene symbol: ZNF720
  hgvsc: ENST00000542684.1:n.284+1170_284+1174delCATTT
  variant of: http://identifiers.org/hgnc/26987
canonical: false
consequence: frameshift
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 25388
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 622
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2137
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6289
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22180
  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: 9.25e1
  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: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1976
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2981
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 554
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21481
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Ser260Ter
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Other
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: ATCATT
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: ClippingRankSum

16-31766395-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31766395
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 31766395
    reference: chr 16
allele count: 0
allele frequency: 0.0e0
allele num: 22770
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000544044
  gene symbol: ZNF720
  hgvsc: ENST00000544044.1:n.278+1174T>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000381694
  ensembl transcript: ENST00000398707
  gene symbol: ZNF720
  hgvsc: ENST00000398707.3:c.*849T>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000542684
  gene symbol: ZNF720
  hgvsc: ENST00000542684.1:n.284+1174T>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000434091
  ensembl transcript: ENST00000534277
  gene symbol: ZNF720
  hgvsc: ENST00000534277.1:c.*835T>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000440701
  ensembl transcript: ENST00000399681
  gene symbol: ZNF720
  hgvsc: ENST00000399681.3:c.783T>G
  hgvsp: ENSP00000440701.1:p.Phe261Leu
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000441893
  ensembl transcript: ENST00000539915
  gene symbol: ZNF720
  hgvsc: ENST00000539915.1:c.151+1174T>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000531864
  gene symbol: ZNF720
  hgvsc: ENST00000531864.2:n.324+1174T>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000319222
  ensembl transcript: ENST00000316491
  gene symbol: ZNF720
  hgvsc: ENST00000316491.9:c.361+1174T>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000431546
  ensembl transcript: ENST00000534369
  gene symbol: ZNF720
  hgvsc: ENST00000534369.1:c.4-37556T>G
  variant of: http://identifiers.org/hgnc/26987
canonical: false
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 2037
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26310
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6323
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21142
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2256
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 645
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1139
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 134
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 575
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Phe261Leu
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum

16-31766398-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31766398
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 31766398
    reference: chr 16
allele count: 0
allele frequency: 0.0e0
allele num: 22928
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000440701
  ensembl transcript: ENST00000399681
  gene symbol: ZNF720
  hgvsc: ENST00000399681.3:c.786A>T
  hgvsp: ENSP00000440701.1:p.Lys262Asn
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000542684
  gene symbol: ZNF720
  hgvsc: ENST00000542684.1:n.284+1177A>T
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000431546
  ensembl transcript: ENST00000534369
  gene symbol: ZNF720
  hgvsc: ENST00000534369.1:c.4-37553A>T
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000381694
  ensembl transcript: ENST00000398707
  gene symbol: ZNF720
  hgvsc: ENST00000398707.3:c.*852A>T
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000434091
  ensembl transcript: ENST00000534277
  gene symbol: ZNF720
  hgvsc: ENST00000534277.1:c.*838A>T
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000531864
  gene symbol: ZNF720
  hgvsc: ENST00000531864.2:n.324+1177A>T
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000544044
  gene symbol: ZNF720
  hgvsc: ENST00000544044.1:n.278+1177A>T
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000441893
  ensembl transcript: ENST00000539915
  gene symbol: ZNF720
  hgvsc: ENST00000539915.1:c.151+1177A>T
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000319222
  ensembl transcript: ENST00000316491
  gene symbol: ZNF720
  hgvsc: ENST00000316491.9:c.361+1177A>T
  variant of: http://identifiers.org/hgnc/26987
canonical: false
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 26826
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2338
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 4.25e1
  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: 6350
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2053
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20539
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 667
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 617
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2443
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19834
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 189
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 118
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Lys262Asn
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
population: South Asian
reference allele: A
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: ClippingRankSum

16-31766399-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31766399
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 31766399
    reference: chr 16
allele count: 0
allele frequency: 0.0e0
allele num: 22982
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000440701
  ensembl transcript: ENST00000399681
  gene symbol: ZNF720
  hgvsc: ENST00000399681.3:c.787G>A
  hgvsp: ENSP00000440701.1:p.Val263Met
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000441893
  ensembl transcript: ENST00000539915
  gene symbol: ZNF720
  hgvsc: ENST00000539915.1:c.151+1178G>A
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000381694
  ensembl transcript: ENST00000398707
  gene symbol: ZNF720
  hgvsc: ENST00000398707.3:c.*853G>A
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000431546
  ensembl transcript: ENST00000534369
  gene symbol: ZNF720
  hgvsc: ENST00000534369.1:c.4-37552G>A
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000544044
  gene symbol: ZNF720
  hgvsc: ENST00000544044.1:n.278+1178G>A
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000542684
  gene symbol: ZNF720
  hgvsc: ENST00000542684.1:n.284+1178G>A
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000434091
  ensembl transcript: ENST00000534277
  gene symbol: ZNF720
  hgvsc: ENST00000534277.1:c.*839G>A
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000531864
  gene symbol: ZNF720
  hgvsc: ENST00000531864.2:n.324+1178G>A
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000319222
  ensembl transcript: ENST00000316491
  gene symbol: ZNF720
  hgvsc: ENST00000316491.9:c.361+1178G>A
  variant of: http://identifiers.org/hgnc/26987
canonical: false
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2366
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20350
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  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: 24
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6368
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27001
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3
  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: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 1.75e1
  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: 2051
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 619
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19695
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 130
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2377
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 5.75e1
  variant carriers: 1
hgvs: p.Val263Met
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: G
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum

16-31766413-T-TA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31766413
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 31766414
    reference: chr 16
allele count: 1
allele frequency: 3.992334717342702e-5
allele num: 25048
alternate allele: TA
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000441893
  ensembl transcript: ENST00000539915
  gene symbol: ZNF720
  hgvsc: ENST00000539915.1:c.151+1193dupA
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000431546
  ensembl transcript: ENST00000534369
  gene symbol: ZNF720
  hgvsc: ENST00000534369.1:c.4-37537dupA
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000531864
  gene symbol: ZNF720
  hgvsc: ENST00000531864.2:n.324+1193dupA
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000544044
  gene symbol: ZNF720
  hgvsc: ENST00000544044.1:n.278+1193dupA
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000542684
  gene symbol: ZNF720
  hgvsc: ENST00000542684.1:n.284+1193dupA
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000440701
  ensembl transcript: ENST00000399681
  gene symbol: ZNF720
  hgvsc: ENST00000399681.3:c.802dupA
  hgvsp: ENSP00000440701.1:p.Thr268AsnfsTer4
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000381694
  ensembl transcript: ENST00000398707
  gene symbol: ZNF720
  hgvsc: ENST00000398707.3:c.*868dupA
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000434091
  ensembl transcript: ENST00000534277
  gene symbol: ZNF720
  hgvsc: ENST00000534277.1:c.*854dupA
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000319222
  ensembl transcript: ENST00000316491
  gene symbol: ZNF720
  hgvsc: ENST00000316491.9:c.361+1193dupA
  variant of: http://identifiers.org/hgnc/26987
canonical: false
consequence: frameshift
filter: VQSRTrancheINDEL95.00to96.00
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: 750
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2724
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17005
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2203
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6684
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29765
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.25e1
  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: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 679
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 141
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 87
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16548
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Thr268AsnfsTer4
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
population: Latino
population: Other
reference allele: T
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: QD

http://identifiers.org/exac.variant/16-31766420-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31766420
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 31766420
    reference: chr 16
allele count: 0
allele frequency: 0.0e0
allele num: 26066
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000381694
  ensembl transcript: ENST00000398707
  gene symbol: ZNF720
  hgvsc: ENST00000398707.3:c.*874C>A
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000441893
  ensembl transcript: ENST00000539915
  gene symbol: ZNF720
  hgvsc: ENST00000539915.1:c.151+1199C>A
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000440701
  ensembl transcript: ENST00000399681
  gene symbol: ZNF720
  hgvsc: ENST00000399681.3:c.808C>A
  hgvsp: ENSP00000440701.1:p.His270Asn
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000531864
  gene symbol: ZNF720
  hgvsc: ENST00000531864.2:n.324+1199C>A
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000542684
  gene symbol: ZNF720
  hgvsc: ENST00000542684.1:n.284+1199C>A
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000431546
  ensembl transcript: ENST00000534369
  gene symbol: ZNF720
  hgvsc: ENST00000534369.1:c.4-37531C>A
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000434091
  ensembl transcript: ENST00000534277
  gene symbol: ZNF720
  hgvsc: ENST00000534277.1:c.*860C>A
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000319222
  ensembl transcript: ENST00000316491
  gene symbol: ZNF720
  hgvsc: ENST00000316491.9:c.361+1199C>A
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000544044
  gene symbol: ZNF720
  hgvsc: ENST00000544044.1:n.278+1199C>A
  variant of: http://identifiers.org/hgnc/26987
canonical: false
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30731
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15552
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 895
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6939
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2867
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  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: 2
  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: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2218
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  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: 0
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15167
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 171
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 778
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2190
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28609
  bin: 2.25e1
  variant carriers: 0
hgvs: p.His270Asn
num of homozygotes: 0
population: Other
population: European (Finnish)
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: MQ
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff

16-31766422-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31766422
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 31766422
    reference: chr 16
allele count: 1
allele frequency: 3.793626707132018e-5
allele num: 26360
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000441893
  ensembl transcript: ENST00000539915
  gene symbol: ZNF720
  hgvsc: ENST00000539915.1:c.151+1201T>C
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000440701
  ensembl transcript: ENST00000399681
  gene symbol: ZNF720
  hgvsc: ENST00000399681.3:c.810T>C
  hgvsp: ENST00000399681.3:c.810T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000381694
  ensembl transcript: ENST00000398707
  gene symbol: ZNF720
  hgvsc: ENST00000398707.3:c.*876T>C
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000431546
  ensembl transcript: ENST00000534369
  gene symbol: ZNF720
  hgvsc: ENST00000534369.1:c.4-37529T>C
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000544044
  gene symbol: ZNF720
  hgvsc: ENST00000544044.1:n.278+1201T>C
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000434091
  ensembl transcript: ENST00000534277
  gene symbol: ZNF720
  hgvsc: ENST00000534277.1:c.*862T>C
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000319222
  ensembl transcript: ENST00000316491
  gene symbol: ZNF720
  hgvsc: ENST00000316491.9:c.361+1201T>C
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000542684
  gene symbol: ZNF720
  hgvsc: ENST00000542684.1:n.284+1201T>C
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000531864
  gene symbol: ZNF720
  hgvsc: ENST00000531864.2:n.324+1201T>C
  variant of: http://identifiers.org/hgnc/26987
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 31026
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15177
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2216
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2887
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 897
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7057
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  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: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 788
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 165
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 641
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29225
  bin: 2.25e1
  variant carriers: 0
hgvs: p.His270His
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum

16-31766422-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31766422
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 31766422
    reference: chr 16
allele count: 1
allele frequency: 3.793626707132018e-5
allele num: 26360
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000381694
  ensembl transcript: ENST00000398707
  gene symbol: ZNF720
  hgvsc: ENST00000398707.3:c.*876T>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000431546
  ensembl transcript: ENST00000534369
  gene symbol: ZNF720
  hgvsc: ENST00000534369.1:c.4-37529T>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000531864
  gene symbol: ZNF720
  hgvsc: ENST00000531864.2:n.324+1201T>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000319222
  ensembl transcript: ENST00000316491
  gene symbol: ZNF720
  hgvsc: ENST00000316491.9:c.361+1201T>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000440701
  ensembl transcript: ENST00000399681
  gene symbol: ZNF720
  hgvsc: ENST00000399681.3:c.810T>G
  hgvsp: ENSP00000440701.1:p.His270Gln
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000434091
  ensembl transcript: ENST00000534277
  gene symbol: ZNF720
  hgvsc: ENST00000534277.1:c.*862T>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000441893
  ensembl transcript: ENST00000539915
  gene symbol: ZNF720
  hgvsc: ENST00000539915.1:c.151+1201T>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000542684
  gene symbol: ZNF720
  hgvsc: ENST00000542684.1:n.284+1201T>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000544044
  gene symbol: ZNF720
  hgvsc: ENST00000544044.1:n.278+1201T>G
  variant of: http://identifiers.org/hgnc/26987
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 897
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7057
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31026
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2216
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15177
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2887
  bin: 1.25e1
  variant carriers: 1
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: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  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 quality: GenotypeQuality
  all individuals: 29225
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 165
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 208
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1998
  bin: 1.75e1
  variant carriers: 0
hgvs: p.His270Gln
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
population: Other
population: European (Finnish)
population: Latino
reference allele: T
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum

16-31766427-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31766427
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 31766427
    reference: chr 16
allele count: 0
allele frequency: 0.0e0
allele num: 26788
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000440701
  ensembl transcript: ENST00000399681
  gene symbol: ZNF720
  hgvsc: ENST00000399681.3:c.815G>A
  hgvsp: ENSP00000440701.1:p.Arg272Lys
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000542684
  gene symbol: ZNF720
  hgvsc: ENST00000542684.1:n.284+1206G>A
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000431546
  ensembl transcript: ENST00000534369
  gene symbol: ZNF720
  hgvsc: ENST00000534369.1:c.4-37524G>A
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000441893
  ensembl transcript: ENST00000539915
  gene symbol: ZNF720
  hgvsc: ENST00000539915.1:c.151+1206G>A
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000434091
  ensembl transcript: ENST00000534277
  gene symbol: ZNF720
  hgvsc: ENST00000534277.1:c.*867G>A
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000381694
  ensembl transcript: ENST00000398707
  gene symbol: ZNF720
  hgvsc: ENST00000398707.3:c.*881G>A
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000531864
  gene symbol: ZNF720
  hgvsc: ENST00000531864.2:n.324+1206G>A
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000544044
  gene symbol: ZNF720
  hgvsc: ENST00000544044.1:n.278+1206G>A
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000319222
  ensembl transcript: ENST00000316491
  gene symbol: ZNF720
  hgvsc: ENST00000316491.9:c.361+1206G>A
  variant of: http://identifiers.org/hgnc/26987
canonical: false
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31294
  bin: 7.5e0
  variant carriers: 1
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: 26
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7153
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2940
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2204
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14695
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1015
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 181
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29444
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 573
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 261
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Arg272Lys
num of homozygotes: 0
population: Latino
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: DP

16-31766435-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31766435
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 31766435
    reference: chr 16
allele count: 0
allele frequency: 0.0e0
allele num: 27274
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000531864
  gene symbol: ZNF720
  hgvsc: ENST00000531864.2:n.324+1214A>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000544044
  gene symbol: ZNF720
  hgvsc: ENST00000544044.1:n.278+1214A>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000542684
  gene symbol: ZNF720
  hgvsc: ENST00000542684.1:n.284+1214A>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000440701
  ensembl transcript: ENST00000399681
  gene symbol: ZNF720
  hgvsc: ENST00000399681.3:c.823A>G
  hgvsp: ENSP00000440701.1:p.Thr275Ala
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000431546
  ensembl transcript: ENST00000534369
  gene symbol: ZNF720
  hgvsc: ENST00000534369.1:c.4-37516A>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000434091
  ensembl transcript: ENST00000534277
  gene symbol: ZNF720
  hgvsc: ENST00000534277.1:c.*875A>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000381694
  ensembl transcript: ENST00000398707
  gene symbol: ZNF720
  hgvsc: ENST00000398707.3:c.*889A>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000441893
  ensembl transcript: ENST00000539915
  gene symbol: ZNF720
  hgvsc: ENST00000539915.1:c.151+1214A>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000319222
  ensembl transcript: ENST00000316491
  gene symbol: ZNF720
  hgvsc: ENST00000316491.9:c.361+1214A>G
  variant of: http://identifiers.org/hgnc/26987
canonical: false
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 2196
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3097
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14502
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  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: 243
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1191
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31277
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7024
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 440
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 827
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29017
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 548
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Thr275Ala
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: ReadPosRankSum

16-31766443-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31766443
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 31766443
    reference: chr 16
allele count: 1
allele frequency: 3.644846187490888e-5
allele num: 27436
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000381694
  ensembl transcript: ENST00000398707
  gene symbol: ZNF720
  hgvsc: ENST00000398707.3:c.*897G>A
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000434091
  ensembl transcript: ENST00000534277
  gene symbol: ZNF720
  hgvsc: ENST00000534277.1:c.*883G>A
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000319222
  ensembl transcript: ENST00000316491
  gene symbol: ZNF720
  hgvsc: ENST00000316491.9:c.361+1222G>A
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000441893
  ensembl transcript: ENST00000539915
  gene symbol: ZNF720
  hgvsc: ENST00000539915.1:c.151+1222G>A
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000542684
  gene symbol: ZNF720
  hgvsc: ENST00000542684.1:n.284+1222G>A
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000431546
  ensembl transcript: ENST00000534369
  gene symbol: ZNF720
  hgvsc: ENST00000534369.1:c.4-37508G>A
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000440701
  ensembl transcript: ENST00000399681
  gene symbol: ZNF720
  hgvsc: ENST00000399681.3:c.831G>A
  hgvsp: ENST00000399681.3:c.831G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000531864
  gene symbol: ZNF720
  hgvsc: ENST00000531864.2:n.324+1222G>A
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000544044
  gene symbol: ZNF720
  hgvsc: ENST00000544044.1:n.278+1222G>A
  variant of: http://identifiers.org/hgnc/26987
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6977
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1250
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14463
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2219
  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: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3288
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31071
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1274
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 817
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14166
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 376
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 727
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Glu277Glu
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
population: African
population: South Asian
population: Latino
reference allele: G
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: ReadPosRankSum

16-31766452-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31766452
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 31766452
    reference: chr 16
allele count: 2
allele frequency: 7.18803910293272e-5
allele num: 27824
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000431546
  ensembl transcript: ENST00000534369
  gene symbol: ZNF720
  hgvsc: ENST00000534369.1:c.4-37499T>C
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000531864
  gene symbol: ZNF720
  hgvsc: ENST00000531864.2:n.324+1231T>C
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000440701
  ensembl transcript: ENST00000399681
  gene symbol: ZNF720
  hgvsc: ENST00000399681.3:c.840T>C
  hgvsp: ENST00000399681.3:c.840T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000434091
  ensembl transcript: ENST00000534277
  gene symbol: ZNF720
  hgvsc: ENST00000534277.1:c.*892T>C
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000441893
  ensembl transcript: ENST00000539915
  gene symbol: ZNF720
  hgvsc: ENST00000539915.1:c.151+1231T>C
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000544044
  gene symbol: ZNF720
  hgvsc: ENST00000544044.1:n.278+1231T>C
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000381694
  ensembl transcript: ENST00000398707
  gene symbol: ZNF720
  hgvsc: ENST00000398707.3:c.*906T>C
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000542684
  gene symbol: ZNF720
  hgvsc: ENST00000542684.1:n.284+1231T>C
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000319222
  ensembl transcript: ENST00000316491
  gene symbol: ZNF720
  hgvsc: ENST00000316491.9:c.361+1231T>C
  variant of: http://identifiers.org/hgnc/26987
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6899
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2274
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14626
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3501
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1201
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30710
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  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: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 129
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 196
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 281
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Tyr280Tyr
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
reference allele: T
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD

16-31766487-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31766487
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 31766487
    reference: chr 16
allele count: 0
allele frequency: 0.0e0
allele num: 25894
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000441893
  ensembl transcript: ENST00000539915
  gene symbol: ZNF720
  hgvsc: ENST00000539915.1:c.151+1266G>A
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000434091
  ensembl transcript: ENST00000534277
  gene symbol: ZNF720
  hgvsc: ENST00000534277.1:c.*927G>A
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000531864
  gene symbol: ZNF720
  hgvsc: ENST00000531864.2:n.324+1266G>A
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000440701
  ensembl transcript: ENST00000399681
  gene symbol: ZNF720
  hgvsc: ENST00000399681.3:c.875G>A
  hgvsp: ENSP00000440701.1:p.Arg292Lys
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000544044
  gene symbol: ZNF720
  hgvsc: ENST00000544044.1:n.278+1266G>A
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000381694
  ensembl transcript: ENST00000398707
  gene symbol: ZNF720
  hgvsc: ENST00000398707.3:c.*941G>A
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000431546
  ensembl transcript: ENST00000534369
  gene symbol: ZNF720
  hgvsc: ENST00000534369.1:c.4-37464G>A
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000319222
  ensembl transcript: ENST00000316491
  gene symbol: ZNF720
  hgvsc: ENST00000316491.9:c.361+1266G>A
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000542684
  gene symbol: ZNF720
  hgvsc: ENST00000542684.1:n.284+1266G>A
  variant of: http://identifiers.org/hgnc/26987
canonical: false
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5691
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24850
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20698
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3911
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2554
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 765
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 4.25e1
  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: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7254
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 750
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20171
  bin: 7.5e0
  variant carriers: 1
hgvs: p.Arg292Lys
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: QD

16-31766490-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31766490
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 31766490
    reference: chr 16
allele count: 2
allele frequency: 7.824726134585289e-5
allele num: 25560
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000542684
  gene symbol: ZNF720
  hgvsc: ENST00000542684.1:n.284+1269C>T
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000440701
  ensembl transcript: ENST00000399681
  gene symbol: ZNF720
  hgvsc: ENST00000399681.3:c.878C>T
  hgvsp: ENSP00000440701.1:p.Ser293Leu
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000431546
  ensembl transcript: ENST00000534369
  gene symbol: ZNF720
  hgvsc: ENST00000534369.1:c.4-37461C>T
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000434091
  ensembl transcript: ENST00000534277
  gene symbol: ZNF720
  hgvsc: ENST00000534277.1:c.*930C>T
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000531864
  gene symbol: ZNF720
  hgvsc: ENST00000531864.2:n.324+1269C>T
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000544044
  gene symbol: ZNF720
  hgvsc: ENST00000544044.1:n.278+1269C>T
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000381694
  ensembl transcript: ENST00000398707
  gene symbol: ZNF720
  hgvsc: ENST00000398707.3:c.*944C>T
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000319222
  ensembl transcript: ENST00000316491
  gene symbol: ZNF720
  hgvsc: ENST00000316491.9:c.361+1269C>T
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000441893
  ensembl transcript: ENST00000539915
  gene symbol: ZNF720
  hgvsc: ENST00000539915.1:c.151+1269C>T
  variant of: http://identifiers.org/hgnc/26987
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 738
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2609
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21280
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5586
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24323
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3829
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2875
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3614
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 132
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Ser293Leu
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: C
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum

16-31766491-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31766491
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 31766491
    reference: chr 16
allele count: 1
allele frequency: 3.956635277360133e-5
allele num: 25274
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000434091
  ensembl transcript: ENST00000534277
  gene symbol: ZNF720
  hgvsc: ENST00000534277.1:c.*931G>A
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000544044
  gene symbol: ZNF720
  hgvsc: ENST00000544044.1:n.278+1270G>A
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000381694
  ensembl transcript: ENST00000398707
  gene symbol: ZNF720
  hgvsc: ENST00000398707.3:c.*945G>A
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000440701
  ensembl transcript: ENST00000399681
  gene symbol: ZNF720
  hgvsc: ENST00000399681.3:c.879G>A
  hgvsp: ENST00000399681.3:c.879G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000542684
  gene symbol: ZNF720
  hgvsc: ENST00000542684.1:n.284+1270G>A
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000531864
  gene symbol: ZNF720
  hgvsc: ENST00000531864.2:n.324+1270G>A
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000319222
  ensembl transcript: ENST00000316491
  gene symbol: ZNF720
  hgvsc: ENST00000316491.9:c.361+1270G>A
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000431546
  ensembl transcript: ENST00000534369
  gene symbol: ZNF720
  hgvsc: ENST00000534369.1:c.4-37460G>A
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000441893
  ensembl transcript: ENST00000539915
  gene symbol: ZNF720
  hgvsc: ENST00000539915.1:c.151+1270G>A
  variant of: http://identifiers.org/hgnc/26987
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2624
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5563
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 712
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24194
  bin: 7.5e0
  variant carriers: 3
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: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3815
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21421
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  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: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2831
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 817
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 9.75e1
  variant carriers: 2
hgvs: p.Ser293Ser
num of homozygotes: 0
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
reference allele: G
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff

16-31766494-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31766494
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 31766494
    reference: chr 16
allele count: 4
allele frequency: 1.583531274742676e-4
allele num: 25260
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000319222
  ensembl transcript: ENST00000316491
  gene symbol: ZNF720
  hgvsc: ENST00000316491.9:c.361+1273C>T
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000542684
  gene symbol: ZNF720
  hgvsc: ENST00000542684.1:n.284+1273C>T
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000381694
  ensembl transcript: ENST00000398707
  gene symbol: ZNF720
  hgvsc: ENST00000398707.3:c.*948C>T
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000434091
  ensembl transcript: ENST00000534277
  gene symbol: ZNF720
  hgvsc: ENST00000534277.1:c.*934C>T
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000544044
  gene symbol: ZNF720
  hgvsc: ENST00000544044.1:n.278+1273C>T
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000440701
  ensembl transcript: ENST00000399681
  gene symbol: ZNF720
  hgvsc: ENST00000399681.3:c.882C>T
  hgvsp: ENST00000399681.3:c.882C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000441893
  ensembl transcript: ENST00000539915
  gene symbol: ZNF720
  hgvsc: ENST00000539915.1:c.151+1273C>T
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000431546
  ensembl transcript: ENST00000534369
  gene symbol: ZNF720
  hgvsc: ENST00000534369.1:c.4-37457C>T
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000531864
  gene symbol: ZNF720
  hgvsc: ENST00000531864.2:n.324+1273C>T
  variant of: http://identifiers.org/hgnc/26987
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22011
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  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: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5537
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23764
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3632
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2656
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 653
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 8.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 3240
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 99
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 107
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 824
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Tyr294Tyr
num of homozygotes: 1
population: Other
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: South Asian
reference allele: C
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: QD

http://identifiers.org/exac.variant/16-31766498-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31766498
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 31766498
    reference: chr 16
allele count: 1
allele frequency: 3.98628717212788e-5
allele num: 25086
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000542684
  gene symbol: ZNF720
  hgvsc: ENST00000542684.1:n.284+1277A>C
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000544044
  gene symbol: ZNF720
  hgvsc: ENST00000544044.1:n.278+1277A>C
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000381694
  ensembl transcript: ENST00000398707
  gene symbol: ZNF720
  hgvsc: ENST00000398707.3:c.*952A>C
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000440701
  ensembl transcript: ENST00000399681
  gene symbol: ZNF720
  hgvsc: ENST00000399681.3:c.886A>C
  hgvsp: ENSP00000440701.1:p.Thr296Pro
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000431546
  ensembl transcript: ENST00000534369
  gene symbol: ZNF720
  hgvsc: ENST00000534369.1:c.4-37453A>C
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000434091
  ensembl transcript: ENST00000534277
  gene symbol: ZNF720
  hgvsc: ENST00000534277.1:c.*938A>C
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000441893
  ensembl transcript: ENST00000539915
  gene symbol: ZNF720
  hgvsc: ENST00000539915.1:c.151+1277A>C
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000531864
  gene symbol: ZNF720
  hgvsc: ENST00000531864.2:n.324+1277A>C
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000319222
  ensembl transcript: ENST00000316491
  gene symbol: ZNF720
  hgvsc: ENST00000316491.9:c.361+1277A>C
  variant of: http://identifiers.org/hgnc/26987
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23222
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3531
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22622
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5549
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2684
  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: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7366
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2962
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1196
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Thr296Pro
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: Other
reference allele: A
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum

16-31766506-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31766506
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 31766506
    reference: chr 16
allele count: 1
allele frequency: 4.07797080172906e-5
allele num: 24522
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000542684
  gene symbol: ZNF720
  hgvsc: ENST00000542684.1:n.284+1285T>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000441893
  ensembl transcript: ENST00000539915
  gene symbol: ZNF720
  hgvsc: ENST00000539915.1:c.151+1285T>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000440701
  ensembl transcript: ENST00000399681
  gene symbol: ZNF720
  hgvsc: ENST00000399681.3:c.894T>G
  hgvsp: ENSP00000440701.1:p.His298Gln
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000434091
  ensembl transcript: ENST00000534277
  gene symbol: ZNF720
  hgvsc: ENST00000534277.1:c.*946T>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000531864
  gene symbol: ZNF720
  hgvsc: ENST00000531864.2:n.324+1285T>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000544044
  gene symbol: ZNF720
  hgvsc: ENST00000544044.1:n.278+1285T>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000431546
  ensembl transcript: ENST00000534369
  gene symbol: ZNF720
  hgvsc: ENST00000534369.1:c.4-37445T>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000319222
  ensembl transcript: ENST00000316491
  gene symbol: ZNF720
  hgvsc: ENST00000316491.9:c.361+1285T>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000381694
  ensembl transcript: ENST00000398707
  gene symbol: ZNF720
  hgvsc: ENST00000398707.3:c.*960T>G
  variant of: http://identifiers.org/hgnc/26987
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 22179
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5443
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2729
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23683
  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: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3318
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  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: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16705
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 95
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7314
  bin: 6.25e1
  variant carriers: 0
hgvs: p.His298Gln
num of homozygotes: 0
population: Other
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff

16-31766512-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31766512
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 31766512
    reference: chr 16
allele count: 4
allele frequency: 1.650437365901964e-4
allele num: 24236
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000381694
  ensembl transcript: ENST00000398707
  gene symbol: ZNF720
  hgvsc: ENST00000398707.3:c.*966A>T
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000441893
  ensembl transcript: ENST00000539915
  gene symbol: ZNF720
  hgvsc: ENST00000539915.1:c.151+1291A>T
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000542684
  gene symbol: ZNF720
  hgvsc: ENST00000542684.1:n.284+1291A>T
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000544044
  gene symbol: ZNF720
  hgvsc: ENST00000544044.1:n.278+1291A>T
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000531864
  gene symbol: ZNF720
  hgvsc: ENST00000531864.2:n.324+1291A>T
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000434091
  ensembl transcript: ENST00000534277
  gene symbol: ZNF720
  hgvsc: ENST00000534277.1:c.*952A>T
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000319222
  ensembl transcript: ENST00000316491
  gene symbol: ZNF720
  hgvsc: ENST00000316491.9:c.361+1291A>T
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000440701
  ensembl transcript: ENST00000399681
  gene symbol: ZNF720
  hgvsc: ENST00000399681.3:c.900A>T
  hgvsp: ENSP00000440701.1:p.Arg300Ser
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000431546
  ensembl transcript: ENST00000534369
  gene symbol: ZNF720
  hgvsc: ENST00000534369.1:c.4-37439A>T
  variant of: http://identifiers.org/hgnc/26987
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2746
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24118
  bin: 2.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3138
  bin: 1.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21755
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5425
  bin: 2.25e1
  variant carriers: 0
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 quality: GenotypeQuality
  all individuals: 71
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 674
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 760
  bin: 2.75e1
  variant carriers: 2
hgvs: p.Arg300Ser
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
population: Other
population: Latino
reference allele: A
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQ

16-31766521-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31766521
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 31766521
    reference: chr 16
allele count: 1
allele frequency: 4.247366632687734e-5
allele num: 23544
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000531864
  gene symbol: ZNF720
  hgvsc: ENST00000531864.2:n.324+1300C>T
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000319222
  ensembl transcript: ENST00000316491
  gene symbol: ZNF720
  hgvsc: ENST00000316491.9:c.361+1300C>T
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000431546
  ensembl transcript: ENST00000534369
  gene symbol: ZNF720
  hgvsc: ENST00000534369.1:c.4-37430C>T
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000434091
  ensembl transcript: ENST00000534277
  gene symbol: ZNF720
  hgvsc: ENST00000534277.1:c.*961C>T
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000542684
  gene symbol: ZNF720
  hgvsc: ENST00000542684.1:n.284+1300C>T
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000544044
  gene symbol: ZNF720
  hgvsc: ENST00000544044.1:n.278+1300C>T
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000440701
  ensembl transcript: ENST00000399681
  gene symbol: ZNF720
  hgvsc: ENST00000399681.3:c.909C>T
  hgvsp: ENST00000399681.3:c.909C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000381694
  ensembl transcript: ENST00000398707
  gene symbol: ZNF720
  hgvsc: ENST00000398707.3:c.*975C>T
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000441893
  ensembl transcript: ENST00000539915
  gene symbol: ZNF720
  hgvsc: ENST00000539915.1:c.151+1300C>T
  variant of: http://identifiers.org/hgnc/26987
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2978
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5387
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24544
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21265
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 345
  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: 6.25e1
  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: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2766
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3794
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7356
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Thr303Thr
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum

16-31766522-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31766522
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 31766522
    reference: chr 16
allele count: 5
allele frequency: 2.115059221658206e-4
allele num: 23640
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000381694
  ensembl transcript: ENST00000398707
  gene symbol: ZNF720
  hgvsc: ENST00000398707.3:c.*976G>A
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000440701
  ensembl transcript: ENST00000399681
  gene symbol: ZNF720
  hgvsc: ENST00000399681.3:c.910G>A
  hgvsp: ENSP00000440701.1:p.Gly304Arg
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000544044
  gene symbol: ZNF720
  hgvsc: ENST00000544044.1:n.278+1301G>A
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000542684
  gene symbol: ZNF720
  hgvsc: ENST00000542684.1:n.284+1301G>A
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000531864
  gene symbol: ZNF720
  hgvsc: ENST00000531864.2:n.324+1301G>A
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000431546
  ensembl transcript: ENST00000534369
  gene symbol: ZNF720
  hgvsc: ENST00000534369.1:c.4-37429G>A
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000434091
  ensembl transcript: ENST00000534277
  gene symbol: ZNF720
  hgvsc: ENST00000534277.1:c.*962G>A
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000441893
  ensembl transcript: ENST00000539915
  gene symbol: ZNF720
  hgvsc: ENST00000539915.1:c.151+1301G>A
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000319222
  ensembl transcript: ENST00000316491
  gene symbol: ZNF720
  hgvsc: ENST00000316491.9:c.361+1301G>A
  variant of: http://identifiers.org/hgnc/26987
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21312
  bin: 7.5e0
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 1.75e1
  variant carriers: 2
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: 24549
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2771
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5407
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2973
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 249
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 4.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 745
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 5.75e1
  variant carriers: 1
hgvs: p.Gly304Arg
num of homozygotes: 0
population: Latino
population: Other
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: FS

16-31766531-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31766531
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 31766531
    reference: chr 16
allele count: 1
allele frequency: 4.232983406705046e-5
allele num: 23624
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000434091
  ensembl transcript: ENST00000534277
  gene symbol: ZNF720
  hgvsc: ENST00000534277.1:c.*971C>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000542684
  gene symbol: ZNF720
  hgvsc: ENST00000542684.1:n.284+1310C>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000431546
  ensembl transcript: ENST00000534369
  gene symbol: ZNF720
  hgvsc: ENST00000534369.1:c.4-37420C>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000441893
  ensembl transcript: ENST00000539915
  gene symbol: ZNF720
  hgvsc: ENST00000539915.1:c.151+1310C>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000440701
  ensembl transcript: ENST00000399681
  gene symbol: ZNF720
  hgvsc: ENST00000399681.3:c.919C>G
  hgvsp: ENSP00000440701.1:p.Leu307Val
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000531864
  gene symbol: ZNF720
  hgvsc: ENST00000531864.2:n.324+1310C>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000319222
  ensembl transcript: ENST00000316491
  gene symbol: ZNF720
  hgvsc: ENST00000316491.9:c.361+1310C>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000544044
  gene symbol: ZNF720
  hgvsc: ENST00000544044.1:n.278+1310C>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000381694
  ensembl transcript: ENST00000398707
  gene symbol: ZNF720
  hgvsc: ENST00000398707.3:c.*985C>G
  variant of: http://identifiers.org/hgnc/26987
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2796
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21638
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5443
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24478
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2802
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 4.25e1
  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: 0
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 630
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15871
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3710
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 257
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2906
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Leu307Val
num of homozygotes: 0
population: Latino
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: FS

16-31766535-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31766535
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 31766535
    reference: chr 16
allele count: 0
allele frequency: 0.0e0
allele num: 23618
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000440701
  ensembl transcript: ENST00000399681
  gene symbol: ZNF720
  hgvsc: ENST00000399681.3:c.923A>G
  hgvsp: ENSP00000440701.1:p.Tyr308Cys
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000381694
  ensembl transcript: ENST00000398707
  gene symbol: ZNF720
  hgvsc: ENST00000398707.3:c.*989A>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000319222
  ensembl transcript: ENST00000316491
  gene symbol: ZNF720
  hgvsc: ENST00000316491.9:c.361+1314A>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000431546
  ensembl transcript: ENST00000534369
  gene symbol: ZNF720
  hgvsc: ENST00000534369.1:c.4-37416A>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000531864
  gene symbol: ZNF720
  hgvsc: ENST00000531864.2:n.324+1314A>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000542684
  gene symbol: ZNF720
  hgvsc: ENST00000542684.1:n.284+1314A>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000434091
  ensembl transcript: ENST00000534277
  gene symbol: ZNF720
  hgvsc: ENST00000534277.1:c.*975A>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000441893
  ensembl transcript: ENST00000539915
  gene symbol: ZNF720
  hgvsc: ENST00000539915.1:c.151+1314A>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000544044
  gene symbol: ZNF720
  hgvsc: ENST00000544044.1:n.278+1314A>G
  variant of: http://identifiers.org/hgnc/26987
canonical: false
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2814
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2817
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21712
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24363
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5456
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  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: 7
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 751
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 254
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 628
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 751
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Tyr308Cys
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: A
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: MQ

http://identifiers.org/exac.variant/16-31766547-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31766547
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 31766547
    reference: chr 16
allele count: 1
allele frequency: 4.200621692010418e-5
allele num: 23806
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000544044
  gene symbol: ZNF720
  hgvsc: ENST00000544044.1:n.278+1326C>A
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000381694
  ensembl transcript: ENST00000398707
  gene symbol: ZNF720
  hgvsc: ENST00000398707.3:c.*1001C>A
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000441893
  ensembl transcript: ENST00000539915
  gene symbol: ZNF720
  hgvsc: ENST00000539915.1:c.151+1326C>A
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000531864
  gene symbol: ZNF720
  hgvsc: ENST00000531864.2:n.324+1326C>A
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000440701
  ensembl transcript: ENST00000399681
  gene symbol: ZNF720
  hgvsc: ENST00000399681.3:c.935C>A
  hgvsp: ENSP00000440701.1:p.Ser312Ter
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000434091
  ensembl transcript: ENST00000534277
  gene symbol: ZNF720
  hgvsc: ENST00000534277.1:c.*987C>A
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000319222
  ensembl transcript: ENST00000316491
  gene symbol: ZNF720
  hgvsc: ENST00000316491.9:c.361+1326C>A
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000431546
  ensembl transcript: ENST00000534369
  gene symbol: ZNF720
  hgvsc: ENST00000534369.1:c.4-37404C>A
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000542684
  gene symbol: ZNF720
  hgvsc: ENST00000542684.1:n.284+1326C>A
  variant of: http://identifiers.org/hgnc/26987
canonical: false
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5538
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23196
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2853
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2845
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23171
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  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: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1589
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22255
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 776
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17438
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3089
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Ser312Ter
num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: MQRankSum

16-31766547-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31766547
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 31766547
    reference: chr 16
allele count: 0
allele frequency: 0.0e0
allele num: 23806
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000441893
  ensembl transcript: ENST00000539915
  gene symbol: ZNF720
  hgvsc: ENST00000539915.1:c.151+1326C>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000319222
  ensembl transcript: ENST00000316491
  gene symbol: ZNF720
  hgvsc: ENST00000316491.9:c.361+1326C>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000431546
  ensembl transcript: ENST00000534369
  gene symbol: ZNF720
  hgvsc: ENST00000534369.1:c.4-37404C>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000440701
  ensembl transcript: ENST00000399681
  gene symbol: ZNF720
  hgvsc: ENST00000399681.3:c.935C>G
  hgvsp: ENSP00000440701.1:p.Ser312Ter
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000531864
  gene symbol: ZNF720
  hgvsc: ENST00000531864.2:n.324+1326C>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000542684
  gene symbol: ZNF720
  hgvsc: ENST00000542684.1:n.284+1326C>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000544044
  gene symbol: ZNF720
  hgvsc: ENST00000544044.1:n.278+1326C>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000381694
  ensembl transcript: ENST00000398707
  gene symbol: ZNF720
  hgvsc: ENST00000398707.3:c.*1001C>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000434091
  ensembl transcript: ENST00000534277
  gene symbol: ZNF720
  hgvsc: ENST00000534277.1:c.*987C>G
  variant of: http://identifiers.org/hgnc/26987
canonical: false
consequence: stop gained
filter: AC_Adj0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2845
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5538
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23171
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23196
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2853
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 758
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17438
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22255
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Ser312Ter
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: South Asian
reference allele: C
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum

16-31766567-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31766567
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 31766567
    reference: chr 16
allele count: 2
allele frequency: 7.95291872117067e-5
allele num: 25148
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000440701
  ensembl transcript: ENST00000399681
  gene symbol: ZNF720
  hgvsc: ENST00000399681.3:c.955C>T
  hgvsp: ENSP00000440701.1:p.Arg319Cys
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000431546
  ensembl transcript: ENST00000534369
  gene symbol: ZNF720
  hgvsc: ENST00000534369.1:c.4-37384C>T
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000441893
  ensembl transcript: ENST00000539915
  gene symbol: ZNF720
  hgvsc: ENST00000539915.1:c.151+1346C>T
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000434091
  ensembl transcript: ENST00000534277
  gene symbol: ZNF720
  hgvsc: ENST00000534277.1:c.*1007C>T
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000381694
  ensembl transcript: ENST00000398707
  gene symbol: ZNF720
  hgvsc: ENST00000398707.3:c.*1021C>T
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000531864
  gene symbol: ZNF720
  hgvsc: ENST00000531864.2:n.324+1346C>T
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000542684
  gene symbol: ZNF720
  hgvsc: ENST00000542684.1:n.284+1346C>T
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000544044
  gene symbol: ZNF720
  hgvsc: ENST00000544044.1:n.278+1346C>T
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000319222
  ensembl transcript: ENST00000316491
  gene symbol: ZNF720
  hgvsc: ENST00000316491.9:c.361+1346C>T
  variant of: http://identifiers.org/hgnc/26987
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27778
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3099
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5966
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18654
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  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: 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: 2900
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 3096
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18028
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Arg319Cys
num of homozygotes: 0
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
population: East Asian
reference allele: C
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff

16-31766568-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31766568
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 31766568
    reference: chr 16
allele count: 11
allele frequency: 4.338908172925213e-4
allele num: 25352
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000381694
  ensembl transcript: ENST00000398707
  gene symbol: ZNF720
  hgvsc: ENST00000398707.3:c.*1022G>A
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000434091
  ensembl transcript: ENST00000534277
  gene symbol: ZNF720
  hgvsc: ENST00000534277.1:c.*1008G>A
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000440701
  ensembl transcript: ENST00000399681
  gene symbol: ZNF720
  hgvsc: ENST00000399681.3:c.956G>A
  hgvsp: ENSP00000440701.1:p.Arg319His
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000531864
  gene symbol: ZNF720
  hgvsc: ENST00000531864.2:n.324+1347G>A
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000441893
  ensembl transcript: ENST00000539915
  gene symbol: ZNF720
  hgvsc: ENST00000539915.1:c.151+1347G>A
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000319222
  ensembl transcript: ENST00000316491
  gene symbol: ZNF720
  hgvsc: ENST00000316491.9:c.361+1347G>A
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000431546
  ensembl transcript: ENST00000534369
  gene symbol: ZNF720
  hgvsc: ENST00000534369.1:c.4-37383G>A
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000544044
  gene symbol: ZNF720
  hgvsc: ENST00000544044.1:n.278+1347G>A
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000542684
  gene symbol: ZNF720
  hgvsc: ENST00000542684.1:n.284+1347G>A
  variant of: http://identifiers.org/hgnc/26987
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3140
  bin: 1.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6066
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28291
  bin: 7.5e0
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18061
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2895
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 499
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  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
  all individuals: 81
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 8125
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 160
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17487
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Arg319His
num of homozygotes: 1
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/16-31766574-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31766574
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 31766574
    reference: chr 16
allele count: 1
allele frequency: 3.75685626267939e-5
allele num: 26618
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000441893
  ensembl transcript: ENST00000539915
  gene symbol: ZNF720
  hgvsc: ENST00000539915.1:c.151+1353C>A
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000319222
  ensembl transcript: ENST00000316491
  gene symbol: ZNF720
  hgvsc: ENST00000316491.9:c.361+1353C>A
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000431546
  ensembl transcript: ENST00000534369
  gene symbol: ZNF720
  hgvsc: ENST00000534369.1:c.4-37377C>A
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000544044
  gene symbol: ZNF720
  hgvsc: ENST00000544044.1:n.278+1353C>A
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000434091
  ensembl transcript: ENST00000534277
  gene symbol: ZNF720
  hgvsc: ENST00000534277.1:c.*1014C>A
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000542684
  gene symbol: ZNF720
  hgvsc: ENST00000542684.1:n.284+1353C>A
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000531864
  gene symbol: ZNF720
  hgvsc: ENST00000531864.2:n.324+1353C>A
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000440701
  ensembl transcript: ENST00000399681
  gene symbol: ZNF720
  hgvsc: ENST00000399681.3:c.962C>A
  hgvsp: ENSP00000440701.1:p.Ser321Ter
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000381694
  ensembl transcript: ENST00000398707
  gene symbol: ZNF720
  hgvsc: ENST00000398707.3:c.*1028C>A
  variant of: http://identifiers.org/hgnc/26987
canonical: false
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3236
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15690
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2918
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6511
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30330
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2120
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15245
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 751
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Ser321Ter
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
population: African
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ

16-31766584-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31766584
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 31766584
    reference: chr 16
allele count: 0
allele frequency: 0.0e0
allele num: 28778
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000319222
  ensembl transcript: ENST00000316491
  gene symbol: ZNF720
  hgvsc: ENST00000316491.9:c.361+1363T>C
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000381694
  ensembl transcript: ENST00000398707
  gene symbol: ZNF720
  hgvsc: ENST00000398707.3:c.*1038T>C
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000431546
  ensembl transcript: ENST00000534369
  gene symbol: ZNF720
  hgvsc: ENST00000534369.1:c.4-37367T>C
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000531864
  gene symbol: ZNF720
  hgvsc: ENST00000531864.2:n.324+1363T>C
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000434091
  ensembl transcript: ENST00000534277
  gene symbol: ZNF720
  hgvsc: ENST00000534277.1:c.*1024T>C
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000441893
  ensembl transcript: ENST00000539915
  gene symbol: ZNF720
  hgvsc: ENST00000539915.1:c.151+1363T>C
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000542684
  gene symbol: ZNF720
  hgvsc: ENST00000542684.1:n.284+1363T>C
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000440701
  ensembl transcript: ENST00000399681
  gene symbol: ZNF720
  hgvsc: ENST00000399681.3:c.972T>C
  hgvsp: ENST00000399681.3:c.972T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000544044
  gene symbol: ZNF720
  hgvsc: ENST00000544044.1:n.278+1363T>C
  variant of: http://identifiers.org/hgnc/26987
canonical: false
consequence: synonymous
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 3269
  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: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12655
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2973
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32566
  bin: 7.5e0
  variant carriers: 2
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: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7413
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  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: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1812
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12327
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 116
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 8.75e1
  variant carriers: 2
hgvs: p.Ile324Ile
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
population: African
population: European (Finnish)
population: East Asian
reference allele: T
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: QD

16-31766585-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31766585
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 31766585
    reference: chr 16
allele count: 3
allele frequency: 1.041811362689262e-4
allele num: 28796
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000441893
  ensembl transcript: ENST00000539915
  gene symbol: ZNF720
  hgvsc: ENST00000539915.1:c.151+1364G>T
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000431546
  ensembl transcript: ENST00000534369
  gene symbol: ZNF720
  hgvsc: ENST00000534369.1:c.4-37366G>T
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000381694
  ensembl transcript: ENST00000398707
  gene symbol: ZNF720
  hgvsc: ENST00000398707.3:c.*1039G>T
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000542684
  gene symbol: ZNF720
  hgvsc: ENST00000542684.1:n.284+1364G>T
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000319222
  ensembl transcript: ENST00000316491
  gene symbol: ZNF720
  hgvsc: ENST00000316491.9:c.361+1364G>T
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000531864
  gene symbol: ZNF720
  hgvsc: ENST00000531864.2:n.324+1364G>T
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000440701
  ensembl transcript: ENST00000399681
  gene symbol: ZNF720
  hgvsc: ENST00000399681.3:c.973G>T
  hgvsp: ENSP00000440701.1:p.Val325Phe
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000434091
  ensembl transcript: ENST00000534277
  gene symbol: ZNF720
  hgvsc: ENST00000534277.1:c.*1025G>T
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000544044
  gene symbol: ZNF720
  hgvsc: ENST00000544044.1:n.278+1364G>T
  variant of: http://identifiers.org/hgnc/26987
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2976
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3349
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7512
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12355
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32657
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 727
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 337
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 167
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Val325Phe
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
population: European (Finnish)
population: Latino
population: African
reference allele: G
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum

16-31766587-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31766587
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 31766587
    reference: chr 16
allele count: 1
allele frequency: 3.424188467333242e-5
allele num: 29204
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000544044
  gene symbol: ZNF720
  hgvsc: ENST00000544044.1:n.278+1366C>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000440701
  ensembl transcript: ENST00000399681
  gene symbol: ZNF720
  hgvsc: ENST00000399681.3:c.975C>G
  hgvsp: ENST00000399681.3:c.975C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000542684
  gene symbol: ZNF720
  hgvsc: ENST00000542684.1:n.284+1366C>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000319222
  ensembl transcript: ENST00000316491
  gene symbol: ZNF720
  hgvsc: ENST00000316491.9:c.361+1366C>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000431546
  ensembl transcript: ENST00000534369
  gene symbol: ZNF720
  hgvsc: ENST00000534369.1:c.4-37364C>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000531864
  gene symbol: ZNF720
  hgvsc: ENST00000531864.2:n.324+1366C>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000441893
  ensembl transcript: ENST00000539915
  gene symbol: ZNF720
  hgvsc: ENST00000539915.1:c.151+1366C>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000434091
  ensembl transcript: ENST00000534277
  gene symbol: ZNF720
  hgvsc: ENST00000534277.1:c.*1027C>G
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000381694
  ensembl transcript: ENST00000398707
  gene symbol: ZNF720
  hgvsc: ENST00000398707.3:c.*1041C>G
  variant of: http://identifiers.org/hgnc/26987
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: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11903
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3401
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32844
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2996
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7672
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 141
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1817
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 802
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Val325Val
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum

16-31766588-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31766588
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 31766588
    reference: chr 16
allele count: 2
allele frequency: 6.710958996040534e-5
allele num: 29802
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000542684
  gene symbol: ZNF720
  hgvsc: ENST00000542684.1:n.284+1367C>T
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000431546
  ensembl transcript: ENST00000534369
  gene symbol: ZNF720
  hgvsc: ENST00000534369.1:c.4-37363C>T
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000319222
  ensembl transcript: ENST00000316491
  gene symbol: ZNF720
  hgvsc: ENST00000316491.9:c.361+1367C>T
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000531864
  gene symbol: ZNF720
  hgvsc: ENST00000531864.2:n.324+1367C>T
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000441893
  ensembl transcript: ENST00000539915
  gene symbol: ZNF720
  hgvsc: ENST00000539915.1:c.151+1367C>T
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000440701
  ensembl transcript: ENST00000399681
  gene symbol: ZNF720
  hgvsc: ENST00000399681.3:c.976C>T
  hgvsp: ENSP00000440701.1:p.His326Tyr
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000434091
  ensembl transcript: ENST00000534277
  gene symbol: ZNF720
  hgvsc: ENST00000534277.1:c.*1028C>T
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000544044
  gene symbol: ZNF720
  hgvsc: ENST00000544044.1:n.278+1367C>T
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000381694
  ensembl transcript: ENST00000398707
  gene symbol: ZNF720
  hgvsc: ENST00000398707.3:c.*1042C>T
  variant of: http://identifiers.org/hgnc/26987
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 612
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 32898
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3456
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 3.25e1
  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: 3003
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11702
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7743
  bin: 2.25e1
  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: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1925
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 798
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 379
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1197
  bin: 1.25e1
  variant carriers: 0
hgvs: p.His326Tyr
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
population: African
population: European (Finnish)
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum

16-31766593-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31766593
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 31766593
    reference: chr 16
allele count: 0
allele frequency: 0.0e0
allele num: 30982
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000531864
  gene symbol: ZNF720
  hgvsc: ENST00000531864.2:n.324+1372G>C
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000544044
  gene symbol: ZNF720
  hgvsc: ENST00000544044.1:n.278+1372G>C
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000434091
  ensembl transcript: ENST00000534277
  gene symbol: ZNF720
  hgvsc: ENST00000534277.1:c.*1033G>C
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000440701
  ensembl transcript: ENST00000399681
  gene symbol: ZNF720
  hgvsc: ENST00000399681.3:c.981G>C
  hgvsp: ENSP00000440701.1:p.Gln327His
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000542684
  gene symbol: ZNF720
  hgvsc: ENST00000542684.1:n.284+1372G>C
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000381694
  ensembl transcript: ENST00000398707
  gene symbol: ZNF720
  hgvsc: ENST00000398707.3:c.*1047G>C
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000431546
  ensembl transcript: ENST00000534369
  gene symbol: ZNF720
  hgvsc: ENST00000534369.1:c.4-37358G>C
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000319222
  ensembl transcript: ENST00000316491
  gene symbol: ZNF720
  hgvsc: ENST00000316491.9:c.361+1372G>C
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000441893
  ensembl transcript: ENST00000539915
  gene symbol: ZNF720
  hgvsc: ENST00000539915.1:c.151+1372G>C
  variant of: http://identifiers.org/hgnc/26987
canonical: false
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 8101
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10801
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3526
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  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: 33311
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3046
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  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 quality: GenotypeQuality
  all individuals: 208
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1108
  bin: 1.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 10508
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 975
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 595
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Gln327His
num of homozygotes: 0
population: Other
population: South Asian
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum

16-31766605-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31766605
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 31766605
    reference: chr 16
allele count: 1
allele frequency: 3.017501508750754e-5
allele num: 33140
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000440701
  ensembl transcript: ENST00000399681
  gene symbol: ZNF720
  hgvsc: ENST00000399681.3:c.993T>C
  hgvsp: ENST00000399681.3:c.993T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000544044
  gene symbol: ZNF720
  hgvsc: ENST00000544044.1:n.278+1384T>C
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000319222
  ensembl transcript: ENST00000316491
  gene symbol: ZNF720
  hgvsc: ENST00000316491.9:c.361+1384T>C
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000431546
  ensembl transcript: ENST00000534369
  gene symbol: ZNF720
  hgvsc: ENST00000534369.1:c.4-37346T>C
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000542684
  gene symbol: ZNF720
  hgvsc: ENST00000542684.1:n.284+1384T>C
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000531864
  gene symbol: ZNF720
  hgvsc: ENST00000531864.2:n.324+1384T>C
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000381694
  ensembl transcript: ENST00000398707
  gene symbol: ZNF720
  hgvsc: ENST00000398707.3:c.*1059T>C
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000441893
  ensembl transcript: ENST00000539915
  gene symbol: ZNF720
  hgvsc: ENST00000539915.1:c.151+1384T>C
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000434091
  ensembl transcript: ENST00000534277
  gene symbol: ZNF720
  hgvsc: ENST00000534277.1:c.*1045T>C
  variant of: http://identifiers.org/hgnc/26987
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9400
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 857
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8793
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33777
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3075
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3717
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28
  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: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 494
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 253
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 179
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32509
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1861
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Thr331Thr
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
reference allele: T
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: QD

http://identifiers.org/exac.variant/16-31766622-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31766622
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 31766622
    reference: chr 16
allele count: 1
allele frequency: 2.81785392245266e-5
allele num: 35488
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000434091
  ensembl transcript: ENST00000534277
  gene symbol: ZNF720
  hgvsc: ENST00000534277.1:c.*1062A>C
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl transcript: ENST00000531864
  gene symbol: ZNF720
  hgvsc: ENST00000531864.2:n.324+1401A>C
  variant of: http://identifiers.org/hgnc/26987
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197302
  ensembl protein: ENSP00000441893
  ensembl transcript: ENST00000539915
  gene symbol: ZNF720
  hgvsc: ENST00000539915.1:c.151+1401A>C
  variant of: http://identifiers.org/hgnc/26987
canonical: false
consequence: missense
filter: PASS
hgvs: p.Lys337Thr
num of homozygotes: 0
reference allele: A

GenotypeQuality
all individuals: 80
bin: 7.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 10
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 276
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6271
bin: 6.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 27
bin: 9.75e1
variant carriers: 11

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

GenotypeQuality
all individuals: 2873
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 543
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 118
bin: 7.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 204
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7616
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: 3918
num of homozygotes: 0

African
type: Population
allele count: 10
allele frequency: 1.785714285714286e-2
allele num: 560
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1590
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 1.737e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.44e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.67e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.45e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.49e-1

DP
type: SiteQuality
SIO_000300: 1.77102e5

MQ
type: SiteQuality
SIO_000300: 5.938e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.55e0

VQSLOD
type: SiteQuality
SIO_000300: 1.58e0

QD
type: SiteQuality
SIO_000300: 1.232e1

GenotypeQuality
all individuals: 3
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 375
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6298
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3667
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 117
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 586
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 80
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 549
bin: 6.75e1
variant carriers: 1

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4000
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1594
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 584
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 212
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 1.313025210084034e-4
allele num: 7616
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -6.026e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.0e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.38e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.85e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.38e0

FS
type: SiteQuality
SIO_000300: 9.25e-1

QD
type: SiteQuality
SIO_000300: 1.422e1

DP
type: SiteQuality
SIO_000300: 1.81414e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.2e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 33
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6329
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 86
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 117
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 493
bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
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GenotypeQuality
all individuals: 81
bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 30
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 8.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4070
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1592
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 196
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.311991603253739e-4
allele num: 7622
num of homozygotes: 0

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

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

QD
type: SiteQuality
SIO_000300: 1.026e1

MQ
type: SiteQuality
SIO_000300: 5.751e1

MQRankSum
type: SiteQuality
SIO_000300: 6.78e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.266e0

FS
type: SiteQuality
SIO_000300: 1.105e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.999999999999999e-3

VQSLOD
type: SiteQuality
SIO_000300: -1.181e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.43e-1

DP
type: SiteQuality
SIO_000300: 1.86307e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.22e-2

GenotypeQuality
all individuals: 5
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12803
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variant carriers: 0

GenotypeQuality
all individuals: 85
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variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 120
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variant carriers: 0

GenotypeQuality
all individuals: 71
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 135
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1360
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 1144
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6500
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 9.75e1
variant carriers: 6

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

GenotypeQuality
all individuals: 35
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4482
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1598
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 714
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 242
num of homozygotes: 0

South Asian
type: Population
allele count: 4
allele frequency: 5.198856251624642e-4
allele num: 7694
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 198
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 7.751937984496124e-3
allele num: 258
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.682e1

DP
type: SiteQuality
SIO_000300: 2.14211e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.28e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.850000000000001e-2

FS
type: SiteQuality
SIO_000300: 1.166e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.824e0

MQRankSum
type: SiteQuality
SIO_000300: -1.87e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.86e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.67e-1

QD
type: SiteQuality
SIO_000300: 1.086e1

GenotypeQuality
all individuals: 86
bin: 2.75e1
variant carriers: 4

GenotypeQuality
all individuals: 151
bin: 1.75e1
variant carriers: 3

GenotypeQuality
all individuals: 20
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 17255
bin: 7.5e0
variant carriers: 4

GenotypeQuality
all individuals: 72
bin: 7.75e1
variant carriers: 3

GenotypeQuality
all individuals: 82
bin: 3.25e1
variant carriers: 2

GenotypeQuality
all individuals: 311
bin: 9.75e1
variant carriers: 309

GenotypeQuality
all individuals: 26
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 109
bin: 7.25e1
variant carriers: 2

GenotypeQuality
all individuals: 29
bin: 4.75e1
variant carriers: 3

GenotypeQuality
all individuals: 1812
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1320
bin: 2.25e1
variant carriers: 5

GenotypeQuality
all individuals: 111
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 8.75e1
variant carriers: 5

GenotypeQuality
all individuals: 33
bin: 8.25e1
variant carriers: 4

GenotypeQuality
all individuals: 534
bin: 6.75e1
variant carriers: 3

GenotypeQuality
all individuals: 7
bin: 9.25e1
variant carriers: 6

GenotypeQuality
all individuals: 10
bin: 5.75e1
variant carriers: 3

GenotypeQuality
all individuals: 48
bin: 3.75e1
variant carriers: 3

South Asian
type: Population
allele count: 80
allele frequency: 1.035732780942517e-2
allele num: 7724
num of homozygotes: 2

African
type: Population
allele count: 6
allele frequency: 7.614213197969543e-3
allele num: 788
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 272
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 268
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 91
allele frequency: 5.6875e-2
allele num: 1600
num of homozygotes: 1

European (Non-Finnish)
type: Population
allele count: 126
allele frequency: 2.645947081058379e-2
allele num: 4762
num of homozygotes: 1

Other
type: Population
allele count: 7
allele frequency: 3.465346534653466e-2
allele num: 202
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 4.832e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.52e-2

VQSLOD
type: SiteQuality
SIO_000300: -7.837e-1

QD
type: SiteQuality
SIO_000300: 1.177e1

FS
type: SiteQuality
SIO_000300: 5.357e0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.33e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.938e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.6e-2

DP
type: SiteQuality
SIO_000300: 2.44521e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.26e-1

GenotypeQuality
all individuals: 22288
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 86
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variant carriers: 0

GenotypeQuality
all individuals: 17
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variant carriers: 0

GenotypeQuality
all individuals: 60
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variant carriers: 0

GenotypeQuality
all individuals: 32
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variant carriers: 0

GenotypeQuality
all individuals: 3
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variant carriers: 0

GenotypeQuality
all individuals: 595
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variant carriers: 0

GenotypeQuality
all individuals: 35
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variant carriers: 0

GenotypeQuality
all individuals: 6776
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variant carriers: 0

GenotypeQuality
all individuals: 2259
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variant carriers: 0

GenotypeQuality
all individuals: 94
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variant carriers: 0

GenotypeQuality
all individuals: 207
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variant carriers: 0

GenotypeQuality
all individuals: 19
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variant carriers: 0

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

GenotypeQuality
all individuals: 104
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1707
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 117
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 9.75e1
variant carriers: 1

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7762
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 284
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 852
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.985702938840349e-4
allele num: 5036
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 204
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1600
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.454e1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.46e-1

DP
type: SiteQuality
SIO_000300: 2.48642e5

FS
type: SiteQuality
SIO_000300: 1.579e0

MQ
type: SiteQuality
SIO_000300: 5.511e1

MQRankSum
type: SiteQuality
SIO_000300: 1.12e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.9e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.02e0

BaseQRankSum
type: SiteQuality
SIO_000300: 6.38e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.919999999999999e-1

GenotypeQuality
all individuals: 63
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2249
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variant carriers: 0

GenotypeQuality
all individuals: 84
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variant carriers: 0

GenotypeQuality
all individuals: 63
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variant carriers: 0

GenotypeQuality
all individuals: 2
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GenotypeQuality
all individuals: 271
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 123
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variant carriers: 0

GenotypeQuality
all individuals: 355
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variant carriers: 0

GenotypeQuality
all individuals: 2604
bin: 2.25e1
variant carriers: 1

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 8.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5228
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 206
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 308
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 310
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1602
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 2.70278e5

MQ
type: SiteQuality
SIO_000300: 5.671e1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.99e-2

QD
type: SiteQuality
SIO_000300: 2.938e1

VQSLOD
type: SiteQuality
SIO_000300: 2.22e0

GenotypeQuality
all individuals: 109
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 380
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1745
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GenotypeQuality
all individuals: 119
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variant carriers: 0

GenotypeQuality
all individuals: 5926
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variant carriers: 0

GenotypeQuality
all individuals: 122
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variant carriers: 0

GenotypeQuality
all individuals: 3
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GenotypeQuality
all individuals: 178
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GenotypeQuality
all individuals: 2
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GenotypeQuality
all individuals: 93
bin: 5.25e1
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GenotypeQuality
all individuals: 32651
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 169
bin: 2.75e1
variant carriers: 1

GenotypeQuality
all individuals: 711
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 63
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 85
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GenotypeQuality
all individuals: 6714
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 577
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 8.25e1
variant carriers: 0

East Asian
type: Population
allele count: 1
allele frequency: 2.923976608187134e-3
allele num: 342
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 212
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 346
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1048
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1606
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5854
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.166e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.39e0

VQSLOD
type: SiteQuality
SIO_000300: -1.924e0

DP
type: SiteQuality
SIO_000300: 3.12996e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.3e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.41e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.878e1

MQRankSum
type: SiteQuality
SIO_000300: 1.64e0

QD
type: SiteQuality
SIO_000300: 9.539999999999999e0

GenotypeQuality
all individuals: 593
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32797
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variant carriers: 0

GenotypeQuality
all individuals: 2
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GenotypeQuality
all individuals: 179
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GenotypeQuality
all individuals: 93
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variant carriers: 0

GenotypeQuality
all individuals: 102
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6250
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variant carriers: 0

GenotypeQuality
all individuals: 107
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6758
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variant carriers: 0

GenotypeQuality
all individuals: 40
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GenotypeQuality
all individuals: 378
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GenotypeQuality
all individuals: 125
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variant carriers: 0

GenotypeQuality
all individuals: 1625
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 49
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variant carriers: 0

GenotypeQuality
all individuals: 88
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GenotypeQuality
all individuals: 177
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GenotypeQuality
all individuals: 3
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variant carriers: 0

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

GenotypeQuality
all individuals: 32
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5922
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 342
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 346
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7676
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1068
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 214
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

BaseQRankSum
type: SiteQuality
SIO_000300: -1.589e0

MQ
type: SiteQuality
SIO_000300: 4.918e1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 3.15119e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.3e-2

MQRankSum
type: SiteQuality
SIO_000300: -5.29e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.72e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.0e-3

QD
type: SiteQuality
SIO_000300: 1.206e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.49e0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 1

GenotypeQuality
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bin: 9.75e1
variant carriers: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 7672
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 214
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 348
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 346
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1066
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5948
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 1608
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.290000000000001e-2

BaseQRankSum
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SIO_000300: 1.23e0

DP
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SIO_000300: 3.17437e5

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 1.23e-1

QD
type: SiteQuality
SIO_000300: 7.99e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.58e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.58e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.58e-1

MQ
type: SiteQuality
SIO_000300: 5.203e1

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

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 105
bin: 5.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6208
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.311991603253739e-4
allele num: 7622
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 214
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1124
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 358
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1614
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.121e1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.639999999999999e-1

VQSLOD
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SIO_000300: -6.795e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.72e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.27e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 3.31338e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.01e-2

MQ
type: SiteQuality
SIO_000300: 5.708e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.33e0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6731
bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6824
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7412
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1628
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 214
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 400
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1254
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 376
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 4.261e1

VQSLOD
type: SiteQuality
SIO_000300: -1.068e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.33e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 3.62937e5

QD
type: SiteQuality
SIO_000300: 2.026e1

GenotypeQuality
all individuals: 127
bin: 5.25e1
variant carriers: 5

GenotypeQuality
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variant carriers: 4

GenotypeQuality
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variant carriers: 3

GenotypeQuality
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GenotypeQuality
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variant carriers: 5

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 9

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 53

GenotypeQuality
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GenotypeQuality
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bin: 7.25e1
variant carriers: 4

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 428
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 2.450980392156863e-3
allele num: 408
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.376273052573631e-4
allele num: 7266
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 1.390047261606895e-4
allele num: 7194
num of homozygotes: 0

African
type: Population
allele count: 49
allele frequency: 3.55072463768116e-2
allele num: 1380
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1642
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.89e-1

DP
type: SiteQuality
SIO_000300: 3.82967e5

BaseQRankSum
type: SiteQuality
SIO_000300: 1.07e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.96e-1

MQ
type: SiteQuality
SIO_000300: 5.107e1

VQSLOD
type: SiteQuality
SIO_000300: 5.82e-1

FS
type: SiteQuality
SIO_000300: 5.39e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.84e-2

QD
type: SiteQuality
SIO_000300: 1.478e1

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 7320
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 1642
num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 412
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 218
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 3.83617e5

InbreedingCoeff
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SIO_000300: -5.85e-2

VQSLOD
type: SiteQuality
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ReadPosRankSum
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ClippingRankSum
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SIO_000300: -5.38e-1

MQRankSum
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BaseQRankSum
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FS
type: SiteQuality
SIO_000300: 9.23e0

QD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 4.878e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

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
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.355748373101952e-4
allele num: 7376
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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Other
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South Asian
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ReadPosRankSum
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ClippingRankSum
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MQRankSum
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FS
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VQSLOD
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InbreedingCoeff
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MQ
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DP
type: SiteQuality
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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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variant carriers: 0

European (Finnish)
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allele count: 0
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num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 216
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7338
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.485884101040119e-4
allele num: 6730
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 436
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1662
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.227e0

ReadPosRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 3.8009e5

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.51e-2

MQ
type: SiteQuality
SIO_000300: 4.198e1

MQRankSum
type: SiteQuality
SIO_000300: 3.53e-1

ClippingRankSum
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SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -1.633e0

QD
type: SiteQuality
SIO_000300: 5.22e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.82e-1

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 2

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 442
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 438
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.486325802615933e-4
allele num: 6728
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1374
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.352447930754666e-4
allele num: 7394
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1662
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 218
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 7.27e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.83e-2

MQRankSum
type: SiteQuality
SIO_000300: 4.1e-1

VQSLOD
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SIO_000300: -7.332e-1

FS
type: SiteQuality
SIO_000300: 1.216e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.27e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.7e-2

MQ
type: SiteQuality
SIO_000300: 4.85e1

DP
type: SiteQuality
SIO_000300: 3.80847e5

QD
type: SiteQuality
SIO_000300: 1.068e1

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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bin: 3.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 210
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6524
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7394
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 1666
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 458
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 448
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1376
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 4.984e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.74e-2

QD
type: SiteQuality
SIO_000300: 1.977e1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 3.77752e5

VQSLOD
type: SiteQuality
SIO_000300: -4.142e-1

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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bin: 5.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 214
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 454
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1376
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1668
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 462
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7406
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6502
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 3.79328e5

QD
type: SiteQuality
SIO_000300: 8.99e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.06e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.48e-1

FS
type: SiteQuality
SIO_000300: 1.1273e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.42e0

VQSLOD
type: SiteQuality
SIO_000300: -1.913e0

MQ
type: SiteQuality
SIO_000300: 4.486e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.001e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.73e-2

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 218
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7098
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 7.363770250368188e-4
allele num: 1358
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 430
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1680
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: -1.701e0

QD
type: SiteQuality
SIO_000300: 8.31e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.01e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.85e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.25e0

BaseQRankSum
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 1.093e0

MQ
type: SiteQuality
SIO_000300: 4.665e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.4e0

DP
type: SiteQuality
SIO_000300: 3.57465e5

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 6.25e1
variant carriers: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.618646811265782e-4
allele num: 6178
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 1632
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 398
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 1222
num of homozygotes: 0

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

East 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
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num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
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DP
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ClippingRankSum
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BaseQRankSum
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MQRankSum
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InbreedingCoeff
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ReadPosRankSum
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MQ
type: SiteQuality
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QD
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SIO_000300: 1.277e1

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

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

European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 6100
num of homozygotes: 0

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

South Asian
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allele frequency: 2.186270222999563e-4
allele num: 4574
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QD
type: SiteQuality
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BaseQRankSum
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ClippingRankSum
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DP
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MQRankSum
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VQSLOD
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FS
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MQ
type: SiteQuality
SIO_000300: 5.111e1

InbreedingCoeff
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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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bin: 6.25e1
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Latino
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East Asian
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South Asian
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European (Finnish)
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African
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Other
type: Population
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European (Non-Finnish)
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DP
type: SiteQuality
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VQSLOD
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BaseQRankSum
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ClippingRankSum
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QD
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MQRankSum
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FS
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InbreedingCoeff
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MQ
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.25e1
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Other
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num of homozygotes: 0

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

European (Finnish)
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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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 396
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 3.08417e5

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.2e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.64e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.38e0

MQRankSum
type: SiteQuality
SIO_000300: -1.38e0

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -2.09e-1

MQ
type: SiteQuality
SIO_000300: 4.883e1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 8.75e0

GenotypeQuality
all individuals: 135
bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
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GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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GenotypeQuality
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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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bin: 8.75e1
variant carriers: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6252
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 206
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1638
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 406
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1234
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 446
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.23e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.38e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.23e0

MQRankSum
type: SiteQuality
SIO_000300: 3.58e-1

QD
type: SiteQuality
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VQSLOD
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SIO_000300: -1.298e-1

DP
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SIO_000300: 3.25369e5

ClippingRankSum
type: SiteQuality
SIO_000300: -1.231e0

MQ
type: SiteQuality
SIO_000300: 5.616e1

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6284
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5032
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 416
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1232
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1648
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 204
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 3.33252e5

BaseQRankSum
type: SiteQuality
SIO_000300: -7.2e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.335e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 4.261e1

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.33e-2

QD
type: SiteQuality
SIO_000300: 1.101e1

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
all individuals: 3
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 430
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1650
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6518
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5436
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 204
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 2.127659574468085e-3
allele num: 470
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1250
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.21e0

MQRankSum
type: SiteQuality
SIO_000300: 5.24e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.32e0

VQSLOD
type: SiteQuality
SIO_000300: -1.291e0

QD
type: SiteQuality
SIO_000300: 1.018e1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.699999999999999e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.98e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 3.44156e5

MQ
type: SiteQuality
SIO_000300: 5.763e1

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 4.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6806
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 214
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 474
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1662
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1294
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.717032967032967e-4
allele num: 5824
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 448
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.134e0

DP
type: SiteQuality
SIO_000300: 3.63283e5

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.635e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.76e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.46e0

QD
type: SiteQuality
SIO_000300: 1.043e1

VQSLOD
type: SiteQuality
SIO_000300: -1.649e0

MQRankSum
type: SiteQuality
SIO_000300: 3.8e-1

MQ
type: SiteQuality
SIO_000300: 5.322e1

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7060
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 496
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 1676
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 466
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South Asian
type: Population
allele count: 1
allele frequency: 1.622849724115547e-4
allele num: 6162
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: 9.21e-1

MQ
type: SiteQuality
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VQSLOD
type: SiteQuality
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DP
type: SiteQuality
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MQRankSum
type: SiteQuality
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BaseQRankSum
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ReadPosRankSum
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FS
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.91e1

GenotypeQuality
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variant carriers: 0

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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
type: Population
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num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 2.74423710208562e-4
allele num: 7288
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European (Finnish)
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South Asian
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DP
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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FS
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QD
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VQSLOD
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BaseQRankSum
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MQRankSum
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MQ
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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African
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East Asian
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European (Non-Finnish)
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South Asian
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European (Finnish)
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Other
type: Population
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VQSLOD
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FS
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MQ
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MQRankSum
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QD
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BaseQRankSum
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DP
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ClippingRankSum
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InbreedingCoeff
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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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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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Latino
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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
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Other
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InbreedingCoeff
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MQRankSum
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QD
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MQ
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BaseQRankSum
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DP
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FS
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ClippingRankSum
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VQSLOD
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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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South Asian
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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

European (Non-Finnish)
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African
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East Asian
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allele frequency: 3.623188405797101e-3
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European (Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

QD
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DP
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ReadPosRankSum
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BaseQRankSum
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VQSLOD
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InbreedingCoeff
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MQ
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MQRankSum
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ClippingRankSum
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FS
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

South Asian
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East Asian
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Other
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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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Latino
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allele frequency: 1.818181818181818e-3
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European (Non-Finnish)
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allele frequency: 0.0e0
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ReadPosRankSum
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VQSLOD
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BaseQRankSum
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MQRankSum
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FS
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DP
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QD
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ClippingRankSum
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MQ
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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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GenotypeQuality
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European (Finnish)
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allele frequency: 0.0e0
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East Asian
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Other
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Latino
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South Asian
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allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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European (Non-Finnish)
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ReadPosRankSum
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FS
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DP
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MQRankSum
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BaseQRankSum
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VQSLOD
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InbreedingCoeff
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MQ
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QD
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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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African
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European (Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 276
num of homozygotes: 0

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

FS
type: SiteQuality
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MQ
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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InbreedingCoeff
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QD
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MQRankSum
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DP
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VQSLOD
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ReadPosRankSum
type: SiteQuality
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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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African
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allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

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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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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num of homozygotes: 0

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

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

European (Non-Finnish)
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European (Finnish)
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African
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South Asian
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Latino
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Other
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ClippingRankSum
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ReadPosRankSum
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InbreedingCoeff
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BaseQRankSum
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MQ
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FS
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MQRankSum
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VQSLOD
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DP
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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South Asian
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African
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East Asian
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European (Non-Finnish)
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Latino
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MQ
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FS
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DP
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ReadPosRankSum
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QD
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MQRankSum
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VQSLOD
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BaseQRankSum
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ClippingRankSum
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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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East Asian
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Latino
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African
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European (Finnish)
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Other
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European (Non-Finnish)
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allele num: 12068
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8066
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -7.31e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.46e-2

DP
type: SiteQuality
SIO_000300: 5.37199e5

QD
type: SiteQuality
SIO_000300: 1.167e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.5e-1

FS
type: SiteQuality
SIO_000300: 1.3442e1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.97e-1

MQ
type: SiteQuality
SIO_000300: 5.561e1

VQSLOD
type: SiteQuality
SIO_000300: -8.367e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 8.25e-1

GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12068
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2036
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8066
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.108647450110865e-3
allele num: 902
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 306
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 2068
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.46e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 8.25e-1

FS
type: SiteQuality
SIO_000300: 1.3442e1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.97e-1

VQSLOD
type: SiteQuality
SIO_000300: -8.367e-1

MQ
type: SiteQuality
SIO_000300: 5.561e1

DP
type: SiteQuality
SIO_000300: 5.37199e5

QD
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SIO_000300: 1.167e1

MQRankSum
type: SiteQuality
SIO_000300: -7.31e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.5e-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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variant carriers: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 930
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 312
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2068
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 12376
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 2096
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 914
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
allele num: 8092
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 7.52e-1

QD
type: SiteQuality
SIO_000300: 1.676e1

VQSLOD
type: SiteQuality
SIO_000300: -1.181e0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
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SIO_000300: -2.017e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.91e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.76e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.07e-1

MQ
type: SiteQuality
SIO_000300: 5.763e1

DP
type: SiteQuality
SIO_000300: 5.418e5

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 0
allele frequency: 0.0e0
allele num: 2100
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 972
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8110
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 982
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2116
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12678
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 316
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 3.56e0

VQSLOD
type: SiteQuality
SIO_000300: -1.134e0

DP
type: SiteQuality
SIO_000300: 5.43045e5

BaseQRankSum
type: SiteQuality
SIO_000300: 2.05e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.71e-2

MQRankSum
type: SiteQuality
SIO_000300: 2.48e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.5e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.48e-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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variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2124
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 7.835762419683435e-5
allele num: 12762
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 994
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 310
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2118
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8132
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 996
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.18e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.93e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.73e-1

QD
type: SiteQuality
SIO_000300: 1.472e1

DP
type: SiteQuality
SIO_000300: 5.45098e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.78e-2

VQSLOD
type: SiteQuality
SIO_000300: -1.54e0

FS
type: SiteQuality
SIO_000300: 6.242e0

MQ
type: SiteQuality
SIO_000300: 5.763e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.1e0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 2128
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 316
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1014
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 7.688759034291866e-5
allele num: 13006
num of homozygotes: 0

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

Latino
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allele count: 1
allele frequency: 9.671179883945841e-4
allele num: 1034
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 2144
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -7.42e-1

QD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.85e-2

DP
type: SiteQuality
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ClippingRankSum
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MQ
type: SiteQuality
SIO_000300: 5.321e1

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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East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 870
num of homozygotes: 0

African
type: Population
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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Latino
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num of homozygotes: 0

Other
type: Population
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allele frequency: 0.0e0
allele num: 288
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European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 11762
num of homozygotes: 0

South Asian
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BaseQRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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ClippingRankSum
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MQ
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FS
type: SiteQuality
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InbreedingCoeff
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DP
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ReadPosRankSum
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QD
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.75e1
variant carriers: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 2042
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.226993865030675e-4
allele num: 8150
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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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 11546
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East Asian
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allele frequency: 1.179245283018868e-3
allele num: 848
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Other
type: Population
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allele num: 286
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MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 9.29e-1

FS
type: SiteQuality
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DP
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 3.29e-2

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 3.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2028
num of homozygotes: 0

African
type: Population
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Other
type: Population
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allele frequency: 3.546099290780142e-3
allele num: 282
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 11320
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 802
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South Asian
type: Population
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QD
type: SiteQuality
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MQRankSum
type: SiteQuality
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ClippingRankSum
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FS
type: SiteQuality
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MQ
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BaseQRankSum
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DP
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ReadPosRankSum
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VQSLOD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 1

GenotypeQuality
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bin: 9.75e1
variant carriers: 2

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 712
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 124
bin: 5.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 282
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11320
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1862
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 758
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2008
num of homozygotes: 0

South Asian
type: Population
allele count: 4
allele frequency: 4.887585532746823e-4
allele num: 8184
num of homozygotes: 1

MQ
type: SiteQuality
SIO_000300: 5.936e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.186e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.08e-2

VQSLOD
type: SiteQuality
SIO_000300: -1.008e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.9e-2

DP
type: SiteQuality
SIO_000300: 4.87694e5

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.9e-2

MQRankSum
type: SiteQuality
SIO_000300: 3.22e-1

FS
type: SiteQuality
SIO_000300: 3.198e0

QD
type: SiteQuality
SIO_000300: 1.799e1

GenotypeQuality
all individuals: 18771
bin: 2.25e1
variant carriers: 1

GenotypeQuality
all individuals: 25
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
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GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8178
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 8.941344778254649e-5
allele num: 11184
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2012
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 832
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1858
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 282
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.774e1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.659999999999999e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.76e0

DP
type: SiteQuality
SIO_000300: 4.8319e5

QD
type: SiteQuality
SIO_000300: 2.059e1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.11e-2

MQRankSum
type: SiteQuality
SIO_000300: 7.15e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.82e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.15e-1

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 727
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variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 282
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 698
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1814
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1986
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 770
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 9.262689885142645e-5
allele num: 10796
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8176
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.02e0

VQSLOD
type: SiteQuality
SIO_000300: -8.222e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.12e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.01e-1

FS
type: SiteQuality
SIO_000300: 1.016e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.249e1

MQRankSum
type: SiteQuality
SIO_000300: 3.77e-1

DP
type: SiteQuality
SIO_000300: 4.7369e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.37e-2

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 739
bin: 6.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8162
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10588
num of homozygotes: 0

East Asian
type: Population
allele count: 4
allele frequency: 5.181347150259068e-3
allele num: 772
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1782
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1970
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 282
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 680
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 3.52e0

MQRankSum
type: SiteQuality
SIO_000300: 6.96e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.5e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.39e-2

QD
type: SiteQuality
SIO_000300: 1.2e1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.37e-1

DP
type: SiteQuality
SIO_000300: 4.69501e5

BaseQRankSum
type: SiteQuality
SIO_000300: -1.754e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 3857
bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 1

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 257
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variant carriers: 0

GenotypeQuality
all individuals: 90
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1710
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10168
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 1.2306177701206e-4
allele num: 8126
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 634
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 700
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 276
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 9.22e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -1.354e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.74e-2

MQ
type: SiteQuality
SIO_000300: 5.951e1

DP
type: SiteQuality
SIO_000300: 4.65108e5

QD
type: SiteQuality
SIO_000300: 1.436e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.7e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.36e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
all individuals: 15064
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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GenotypeQuality
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variant carriers: 6

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 738
bin: 2.75e1
variant carriers: 2

Latino
type: Population
allele count: 1
allele frequency: 1.5625e-3
allele num: 640
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 280
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 718
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1950
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1730
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10188
num of homozygotes: 0

South Asian
type: Population
allele count: 4
allele frequency: 4.917629702483403e-4
allele num: 8134
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.862e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.26e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 9.22e-1

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -4.55e-2

QD
type: SiteQuality
SIO_000300: 1.317e1

DP
type: SiteQuality
SIO_000300: 4.66087e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.71e-2

FS
type: SiteQuality
SIO_000300: 2.253e0

GenotypeQuality
all individuals: 50
bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 7.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 636
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 280
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1938
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10238
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 696
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1724
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.232741617357002e-4
allele num: 8112
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.53e-2

MQRankSum
type: SiteQuality
SIO_000300: 8.090000000000001e-1

MQ
type: SiteQuality
SIO_000300: 5.947e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.337e0

VQSLOD
type: SiteQuality
SIO_000300: -1.053e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.21e-1

DP
type: SiteQuality
SIO_000300: 4.66835e5

ClippingRankSum
type: SiteQuality
SIO_000300: 3.42e-1

QD
type: SiteQuality
SIO_000300: 1.387e1

FS
type: SiteQuality
SIO_000300: 8.875e0

GenotypeQuality
all individuals: 3828
bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 1

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 1.75e1
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GenotypeQuality
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GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.25e1
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GenotypeQuality
all individuals: 74
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 5.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1718
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 632
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 290
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10254
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8110
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 7.31e-1

QD
type: SiteQuality
SIO_000300: 1.574e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.5e-2

VQSLOD
type: SiteQuality
SIO_000300: -7.05e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.31e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.31e-1

DP
type: SiteQuality
SIO_000300: 4.67179e5

BaseQRankSum
type: SiteQuality
SIO_000300: 7.31e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.616e1

GenotypeQuality
all individuals: 21
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 62
bin: 4.25e1
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GenotypeQuality
all individuals: 48
bin: 5.25e1
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GenotypeQuality
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GenotypeQuality
all individuals: 668
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 650
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 688
num of homozygotes: 0

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

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8136
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 9.656237929702588e-5
allele num: 10356
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.36e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.31e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.55e-2

FS
type: SiteQuality
SIO_000300: 2.341e0

VQSLOD
type: SiteQuality
SIO_000300: -6.681e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.31e-1

DP
type: SiteQuality
SIO_000300: 4.78267e5

QD
type: SiteQuality
SIO_000300: 9.25e0

MQRankSum
type: SiteQuality
SIO_000300: 8.51e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 3.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 650
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1750
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 688
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10356
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8136
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 4.78267e5

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.55e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 2.341e0

BaseQRankSum
type: SiteQuality
SIO_000300: 7.31e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.31e-1

VQSLOD
type: SiteQuality
SIO_000300: -6.681e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.36e-1

QD
type: SiteQuality
SIO_000300: 9.25e0

MQRankSum
type: SiteQuality
SIO_000300: 8.51e-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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variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1854
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8218
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11258
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1992
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 742
num of homozygotes: 0

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

East Asian
type: Population
allele count: 2
allele frequency: 2.531645569620253e-3
allele num: 790
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.912e1

DP
type: SiteQuality
SIO_000300: 5.16027e5

VQSLOD
type: SiteQuality
SIO_000300: -1.304e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.268e0

QD
type: SiteQuality
SIO_000300: 8.359999999999999e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.73e-1

MQRankSum
type: SiteQuality
SIO_000300: -5.3e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.73e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.53e-2

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 8

GenotypeQuality
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GenotypeQuality
all individuals: 2
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GenotypeQuality
all individuals: 699
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variant carriers: 1

European (Finnish)
type: Population
allele count: 3
allele frequency: 1.495513459621137e-3
allele num: 2006
num of homozygotes: 1

African
type: Population
allele count: 2
allele frequency: 1.062699256110521e-3
allele num: 1882
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.30890052356021e-3
allele num: 764
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 810
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 296
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 3.518029903254178e-4
allele num: 11370
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.215953307392996e-4
allele num: 8224
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.562e1

DP
type: SiteQuality
SIO_000300: 5.21578e5

VQSLOD
type: SiteQuality
SIO_000300: -8.216e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.27e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.53e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -8.78e-1

QD
type: SiteQuality
SIO_000300: 1.094e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.87e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.39e-2

GenotypeQuality
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variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 918
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 8.203445447087777e-5
allele num: 12190
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8292
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2064
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1990
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 304
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BaseQRankSum
type: SiteQuality
SIO_000300: -1.157e0

MQRankSum
type: SiteQuality
SIO_000300: 6.94e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.93e-2

QD
type: SiteQuality
SIO_000300: 3.39e0

DP
type: SiteQuality
SIO_000300: 5.42506e5

VQSLOD
type: SiteQuality
SIO_000300: -1.892e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.32e-1

FS
type: SiteQuality
SIO_000300: 2.757e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.4e-1

MQ
type: SiteQuality
SIO_000300: 5.977e1

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1022
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13646
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8412
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 320
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African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2156
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 2164
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1058
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InbreedingCoeff
type: SiteQuality
SIO_000300: -2.39e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 1.2e0

VQSLOD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 2.336e0

MQRankSum
type: SiteQuality
SIO_000300: 1.42e0

MQ
type: SiteQuality
SIO_000300: 5.749e1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.840000000000001e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.73e-1

DP
type: SiteQuality
SIO_000300: 5.72934e5

QD
type: SiteQuality
SIO_000300: 1.152e1

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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bin: 2.25e1
variant carriers: 0

East Asian
type: Population
allele count: 2
allele frequency: 1.904761904761905e-3
allele num: 1050
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13666
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 320
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2180
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Latino
type: Population
allele count: 1
allele frequency: 9.84251968503937e-4
allele num: 1016
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2142
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.48e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -5.92e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -2.26e-1

VQSLOD
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MQ
type: SiteQuality
SIO_000300: 5.712e1

DP
type: SiteQuality
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QD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 9.22e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.017e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1080
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1056
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African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2178
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European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2194
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 320
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8430
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European (Non-Finnish)
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allele count: 1
allele frequency: 7.170514842965726e-5
allele num: 13946
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 3.511e0

ClippingRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: 2.12e0

QD
type: SiteQuality
SIO_000300: 2.655e1

DP
type: SiteQuality
SIO_000300: 5.8272e5

VQSLOD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -2.47e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.41e0

MQ
type: SiteQuality
SIO_000300: 5.951e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.3e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 4
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GenotypeQuality
all individuals: 98
bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14304
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1122
num of homozygotes: 0

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

South Asian
type: Population
allele count: 2
allele frequency: 2.359603586597452e-4
allele num: 8476
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African
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allele count: 0
allele frequency: 0.0e0
allele num: 2226
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 2218
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Other
type: Population
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allele frequency: 0.0e0
allele num: 324
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ReadPosRankSum
type: SiteQuality
SIO_000300: 5.4e-1

MQ
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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VQSLOD
type: SiteQuality
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MQRankSum
type: SiteQuality
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DP
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QD
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FS
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BaseQRankSum
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ClippingRankSum
type: SiteQuality
SIO_000300: -3.86e-1

GenotypeQuality
all individuals: 4
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 99
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1983
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 819
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 10070
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 123
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 168
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 130
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 809
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31694
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 389
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 176
bin: 7.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 332
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8534
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1232
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2266
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2330
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15050
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1238
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.08e-2

FS
type: SiteQuality
SIO_000300: 2.128e0

MQ
type: SiteQuality
SIO_000300: 5.583e1

VQSLOD
type: SiteQuality
SIO_000300: -1.202e0

DP
type: SiteQuality
SIO_000300: 5.97376e5

BaseQRankSum
type: SiteQuality
SIO_000300: 1.54e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.340000000000001e-1

QD
type: SiteQuality
SIO_000300: 5.07e0

MQRankSum
type: SiteQuality
SIO_000300: 4.06e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.06e-1

GenotypeQuality
all individuals: 208
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10714
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9212
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1052
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1017
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 822
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 435
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 156
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 841
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 140
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 99
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 8.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 344
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 3.993610223642172e-4
allele num: 2504
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8632
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16458
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1388
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2386
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -2.014e0

MQRankSum
type: SiteQuality
SIO_000300: 4.52e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.81e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.39e-1

FS
type: SiteQuality
SIO_000300: 2.688e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.94e-2

DP
type: SiteQuality
SIO_000300: 6.17821e5

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.226e0

MQ
type: SiteQuality
SIO_000300: 5.646e1

QD
type: SiteQuality
SIO_000300: 6.86e0