19-58145304-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58145304
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 58145304
    reference: chr 19
allele count: 3
allele frequency: 2.501751225858101e-5
allele num: 119916
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000240731
  ensembl transcript: ENST00000240731
  gene symbol: ZNF211
  hgvsc: ENST00000240731.4:c.91-87C>T
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000375584
  ensembl transcript: ENST00000391703
  gene symbol: ZNF211
  hgvsc: ENST00000391703.3:c.-94+690C>T
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000254182
  ensembl transcript: ENST00000254182
  gene symbol: ZNF211
  hgvsc: ENST00000254182.7:c.-132-87C>T
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000121417
  ensembl transcript: ENST00000541072
  gene symbol: ZNF211
  hgvsc: ENST00000541072.1:n.493C>T
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000442601
  ensembl transcript: ENST00000541801
  gene symbol: ZNF211
  hgvsc: ENST00000541801.1:c.-94+690C>T
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000441386
  ensembl transcript: ENST00000544273
  gene symbol: ZNF211
  hgvsc: ENST00000544273.1:c.87+31C>T
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000442740
  ensembl transcript: ENST00000535785
  gene symbol: ZNF211
  hgvsc: ENST00000535785.1:c.*145+31C>T
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000399193
  ensembl transcript: ENST00000420680
  gene symbol: ZNF211
  hgvsc: ENST00000420680.1:c.103-693C>T
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl transcript: ENST00000540780
  gene symbol: ZNF211
  hgvsc: ENST00000540780.1:n.405+31C>T
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl transcript: ENST00000542008
  gene symbol: ZNF211
  hgvsc: ENST00000542008.1:n.270-87C>T
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000440793
  ensembl transcript: ENST00000540556
  gene symbol: ZNF211
  hgvsc: ENST00000540556.1:c.*93+31C>T
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000339562
  ensembl transcript: ENST00000347302
  gene symbol: ZNF211
  hgvsc: ENST00000347302.3:c.90+500C>T
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000299871
  ensembl transcript: ENST00000299871
  gene symbol: ZNF211
  hgvsc: ENST00000299871.5:c.91-87C>T
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000384436
  ensembl transcript: ENST00000407202
  gene symbol: ZNF211
  hgvsc: ENST00000407202.2:c.101-693C>T
  variant of: http://identifiers.org/hgnc/13003
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1984
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1115
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12164
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5739
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36313
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP

19-58145306-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58145306
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 58145306
    reference: chr 19
allele count: 7
allele frequency: 5.837808986889949e-5
allele num: 119908
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000375584
  ensembl transcript: ENST00000391703
  gene symbol: ZNF211
  hgvsc: ENST00000391703.3:c.-93-691G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000254182
  ensembl transcript: ENST00000254182
  gene symbol: ZNF211
  hgvsc: ENST00000254182.7:c.-132-85G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000240731
  ensembl transcript: ENST00000240731
  gene symbol: ZNF211
  hgvsc: ENST00000240731.4:c.91-85G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000339562
  ensembl transcript: ENST00000347302
  gene symbol: ZNF211
  hgvsc: ENST00000347302.3:c.90+502G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000399193
  ensembl transcript: ENST00000420680
  gene symbol: ZNF211
  hgvsc: ENST00000420680.1:c.103-691G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000441386
  ensembl transcript: ENST00000544273
  gene symbol: ZNF211
  hgvsc: ENST00000544273.1:c.87+33G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000384436
  ensembl transcript: ENST00000407202
  gene symbol: ZNF211
  hgvsc: ENST00000407202.2:c.101-691G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl transcript: ENST00000540780
  gene symbol: ZNF211
  hgvsc: ENST00000540780.1:n.405+33G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl transcript: ENST00000542008
  gene symbol: ZNF211
  hgvsc: ENST00000542008.1:n.270-85G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000442740
  ensembl transcript: ENST00000535785
  gene symbol: ZNF211
  hgvsc: ENST00000535785.1:c.*145+33G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000121417
  ensembl transcript: ENST00000541072
  gene symbol: ZNF211
  hgvsc: ENST00000541072.1:n.495G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000440793
  ensembl transcript: ENST00000540556
  gene symbol: ZNF211
  hgvsc: ENST00000540556.1:c.*93+33G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000442601
  ensembl transcript: ENST00000541801
  gene symbol: ZNF211
  hgvsc: ENST00000541801.1:c.-93-691G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000299871
  ensembl transcript: ENST00000299871
  gene symbol: ZNF211
  hgvsc: ENST00000299871.5:c.91-85G>A
  variant of: http://identifiers.org/hgnc/13003
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1727
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5740
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12047
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 638
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1978
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: South Asian
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum

19-58145311-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58145311
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 58145311
    reference: chr 19
allele count: 1
allele frequency: 8.349475652928997e-6
allele num: 119768
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000299871
  ensembl transcript: ENST00000299871
  gene symbol: ZNF211
  hgvsc: ENST00000299871.5:c.91-80G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000240731
  ensembl transcript: ENST00000240731
  gene symbol: ZNF211
  hgvsc: ENST00000240731.4:c.91-80G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000440793
  ensembl transcript: ENST00000540556
  gene symbol: ZNF211
  hgvsc: ENST00000540556.1:c.*93+38G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000384436
  ensembl transcript: ENST00000407202
  gene symbol: ZNF211
  hgvsc: ENST00000407202.2:c.101-686G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000399193
  ensembl transcript: ENST00000420680
  gene symbol: ZNF211
  hgvsc: ENST00000420680.1:c.103-686G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000375584
  ensembl transcript: ENST00000391703
  gene symbol: ZNF211
  hgvsc: ENST00000391703.3:c.-93-686G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl transcript: ENST00000542008
  gene symbol: ZNF211
  hgvsc: ENST00000542008.1:n.270-80G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000254182
  ensembl transcript: ENST00000254182
  gene symbol: ZNF211
  hgvsc: ENST00000254182.7:c.-132-80G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl transcript: ENST00000540780
  gene symbol: ZNF211
  hgvsc: ENST00000540780.1:n.405+38G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000121417
  ensembl transcript: ENST00000541072
  gene symbol: ZNF211
  hgvsc: ENST00000541072.1:n.500G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000441386
  ensembl transcript: ENST00000544273
  gene symbol: ZNF211
  hgvsc: ENST00000544273.1:c.87+38G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000339562
  ensembl transcript: ENST00000347302
  gene symbol: ZNF211
  hgvsc: ENST00000347302.3:c.90+507G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000442740
  ensembl transcript: ENST00000535785
  gene symbol: ZNF211
  hgvsc: ENST00000535785.1:c.*145+38G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000442601
  ensembl transcript: ENST00000541801
  gene symbol: ZNF211
  hgvsc: ENST00000541801.1:c.-93-686G>A
  variant of: http://identifiers.org/hgnc/13003
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 655
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36147
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5786
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11902
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1981
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1165
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1826
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
population: European (Finnish)
population: Other
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum

19-58145314-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58145314
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 58145314
    reference: chr 19
allele count: 9
allele frequency: 7.514151652278458e-5
allele num: 119774
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000399193
  ensembl transcript: ENST00000420680
  gene symbol: ZNF211
  hgvsc: ENST00000420680.1:c.103-683G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000121417
  ensembl transcript: ENST00000541072
  gene symbol: ZNF211
  hgvsc: ENST00000541072.1:n.503G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000240731
  ensembl transcript: ENST00000240731
  gene symbol: ZNF211
  hgvsc: ENST00000240731.4:c.91-77G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000440793
  ensembl transcript: ENST00000540556
  gene symbol: ZNF211
  hgvsc: ENST00000540556.1:c.*93+41G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000384436
  ensembl transcript: ENST00000407202
  gene symbol: ZNF211
  hgvsc: ENST00000407202.2:c.101-683G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl transcript: ENST00000540780
  gene symbol: ZNF211
  hgvsc: ENST00000540780.1:n.405+41G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000442740
  ensembl transcript: ENST00000535785
  gene symbol: ZNF211
  hgvsc: ENST00000535785.1:c.*145+41G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000299871
  ensembl transcript: ENST00000299871
  gene symbol: ZNF211
  hgvsc: ENST00000299871.5:c.91-77G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000254182
  ensembl transcript: ENST00000254182
  gene symbol: ZNF211
  hgvsc: ENST00000254182.7:c.-132-77G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000442601
  ensembl transcript: ENST00000541801
  gene symbol: ZNF211
  hgvsc: ENST00000541801.1:c.-93-683G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000375584
  ensembl transcript: ENST00000391703
  gene symbol: ZNF211
  hgvsc: ENST00000391703.3:c.-93-683G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl transcript: ENST00000542008
  gene symbol: ZNF211
  hgvsc: ENST00000542008.1:n.270-77G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000441386
  ensembl transcript: ENST00000544273
  gene symbol: ZNF211
  hgvsc: ENST00000544273.1:c.87+41G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000339562
  ensembl transcript: ENST00000347302
  gene symbol: ZNF211
  hgvsc: ENST00000347302.3:c.90+510G>A
  variant of: http://identifiers.org/hgnc/13003
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1807
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1964
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5813
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 36154
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 688
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1167
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: African
population: Other
population: East Asian
population: Latino
reference allele: G
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum

19-58145340-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58145340
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 58145340
    reference: chr 19
allele count: 10
allele frequency: 8.681761355743853e-5
allele num: 115184
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl transcript: ENST00000540780
  gene symbol: ZNF211
  hgvsc: ENST00000540780.1:n.406-51C>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl transcript: ENST00000542008
  gene symbol: ZNF211
  hgvsc: ENST00000542008.1:n.270-51C>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000299871
  ensembl transcript: ENST00000299871
  gene symbol: ZNF211
  hgvsc: ENST00000299871.5:c.91-51C>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000339562
  ensembl transcript: ENST00000347302
  gene symbol: ZNF211
  hgvsc: ENST00000347302.3:c.90+536C>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000240731
  ensembl transcript: ENST00000240731
  gene symbol: ZNF211
  hgvsc: ENST00000240731.4:c.91-51C>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000440793
  ensembl transcript: ENST00000540556
  gene symbol: ZNF211
  hgvsc: ENST00000540556.1:c.*94-51C>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000254182
  ensembl transcript: ENST00000254182
  gene symbol: ZNF211
  hgvsc: ENST00000254182.7:c.-132-51C>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000399193
  ensembl transcript: ENST00000420680
  gene symbol: ZNF211
  hgvsc: ENST00000420680.1:c.103-657C>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000121417
  ensembl transcript: ENST00000541072
  gene symbol: ZNF211
  hgvsc: ENST00000541072.1:n.529C>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000375584
  ensembl transcript: ENST00000391703
  gene symbol: ZNF211
  hgvsc: ENST00000391703.3:c.-93-657C>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000384436
  ensembl transcript: ENST00000407202
  gene symbol: ZNF211
  hgvsc: ENST00000407202.2:c.101-657C>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000442601
  ensembl transcript: ENST00000541801
  gene symbol: ZNF211
  hgvsc: ENST00000541801.1:c.-93-657C>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000442740
  ensembl transcript: ENST00000535785
  gene symbol: ZNF211
  hgvsc: ENST00000535785.1:c.*146-51C>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000441386
  ensembl transcript: ENST00000544273
  gene symbol: ZNF211
  hgvsc: ENST00000544273.1:c.88-51C>G
  variant of: http://identifiers.org/hgnc/13003
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9299
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1002
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2068
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14525
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2598
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 993
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1800
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1778
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5846
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD

19-58145342-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58145342
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 58145342
    reference: chr 19
allele count: 1
allele frequency: 8.687795385043092e-6
allele num: 115104
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl transcript: ENST00000542008
  gene symbol: ZNF211
  hgvsc: ENST00000542008.1:n.270-49T>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000399193
  ensembl transcript: ENST00000420680
  gene symbol: ZNF211
  hgvsc: ENST00000420680.1:c.103-655T>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000442740
  ensembl transcript: ENST00000535785
  gene symbol: ZNF211
  hgvsc: ENST00000535785.1:c.*146-49T>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl transcript: ENST00000540780
  gene symbol: ZNF211
  hgvsc: ENST00000540780.1:n.406-49T>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000240731
  ensembl transcript: ENST00000240731
  gene symbol: ZNF211
  hgvsc: ENST00000240731.4:c.91-49T>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000121417
  ensembl transcript: ENST00000541072
  gene symbol: ZNF211
  hgvsc: ENST00000541072.1:n.531T>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000375584
  ensembl transcript: ENST00000391703
  gene symbol: ZNF211
  hgvsc: ENST00000391703.3:c.-93-655T>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000384436
  ensembl transcript: ENST00000407202
  gene symbol: ZNF211
  hgvsc: ENST00000407202.2:c.101-655T>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000442601
  ensembl transcript: ENST00000541801
  gene symbol: ZNF211
  hgvsc: ENST00000541801.1:c.-93-655T>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000441386
  ensembl transcript: ENST00000544273
  gene symbol: ZNF211
  hgvsc: ENST00000544273.1:c.88-49T>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000440793
  ensembl transcript: ENST00000540556
  gene symbol: ZNF211
  hgvsc: ENST00000540556.1:c.*94-49T>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000299871
  ensembl transcript: ENST00000299871
  gene symbol: ZNF211
  hgvsc: ENST00000299871.5:c.91-49T>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000339562
  ensembl transcript: ENST00000347302
  gene symbol: ZNF211
  hgvsc: ENST00000347302.3:c.90+538T>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000254182
  ensembl transcript: ENST00000254182
  gene symbol: ZNF211
  hgvsc: ENST00000254182.7:c.-132-49T>G
  variant of: http://identifiers.org/hgnc/13003
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 999
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1729
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 992
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1798
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12249
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3425
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 618
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5845
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2067
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2673
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9300
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: Other
population: South Asian
population: European (Non-Finnish)
population: Latino
reference allele: T
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ

19-58145354-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58145354
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 58145354
    reference: chr 19
allele count: 20
allele frequency: 1.747152142008526e-4
allele num: 114472
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000121417
  ensembl transcript: ENST00000541072
  gene symbol: ZNF211
  hgvsc: ENST00000541072.1:n.543A>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl transcript: ENST00000540780
  gene symbol: ZNF211
  hgvsc: ENST00000540780.1:n.406-37A>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000399193
  ensembl transcript: ENST00000420680
  gene symbol: ZNF211
  hgvsc: ENST00000420680.1:c.103-643A>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000442740
  ensembl transcript: ENST00000535785
  gene symbol: ZNF211
  hgvsc: ENST00000535785.1:c.*146-37A>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000339562
  ensembl transcript: ENST00000347302
  gene symbol: ZNF211
  hgvsc: ENST00000347302.3:c.90+550A>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000440793
  ensembl transcript: ENST00000540556
  gene symbol: ZNF211
  hgvsc: ENST00000540556.1:c.*94-37A>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000442601
  ensembl transcript: ENST00000541801
  gene symbol: ZNF211
  hgvsc: ENST00000541801.1:c.-93-643A>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000299871
  ensembl transcript: ENST00000299871
  gene symbol: ZNF211
  hgvsc: ENST00000299871.5:c.91-37A>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000375584
  ensembl transcript: ENST00000391703
  gene symbol: ZNF211
  hgvsc: ENST00000391703.3:c.-93-643A>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000441386
  ensembl transcript: ENST00000544273
  gene symbol: ZNF211
  hgvsc: ENST00000544273.1:c.88-37A>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000240731
  ensembl transcript: ENST00000240731
  gene symbol: ZNF211
  hgvsc: ENST00000240731.4:c.91-37A>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000254182
  ensembl transcript: ENST00000254182
  gene symbol: ZNF211
  hgvsc: ENST00000254182.7:c.-132-37A>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000384436
  ensembl transcript: ENST00000407202
  gene symbol: ZNF211
  hgvsc: ENST00000407202.2:c.101-643A>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl transcript: ENST00000542008
  gene symbol: ZNF211
  hgvsc: ENST00000542008.1:n.270-37A>G
  variant of: http://identifiers.org/hgnc/13003
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1270
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1543
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14521
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2065
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5841
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1000
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1778
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2912
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9297
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3421
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
population: African
reference allele: A
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: DP

19-58145354-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58145354
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 58145354
    reference: chr 19
allele count: 1
allele frequency: 8.73576071004263e-6
allele num: 114472
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000442740
  ensembl transcript: ENST00000535785
  gene symbol: ZNF211
  hgvsc: ENST00000535785.1:c.*146-37A>T
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000440793
  ensembl transcript: ENST00000540556
  gene symbol: ZNF211
  hgvsc: ENST00000540556.1:c.*94-37A>T
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000441386
  ensembl transcript: ENST00000544273
  gene symbol: ZNF211
  hgvsc: ENST00000544273.1:c.88-37A>T
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000442601
  ensembl transcript: ENST00000541801
  gene symbol: ZNF211
  hgvsc: ENST00000541801.1:c.-93-643A>T
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000121417
  ensembl transcript: ENST00000541072
  gene symbol: ZNF211
  hgvsc: ENST00000541072.1:n.543A>T
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000339562
  ensembl transcript: ENST00000347302
  gene symbol: ZNF211
  hgvsc: ENST00000347302.3:c.90+550A>T
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000399193
  ensembl transcript: ENST00000420680
  gene symbol: ZNF211
  hgvsc: ENST00000420680.1:c.103-643A>T
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000254182
  ensembl transcript: ENST00000254182
  gene symbol: ZNF211
  hgvsc: ENST00000254182.7:c.-132-37A>T
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl transcript: ENST00000540780
  gene symbol: ZNF211
  hgvsc: ENST00000540780.1:n.406-37A>T
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000240731
  ensembl transcript: ENST00000240731
  gene symbol: ZNF211
  hgvsc: ENST00000240731.4:c.91-37A>T
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000299871
  ensembl transcript: ENST00000299871
  gene symbol: ZNF211
  hgvsc: ENST00000299871.5:c.91-37A>T
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000384436
  ensembl transcript: ENST00000407202
  gene symbol: ZNF211
  hgvsc: ENST00000407202.2:c.101-643A>T
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl transcript: ENST00000542008
  gene symbol: ZNF211
  hgvsc: ENST00000542008.1:n.270-37A>T
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000375584
  ensembl transcript: ENST00000391703
  gene symbol: ZNF211
  hgvsc: ENST00000391703.3:c.-93-643A>T
  variant of: http://identifiers.org/hgnc/13003
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9297
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5841
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2912
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12254
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1000
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1543
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2065
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3421
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14521
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ

19-58145356-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58145356
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 58145356
    reference: chr 19
allele count: 1
allele frequency: 8.739730816290858e-6
allele num: 114420
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000240731
  ensembl transcript: ENST00000240731
  gene symbol: ZNF211
  hgvsc: ENST00000240731.4:c.91-35G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000440793
  ensembl transcript: ENST00000540556
  gene symbol: ZNF211
  hgvsc: ENST00000540556.1:c.*94-35G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000442601
  ensembl transcript: ENST00000541801
  gene symbol: ZNF211
  hgvsc: ENST00000541801.1:c.-93-641G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000442740
  ensembl transcript: ENST00000535785
  gene symbol: ZNF211
  hgvsc: ENST00000535785.1:c.*146-35G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl transcript: ENST00000540780
  gene symbol: ZNF211
  hgvsc: ENST00000540780.1:n.406-35G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000399193
  ensembl transcript: ENST00000420680
  gene symbol: ZNF211
  hgvsc: ENST00000420680.1:c.103-641G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000441386
  ensembl transcript: ENST00000544273
  gene symbol: ZNF211
  hgvsc: ENST00000544273.1:c.88-35G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000299871
  ensembl transcript: ENST00000299871
  gene symbol: ZNF211
  hgvsc: ENST00000299871.5:c.91-35G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl transcript: ENST00000542008
  gene symbol: ZNF211
  hgvsc: ENST00000542008.1:n.270-35G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000254182
  ensembl transcript: ENST00000254182
  gene symbol: ZNF211
  hgvsc: ENST00000254182.7:c.-132-35G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000339562
  ensembl transcript: ENST00000347302
  gene symbol: ZNF211
  hgvsc: ENST00000347302.3:c.90+552G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000121417
  ensembl transcript: ENST00000541072
  gene symbol: ZNF211
  hgvsc: ENST00000541072.1:n.545G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000384436
  ensembl transcript: ENST00000407202
  gene symbol: ZNF211
  hgvsc: ENST00000407202.2:c.101-641G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000375584
  ensembl transcript: ENST00000391703
  gene symbol: ZNF211
  hgvsc: ENST00000391703.3:c.-93-641G>A
  variant of: http://identifiers.org/hgnc/13003
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 999
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14530
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1269
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2066
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 988
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2914
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 614
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12257
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9297
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3423
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/19-58145362-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58145362
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 58145362
    reference: chr 19
allele count: 1
allele frequency: 8.756260726419389e-6
allele num: 114204
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000339562
  ensembl transcript: ENST00000347302
  gene symbol: ZNF211
  hgvsc: ENST00000347302.3:c.90+558A>C
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000399193
  ensembl transcript: ENST00000420680
  gene symbol: ZNF211
  hgvsc: ENST00000420680.1:c.103-635A>C
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000121417
  ensembl transcript: ENST00000541072
  gene symbol: ZNF211
  hgvsc: ENST00000541072.1:n.551A>C
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000442740
  ensembl transcript: ENST00000535785
  gene symbol: ZNF211
  hgvsc: ENST00000535785.1:c.*146-29A>C
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000441386
  ensembl transcript: ENST00000544273
  gene symbol: ZNF211
  hgvsc: ENST00000544273.1:c.88-29A>C
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000384436
  ensembl transcript: ENST00000407202
  gene symbol: ZNF211
  hgvsc: ENST00000407202.2:c.101-635A>C
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl transcript: ENST00000542008
  gene symbol: ZNF211
  hgvsc: ENST00000542008.1:n.270-29A>C
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000442601
  ensembl transcript: ENST00000541801
  gene symbol: ZNF211
  hgvsc: ENST00000541801.1:c.-93-635A>C
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000240731
  ensembl transcript: ENST00000240731
  gene symbol: ZNF211
  hgvsc: ENST00000240731.4:c.91-29A>C
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000299871
  ensembl transcript: ENST00000299871
  gene symbol: ZNF211
  hgvsc: ENST00000299871.5:c.91-29A>C
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000375584
  ensembl transcript: ENST00000391703
  gene symbol: ZNF211
  hgvsc: ENST00000391703.3:c.-93-635A>C
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000440793
  ensembl transcript: ENST00000540556
  gene symbol: ZNF211
  hgvsc: ENST00000540556.1:c.*94-29A>C
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000254182
  ensembl transcript: ENST00000254182
  gene symbol: ZNF211
  hgvsc: ENST00000254182.7:c.-132-29A>C
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl transcript: ENST00000540780
  gene symbol: ZNF211
  hgvsc: ENST00000540780.1:n.406-29A>C
  variant of: http://identifiers.org/hgnc/13003
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2971
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5838
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14532
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 575
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1265
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2058
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1463
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1000
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1763
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1036
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
reference allele: A
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum

19-58145362-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58145362
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 58145362
    reference: chr 19
allele count: 175
allele frequency: 1.532345627123393e-3
allele num: 114204
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000441386
  ensembl transcript: ENST00000544273
  gene symbol: ZNF211
  hgvsc: ENST00000544273.1:c.88-29A>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000299871
  ensembl transcript: ENST00000299871
  gene symbol: ZNF211
  hgvsc: ENST00000299871.5:c.91-29A>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl transcript: ENST00000540780
  gene symbol: ZNF211
  hgvsc: ENST00000540780.1:n.406-29A>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000121417
  ensembl transcript: ENST00000541072
  gene symbol: ZNF211
  hgvsc: ENST00000541072.1:n.551A>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000384436
  ensembl transcript: ENST00000407202
  gene symbol: ZNF211
  hgvsc: ENST00000407202.2:c.101-635A>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000440793
  ensembl transcript: ENST00000540556
  gene symbol: ZNF211
  hgvsc: ENST00000540556.1:c.*94-29A>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000339562
  ensembl transcript: ENST00000347302
  gene symbol: ZNF211
  hgvsc: ENST00000347302.3:c.90+558A>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000399193
  ensembl transcript: ENST00000420680
  gene symbol: ZNF211
  hgvsc: ENST00000420680.1:c.103-635A>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000442740
  ensembl transcript: ENST00000535785
  gene symbol: ZNF211
  hgvsc: ENST00000535785.1:c.*146-29A>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000442601
  ensembl transcript: ENST00000541801
  gene symbol: ZNF211
  hgvsc: ENST00000541801.1:c.-93-635A>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000254182
  ensembl transcript: ENST00000254182
  gene symbol: ZNF211
  hgvsc: ENST00000254182.7:c.-132-29A>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000375584
  ensembl transcript: ENST00000391703
  gene symbol: ZNF211
  hgvsc: ENST00000391703.3:c.-93-635A>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000240731
  ensembl transcript: ENST00000240731
  gene symbol: ZNF211
  hgvsc: ENST00000240731.4:c.91-29A>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl transcript: ENST00000542008
  gene symbol: ZNF211
  hgvsc: ENST00000542008.1:n.270-29A>G
  variant of: http://identifiers.org/hgnc/13003
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 7.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 1265
  bin: 5.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14532
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1463
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 9.25e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 850
  bin: 6.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 2971
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1000
  bin: 6.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 1763
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5838
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1036
  bin: 9.75e1
  variant carriers: 91
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 8.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 12253
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 1
population: East Asian
population: African
population: South Asian
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: A
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: QD

19-58145365-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58145365
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 58145365
    reference: chr 19
allele count: 1
allele frequency: 8.777011252128426e-6
allele num: 113934
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000442601
  ensembl transcript: ENST00000541801
  gene symbol: ZNF211
  hgvsc: ENST00000541801.1:c.-93-632C>T
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000442740
  ensembl transcript: ENST00000535785
  gene symbol: ZNF211
  hgvsc: ENST00000535785.1:c.*146-26C>T
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000440793
  ensembl transcript: ENST00000540556
  gene symbol: ZNF211
  hgvsc: ENST00000540556.1:c.*94-26C>T
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000299871
  ensembl transcript: ENST00000299871
  gene symbol: ZNF211
  hgvsc: ENST00000299871.5:c.91-26C>T
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000375584
  ensembl transcript: ENST00000391703
  gene symbol: ZNF211
  hgvsc: ENST00000391703.3:c.-93-632C>T
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000399193
  ensembl transcript: ENST00000420680
  gene symbol: ZNF211
  hgvsc: ENST00000420680.1:c.103-632C>T
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000441386
  ensembl transcript: ENST00000544273
  gene symbol: ZNF211
  hgvsc: ENST00000544273.1:c.88-26C>T
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000240731
  ensembl transcript: ENST00000240731
  gene symbol: ZNF211
  hgvsc: ENST00000240731.4:c.91-26C>T
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000121417
  ensembl transcript: ENST00000541072
  gene symbol: ZNF211
  hgvsc: ENST00000541072.1:n.554C>T
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000339562
  ensembl transcript: ENST00000347302
  gene symbol: ZNF211
  hgvsc: ENST00000347302.3:c.90+561C>T
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000384436
  ensembl transcript: ENST00000407202
  gene symbol: ZNF211
  hgvsc: ENST00000407202.2:c.101-632C>T
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl transcript: ENST00000540780
  gene symbol: ZNF211
  hgvsc: ENST00000540780.1:n.406-26C>T
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000254182
  ensembl transcript: ENST00000254182
  gene symbol: ZNF211
  hgvsc: ENST00000254182.7:c.-132-26C>T
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl transcript: ENST00000542008
  gene symbol: ZNF211
  hgvsc: ENST00000542008.1:n.270-26C>T
  variant of: http://identifiers.org/hgnc/13003
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1751
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3430
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1265
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2064
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 846
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 993
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3000
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14574
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12297
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: Other
population: African
population: European (Finnish)
population: South Asian
population: East Asian
reference allele: C
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff

19-58145366-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58145366
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 58145366
    reference: chr 19
allele count: 1
allele frequency: 8.775624824487504e-6
allele num: 113952
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000339562
  ensembl transcript: ENST00000347302
  gene symbol: ZNF211
  hgvsc: ENST00000347302.3:c.90+562C>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl transcript: ENST00000540780
  gene symbol: ZNF211
  hgvsc: ENST00000540780.1:n.406-25C>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000384436
  ensembl transcript: ENST00000407202
  gene symbol: ZNF211
  hgvsc: ENST00000407202.2:c.101-631C>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000240731
  ensembl transcript: ENST00000240731
  gene symbol: ZNF211
  hgvsc: ENST00000240731.4:c.91-25C>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000442601
  ensembl transcript: ENST00000541801
  gene symbol: ZNF211
  hgvsc: ENST00000541801.1:c.-93-631C>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000441386
  ensembl transcript: ENST00000544273
  gene symbol: ZNF211
  hgvsc: ENST00000544273.1:c.88-25C>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000254182
  ensembl transcript: ENST00000254182
  gene symbol: ZNF211
  hgvsc: ENST00000254182.7:c.-132-25C>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000399193
  ensembl transcript: ENST00000420680
  gene symbol: ZNF211
  hgvsc: ENST00000420680.1:c.103-631C>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000442740
  ensembl transcript: ENST00000535785
  gene symbol: ZNF211
  hgvsc: ENST00000535785.1:c.*146-25C>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000121417
  ensembl transcript: ENST00000541072
  gene symbol: ZNF211
  hgvsc: ENST00000541072.1:n.555C>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000299871
  ensembl transcript: ENST00000299871
  gene symbol: ZNF211
  hgvsc: ENST00000299871.5:c.91-25C>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl transcript: ENST00000542008
  gene symbol: ZNF211
  hgvsc: ENST00000542008.1:n.270-25C>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000440793
  ensembl transcript: ENST00000540556
  gene symbol: ZNF211
  hgvsc: ENST00000540556.1:c.*94-25C>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000375584
  ensembl transcript: ENST00000391703
  gene symbol: ZNF211
  hgvsc: ENST00000391703.3:c.-93-631C>G
  variant of: http://identifiers.org/hgnc/13003
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2064
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1400
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12293
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14575
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1266
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9319
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3429
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 948
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3025
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff

19-58145371-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58145371
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 58145371
    reference: chr 19
allele count: 1
allele frequency: 8.785184664581649e-6
allele num: 113828
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000121417
  ensembl transcript: ENST00000541072
  gene symbol: ZNF211
  hgvsc: ENST00000541072.1:n.560A>T
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000440793
  ensembl transcript: ENST00000540556
  gene symbol: ZNF211
  hgvsc: ENST00000540556.1:c.*94-20A>T
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000441386
  ensembl transcript: ENST00000544273
  gene symbol: ZNF211
  hgvsc: ENST00000544273.1:c.88-20A>T
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000240731
  ensembl transcript: ENST00000240731
  gene symbol: ZNF211
  hgvsc: ENST00000240731.4:c.91-20A>T
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000299871
  ensembl transcript: ENST00000299871
  gene symbol: ZNF211
  hgvsc: ENST00000299871.5:c.91-20A>T
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl transcript: ENST00000542008
  gene symbol: ZNF211
  hgvsc: ENST00000542008.1:n.270-20A>T
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000442601
  ensembl transcript: ENST00000541801
  gene symbol: ZNF211
  hgvsc: ENST00000541801.1:c.-93-626A>T
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000384436
  ensembl transcript: ENST00000407202
  gene symbol: ZNF211
  hgvsc: ENST00000407202.2:c.101-626A>T
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000339562
  ensembl transcript: ENST00000347302
  gene symbol: ZNF211
  hgvsc: ENST00000347302.3:c.90+567A>T
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000399193
  ensembl transcript: ENST00000420680
  gene symbol: ZNF211
  hgvsc: ENST00000420680.1:c.103-626A>T
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000442740
  ensembl transcript: ENST00000535785
  gene symbol: ZNF211
  hgvsc: ENST00000535785.1:c.*146-20A>T
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl transcript: ENST00000540780
  gene symbol: ZNF211
  hgvsc: ENST00000540780.1:n.406-20A>T
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000254182
  ensembl transcript: ENST00000254182
  gene symbol: ZNF211
  hgvsc: ENST00000254182.7:c.-132-20A>T
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000375584
  ensembl transcript: ENST00000391703
  gene symbol: ZNF211
  hgvsc: ENST00000391703.3:c.-93-626A>T
  variant of: http://identifiers.org/hgnc/13003
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9317
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14575
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 992
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3081
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5859
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1265
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3429
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Other
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
reference allele: A
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD

19-58145373-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58145373
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 58145373
    reference: chr 19
allele count: 1
allele frequency: 8.788118463836893e-6
allele num: 113790
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000442740
  ensembl transcript: ENST00000535785
  gene symbol: ZNF211
  hgvsc: ENST00000535785.1:c.*146-18G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000441386
  ensembl transcript: ENST00000544273
  gene symbol: ZNF211
  hgvsc: ENST00000544273.1:c.88-18G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl transcript: ENST00000542008
  gene symbol: ZNF211
  hgvsc: ENST00000542008.1:n.270-18G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000240731
  ensembl transcript: ENST00000240731
  gene symbol: ZNF211
  hgvsc: ENST00000240731.4:c.91-18G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000442601
  ensembl transcript: ENST00000541801
  gene symbol: ZNF211
  hgvsc: ENST00000541801.1:c.-93-624G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000384436
  ensembl transcript: ENST00000407202
  gene symbol: ZNF211
  hgvsc: ENST00000407202.2:c.101-624G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000399193
  ensembl transcript: ENST00000420680
  gene symbol: ZNF211
  hgvsc: ENST00000420680.1:c.103-624G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000254182
  ensembl transcript: ENST00000254182
  gene symbol: ZNF211
  hgvsc: ENST00000254182.7:c.-132-18G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000299871
  ensembl transcript: ENST00000299871
  gene symbol: ZNF211
  hgvsc: ENST00000299871.5:c.91-18G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl transcript: ENST00000540780
  gene symbol: ZNF211
  hgvsc: ENST00000540780.1:n.406-18G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000121417
  ensembl transcript: ENST00000541072
  gene symbol: ZNF211
  hgvsc: ENST00000541072.1:n.562G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000375584
  ensembl transcript: ENST00000391703
  gene symbol: ZNF211
  hgvsc: ENST00000391703.3:c.-93-624G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000339562
  ensembl transcript: ENST00000347302
  gene symbol: ZNF211
  hgvsc: ENST00000347302.3:c.90+569G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000440793
  ensembl transcript: ENST00000540556
  gene symbol: ZNF211
  hgvsc: ENST00000540556.1:c.*94-18G>A
  variant of: http://identifiers.org/hgnc/13003
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9317
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 846
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 992
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3429
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 661
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1329
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 948
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3087
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1766
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12293
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14575
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
population: African
reference allele: G
site quality: FS
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/19-58145374-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58145374
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 58145374
    reference: chr 19
allele count: 1
allele frequency: 8.794610662585968e-6
allele num: 113706
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000442601
  ensembl transcript: ENST00000541801
  gene symbol: ZNF211
  hgvsc: ENST00000541801.1:c.-93-623C>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000254182
  ensembl transcript: ENST00000254182
  gene symbol: ZNF211
  hgvsc: ENST00000254182.7:c.-132-17C>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000440793
  ensembl transcript: ENST00000540556
  gene symbol: ZNF211
  hgvsc: ENST00000540556.1:c.*94-17C>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000299871
  ensembl transcript: ENST00000299871
  gene symbol: ZNF211
  hgvsc: ENST00000299871.5:c.91-17C>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000121417
  ensembl transcript: ENST00000541072
  gene symbol: ZNF211
  hgvsc: ENST00000541072.1:n.563C>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl transcript: ENST00000540780
  gene symbol: ZNF211
  hgvsc: ENST00000540780.1:n.406-17C>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl transcript: ENST00000542008
  gene symbol: ZNF211
  hgvsc: ENST00000542008.1:n.270-17C>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000240731
  ensembl transcript: ENST00000240731
  gene symbol: ZNF211
  hgvsc: ENST00000240731.4:c.91-17C>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000375584
  ensembl transcript: ENST00000391703
  gene symbol: ZNF211
  hgvsc: ENST00000391703.3:c.-93-623C>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000442740
  ensembl transcript: ENST00000535785
  gene symbol: ZNF211
  hgvsc: ENST00000535785.1:c.*146-17C>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000339562
  ensembl transcript: ENST00000347302
  gene symbol: ZNF211
  hgvsc: ENST00000347302.3:c.90+570C>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000399193
  ensembl transcript: ENST00000420680
  gene symbol: ZNF211
  hgvsc: ENST00000420680.1:c.103-623C>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000384436
  ensembl transcript: ENST00000407202
  gene symbol: ZNF211
  hgvsc: ENST00000407202.2:c.101-623C>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000441386
  ensembl transcript: ENST00000544273
  gene symbol: ZNF211
  hgvsc: ENST00000544273.1:c.88-17C>A
  variant of: http://identifiers.org/hgnc/13003
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1337
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5859
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12292
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3069
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9318
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1766
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 949
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 846
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3429
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff

19-58145375-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58145375
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 58145375
    reference: chr 19
allele count: 3
allele frequency: 2.639218791237794e-5
allele num: 113670
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000442601
  ensembl transcript: ENST00000541801
  gene symbol: ZNF211
  hgvsc: ENST00000541801.1:c.-93-622C>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000121417
  ensembl transcript: ENST00000541072
  gene symbol: ZNF211
  hgvsc: ENST00000541072.1:n.564C>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000339562
  ensembl transcript: ENST00000347302
  gene symbol: ZNF211
  hgvsc: ENST00000347302.3:c.90+571C>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl transcript: ENST00000540780
  gene symbol: ZNF211
  hgvsc: ENST00000540780.1:n.406-16C>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000440793
  ensembl transcript: ENST00000540556
  gene symbol: ZNF211
  hgvsc: ENST00000540556.1:c.*94-16C>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000384436
  ensembl transcript: ENST00000407202
  gene symbol: ZNF211
  hgvsc: ENST00000407202.2:c.101-622C>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000441386
  ensembl transcript: ENST00000544273
  gene symbol: ZNF211
  hgvsc: ENST00000544273.1:c.88-16C>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000375584
  ensembl transcript: ENST00000391703
  gene symbol: ZNF211
  hgvsc: ENST00000391703.3:c.-93-622C>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000240731
  ensembl transcript: ENST00000240731
  gene symbol: ZNF211
  hgvsc: ENST00000240731.4:c.91-16C>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000299871
  ensembl transcript: ENST00000299871
  gene symbol: ZNF211
  hgvsc: ENST00000299871.5:c.91-16C>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000399193
  ensembl transcript: ENST00000420680
  gene symbol: ZNF211
  hgvsc: ENST00000420680.1:c.103-622C>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000254182
  ensembl transcript: ENST00000254182
  gene symbol: ZNF211
  hgvsc: ENST00000254182.7:c.-132-16C>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl transcript: ENST00000542008
  gene symbol: ZNF211
  hgvsc: ENST00000542008.1:n.270-16C>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000442740
  ensembl transcript: ENST00000535785
  gene symbol: ZNF211
  hgvsc: ENST00000535785.1:c.*146-16C>G
  variant of: http://identifiers.org/hgnc/13003
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1763
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12293
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3429
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 845
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2062
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5858
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 993
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3080
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1309
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP

19-58145375-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58145375
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 58145375
    reference: chr 19
allele count: 6
allele frequency: 5.278437582475587e-5
allele num: 113670
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000442740
  ensembl transcript: ENST00000535785
  gene symbol: ZNF211
  hgvsc: ENST00000535785.1:c.*146-16C>T
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000254182
  ensembl transcript: ENST00000254182
  gene symbol: ZNF211
  hgvsc: ENST00000254182.7:c.-132-16C>T
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000384436
  ensembl transcript: ENST00000407202
  gene symbol: ZNF211
  hgvsc: ENST00000407202.2:c.101-622C>T
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl transcript: ENST00000542008
  gene symbol: ZNF211
  hgvsc: ENST00000542008.1:n.270-16C>T
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000121417
  ensembl transcript: ENST00000541072
  gene symbol: ZNF211
  hgvsc: ENST00000541072.1:n.564C>T
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000440793
  ensembl transcript: ENST00000540556
  gene symbol: ZNF211
  hgvsc: ENST00000540556.1:c.*94-16C>T
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000299871
  ensembl transcript: ENST00000299871
  gene symbol: ZNF211
  hgvsc: ENST00000299871.5:c.91-16C>T
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000240731
  ensembl transcript: ENST00000240731
  gene symbol: ZNF211
  hgvsc: ENST00000240731.4:c.91-16C>T
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl transcript: ENST00000540780
  gene symbol: ZNF211
  hgvsc: ENST00000540780.1:n.406-16C>T
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000399193
  ensembl transcript: ENST00000420680
  gene symbol: ZNF211
  hgvsc: ENST00000420680.1:c.103-622C>T
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000339562
  ensembl transcript: ENST00000347302
  gene symbol: ZNF211
  hgvsc: ENST00000347302.3:c.90+571C>T
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000442601
  ensembl transcript: ENST00000541801
  gene symbol: ZNF211
  hgvsc: ENST00000541801.1:c.-93-622C>T
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000375584
  ensembl transcript: ENST00000391703
  gene symbol: ZNF211
  hgvsc: ENST00000391703.3:c.-93-622C>T
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000441386
  ensembl transcript: ENST00000544273
  gene symbol: ZNF211
  hgvsc: ENST00000544273.1:c.88-16C>T
  variant of: http://identifiers.org/hgnc/13003
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1763
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14576
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1309
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 952
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 993
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2062
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5858
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3080
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12293
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
population: European (Finnish)
population: East Asian
population: Other
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ

19-58145377-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58145377
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 58145377
    reference: chr 19
allele count: 4
allele frequency: 3.520197131039338e-5
allele num: 113630
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000375584
  ensembl transcript: ENST00000391703
  gene symbol: ZNF211
  hgvsc: ENST00000391703.3:c.-93-620G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000442740
  ensembl transcript: ENST00000535785
  gene symbol: ZNF211
  hgvsc: ENST00000535785.1:c.*146-14G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000441386
  ensembl transcript: ENST00000544273
  gene symbol: ZNF211
  hgvsc: ENST00000544273.1:c.88-14G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000254182
  ensembl transcript: ENST00000254182
  gene symbol: ZNF211
  hgvsc: ENST00000254182.7:c.-132-14G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl transcript: ENST00000540780
  gene symbol: ZNF211
  hgvsc: ENST00000540780.1:n.406-14G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000240731
  ensembl transcript: ENST00000240731
  gene symbol: ZNF211
  hgvsc: ENST00000240731.4:c.91-14G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000339562
  ensembl transcript: ENST00000347302
  gene symbol: ZNF211
  hgvsc: ENST00000347302.3:c.90+573G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000384436
  ensembl transcript: ENST00000407202
  gene symbol: ZNF211
  hgvsc: ENST00000407202.2:c.101-620G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000442601
  ensembl transcript: ENST00000541801
  gene symbol: ZNF211
  hgvsc: ENST00000541801.1:c.-93-620G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000121417
  ensembl transcript: ENST00000541072
  gene symbol: ZNF211
  hgvsc: ENST00000541072.1:n.566G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000399193
  ensembl transcript: ENST00000420680
  gene symbol: ZNF211
  hgvsc: ENST00000420680.1:c.103-620G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000299871
  ensembl transcript: ENST00000299871
  gene symbol: ZNF211
  hgvsc: ENST00000299871.5:c.91-14G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl transcript: ENST00000542008
  gene symbol: ZNF211
  hgvsc: ENST00000542008.1:n.270-14G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000440793
  ensembl transcript: ENST00000540556
  gene symbol: ZNF211
  hgvsc: ENST00000540556.1:c.*94-14G>A
  variant of: http://identifiers.org/hgnc/13003
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3429
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 993
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1286
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2063
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 845
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 947
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3111
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1264
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14578
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1759
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
reference allele: G
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: MQ

19-58145384-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58145384
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 58145384
    reference: chr 19
allele count: 1
allele frequency: 8.821298142234612e-6
allele num: 113362
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000440793
  ensembl transcript: ENST00000540556
  gene symbol: ZNF211
  hgvsc: ENST00000540556.1:c.*94-7T>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000254182
  ensembl transcript: ENST00000254182
  gene symbol: ZNF211
  hgvsc: ENST00000254182.7:c.-132-7T>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000442601
  ensembl transcript: ENST00000541801
  gene symbol: ZNF211
  hgvsc: ENST00000541801.1:c.-93-613T>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl transcript: ENST00000542008
  gene symbol: ZNF211
  hgvsc: ENST00000542008.1:n.270-7T>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000240731
  ensembl transcript: ENST00000240731
  gene symbol: ZNF211
  hgvsc: ENST00000240731.4:c.91-7T>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl transcript: ENST00000540780
  gene symbol: ZNF211
  hgvsc: ENST00000540780.1:n.406-7T>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000441386
  ensembl transcript: ENST00000544273
  gene symbol: ZNF211
  hgvsc: ENST00000544273.1:c.88-7T>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000339562
  ensembl transcript: ENST00000347302
  gene symbol: ZNF211
  hgvsc: ENST00000347302.3:c.90+580T>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000442740
  ensembl transcript: ENST00000535785
  gene symbol: ZNF211
  hgvsc: ENST00000535785.1:c.*146-7T>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000299871
  ensembl transcript: ENST00000299871
  gene symbol: ZNF211
  hgvsc: ENST00000299871.5:c.91-7T>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000375584
  ensembl transcript: ENST00000391703
  gene symbol: ZNF211
  hgvsc: ENST00000391703.3:c.-93-613T>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000399193
  ensembl transcript: ENST00000420680
  gene symbol: ZNF211
  hgvsc: ENST00000420680.1:c.103-613T>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000121417
  ensembl transcript: ENST00000541072
  gene symbol: ZNF211
  hgvsc: ENST00000541072.1:n.573T>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000384436
  ensembl transcript: ENST00000407202
  gene symbol: ZNF211
  hgvsc: ENST00000407202.2:c.101-613T>A
  variant of: http://identifiers.org/hgnc/13003
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3166
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 945
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3429
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 804
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5858
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9321
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1774
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.91-7T>A
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
population: Other
reference allele: T
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum

19-58145389-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58145389
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 58145389
    reference: chr 19
allele count: 1
allele frequency: 8.83158173628897e-6
allele num: 113230
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000299871
  ensembl transcript: ENST00000299871
  gene symbol: ZNF211
  hgvsc: ENST00000299871.5:c.91-2A>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000399193
  ensembl transcript: ENST00000420680
  gene symbol: ZNF211
  hgvsc: ENST00000420680.1:c.103-608A>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000375584
  ensembl transcript: ENST00000391703
  gene symbol: ZNF211
  hgvsc: ENST00000391703.3:c.-93-608A>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000121417
  ensembl transcript: ENST00000540780
  gene symbol: ZNF211
  hgvsc: ENST00000540780.1:n.406-2A>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000441386
  ensembl transcript: ENST00000544273
  gene symbol: ZNF211
  hgvsc: ENST00000544273.1:c.88-2A>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000440793
  ensembl transcript: ENST00000540556
  gene symbol: ZNF211
  hgvsc: ENST00000540556.1:c.*94-2A>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000254182
  ensembl transcript: ENST00000254182
  gene symbol: ZNF211
  hgvsc: ENST00000254182.7:c.-132-2A>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000442601
  ensembl transcript: ENST00000541801
  gene symbol: ZNF211
  hgvsc: ENST00000541801.1:c.-93-608A>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000442740
  ensembl transcript: ENST00000535785
  gene symbol: ZNF211
  hgvsc: ENST00000535785.1:c.*146-2A>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000121417
  ensembl transcript: ENST00000542008
  gene symbol: ZNF211
  hgvsc: ENST00000542008.1:n.270-2A>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000384436
  ensembl transcript: ENST00000407202
  gene symbol: ZNF211
  hgvsc: ENST00000407202.2:c.101-608A>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000121417
  ensembl transcript: ENST00000541072
  gene symbol: ZNF211
  hgvsc: ENST00000541072.1:n.578A>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000240731
  ensembl transcript: ENST00000240731
  gene symbol: ZNF211
  hgvsc: ENST00000240731.4:c.91-2A>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000339562
  ensembl transcript: ENST00000347302
  gene symbol: ZNF211
  hgvsc: ENST00000347302.3:c.90+585A>G
  variant of: http://identifiers.org/hgnc/13003
canonical: true
consequence: splice acceptor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14582
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12290
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1132
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1783
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9321
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1264
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 845
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 993
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.91-2A>G
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD

http://identifiers.org/exac.variant/19-58145396-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58145396
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 58145396
    reference: chr 19
allele count: 2
allele frequency: 1.768065206244806e-5
allele num: 113118
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000299871
  ensembl transcript: ENST00000299871
  gene symbol: ZNF211
  hgvsc: ENST00000299871.5:c.96C>A
  hgvsp: ENST00000299871.5:c.96C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000441386
  ensembl transcript: ENST00000544273
  gene symbol: ZNF211
  hgvsc: ENST00000544273.1:c.93C>A
  hgvsp: ENST00000544273.1:c.93C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000375584
  ensembl transcript: ENST00000391703
  gene symbol: ZNF211
  hgvsc: ENST00000391703.3:c.-93-601C>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000440793
  ensembl transcript: ENST00000540556
  gene symbol: ZNF211
  hgvsc: ENST00000540556.1:c.*99C>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000442740
  ensembl transcript: ENST00000535785
  gene symbol: ZNF211
  hgvsc: ENST00000535785.1:c.*151C>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000254182
  ensembl transcript: ENST00000254182
  gene symbol: ZNF211
  hgvsc: ENST00000254182.7:c.-127C>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000240731
  ensembl transcript: ENST00000240731
  gene symbol: ZNF211
  hgvsc: ENST00000240731.4:c.96C>A
  hgvsp: ENST00000240731.4:c.96C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000121417
  ensembl transcript: ENST00000540780
  gene symbol: ZNF211
  hgvsc: ENST00000540780.1:n.411C>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000339562
  ensembl transcript: ENST00000347302
  gene symbol: ZNF211
  hgvsc: ENST00000347302.3:c.90+592C>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000384436
  ensembl transcript: ENST00000407202
  gene symbol: ZNF211
  hgvsc: ENST00000407202.2:c.101-601C>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000121417
  ensembl transcript: ENST00000541072
  gene symbol: ZNF211
  hgvsc: ENST00000541072.1:n.585C>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000121417
  ensembl transcript: ENST00000542008
  gene symbol: ZNF211
  hgvsc: ENST00000542008.1:n.275C>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000442601
  ensembl transcript: ENST00000541801
  gene symbol: ZNF211
  hgvsc: ENST00000541801.1:c.-93-601C>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000399193
  ensembl transcript: ENST00000420680
  gene symbol: ZNF211
  hgvsc: ENST00000420680.1:c.103-601C>A
  variant of: http://identifiers.org/hgnc/13003
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14581
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2062
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5858
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1084
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 945
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1775
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 846
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3429
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 993
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12293
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro32Pro
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: QD

19-58145397-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58145397
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 58145397
    reference: chr 19
allele count: 1
allele frequency: 8.841732979664014e-6
allele num: 113100
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000441386
  ensembl transcript: ENST00000544273
  gene symbol: ZNF211
  hgvsc: ENST00000544273.1:c.94A>G
  hgvsp: ENSP00000441386.1:p.Ile32Val
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000240731
  ensembl transcript: ENST00000240731
  gene symbol: ZNF211
  hgvsc: ENST00000240731.4:c.97A>G
  hgvsp: ENSP00000240731.4:p.Ile33Val
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000299871
  ensembl transcript: ENST00000299871
  gene symbol: ZNF211
  hgvsc: ENST00000299871.5:c.97A>G
  hgvsp: ENSP00000299871.5:p.Ile33Val
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000442740
  ensembl transcript: ENST00000535785
  gene symbol: ZNF211
  hgvsc: ENST00000535785.1:c.*152A>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000440793
  ensembl transcript: ENST00000540556
  gene symbol: ZNF211
  hgvsc: ENST00000540556.1:c.*100A>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000121417
  ensembl transcript: ENST00000541072
  gene symbol: ZNF211
  hgvsc: ENST00000541072.1:n.586A>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000254182
  ensembl transcript: ENST00000254182
  gene symbol: ZNF211
  hgvsc: ENST00000254182.7:c.-126A>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000375584
  ensembl transcript: ENST00000391703
  gene symbol: ZNF211
  hgvsc: ENST00000391703.3:c.-93-600A>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000339562
  ensembl transcript: ENST00000347302
  gene symbol: ZNF211
  hgvsc: ENST00000347302.3:c.90+593A>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000399193
  ensembl transcript: ENST00000420680
  gene symbol: ZNF211
  hgvsc: ENST00000420680.1:c.103-600A>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000442601
  ensembl transcript: ENST00000541801
  gene symbol: ZNF211
  hgvsc: ENST00000541801.1:c.-93-600A>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000121417
  ensembl transcript: ENST00000542008
  gene symbol: ZNF211
  hgvsc: ENST00000542008.1:n.276A>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000121417
  ensembl transcript: ENST00000540780
  gene symbol: ZNF211
  hgvsc: ENST00000540780.1:n.412A>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000384436
  ensembl transcript: ENST00000407202
  gene symbol: ZNF211
  hgvsc: ENST00000407202.2:c.101-600A>G
  variant of: http://identifiers.org/hgnc/13003
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14583
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1071
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2062
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12292
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 996
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9320
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 945
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3108
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1771
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile33Val
num of homozygotes: 0
population: European (Finnish)
population: African
population: Other
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: QD

19-58145405-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58145405
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 58145405
    reference: chr 19
allele count: 1
allele frequency: 8.854258898530193e-6
allele num: 112940
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000339562
  ensembl transcript: ENST00000347302
  gene symbol: ZNF211
  hgvsc: ENST00000347302.3:c.91-592A>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000240731
  ensembl transcript: ENST00000240731
  gene symbol: ZNF211
  hgvsc: ENST00000240731.4:c.105A>G
  hgvsp: ENST00000240731.4:c.105A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000121417
  ensembl transcript: ENST00000540780
  gene symbol: ZNF211
  hgvsc: ENST00000540780.1:n.420A>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000375584
  ensembl transcript: ENST00000391703
  gene symbol: ZNF211
  hgvsc: ENST00000391703.3:c.-93-592A>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000442601
  ensembl transcript: ENST00000541801
  gene symbol: ZNF211
  hgvsc: ENST00000541801.1:c.-93-592A>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000440793
  ensembl transcript: ENST00000540556
  gene symbol: ZNF211
  hgvsc: ENST00000540556.1:c.*108A>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000399193
  ensembl transcript: ENST00000420680
  gene symbol: ZNF211
  hgvsc: ENST00000420680.1:c.103-592A>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000254182
  ensembl transcript: ENST00000254182
  gene symbol: ZNF211
  hgvsc: ENST00000254182.7:c.-118A>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000441386
  ensembl transcript: ENST00000544273
  gene symbol: ZNF211
  hgvsc: ENST00000544273.1:c.102A>G
  hgvsp: ENST00000544273.1:c.102A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000299871
  ensembl transcript: ENST00000299871
  gene symbol: ZNF211
  hgvsc: ENST00000299871.5:c.105A>G
  hgvsp: ENST00000299871.5:c.105A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000442740
  ensembl transcript: ENST00000535785
  gene symbol: ZNF211
  hgvsc: ENST00000535785.1:c.*160A>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000121417
  ensembl transcript: ENST00000542008
  gene symbol: ZNF211
  hgvsc: ENST00000542008.1:n.284A>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000384436
  ensembl transcript: ENST00000407202
  gene symbol: ZNF211
  hgvsc: ENST00000407202.2:c.101-592A>G
  variant of: http://identifiers.org/hgnc/13003
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1142
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5859
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 992
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2062
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3044
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1744
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1264
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9319
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1021
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 945
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3429
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12292
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14582
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr35Thr
num of homozygotes: 0
population: Other
population: South Asian
population: African
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD

19-58145430-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58145430
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 58145430
    reference: chr 19
allele count: 5
allele frequency: 4.460064581735143e-5
allele num: 112106
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000121417
  ensembl transcript: ENST00000542008
  gene symbol: ZNF211
  hgvsc: ENST00000542008.1:n.309G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000384436
  ensembl transcript: ENST00000407202
  gene symbol: ZNF211
  hgvsc: ENST00000407202.2:c.101-567G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000440793
  ensembl transcript: ENST00000540556
  gene symbol: ZNF211
  hgvsc: ENST00000540556.1:c.*132+1G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000441386
  ensembl transcript: ENST00000544273
  gene symbol: ZNF211
  hgvsc: ENST00000544273.1:c.126+1G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000121417
  ensembl transcript: ENST00000540780
  gene symbol: ZNF211
  hgvsc: ENST00000540780.1:n.445G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000240731
  ensembl transcript: ENST00000240731
  gene symbol: ZNF211
  hgvsc: ENST00000240731.4:c.129+1G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000399193
  ensembl transcript: ENST00000420680
  gene symbol: ZNF211
  hgvsc: ENST00000420680.1:c.103-567G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000442740
  ensembl transcript: ENST00000535785
  gene symbol: ZNF211
  hgvsc: ENST00000535785.1:c.*184+1G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000442601
  ensembl transcript: ENST00000541801
  gene symbol: ZNF211
  hgvsc: ENST00000541801.1:c.-93-567G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000254182
  ensembl transcript: ENST00000254182
  gene symbol: ZNF211
  hgvsc: ENST00000254182.7:c.-94+1G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000375584
  ensembl transcript: ENST00000391703
  gene symbol: ZNF211
  hgvsc: ENST00000391703.3:c.-93-567G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000339562
  ensembl transcript: ENST00000347302
  gene symbol: ZNF211
  hgvsc: ENST00000347302.3:c.91-567G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: true
  consequence: splice_donor_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000299871
  ensembl transcript: ENST00000299871
  gene symbol: ZNF211
  hgvsc: ENST00000299871.5:c.129+1G>A
  variant of: http://identifiers.org/hgnc/13003
canonical: true
consequence: splice donor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1263
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2096
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5858
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12269
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2062
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2396
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 944
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 14566
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9317
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1664
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 844
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3429
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.129+1G>A
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum

19-58145434-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58145434
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 58145434
    reference: chr 19
allele count: 1
allele frequency: 8.922198429693077e-6
allele num: 112080
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000299871
  ensembl transcript: ENST00000299871
  gene symbol: ZNF211
  hgvsc: ENST00000299871.5:c.129+5G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000339562
  ensembl transcript: ENST00000347302
  gene symbol: ZNF211
  hgvsc: ENST00000347302.3:c.91-563G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000442601
  ensembl transcript: ENST00000541801
  gene symbol: ZNF211
  hgvsc: ENST00000541801.1:c.-93-563G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000121417
  ensembl transcript: ENST00000540780
  gene symbol: ZNF211
  hgvsc: ENST00000540780.1:n.449G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000121417
  ensembl transcript: ENST00000542008
  gene symbol: ZNF211
  hgvsc: ENST00000542008.1:n.313G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000399193
  ensembl transcript: ENST00000420680
  gene symbol: ZNF211
  hgvsc: ENST00000420680.1:c.103-563G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000254182
  ensembl transcript: ENST00000254182
  gene symbol: ZNF211
  hgvsc: ENST00000254182.7:c.-94+5G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000442740
  ensembl transcript: ENST00000535785
  gene symbol: ZNF211
  hgvsc: ENST00000535785.1:c.*184+5G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000384436
  ensembl transcript: ENST00000407202
  gene symbol: ZNF211
  hgvsc: ENST00000407202.2:c.101-563G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000240731
  ensembl transcript: ENST00000240731
  gene symbol: ZNF211
  hgvsc: ENST00000240731.4:c.129+5G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000375584
  ensembl transcript: ENST00000391703
  gene symbol: ZNF211
  hgvsc: ENST00000391703.3:c.-93-563G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000441386
  ensembl transcript: ENST00000544273
  gene symbol: ZNF211
  hgvsc: ENST00000544273.1:c.126+5G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000440793
  ensembl transcript: ENST00000540556
  gene symbol: ZNF211
  hgvsc: ENST00000540556.1:c.*132+5G>A
  variant of: http://identifiers.org/hgnc/13003
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2063
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2358
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1263
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3429
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12265
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1668
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5858
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9317
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 737
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 942
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 991
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.129+5G>A
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum

19-58145436-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58145436
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 58145436
    reference: chr 19
allele count: 1
allele frequency: 8.928252562408485e-6
allele num: 112004
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000121417
  ensembl transcript: ENST00000540780
  gene symbol: ZNF211
  hgvsc: ENST00000540780.1:n.451G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000440793
  ensembl transcript: ENST00000540556
  gene symbol: ZNF211
  hgvsc: ENST00000540556.1:c.*132+7G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000254182
  ensembl transcript: ENST00000254182
  gene symbol: ZNF211
  hgvsc: ENST00000254182.7:c.-94+7G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000384436
  ensembl transcript: ENST00000407202
  gene symbol: ZNF211
  hgvsc: ENST00000407202.2:c.101-561G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000339562
  ensembl transcript: ENST00000347302
  gene symbol: ZNF211
  hgvsc: ENST00000347302.3:c.91-561G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000442740
  ensembl transcript: ENST00000535785
  gene symbol: ZNF211
  hgvsc: ENST00000535785.1:c.*184+7G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000240731
  ensembl transcript: ENST00000240731
  gene symbol: ZNF211
  hgvsc: ENST00000240731.4:c.129+7G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000442601
  ensembl transcript: ENST00000541801
  gene symbol: ZNF211
  hgvsc: ENST00000541801.1:c.-93-561G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000121417
  ensembl transcript: ENST00000542008
  gene symbol: ZNF211
  hgvsc: ENST00000542008.1:n.315G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000399193
  ensembl transcript: ENST00000420680
  gene symbol: ZNF211
  hgvsc: ENST00000420680.1:c.103-561G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000375584
  ensembl transcript: ENST00000391703
  gene symbol: ZNF211
  hgvsc: ENST00000391703.3:c.-93-561G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000299871
  ensembl transcript: ENST00000299871
  gene symbol: ZNF211
  hgvsc: ENST00000299871.5:c.129+7G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000441386
  ensembl transcript: ENST00000544273
  gene symbol: ZNF211
  hgvsc: ENST00000544273.1:c.126+7G>A
  variant of: http://identifiers.org/hgnc/13003
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12267
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2264
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2063
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3429
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1264
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9317
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 942
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2280
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 844
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14555
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1665
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.129+7G>A
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: G
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: VQSLOD

19-58145444-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58145444
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 58145444
    reference: chr 19
allele count: 1
allele frequency: 8.970862638151285e-6
allele num: 111472
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000121417
  ensembl transcript: ENST00000542008
  gene symbol: ZNF211
  hgvsc: ENST00000542008.1:n.323C>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000399193
  ensembl transcript: ENST00000420680
  gene symbol: ZNF211
  hgvsc: ENST00000420680.1:c.103-553C>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000442601
  ensembl transcript: ENST00000541801
  gene symbol: ZNF211
  hgvsc: ENST00000541801.1:c.-93-553C>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000121417
  ensembl transcript: ENST00000540780
  gene symbol: ZNF211
  hgvsc: ENST00000540780.1:n.459C>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000375584
  ensembl transcript: ENST00000391703
  gene symbol: ZNF211
  hgvsc: ENST00000391703.3:c.-93-553C>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000240731
  ensembl transcript: ENST00000240731
  gene symbol: ZNF211
  hgvsc: ENST00000240731.4:c.129+15C>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000299871
  ensembl transcript: ENST00000299871
  gene symbol: ZNF211
  hgvsc: ENST00000299871.5:c.129+15C>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000339562
  ensembl transcript: ENST00000347302
  gene symbol: ZNF211
  hgvsc: ENST00000347302.3:c.91-553C>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000442740
  ensembl transcript: ENST00000535785
  gene symbol: ZNF211
  hgvsc: ENST00000535785.1:c.*184+15C>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000254182
  ensembl transcript: ENST00000254182
  gene symbol: ZNF211
  hgvsc: ENST00000254182.7:c.-94+15C>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000384436
  ensembl transcript: ENST00000407202
  gene symbol: ZNF211
  hgvsc: ENST00000407202.2:c.101-553C>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000440793
  ensembl transcript: ENST00000540556
  gene symbol: ZNF211
  hgvsc: ENST00000540556.1:c.*132+15C>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000441386
  ensembl transcript: ENST00000544273
  gene symbol: ZNF211
  hgvsc: ENST00000544273.1:c.126+15C>G
  variant of: http://identifiers.org/hgnc/13003
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 989
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1875
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5848
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2814
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 942
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3424
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9306
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12185
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 844
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2061
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
population: African
reference allele: C
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/19-58145450-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58145450
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 58145450
    reference: chr 19
allele count: 1
allele frequency: 8.987956138774043e-6
allele num: 111260
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000121417
  ensembl transcript: ENST00000542008
  gene symbol: ZNF211
  hgvsc: ENST00000542008.1:n.329C>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000254182
  ensembl transcript: ENST00000254182
  gene symbol: ZNF211
  hgvsc: ENST00000254182.7:c.-94+21C>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000375584
  ensembl transcript: ENST00000391703
  gene symbol: ZNF211
  hgvsc: ENST00000391703.3:c.-93-547C>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000442740
  ensembl transcript: ENST00000535785
  gene symbol: ZNF211
  hgvsc: ENST00000535785.1:c.*184+21C>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000399193
  ensembl transcript: ENST00000420680
  gene symbol: ZNF211
  hgvsc: ENST00000420680.1:c.103-547C>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000440793
  ensembl transcript: ENST00000540556
  gene symbol: ZNF211
  hgvsc: ENST00000540556.1:c.*132+21C>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000240731
  ensembl transcript: ENST00000240731
  gene symbol: ZNF211
  hgvsc: ENST00000240731.4:c.129+21C>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000442601
  ensembl transcript: ENST00000541801
  gene symbol: ZNF211
  hgvsc: ENST00000541801.1:c.-93-547C>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000299871
  ensembl transcript: ENST00000299871
  gene symbol: ZNF211
  hgvsc: ENST00000299871.5:c.129+21C>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000441386
  ensembl transcript: ENST00000544273
  gene symbol: ZNF211
  hgvsc: ENST00000544273.1:c.126+21C>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000339562
  ensembl transcript: ENST00000347302
  gene symbol: ZNF211
  hgvsc: ENST00000347302.3:c.91-547C>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000384436
  ensembl transcript: ENST00000407202
  gene symbol: ZNF211
  hgvsc: ENST00000407202.2:c.101-547C>A
  variant of: http://identifiers.org/hgnc/13003
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3051
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5835
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2061
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 989
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1262
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14419
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9280
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1692
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 844
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1727
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3422
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 942
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: FS
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD

19-58145461-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58145461
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 58145461
    reference: chr 19
allele count: 2
allele frequency: 1.8045004240576e-5
allele num: 110834
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000399193
  ensembl transcript: ENST00000420680
  gene symbol: ZNF211
  hgvsc: ENST00000420680.1:c.103-536C>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000442601
  ensembl transcript: ENST00000541801
  gene symbol: ZNF211
  hgvsc: ENST00000541801.1:c.-93-536C>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000375584
  ensembl transcript: ENST00000391703
  gene symbol: ZNF211
  hgvsc: ENST00000391703.3:c.-93-536C>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000240731
  ensembl transcript: ENST00000240731
  gene symbol: ZNF211
  hgvsc: ENST00000240731.4:c.129+32C>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000121417
  ensembl transcript: ENST00000542008
  gene symbol: ZNF211
  hgvsc: ENST00000542008.1:n.340C>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000254182
  ensembl transcript: ENST00000254182
  gene symbol: ZNF211
  hgvsc: ENST00000254182.7:c.-94+32C>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000339562
  ensembl transcript: ENST00000347302
  gene symbol: ZNF211
  hgvsc: ENST00000347302.3:c.91-536C>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000441386
  ensembl transcript: ENST00000544273
  gene symbol: ZNF211
  hgvsc: ENST00000544273.1:c.126+32C>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000299871
  ensembl transcript: ENST00000299871
  gene symbol: ZNF211
  hgvsc: ENST00000299871.5:c.129+32C>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000384436
  ensembl transcript: ENST00000407202
  gene symbol: ZNF211
  hgvsc: ENST00000407202.2:c.101-536C>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000440793
  ensembl transcript: ENST00000540556
  gene symbol: ZNF211
  hgvsc: ENST00000540556.1:c.*132+32C>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000442740
  ensembl transcript: ENST00000535785
  gene symbol: ZNF211
  hgvsc: ENST00000535785.1:c.*184+32C>G
  variant of: http://identifiers.org/hgnc/13003
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3354
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11711
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1260
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 624
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 871
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1867
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3409
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1490
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2060
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 844
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9120
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 942
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13870
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5792
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: African
population: Other
population: European (Finnish)
population: Latino
reference allele: C
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: DP

19-58145467-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58145467
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 58145467
    reference: chr 19
allele count: 3
allele frequency: 2.708363426260292e-5
allele num: 110768
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000299871
  ensembl transcript: ENST00000299871
  gene symbol: ZNF211
  hgvsc: ENST00000299871.5:c.129+38T>C
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000442740
  ensembl transcript: ENST00000535785
  gene symbol: ZNF211
  hgvsc: ENST00000535785.1:c.*184+38T>C
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000399193
  ensembl transcript: ENST00000420680
  gene symbol: ZNF211
  hgvsc: ENST00000420680.1:c.103-530T>C
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000442601
  ensembl transcript: ENST00000541801
  gene symbol: ZNF211
  hgvsc: ENST00000541801.1:c.-93-530T>C
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000375584
  ensembl transcript: ENST00000391703
  gene symbol: ZNF211
  hgvsc: ENST00000391703.3:c.-93-530T>C
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000254182
  ensembl transcript: ENST00000254182
  gene symbol: ZNF211
  hgvsc: ENST00000254182.7:c.-94+38T>C
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000121417
  ensembl transcript: ENST00000542008
  gene symbol: ZNF211
  hgvsc: ENST00000542008.1:n.346T>C
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000440793
  ensembl transcript: ENST00000540556
  gene symbol: ZNF211
  hgvsc: ENST00000540556.1:c.*132+38T>C
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000384436
  ensembl transcript: ENST00000407202
  gene symbol: ZNF211
  hgvsc: ENST00000407202.2:c.101-530T>C
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000240731
  ensembl transcript: ENST00000240731
  gene symbol: ZNF211
  hgvsc: ENST00000240731.4:c.129+38T>C
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000339562
  ensembl transcript: ENST00000347302
  gene symbol: ZNF211
  hgvsc: ENST00000347302.3:c.91-530T>C
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000441386
  ensembl transcript: ENST00000544273
  gene symbol: ZNF211
  hgvsc: ENST00000544273.1:c.126+38T>C
  variant of: http://identifiers.org/hgnc/13003
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2058
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3403
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3393
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2038
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1438
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11058
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 942
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1875
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5780
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9043
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13359
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 843
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1259
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: Other
reference allele: T
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum

19-58145469-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58145469
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 58145469
    reference: chr 19
allele count: 17
allele frequency: 1.53493327554761e-4
allele num: 110754
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000121417
  ensembl transcript: ENST00000542008
  gene symbol: ZNF211
  hgvsc: ENST00000542008.1:n.348T>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000441386
  ensembl transcript: ENST00000544273
  gene symbol: ZNF211
  hgvsc: ENST00000544273.1:c.126+40T>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000399193
  ensembl transcript: ENST00000420680
  gene symbol: ZNF211
  hgvsc: ENST00000420680.1:c.103-528T>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000442740
  ensembl transcript: ENST00000535785
  gene symbol: ZNF211
  hgvsc: ENST00000535785.1:c.*184+40T>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000375584
  ensembl transcript: ENST00000391703
  gene symbol: ZNF211
  hgvsc: ENST00000391703.3:c.-93-528T>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000240731
  ensembl transcript: ENST00000240731
  gene symbol: ZNF211
  hgvsc: ENST00000240731.4:c.129+40T>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000442601
  ensembl transcript: ENST00000541801
  gene symbol: ZNF211
  hgvsc: ENST00000541801.1:c.-93-528T>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000254182
  ensembl transcript: ENST00000254182
  gene symbol: ZNF211
  hgvsc: ENST00000254182.7:c.-94+40T>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000299871
  ensembl transcript: ENST00000299871
  gene symbol: ZNF211
  hgvsc: ENST00000299871.5:c.129+40T>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000384436
  ensembl transcript: ENST00000407202
  gene symbol: ZNF211
  hgvsc: ENST00000407202.2:c.101-528T>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000440793
  ensembl transcript: ENST00000540556
  gene symbol: ZNF211
  hgvsc: ENST00000540556.1:c.*132+40T>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000339562
  ensembl transcript: ENST00000347302
  gene symbol: ZNF211
  hgvsc: ENST00000347302.3:c.91-528T>G
  variant of: http://identifiers.org/hgnc/13003
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3402
  bin: 4.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 13161
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5772
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1259
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2058
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 989
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3398
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2203
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1427
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2274
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 943
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9006
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 843
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10729
  bin: 2.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: T
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum

19-58145471-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58145471
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 58145471
    reference: chr 19
allele count: 1
allele frequency: 9.037342298376894e-6
allele num: 110652
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000254182
  ensembl transcript: ENST00000254182
  gene symbol: ZNF211
  hgvsc: ENST00000254182.7:c.-94+42C>T
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000399193
  ensembl transcript: ENST00000420680
  gene symbol: ZNF211
  hgvsc: ENST00000420680.1:c.103-526C>T
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000121417
  ensembl transcript: ENST00000542008
  gene symbol: ZNF211
  hgvsc: ENST00000542008.1:n.350C>T
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000442740
  ensembl transcript: ENST00000535785
  gene symbol: ZNF211
  hgvsc: ENST00000535785.1:c.*184+42C>T
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000384436
  ensembl transcript: ENST00000407202
  gene symbol: ZNF211
  hgvsc: ENST00000407202.2:c.101-526C>T
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000440793
  ensembl transcript: ENST00000540556
  gene symbol: ZNF211
  hgvsc: ENST00000540556.1:c.*132+42C>T
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000339562
  ensembl transcript: ENST00000347302
  gene symbol: ZNF211
  hgvsc: ENST00000347302.3:c.91-526C>T
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000441386
  ensembl transcript: ENST00000544273
  gene symbol: ZNF211
  hgvsc: ENST00000544273.1:c.126+42C>T
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000375584
  ensembl transcript: ENST00000391703
  gene symbol: ZNF211
  hgvsc: ENST00000391703.3:c.-93-526C>T
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000299871
  ensembl transcript: ENST00000299871
  gene symbol: ZNF211
  hgvsc: ENST00000299871.5:c.129+42C>T
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000240731
  ensembl transcript: ENST00000240731
  gene symbol: ZNF211
  hgvsc: ENST00000240731.4:c.129+42C>T
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000442601
  ensembl transcript: ENST00000541801
  gene symbol: ZNF211
  hgvsc: ENST00000541801.1:c.-93-526C>T
  variant of: http://identifiers.org/hgnc/13003
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3368
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8883
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3369
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3396
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 659
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1434
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1259
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5749
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12555
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2053
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9931
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2656
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 942
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 842
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
population: East Asian
population: Other
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

19-58145472-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58145472
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 58145472
    reference: chr 19
allele count: 1
allele frequency: 9.038159107752934e-6
allele num: 110642
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000399193
  ensembl transcript: ENST00000420680
  gene symbol: ZNF211
  hgvsc: ENST00000420680.1:c.103-525C>T
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000254182
  ensembl transcript: ENST00000254182
  gene symbol: ZNF211
  hgvsc: ENST00000254182.7:c.-94+43C>T
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000441386
  ensembl transcript: ENST00000544273
  gene symbol: ZNF211
  hgvsc: ENST00000544273.1:c.126+43C>T
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000240731
  ensembl transcript: ENST00000240731
  gene symbol: ZNF211
  hgvsc: ENST00000240731.4:c.129+43C>T
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000375584
  ensembl transcript: ENST00000391703
  gene symbol: ZNF211
  hgvsc: ENST00000391703.3:c.-93-525C>T
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000442740
  ensembl transcript: ENST00000535785
  gene symbol: ZNF211
  hgvsc: ENST00000535785.1:c.*184+43C>T
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000442601
  ensembl transcript: ENST00000541801
  gene symbol: ZNF211
  hgvsc: ENST00000541801.1:c.-93-525C>T
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000121417
  ensembl transcript: ENST00000542008
  gene symbol: ZNF211
  hgvsc: ENST00000542008.1:n.351C>T
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000440793
  ensembl transcript: ENST00000540556
  gene symbol: ZNF211
  hgvsc: ENST00000540556.1:c.*132+43C>T
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000339562
  ensembl transcript: ENST00000347302
  gene symbol: ZNF211
  hgvsc: ENST00000347302.3:c.91-525C>T
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000384436
  ensembl transcript: ENST00000407202
  gene symbol: ZNF211
  hgvsc: ENST00000407202.2:c.101-525C>T
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000299871
  ensembl transcript: ENST00000299871
  gene symbol: ZNF211
  hgvsc: ENST00000299871.5:c.129+43C>T
  variant of: http://identifiers.org/hgnc/13003
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2661
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 664
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9946
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12514
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3378
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 988
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1425
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 842
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2053
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8868
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5742
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3409
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3395
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 942
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1259
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
reference allele: C
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD

http://identifiers.org/exac.variant/19-58145474-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58145474
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 58145474
    reference: chr 19
allele count: 4
allele frequency: 3.616571128912678e-5
allele num: 110602
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000440793
  ensembl transcript: ENST00000540556
  gene symbol: ZNF211
  hgvsc: ENST00000540556.1:c.*132+45C>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000399193
  ensembl transcript: ENST00000420680
  gene symbol: ZNF211
  hgvsc: ENST00000420680.1:c.103-523C>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000441386
  ensembl transcript: ENST00000544273
  gene symbol: ZNF211
  hgvsc: ENST00000544273.1:c.126+45C>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000299871
  ensembl transcript: ENST00000299871
  gene symbol: ZNF211
  hgvsc: ENST00000299871.5:c.129+45C>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000442740
  ensembl transcript: ENST00000535785
  gene symbol: ZNF211
  hgvsc: ENST00000535785.1:c.*184+45C>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000240731
  ensembl transcript: ENST00000240731
  gene symbol: ZNF211
  hgvsc: ENST00000240731.4:c.129+45C>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000254182
  ensembl transcript: ENST00000254182
  gene symbol: ZNF211
  hgvsc: ENST00000254182.7:c.-94+45C>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000442601
  ensembl transcript: ENST00000541801
  gene symbol: ZNF211
  hgvsc: ENST00000541801.1:c.-93-523C>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000339562
  ensembl transcript: ENST00000347302
  gene symbol: ZNF211
  hgvsc: ENST00000347302.3:c.91-523C>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000121417
  ensembl transcript: ENST00000542008
  gene symbol: ZNF211
  hgvsc: ENST00000542008.1:n.353C>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000375584
  ensembl transcript: ENST00000391703
  gene symbol: ZNF211
  hgvsc: ENST00000391703.3:c.-93-523C>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000384436
  ensembl transcript: ENST00000407202
  gene symbol: ZNF211
  hgvsc: ENST00000407202.2:c.101-523C>A
  variant of: http://identifiers.org/hgnc/13003
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3350
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 661
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1257
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5709
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9228
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11600
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 842
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 942
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2051
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1428
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5215
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 988
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8715
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2661
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3392
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: South Asian
reference allele: C
site quality: FS
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD

19-58145479-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58145479
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 58145479
    reference: chr 19
allele count: 1
allele frequency: 9.055182280819313e-6
allele num: 110434
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000339562
  ensembl transcript: ENST00000347302
  gene symbol: ZNF211
  hgvsc: ENST00000347302.3:c.91-518C>T
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000441386
  ensembl transcript: ENST00000544273
  gene symbol: ZNF211
  hgvsc: ENST00000544273.1:c.126+50C>T
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000384436
  ensembl transcript: ENST00000407202
  gene symbol: ZNF211
  hgvsc: ENST00000407202.2:c.101-518C>T
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000121417
  ensembl transcript: ENST00000542008
  gene symbol: ZNF211
  hgvsc: ENST00000542008.1:n.358C>T
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000375584
  ensembl transcript: ENST00000391703
  gene symbol: ZNF211
  hgvsc: ENST00000391703.3:c.-93-518C>T
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000442601
  ensembl transcript: ENST00000541801
  gene symbol: ZNF211
  hgvsc: ENST00000541801.1:c.-93-518C>T
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000240731
  ensembl transcript: ENST00000240731
  gene symbol: ZNF211
  hgvsc: ENST00000240731.4:c.129+50C>T
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000399193
  ensembl transcript: ENST00000420680
  gene symbol: ZNF211
  hgvsc: ENST00000420680.1:c.103-518C>T
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000254182
  ensembl transcript: ENST00000254182
  gene symbol: ZNF211
  hgvsc: ENST00000254182.7:c.-94+50C>T
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000442740
  ensembl transcript: ENST00000535785
  gene symbol: ZNF211
  hgvsc: ENST00000535785.1:c.*184+50C>T
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000299871
  ensembl transcript: ENST00000299871
  gene symbol: ZNF211
  hgvsc: ENST00000299871.5:c.129+50C>T
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000440793
  ensembl transcript: ENST00000540556
  gene symbol: ZNF211
  hgvsc: ENST00000540556.1:c.*132+50C>T
  variant of: http://identifiers.org/hgnc/13003
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3347
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6107
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9439
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1257
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2050
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3383
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 989
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10695
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5692
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2640
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1429
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 684
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 942
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8528
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 842
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
population: African
reference allele: C
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum

19-58145480-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58145480
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 58145480
    reference: chr 19
allele count: 3
allele frequency: 2.717440533342995e-5
allele num: 110398
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000254182
  ensembl transcript: ENST00000254182
  gene symbol: ZNF211
  hgvsc: ENST00000254182.7:c.-94+51T>C
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000440793
  ensembl transcript: ENST00000540556
  gene symbol: ZNF211
  hgvsc: ENST00000540556.1:c.*132+51T>C
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000442740
  ensembl transcript: ENST00000535785
  gene symbol: ZNF211
  hgvsc: ENST00000535785.1:c.*184+51T>C
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000441386
  ensembl transcript: ENST00000544273
  gene symbol: ZNF211
  hgvsc: ENST00000544273.1:c.126+51T>C
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000442601
  ensembl transcript: ENST00000541801
  gene symbol: ZNF211
  hgvsc: ENST00000541801.1:c.-93-517T>C
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000121417
  ensembl transcript: ENST00000542008
  gene symbol: ZNF211
  hgvsc: ENST00000542008.1:n.359T>C
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000384436
  ensembl transcript: ENST00000407202
  gene symbol: ZNF211
  hgvsc: ENST00000407202.2:c.101-517T>C
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000240731
  ensembl transcript: ENST00000240731
  gene symbol: ZNF211
  hgvsc: ENST00000240731.4:c.129+51T>C
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000399193
  ensembl transcript: ENST00000420680
  gene symbol: ZNF211
  hgvsc: ENST00000420680.1:c.103-517T>C
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000299871
  ensembl transcript: ENST00000299871
  gene symbol: ZNF211
  hgvsc: ENST00000299871.5:c.129+51T>C
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000375584
  ensembl transcript: ENST00000391703
  gene symbol: ZNF211
  hgvsc: ENST00000391703.3:c.-93-517T>C
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000339562
  ensembl transcript: ENST00000347302
  gene symbol: ZNF211
  hgvsc: ENST00000347302.3:c.91-517T>C
  variant of: http://identifiers.org/hgnc/13003
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 942
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3352
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9571
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2633
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8484
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 989
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5682
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1257
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1426
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10510
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 6210
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3383
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 842
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
reference allele: T
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/19-58145949-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58145949
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 58145949
    reference: chr 19
allele count: 1
allele frequency: 8.898697230725422e-6
allele num: 112376
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000442601
  ensembl transcript: ENST00000541801
  gene symbol: ZNF211
  hgvsc: ENST00000541801.1:c.-93-48C>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000254182
  ensembl transcript: ENST00000254182
  gene symbol: ZNF211
  hgvsc: ENST00000254182.7:c.-93-48C>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000441386
  ensembl transcript: ENST00000544273
  gene symbol: ZNF211
  hgvsc: ENST00000544273.1:c.127-48C>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000440793
  ensembl transcript: ENST00000540556
  gene symbol: ZNF211
  hgvsc: ENST00000540556.1:c.*133-48C>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000339562
  ensembl transcript: ENST00000347302
  gene symbol: ZNF211
  hgvsc: ENST00000347302.3:c.91-48C>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000399193
  ensembl transcript: ENST00000420680
  gene symbol: ZNF211
  hgvsc: ENST00000420680.1:c.103-48C>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000384436
  ensembl transcript: ENST00000407202
  gene symbol: ZNF211
  hgvsc: ENST00000407202.2:c.101-48C>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000240731
  ensembl transcript: ENST00000240731
  gene symbol: ZNF211
  hgvsc: ENST00000240731.4:c.130-48C>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000442740
  ensembl transcript: ENST00000535785
  gene symbol: ZNF211
  hgvsc: ENST00000535785.1:c.*185-48C>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000299871
  ensembl transcript: ENST00000299871
  gene symbol: ZNF211
  hgvsc: ENST00000299871.5:c.130-48C>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000375584
  ensembl transcript: ENST00000391703
  gene symbol: ZNF211
  hgvsc: ENST00000391703.3:c.-93-48C>A
  variant of: http://identifiers.org/hgnc/13003
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4000
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2939
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1375
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6607
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4587
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1000
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5566
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1401
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1999
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2554
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3058
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6355
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 831
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 831
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6931
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5206
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4481
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 314
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
population: East Asian
population: African
population: European (Finnish)
reference allele: C
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum

19-58145949-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58145949
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 58145949
    reference: chr 19
allele count: 1
allele frequency: 8.898697230725422e-6
allele num: 112376
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000384436
  ensembl transcript: ENST00000407202
  gene symbol: ZNF211
  hgvsc: ENST00000407202.2:c.101-48C>T
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000240731
  ensembl transcript: ENST00000240731
  gene symbol: ZNF211
  hgvsc: ENST00000240731.4:c.130-48C>T
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000442601
  ensembl transcript: ENST00000541801
  gene symbol: ZNF211
  hgvsc: ENST00000541801.1:c.-93-48C>T
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000299871
  ensembl transcript: ENST00000299871
  gene symbol: ZNF211
  hgvsc: ENST00000299871.5:c.130-48C>T
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000440793
  ensembl transcript: ENST00000540556
  gene symbol: ZNF211
  hgvsc: ENST00000540556.1:c.*133-48C>T
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000375584
  ensembl transcript: ENST00000391703
  gene symbol: ZNF211
  hgvsc: ENST00000391703.3:c.-93-48C>T
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000339562
  ensembl transcript: ENST00000347302
  gene symbol: ZNF211
  hgvsc: ENST00000347302.3:c.91-48C>T
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000442740
  ensembl transcript: ENST00000535785
  gene symbol: ZNF211
  hgvsc: ENST00000535785.1:c.*185-48C>T
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000254182
  ensembl transcript: ENST00000254182
  gene symbol: ZNF211
  hgvsc: ENST00000254182.7:c.-93-48C>T
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000399193
  ensembl transcript: ENST00000420680
  gene symbol: ZNF211
  hgvsc: ENST00000420680.1:c.103-48C>T
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000441386
  ensembl transcript: ENST00000544273
  gene symbol: ZNF211
  hgvsc: ENST00000544273.1:c.127-48C>T
  variant of: http://identifiers.org/hgnc/13003
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3058
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1000
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2554
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2939
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6931
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1401
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 831
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4481
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4000
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1375
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5206
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 831
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6355
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6607
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1999
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5566
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4587
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Other
population: Latino
reference allele: C
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP

19-58145957-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58145957
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 58145957
    reference: chr 19
allele count: 2
allele frequency: 1.777682968019483e-5
allele num: 112506
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000299871
  ensembl transcript: ENST00000299871
  gene symbol: ZNF211
  hgvsc: ENST00000299871.5:c.130-40T>C
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000384436
  ensembl transcript: ENST00000407202
  gene symbol: ZNF211
  hgvsc: ENST00000407202.2:c.101-40T>C
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000441386
  ensembl transcript: ENST00000544273
  gene symbol: ZNF211
  hgvsc: ENST00000544273.1:c.127-40T>C
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000254182
  ensembl transcript: ENST00000254182
  gene symbol: ZNF211
  hgvsc: ENST00000254182.7:c.-93-40T>C
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000399193
  ensembl transcript: ENST00000420680
  gene symbol: ZNF211
  hgvsc: ENST00000420680.1:c.103-40T>C
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000442601
  ensembl transcript: ENST00000541801
  gene symbol: ZNF211
  hgvsc: ENST00000541801.1:c.-93-40T>C
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000442740
  ensembl transcript: ENST00000535785
  gene symbol: ZNF211
  hgvsc: ENST00000535785.1:c.*185-40T>C
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000240731
  ensembl transcript: ENST00000240731
  gene symbol: ZNF211
  hgvsc: ENST00000240731.4:c.130-40T>C
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000375584
  ensembl transcript: ENST00000391703
  gene symbol: ZNF211
  hgvsc: ENST00000391703.3:c.-93-40T>C
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000339562
  ensembl transcript: ENST00000347302
  gene symbol: ZNF211
  hgvsc: ENST00000347302.3:c.91-40T>C
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000440793
  ensembl transcript: ENST00000540556
  gene symbol: ZNF211
  hgvsc: ENST00000540556.1:c.*133-40T>C
  variant of: http://identifiers.org/hgnc/13003
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6931
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1376
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5208
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1000
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2554
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3173
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4587
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6355
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 831
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3999
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1998
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4486
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2939
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5563
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1239
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 865
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6605
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 512
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: T
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: QD

19-58145959-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58145959
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 58145959
    reference: chr 19
allele count: 2
allele frequency: 1.77724065615725e-5
allele num: 112534
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000440793
  ensembl transcript: ENST00000540556
  gene symbol: ZNF211
  hgvsc: ENST00000540556.1:c.*133-38G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000384436
  ensembl transcript: ENST00000407202
  gene symbol: ZNF211
  hgvsc: ENST00000407202.2:c.101-38G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000240731
  ensembl transcript: ENST00000240731
  gene symbol: ZNF211
  hgvsc: ENST00000240731.4:c.130-38G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000299871
  ensembl transcript: ENST00000299871
  gene symbol: ZNF211
  hgvsc: ENST00000299871.5:c.130-38G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000399193
  ensembl transcript: ENST00000420680
  gene symbol: ZNF211
  hgvsc: ENST00000420680.1:c.103-38G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000375584
  ensembl transcript: ENST00000391703
  gene symbol: ZNF211
  hgvsc: ENST00000391703.3:c.-93-38G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000442740
  ensembl transcript: ENST00000535785
  gene symbol: ZNF211
  hgvsc: ENST00000535785.1:c.*185-38G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000339562
  ensembl transcript: ENST00000347302
  gene symbol: ZNF211
  hgvsc: ENST00000347302.3:c.91-38G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000254182
  ensembl transcript: ENST00000254182
  gene symbol: ZNF211
  hgvsc: ENST00000254182.7:c.-93-38G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000442601
  ensembl transcript: ENST00000541801
  gene symbol: ZNF211
  hgvsc: ENST00000541801.1:c.-93-38G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000441386
  ensembl transcript: ENST00000544273
  gene symbol: ZNF211
  hgvsc: ENST00000544273.1:c.127-38G>A
  variant of: http://identifiers.org/hgnc/13003
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6606
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 608
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 877
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6355
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1146
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4486
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1997
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3250
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3998
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5208
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6931
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2556
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2940
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4587
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5563
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1000
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 831
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1375
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: African
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff

19-58145960-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58145960
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 58145960
    reference: chr 19
allele count: 1
allele frequency: 8.886992997049519e-6
allele num: 112524
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000299871
  ensembl transcript: ENST00000299871
  gene symbol: ZNF211
  hgvsc: ENST00000299871.5:c.130-37A>T
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000240731
  ensembl transcript: ENST00000240731
  gene symbol: ZNF211
  hgvsc: ENST00000240731.4:c.130-37A>T
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000399193
  ensembl transcript: ENST00000420680
  gene symbol: ZNF211
  hgvsc: ENST00000420680.1:c.103-37A>T
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000442601
  ensembl transcript: ENST00000541801
  gene symbol: ZNF211
  hgvsc: ENST00000541801.1:c.-93-37A>T
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000375584
  ensembl transcript: ENST00000391703
  gene symbol: ZNF211
  hgvsc: ENST00000391703.3:c.-93-37A>T
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000384436
  ensembl transcript: ENST00000407202
  gene symbol: ZNF211
  hgvsc: ENST00000407202.2:c.101-37A>T
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000442740
  ensembl transcript: ENST00000535785
  gene symbol: ZNF211
  hgvsc: ENST00000535785.1:c.*185-37A>T
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000254182
  ensembl transcript: ENST00000254182
  gene symbol: ZNF211
  hgvsc: ENST00000254182.7:c.-93-37A>T
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000441386
  ensembl transcript: ENST00000544273
  gene symbol: ZNF211
  hgvsc: ENST00000544273.1:c.127-37A>T
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000339562
  ensembl transcript: ENST00000347302
  gene symbol: ZNF211
  hgvsc: ENST00000347302.3:c.91-37A>T
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000440793
  ensembl transcript: ENST00000540556
  gene symbol: ZNF211
  hgvsc: ENST00000540556.1:c.*133-37A>T
  variant of: http://identifiers.org/hgnc/13003
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1998
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 887
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3998
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1000
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6606
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6355
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1106
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2557
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3281
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1375
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5207
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6932
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 831
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4485
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2939
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5565
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4587
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1218
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
reference allele: A
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD

http://identifiers.org/exac.variant/19-58145977-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58145977
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 58145977
    reference: chr 19
allele count: 1
allele frequency: 8.843296781039971e-6
allele num: 113080
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000375584
  ensembl transcript: ENST00000391703
  gene symbol: ZNF211
  hgvsc: ENST00000391703.3:c.-93-20A>C
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000442740
  ensembl transcript: ENST00000535785
  gene symbol: ZNF211
  hgvsc: ENST00000535785.1:c.*185-20A>C
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000299871
  ensembl transcript: ENST00000299871
  gene symbol: ZNF211
  hgvsc: ENST00000299871.5:c.130-20A>C
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000384436
  ensembl transcript: ENST00000407202
  gene symbol: ZNF211
  hgvsc: ENST00000407202.2:c.101-20A>C
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000254182
  ensembl transcript: ENST00000254182
  gene symbol: ZNF211
  hgvsc: ENST00000254182.7:c.-93-20A>C
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000440793
  ensembl transcript: ENST00000540556
  gene symbol: ZNF211
  hgvsc: ENST00000540556.1:c.*133-20A>C
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000240731
  ensembl transcript: ENST00000240731
  gene symbol: ZNF211
  hgvsc: ENST00000240731.4:c.130-20A>C
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000399193
  ensembl transcript: ENST00000420680
  gene symbol: ZNF211
  hgvsc: ENST00000420680.1:c.103-20A>C
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000339562
  ensembl transcript: ENST00000347302
  gene symbol: ZNF211
  hgvsc: ENST00000347302.3:c.91-20A>C
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000442601
  ensembl transcript: ENST00000541801
  gene symbol: ZNF211
  hgvsc: ENST00000541801.1:c.-93-20A>C
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000441386
  ensembl transcript: ENST00000544273
  gene symbol: ZNF211
  hgvsc: ENST00000544273.1:c.127-20A>C
  variant of: http://identifiers.org/hgnc/13003
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3581
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5206
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2565
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6356
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1997
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4587
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1001
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6606
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 989
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4485
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 831
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1375
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2939
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6932
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5565
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3998
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 375
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
population: African
population: East Asian
population: South Asian
reference allele: A
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum

19-58145983-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58145983
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 58145983
    reference: chr 19
allele count: 1
allele frequency: 8.824100382965956e-6
allele num: 113326
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000240731
  ensembl transcript: ENST00000240731
  gene symbol: ZNF211
  hgvsc: ENST00000240731.4:c.130-14C>T
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000339562
  ensembl transcript: ENST00000347302
  gene symbol: ZNF211
  hgvsc: ENST00000347302.3:c.91-14C>T
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000442601
  ensembl transcript: ENST00000541801
  gene symbol: ZNF211
  hgvsc: ENST00000541801.1:c.-93-14C>T
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000442740
  ensembl transcript: ENST00000535785
  gene symbol: ZNF211
  hgvsc: ENST00000535785.1:c.*185-14C>T
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000440793
  ensembl transcript: ENST00000540556
  gene symbol: ZNF211
  hgvsc: ENST00000540556.1:c.*133-14C>T
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000384436
  ensembl transcript: ENST00000407202
  gene symbol: ZNF211
  hgvsc: ENST00000407202.2:c.101-14C>T
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000375584
  ensembl transcript: ENST00000391703
  gene symbol: ZNF211
  hgvsc: ENST00000391703.3:c.-93-14C>T
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000441386
  ensembl transcript: ENST00000544273
  gene symbol: ZNF211
  hgvsc: ENST00000544273.1:c.127-14C>T
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000399193
  ensembl transcript: ENST00000420680
  gene symbol: ZNF211
  hgvsc: ENST00000420680.1:c.103-14C>T
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000299871
  ensembl transcript: ENST00000299871
  gene symbol: ZNF211
  hgvsc: ENST00000299871.5:c.130-14C>T
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000254182
  ensembl transcript: ENST00000254182
  gene symbol: ZNF211
  hgvsc: ENST00000254182.7:c.-93-14C>T
  variant of: http://identifiers.org/hgnc/13003
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5206
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1375
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3579
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6932
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1016
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4588
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5565
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6356
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2572
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6607
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2939
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 831
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1996
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1000
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4486
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3998
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 132
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: South Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: QD

19-58145989-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58145989
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 58145989
    reference: chr 19
allele count: 1
allele frequency: 8.793837278834993e-6
allele num: 113716
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000339562
  ensembl transcript: ENST00000347302
  gene symbol: ZNF211
  hgvsc: ENST00000347302.3:c.91-8T>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000375584
  ensembl transcript: ENST00000391703
  gene symbol: ZNF211
  hgvsc: ENST00000391703.3:c.-93-8T>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000240731
  ensembl transcript: ENST00000240731
  gene symbol: ZNF211
  hgvsc: ENST00000240731.4:c.130-8T>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000254182
  ensembl transcript: ENST00000254182
  gene symbol: ZNF211
  hgvsc: ENST00000254182.7:c.-93-8T>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000441386
  ensembl transcript: ENST00000544273
  gene symbol: ZNF211
  hgvsc: ENST00000544273.1:c.127-8T>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000440793
  ensembl transcript: ENST00000540556
  gene symbol: ZNF211
  hgvsc: ENST00000540556.1:c.*133-8T>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000384436
  ensembl transcript: ENST00000407202
  gene symbol: ZNF211
  hgvsc: ENST00000407202.2:c.101-8T>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000442740
  ensembl transcript: ENST00000535785
  gene symbol: ZNF211
  hgvsc: ENST00000535785.1:c.*185-8T>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000399193
  ensembl transcript: ENST00000420680
  gene symbol: ZNF211
  hgvsc: ENST00000420680.1:c.103-8T>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000299871
  ensembl transcript: ENST00000299871
  gene symbol: ZNF211
  hgvsc: ENST00000299871.5:c.130-8T>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000442601
  ensembl transcript: ENST00000541801
  gene symbol: ZNF211
  hgvsc: ENST00000541801.1:c.-93-8T>G
  variant of: http://identifiers.org/hgnc/13003
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3521
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 668
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5565
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4488
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1011
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6932
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1995
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2580
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1375
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2939
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4588
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6357
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 831
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6607
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1000
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.130-8T>G
num of homozygotes: 0
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: African
reference allele: T
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum

19-58145991-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58145991
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 58145991
    reference: chr 19
allele count: 1
allele frequency: 8.783024170882518e-6
allele num: 113856
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000440793
  ensembl transcript: ENST00000540556
  gene symbol: ZNF211
  hgvsc: ENST00000540556.1:c.*133-6T>C
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000384436
  ensembl transcript: ENST00000407202
  gene symbol: ZNF211
  hgvsc: ENST00000407202.2:c.101-6T>C
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000339562
  ensembl transcript: ENST00000347302
  gene symbol: ZNF211
  hgvsc: ENST00000347302.3:c.91-6T>C
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000399193
  ensembl transcript: ENST00000420680
  gene symbol: ZNF211
  hgvsc: ENST00000420680.1:c.103-6T>C
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000254182
  ensembl transcript: ENST00000254182
  gene symbol: ZNF211
  hgvsc: ENST00000254182.7:c.-93-6T>C
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000240731
  ensembl transcript: ENST00000240731
  gene symbol: ZNF211
  hgvsc: ENST00000240731.4:c.130-6T>C
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000442740
  ensembl transcript: ENST00000535785
  gene symbol: ZNF211
  hgvsc: ENST00000535785.1:c.*185-6T>C
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000299871
  ensembl transcript: ENST00000299871
  gene symbol: ZNF211
  hgvsc: ENST00000299871.5:c.130-6T>C
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000375584
  ensembl transcript: ENST00000391703
  gene symbol: ZNF211
  hgvsc: ENST00000391703.3:c.-93-6T>C
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000441386
  ensembl transcript: ENST00000544273
  gene symbol: ZNF211
  hgvsc: ENST00000544273.1:c.127-6T>C
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000442601
  ensembl transcript: ENST00000541801
  gene symbol: ZNF211
  hgvsc: ENST00000541801.1:c.-93-6T>C
  variant of: http://identifiers.org/hgnc/13003
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 731
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5206
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 831
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1995
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3494
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6358
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4490
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1008
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1375
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4588
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3998
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5565
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6932
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1000
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2581
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6607
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.130-6T>C
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
population: Other
reference allele: T
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD

19-58145996-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58145996
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 58145996
    reference: chr 19
allele count: 1
allele frequency: 8.741717222931273e-6
allele num: 114394
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000441386
  ensembl transcript: ENST00000544273
  gene symbol: ZNF211
  hgvsc: ENST00000544273.1:c.127-1G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000254182
  ensembl transcript: ENST00000254182
  gene symbol: ZNF211
  hgvsc: ENST00000254182.7:c.-93-1G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000440793
  ensembl transcript: ENST00000540556
  gene symbol: ZNF211
  hgvsc: ENST00000540556.1:c.*133-1G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000399193
  ensembl transcript: ENST00000420680
  gene symbol: ZNF211
  hgvsc: ENST00000420680.1:c.103-1G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000375584
  ensembl transcript: ENST00000391703
  gene symbol: ZNF211
  hgvsc: ENST00000391703.3:c.-93-1G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000240731
  ensembl transcript: ENST00000240731
  gene symbol: ZNF211
  hgvsc: ENST00000240731.4:c.130-1G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000442740
  ensembl transcript: ENST00000535785
  gene symbol: ZNF211
  hgvsc: ENST00000535785.1:c.*185-1G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000384436
  ensembl transcript: ENST00000407202
  gene symbol: ZNF211
  hgvsc: ENST00000407202.2:c.101-1G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: true
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000299871
  ensembl transcript: ENST00000299871
  gene symbol: ZNF211
  hgvsc: ENST00000299871.5:c.130-1G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000442601
  ensembl transcript: ENST00000541801
  gene symbol: ZNF211
  hgvsc: ENST00000541801.1:c.-93-1G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000339562
  ensembl transcript: ENST00000347302
  gene symbol: ZNF211
  hgvsc: ENST00000347302.3:c.91-1G>A
  variant of: http://identifiers.org/hgnc/13003
canonical: true
consequence: splice acceptor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1995
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3291
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 989
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6607
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 968
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6359
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1000
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 832
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2939
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4492
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5206
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6931
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2598
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5564
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3998
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4587
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1375
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3342
  bin: 6.25e1
  variant carriers: 0
hgvs: c.130-1G>A
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
reference allele: G
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum

http://identifiers.org/exac.variant/19-58145999-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58145999
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 58145999
    reference: chr 19
allele count: 1
allele frequency: 8.720220447172904e-6
allele num: 114676
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000384436
  ensembl transcript: ENST00000407202
  gene symbol: ZNF211
  hgvsc: ENST00000407202.2:c.103A>C
  hgvsp: ENST00000407202.2:c.103A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000442740
  ensembl transcript: ENST00000535785
  gene symbol: ZNF211
  hgvsc: ENST00000535785.1:c.*187A>C
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000442601
  ensembl transcript: ENST00000541801
  gene symbol: ZNF211
  hgvsc: ENST00000541801.1:c.-91A>C
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000339562
  ensembl transcript: ENST00000347302
  gene symbol: ZNF211
  hgvsc: ENST00000347302.3:c.93A>C
  hgvsp: ENST00000347302.3:c.93A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000399193
  ensembl transcript: ENST00000420680
  gene symbol: ZNF211
  hgvsc: ENST00000420680.1:c.105A>C
  hgvsp: ENST00000420680.1:c.105A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000375584
  ensembl transcript: ENST00000391703
  gene symbol: ZNF211
  hgvsc: ENST00000391703.3:c.-91A>C
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000240731
  ensembl transcript: ENST00000240731
  gene symbol: ZNF211
  hgvsc: ENST00000240731.4:c.132A>C
  hgvsp: ENST00000240731.4:c.132A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000440793
  ensembl transcript: ENST00000540556
  gene symbol: ZNF211
  hgvsc: ENST00000540556.1:c.*135A>C
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000441386
  ensembl transcript: ENST00000544273
  gene symbol: ZNF211
  hgvsc: ENST00000544273.1:c.129A>C
  hgvsp: ENST00000544273.1:c.129A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000299871
  ensembl transcript: ENST00000299871
  gene symbol: ZNF211
  hgvsc: ENST00000299871.5:c.132A>C
  hgvsp: ENST00000299871.5:c.132A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000254182
  ensembl transcript: ENST00000254182
  gene symbol: ZNF211
  hgvsc: ENST00000254182.7:c.-91A>C
  variant of: http://identifiers.org/hgnc/13003
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1375
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3196
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6359
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1995
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1109
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5205
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6931
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2608
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6608
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1001
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3998
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5564
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 957
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4493
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.132A>C
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Other
population: European (Finnish)
population: East Asian
population: African
population: Latino
reference allele: A
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum

19-58146023-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58146023
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 58146023
    reference: chr 19
allele count: 1
allele frequency: 8.509624385179638e-6
allele num: 117514
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000440793
  ensembl transcript: ENST00000540556
  gene symbol: ZNF211
  hgvsc: ENST00000540556.1:c.*159C>T
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000442601
  ensembl transcript: ENST00000541801
  gene symbol: ZNF211
  hgvsc: ENST00000541801.1:c.-67C>T
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000339562
  ensembl transcript: ENST00000347302
  gene symbol: ZNF211
  hgvsc: ENST00000347302.3:c.117C>T
  hgvsp: ENST00000347302.3:c.117C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000384436
  ensembl transcript: ENST00000407202
  gene symbol: ZNF211
  hgvsc: ENST00000407202.2:c.127C>T
  hgvsp: ENST00000407202.2:c.127C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000375584
  ensembl transcript: ENST00000391703
  gene symbol: ZNF211
  hgvsc: ENST00000391703.3:c.-67C>T
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000254182
  ensembl transcript: ENST00000254182
  gene symbol: ZNF211
  hgvsc: ENST00000254182.7:c.-67C>T
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000441386
  ensembl transcript: ENST00000544273
  gene symbol: ZNF211
  hgvsc: ENST00000544273.1:c.153C>T
  hgvsp: ENST00000544273.1:c.153C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000399193
  ensembl transcript: ENST00000420680
  gene symbol: ZNF211
  hgvsc: ENST00000420680.1:c.129C>T
  hgvsp: ENST00000420680.1:c.129C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000442740
  ensembl transcript: ENST00000535785
  gene symbol: ZNF211
  hgvsc: ENST00000535785.1:c.*211C>T
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000240731
  ensembl transcript: ENST00000240731
  gene symbol: ZNF211
  hgvsc: ENST00000240731.4:c.156C>T
  hgvsp: ENST00000240731.4:c.156C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000299871
  ensembl transcript: ENST00000299871
  gene symbol: ZNF211
  hgvsc: ENST00000299871.5:c.156C>T
  hgvsp: ENST00000299871.5:c.156C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13003
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1862
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6359
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 831
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6608
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 536
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5205
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2691
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1375
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4516
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2854
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 999
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3998
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2939
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6931
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1995
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4588
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Ala52Ala
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
population: African
population: Latino
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: DP

19-58146036-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58146036
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 58146036
    reference: chr 19
allele count: 1
allele frequency: 8.422613031466883e-6
allele num: 118728
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000299871
  ensembl transcript: ENST00000299871
  gene symbol: ZNF211
  hgvsc: ENST00000299871.5:c.169T>C
  hgvsp: ENSP00000299871.5:p.Trp57Arg
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000440793
  ensembl transcript: ENST00000540556
  gene symbol: ZNF211
  hgvsc: ENST00000540556.1:c.*172T>C
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000375584
  ensembl transcript: ENST00000391703
  gene symbol: ZNF211
  hgvsc: ENST00000391703.3:c.-54T>C
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000384436
  ensembl transcript: ENST00000407202
  gene symbol: ZNF211
  hgvsc: ENST00000407202.2:c.140T>C
  hgvsp: ENSP00000384436.2:p.Trp48Arg
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000399193
  ensembl transcript: ENST00000420680
  gene symbol: ZNF211
  hgvsc: ENST00000420680.1:c.142T>C
  hgvsp: ENSP00000399193.1:p.Trp48Arg
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000254182
  ensembl transcript: ENST00000254182
  gene symbol: ZNF211
  hgvsc: ENST00000254182.7:c.-54T>C
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000240731
  ensembl transcript: ENST00000240731
  gene symbol: ZNF211
  hgvsc: ENST00000240731.4:c.169T>C
  hgvsp: ENSP00000240731.4:p.Trp57Arg
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000442601
  ensembl transcript: ENST00000541801
  gene symbol: ZNF211
  hgvsc: ENST00000541801.1:c.-54T>C
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000442740
  ensembl transcript: ENST00000535785
  gene symbol: ZNF211
  hgvsc: ENST00000535785.1:c.*224T>C
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000441386
  ensembl transcript: ENST00000544273
  gene symbol: ZNF211
  hgvsc: ENST00000544273.1:c.166T>C
  hgvsp: ENSP00000441386.1:p.Trp56Arg
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000339562
  ensembl transcript: ENST00000347302
  gene symbol: ZNF211
  hgvsc: ENST00000347302.3:c.130T>C
  hgvsp: ENSP00000339562.3:p.Trp44Arg
  variant of: http://identifiers.org/hgnc/13003
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5205
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2994
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5567
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 999
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1308
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4588
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6608
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3365
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1375
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1995
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2939
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3998
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 831
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4519
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6931
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Trp57Arg
num of homozygotes: 0
population: East Asian
population: Other
population: South Asian
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: T
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum

19-58146039-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58146039
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 58146039
    reference: chr 19
allele count: 1
allele frequency: 8.40279645065878e-6
allele num: 119008
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000254182
  ensembl transcript: ENST00000254182
  gene symbol: ZNF211
  hgvsc: ENST00000254182.7:c.-51G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000384436
  ensembl transcript: ENST00000407202
  gene symbol: ZNF211
  hgvsc: ENST00000407202.2:c.143G>A
  hgvsp: ENSP00000384436.2:p.Glu49Lys
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000441386
  ensembl transcript: ENST00000544273
  gene symbol: ZNF211
  hgvsc: ENST00000544273.1:c.169G>A
  hgvsp: ENSP00000441386.1:p.Glu57Lys
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000399193
  ensembl transcript: ENST00000420680
  gene symbol: ZNF211
  hgvsc: ENST00000420680.1:c.145G>A
  hgvsp: ENSP00000399193.1:p.Glu49Lys
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000240731
  ensembl transcript: ENST00000240731
  gene symbol: ZNF211
  hgvsc: ENST00000240731.4:c.172G>A
  hgvsp: ENSP00000240731.4:p.Glu58Lys
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000299871
  ensembl transcript: ENST00000299871
  gene symbol: ZNF211
  hgvsc: ENST00000299871.5:c.172G>A
  hgvsp: ENSP00000299871.5:p.Glu58Lys
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000339562
  ensembl transcript: ENST00000347302
  gene symbol: ZNF211
  hgvsc: ENST00000347302.3:c.133G>A
  hgvsp: ENSP00000339562.3:p.Glu45Lys
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000440793
  ensembl transcript: ENST00000540556
  gene symbol: ZNF211
  hgvsc: ENST00000540556.1:c.*175G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000375584
  ensembl transcript: ENST00000391703
  gene symbol: ZNF211
  hgvsc: ENST00000391703.3:c.-51G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000442601
  ensembl transcript: ENST00000541801
  gene symbol: ZNF211
  hgvsc: ENST00000541801.1:c.-51G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000442740
  ensembl transcript: ENST00000535785
  gene symbol: ZNF211
  hgvsc: ENST00000535785.1:c.*227G>A
  variant of: http://identifiers.org/hgnc/13003
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 831
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3537
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5205
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1375
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3997
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6931
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1995
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4588
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1178
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4522
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6609
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6359
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 999
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3019
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2939
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu58Lys
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Other
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff

19-58146047-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58146047
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 58146047
    reference: chr 19
allele count: 1
allele frequency: 8.377454594196099e-6
allele num: 119368
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000442601
  ensembl transcript: ENST00000541801
  gene symbol: ZNF211
  hgvsc: ENST00000541801.1:c.-43G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000441386
  ensembl transcript: ENST00000544273
  gene symbol: ZNF211
  hgvsc: ENST00000544273.1:c.177G>A
  hgvsp: ENSP00000441386.1:p.Trp59Ter
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000442740
  ensembl transcript: ENST00000535785
  gene symbol: ZNF211
  hgvsc: ENST00000535785.1:c.*235G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000384436
  ensembl transcript: ENST00000407202
  gene symbol: ZNF211
  hgvsc: ENST00000407202.2:c.151G>A
  hgvsp: ENSP00000384436.2:p.Trp51Ter
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000339562
  ensembl transcript: ENST00000347302
  gene symbol: ZNF211
  hgvsc: ENST00000347302.3:c.141G>A
  hgvsp: ENSP00000339562.3:p.Trp47Ter
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000375584
  ensembl transcript: ENST00000391703
  gene symbol: ZNF211
  hgvsc: ENST00000391703.3:c.-43G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000399193
  ensembl transcript: ENST00000420680
  gene symbol: ZNF211
  hgvsc: ENST00000420680.1:c.153G>A
  hgvsp: ENSP00000399193.1:p.Trp51Ter
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000240731
  ensembl transcript: ENST00000240731
  gene symbol: ZNF211
  hgvsc: ENST00000240731.4:c.180G>A
  hgvsp: ENSP00000240731.4:p.Trp60Ter
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000254182
  ensembl transcript: ENST00000254182
  gene symbol: ZNF211
  hgvsc: ENST00000254182.7:c.-43G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000440793
  ensembl transcript: ENST00000540556
  gene symbol: ZNF211
  hgvsc: ENST00000540556.1:c.*183G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000299871
  ensembl transcript: ENST00000299871
  gene symbol: ZNF211
  hgvsc: ENST00000299871.5:c.180G>A
  hgvsp: ENSP00000299871.5:p.Trp60Ter
  variant of: http://identifiers.org/hgnc/13003
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6932
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4588
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2939
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 987
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3702
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6609
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5205
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3097
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1375
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1995
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5569
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6358
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3996
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 831
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4525
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Trp60Ter
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum

19-58146050-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58146050
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 58146050
    reference: chr 19
allele count: 1
allele frequency: 8.370021929457456e-6
allele num: 119474
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000442740
  ensembl transcript: ENST00000535785
  gene symbol: ZNF211
  hgvsc: ENST00000535785.1:c.*238T>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000442601
  ensembl transcript: ENST00000541801
  gene symbol: ZNF211
  hgvsc: ENST00000541801.1:c.-40T>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000441386
  ensembl transcript: ENST00000544273
  gene symbol: ZNF211
  hgvsc: ENST00000544273.1:c.180T>G
  hgvsp: ENSP00000441386.1:p.Asp60Glu
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000375584
  ensembl transcript: ENST00000391703
  gene symbol: ZNF211
  hgvsc: ENST00000391703.3:c.-40T>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000440793
  ensembl transcript: ENST00000540556
  gene symbol: ZNF211
  hgvsc: ENST00000540556.1:c.*186T>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000399193
  ensembl transcript: ENST00000420680
  gene symbol: ZNF211
  hgvsc: ENST00000420680.1:c.156T>G
  hgvsp: ENSP00000399193.1:p.Asp52Glu
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000254182
  ensembl transcript: ENST00000254182
  gene symbol: ZNF211
  hgvsc: ENST00000254182.7:c.-40T>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000384436
  ensembl transcript: ENST00000407202
  gene symbol: ZNF211
  hgvsc: ENST00000407202.2:c.154T>G
  hgvsp: ENSP00000384436.2:p.Asp52Glu
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000240731
  ensembl transcript: ENST00000240731
  gene symbol: ZNF211
  hgvsc: ENST00000240731.4:c.183T>G
  hgvsp: ENSP00000240731.4:p.Asp61Glu
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000339562
  ensembl transcript: ENST00000347302
  gene symbol: ZNF211
  hgvsc: ENST00000347302.3:c.144T>G
  hgvsp: ENSP00000339562.3:p.Asp48Glu
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000299871
  ensembl transcript: ENST00000299871
  gene symbol: ZNF211
  hgvsc: ENST00000299871.5:c.183T>G
  hgvsp: ENSP00000299871.5:p.Asp61Glu
  variant of: http://identifiers.org/hgnc/13003
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5567
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 999
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1995
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 949
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6609
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3110
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3750
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6358
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1375
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 608
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2939
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4588
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6932
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5204
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4524
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3996
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp61Glu
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: Other
population: African
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: T
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: ReadPosRankSum

19-58146062-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58146062
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 58146062
    reference: chr 19
allele count: 1
allele frequency: 8.363581620193032e-6
allele num: 119566
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000384436
  ensembl transcript: ENST00000407202
  gene symbol: ZNF211
  hgvsc: ENST00000407202.2:c.166G>A
  hgvsp: ENST00000407202.2:c.166G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000339562
  ensembl transcript: ENST00000347302
  gene symbol: ZNF211
  hgvsc: ENST00000347302.3:c.156G>A
  hgvsp: ENST00000347302.3:c.156G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000442740
  ensembl transcript: ENST00000535785
  gene symbol: ZNF211
  hgvsc: ENST00000535785.1:c.*250G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000375584
  ensembl transcript: ENST00000391703
  gene symbol: ZNF211
  hgvsc: ENST00000391703.3:c.-28G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000441386
  ensembl transcript: ENST00000544273
  gene symbol: ZNF211
  hgvsc: ENST00000544273.1:c.192G>A
  hgvsp: ENST00000544273.1:c.192G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000240731
  ensembl transcript: ENST00000240731
  gene symbol: ZNF211
  hgvsc: ENST00000240731.4:c.195G>A
  hgvsp: ENST00000240731.4:c.195G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000254182
  ensembl transcript: ENST00000254182
  gene symbol: ZNF211
  hgvsc: ENST00000254182.7:c.-28G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000442601
  ensembl transcript: ENST00000541801
  gene symbol: ZNF211
  hgvsc: ENST00000541801.1:c.-28G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000440793
  ensembl transcript: ENST00000540556
  gene symbol: ZNF211
  hgvsc: ENST00000540556.1:c.*198G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000399193
  ensembl transcript: ENST00000420680
  gene symbol: ZNF211
  hgvsc: ENST00000420680.1:c.168G>A
  hgvsp: ENST00000420680.1:c.168G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000299871
  ensembl transcript: ENST00000299871
  gene symbol: ZNF211
  hgvsc: ENST00000299871.5:c.195G>A
  hgvsp: ENST00000299871.5:c.195G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13003
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3640
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5204
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 911
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4587
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4530
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6932
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1995
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3996
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 608
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2939
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6610
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6358
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3204
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5566
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 999
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1375
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu65Glu
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: MQRankSum

19-58146083-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58146083
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 58146083
    reference: chr 19
allele count: 1
allele frequency: 8.406469619018796e-6
allele num: 118956
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000399193
  ensembl transcript: ENST00000420680
  gene symbol: ZNF211
  hgvsc: ENST00000420680.1:c.189C>T
  hgvsp: ENST00000420680.1:c.189C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000442740
  ensembl transcript: ENST00000535785
  gene symbol: ZNF211
  hgvsc: ENST00000535785.1:c.*271C>T
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000384436
  ensembl transcript: ENST00000407202
  gene symbol: ZNF211
  hgvsc: ENST00000407202.2:c.187C>T
  hgvsp: ENST00000407202.2:c.187C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000440793
  ensembl transcript: ENST00000540556
  gene symbol: ZNF211
  hgvsc: ENST00000540556.1:c.*219C>T
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000299871
  ensembl transcript: ENST00000299871
  gene symbol: ZNF211
  hgvsc: ENST00000299871.5:c.216C>T
  hgvsp: ENST00000299871.5:c.216C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000441386
  ensembl transcript: ENST00000544273
  gene symbol: ZNF211
  hgvsc: ENST00000544273.1:c.213C>T
  hgvsp: ENST00000544273.1:c.213C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000240731
  ensembl transcript: ENST00000240731
  gene symbol: ZNF211
  hgvsc: ENST00000240731.4:c.216C>T
  hgvsp: ENST00000240731.4:c.216C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000375584
  ensembl transcript: ENST00000391703
  gene symbol: ZNF211
  hgvsc: ENST00000391703.3:c.-7C>T
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000442601
  ensembl transcript: ENST00000541801
  gene symbol: ZNF211
  hgvsc: ENST00000541801.1:c.-7C>T
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000254182
  ensembl transcript: ENST00000254182
  gene symbol: ZNF211
  hgvsc: ENST00000254182.7:c.-7C>T
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000339562
  ensembl transcript: ENST00000347302
  gene symbol: ZNF211
  hgvsc: ENST00000347302.3:c.177C>T
  hgvsp: ENST00000347302.3:c.177C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13003
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1188
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6932
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4534
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 803
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2939
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3996
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5568
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4588
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2685
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6610
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 999
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3237
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 608
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 831
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5204
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1375
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6358
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Phe72Phe
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
population: African
population: East Asian
population: Other
reference allele: C
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: BaseQRankSum

19-58146084-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58146084
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 58146084
    reference: chr 19
allele count: 2
allele frequency: 1.681322191771609e-5
allele num: 118954
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000384436
  ensembl transcript: ENST00000407202
  gene symbol: ZNF211
  hgvsc: ENST00000407202.2:c.188G>A
  hgvsp: ENSP00000384436.2:p.Asp64Asn
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000442601
  ensembl transcript: ENST00000541801
  gene symbol: ZNF211
  hgvsc: ENST00000541801.1:c.-6G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000299871
  ensembl transcript: ENST00000299871
  gene symbol: ZNF211
  hgvsc: ENST00000299871.5:c.217G>A
  hgvsp: ENSP00000299871.5:p.Asp73Asn
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000339562
  ensembl transcript: ENST00000347302
  gene symbol: ZNF211
  hgvsc: ENST00000347302.3:c.178G>A
  hgvsp: ENSP00000339562.3:p.Asp60Asn
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000254182
  ensembl transcript: ENST00000254182
  gene symbol: ZNF211
  hgvsc: ENST00000254182.7:c.-6G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000375584
  ensembl transcript: ENST00000391703
  gene symbol: ZNF211
  hgvsc: ENST00000391703.3:c.-6G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000441386
  ensembl transcript: ENST00000544273
  gene symbol: ZNF211
  hgvsc: ENST00000544273.1:c.214G>A
  hgvsp: ENSP00000441386.1:p.Asp72Asn
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000240731
  ensembl transcript: ENST00000240731
  gene symbol: ZNF211
  hgvsc: ENST00000240731.4:c.217G>A
  hgvsp: ENSP00000240731.4:p.Asp73Asn
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000399193
  ensembl transcript: ENST00000420680
  gene symbol: ZNF211
  hgvsc: ENST00000420680.1:c.190G>A
  hgvsp: ENSP00000399193.1:p.Asp64Asn
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000440793
  ensembl transcript: ENST00000540556
  gene symbol: ZNF211
  hgvsc: ENST00000540556.1:c.*220G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000442740
  ensembl transcript: ENST00000535785
  gene symbol: ZNF211
  hgvsc: ENST00000535785.1:c.*272G>A
  variant of: http://identifiers.org/hgnc/13003
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 831
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2683
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6611
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3241
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1189
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1995
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6358
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5566
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4531
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 608
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2939
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6932
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3996
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1375
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5204
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 813
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4588
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Asp73Asn
num of homozygotes: 0
population: African
population: Other
population: Latino
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: BaseQRankSum

19-58146106-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58146106
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 58146106
    reference: chr 19
allele count: 8
allele frequency: 6.838425110697007e-5
allele num: 116986
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000254182
  ensembl transcript: ENST00000254182
  gene symbol: ZNF211
  hgvsc: ENST00000254182.7:c.17C>T
  hgvsp: ENSP00000254182.7:p.Ala6Val
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000441386
  ensembl transcript: ENST00000544273
  gene symbol: ZNF211
  hgvsc: ENST00000544273.1:c.236C>T
  hgvsp: ENSP00000441386.1:p.Ala79Val
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000399193
  ensembl transcript: ENST00000420680
  gene symbol: ZNF211
  hgvsc: ENST00000420680.1:c.212C>T
  hgvsp: ENSP00000399193.1:p.Ala71Val
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000375584
  ensembl transcript: ENST00000391703
  gene symbol: ZNF211
  hgvsc: ENST00000391703.3:c.17C>T
  hgvsp: ENSP00000375584.3:p.Ala6Val
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000440793
  ensembl transcript: ENST00000540556
  gene symbol: ZNF211
  hgvsc: ENST00000540556.1:c.*242C>T
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000240731
  ensembl transcript: ENST00000240731
  gene symbol: ZNF211
  hgvsc: ENST00000240731.4:c.239C>T
  hgvsp: ENSP00000240731.4:p.Ala80Val
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000339562
  ensembl transcript: ENST00000347302
  gene symbol: ZNF211
  hgvsc: ENST00000347302.3:c.200C>T
  hgvsp: ENSP00000339562.3:p.Ala67Val
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000299871
  ensembl transcript: ENST00000299871
  gene symbol: ZNF211
  hgvsc: ENST00000299871.5:c.239C>T
  hgvsp: ENSP00000299871.5:p.Ala80Val
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000384436
  ensembl transcript: ENST00000407202
  gene symbol: ZNF211
  hgvsc: ENST00000407202.2:c.210C>T
  hgvsp: ENSP00000384436.2:p.Ala71Val
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000442601
  ensembl transcript: ENST00000541801
  gene symbol: ZNF211
  hgvsc: ENST00000541801.1:c.17C>T
  hgvsp: ENSP00000442601.1:p.Ala6Val
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000442740
  ensembl transcript: ENST00000535785
  gene symbol: ZNF211
  hgvsc: ENST00000535785.1:c.*294C>T
  variant of: http://identifiers.org/hgnc/13003
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2778
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4507
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5565
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1976
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 936
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3996
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1995
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6931
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6611
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1853
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2939
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 830
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4591
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 5204
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6358
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1375
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala80Val
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff

19-58146110-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58146110
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 58146110
    reference: chr 19
allele count: 1
allele frequency: 8.564283512041383e-6
allele num: 116764
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000441386
  ensembl transcript: ENST00000544273
  gene symbol: ZNF211
  hgvsc: ENST00000544273.1:c.240T>C
  hgvsp: ENST00000544273.1:c.240T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000339562
  ensembl transcript: ENST00000347302
  gene symbol: ZNF211
  hgvsc: ENST00000347302.3:c.204T>C
  hgvsp: ENST00000347302.3:c.204T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000299871
  ensembl transcript: ENST00000299871
  gene symbol: ZNF211
  hgvsc: ENST00000299871.5:c.243T>C
  hgvsp: ENST00000299871.5:c.243T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000384436
  ensembl transcript: ENST00000407202
  gene symbol: ZNF211
  hgvsc: ENST00000407202.2:c.214T>C
  hgvsp: ENST00000407202.2:c.214T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000440793
  ensembl transcript: ENST00000540556
  gene symbol: ZNF211
  hgvsc: ENST00000540556.1:c.*246T>C
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000399193
  ensembl transcript: ENST00000420680
  gene symbol: ZNF211
  hgvsc: ENST00000420680.1:c.216T>C
  hgvsp: ENST00000420680.1:c.216T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000442740
  ensembl transcript: ENST00000535785
  gene symbol: ZNF211
  hgvsc: ENST00000535785.1:c.*298T>C
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000442601
  ensembl transcript: ENST00000541801
  gene symbol: ZNF211
  hgvsc: ENST00000541801.1:c.21T>C
  hgvsp: ENST00000541801.1:c.21T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000240731
  ensembl transcript: ENST00000240731
  gene symbol: ZNF211
  hgvsc: ENST00000240731.4:c.243T>C
  hgvsp: ENST00000240731.4:c.243T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000375584
  ensembl transcript: ENST00000391703
  gene symbol: ZNF211
  hgvsc: ENST00000391703.3:c.21T>C
  hgvsp: ENST00000391703.3:c.21T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000254182
  ensembl transcript: ENST00000254182
  gene symbol: ZNF211
  hgvsc: ENST00000254182.7:c.21T>C
  hgvsp: ENST00000254182.7:c.21T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13003
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 808
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 830
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1916
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2938
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4501
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6931
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1995
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 997
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5566
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2095
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6358
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3997
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4587
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6611
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1377
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 608
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2728
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu81Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
population: Other
reference allele: T
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD

19-58146110-T-TA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58146110
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 58146111
    reference: chr 19
allele count: 2
allele frequency: 1.712856702408277e-5
allele num: 116764
alternate allele: TA
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000442601
  ensembl transcript: ENST00000541801
  gene symbol: ZNF211
  hgvsc: ENST00000541801.1:c.22dupA
  hgvsp: ENSP00000442601.1:p.Thr8AsnfsTer47
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000240731
  ensembl transcript: ENST00000240731
  gene symbol: ZNF211
  hgvsc: ENST00000240731.4:c.244dupA
  hgvsp: ENSP00000240731.4:p.Thr82AsnfsTer13
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000384436
  ensembl transcript: ENST00000407202
  gene symbol: ZNF211
  hgvsc: ENST00000407202.2:c.215dupA
  hgvsp: ENSP00000384436.2:p.Thr73AsnfsTer13
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000375584
  ensembl transcript: ENST00000391703
  gene symbol: ZNF211
  hgvsc: ENST00000391703.3:c.22dupA
  hgvsp: ENSP00000375584.3:p.Thr8AsnfsTer13
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000440793
  ensembl transcript: ENST00000540556
  gene symbol: ZNF211
  hgvsc: ENST00000540556.1:c.*247dupA
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000339562
  ensembl transcript: ENST00000347302
  gene symbol: ZNF211
  hgvsc: ENST00000347302.3:c.205dupA
  hgvsp: ENSP00000339562.3:p.Thr69AsnfsTer13
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000441386
  ensembl transcript: ENST00000544273
  gene symbol: ZNF211
  hgvsc: ENST00000544273.1:c.241dupA
  hgvsp: ENSP00000441386.1:p.Thr81AsnfsTer13
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000299871
  ensembl transcript: ENST00000299871
  gene symbol: ZNF211
  hgvsc: ENST00000299871.5:c.244dupA
  hgvsp: ENSP00000299871.5:p.Thr82AsnfsTer47
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000254182
  ensembl transcript: ENST00000254182
  gene symbol: ZNF211
  hgvsc: ENST00000254182.7:c.22dupA
  hgvsp: ENSP00000254182.7:p.Thr8AsnfsTer47
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000399193
  ensembl transcript: ENST00000420680
  gene symbol: ZNF211
  hgvsc: ENST00000420680.1:c.217dupA
  hgvsp: ENSP00000399193.1:p.Thr73AsnfsTer13
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000442740
  ensembl transcript: ENST00000535785
  gene symbol: ZNF211
  hgvsc: ENST00000535785.1:c.*299dupA
  variant of: http://identifiers.org/hgnc/13003
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 997
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 608
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4501
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 808
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1995
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2728
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1916
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6358
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2095
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3997
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 830
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5203
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2938
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4587
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1377
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6611
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5566
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr82AsnfsTer47
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
population: Other
reference allele: T
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD

http://identifiers.org/exac.variant/19-58146111-AC-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58146111
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 58146110
    reference: chr 19
allele count: 1
allele frequency: 8.57030218885518e-6
allele num: 116682
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000442601
  ensembl transcript: ENST00000541801
  gene symbol: ZNF211
  hgvsc: ENST00000541801.1:c.23delC
  hgvsp: ENSP00000442601.1:p.Thr8SerfsTer13
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000339562
  ensembl transcript: ENST00000347302
  gene symbol: ZNF211
  hgvsc: ENST00000347302.3:c.206delC
  hgvsp: ENSP00000339562.3:p.Thr69SerfsTer51
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000254182
  ensembl transcript: ENST00000254182
  gene symbol: ZNF211
  hgvsc: ENST00000254182.7:c.23delC
  hgvsp: ENSP00000254182.7:p.Thr8SerfsTer13
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000384436
  ensembl transcript: ENST00000407202
  gene symbol: ZNF211
  hgvsc: ENST00000407202.2:c.216delC
  hgvsp: ENSP00000384436.2:p.Thr73SerfsTer51
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000299871
  ensembl transcript: ENST00000299871
  gene symbol: ZNF211
  hgvsc: ENST00000299871.5:c.245delC
  hgvsp: ENSP00000299871.5:p.Thr82SerfsTer13
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000440793
  ensembl transcript: ENST00000540556
  gene symbol: ZNF211
  hgvsc: ENST00000540556.1:c.*248delC
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000240731
  ensembl transcript: ENST00000240731
  gene symbol: ZNF211
  hgvsc: ENST00000240731.4:c.245delC
  hgvsp: ENSP00000240731.4:p.Thr82SerfsTer51
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000375584
  ensembl transcript: ENST00000391703
  gene symbol: ZNF211
  hgvsc: ENST00000391703.3:c.23delC
  hgvsp: ENSP00000375584.3:p.Thr8SerfsTer51
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000441386
  ensembl transcript: ENST00000544273
  gene symbol: ZNF211
  hgvsc: ENST00000544273.1:c.242delC
  hgvsp: ENSP00000441386.1:p.Thr81SerfsTer51
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000442740
  ensembl transcript: ENST00000535785
  gene symbol: ZNF211
  hgvsc: ENST00000535785.1:c.*300delC
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000399193
  ensembl transcript: ENST00000420680
  gene symbol: ZNF211
  hgvsc: ENST00000420680.1:c.218delC
  hgvsp: ENSP00000399193.1:p.Thr73SerfsTer51
  variant of: http://identifiers.org/hgnc/13003
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 997
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6358
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5566
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4498
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2713
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2938
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 782
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3998
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1928
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5203
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1377
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4587
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 830
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6931
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6611
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2123
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr82SerfsTer13
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Other
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: AC
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum

19-58146112-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58146112
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 58146112
    reference: chr 19
allele count: 111
allele frequency: 9.532642860823414e-4
allele num: 116442
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000254182
  ensembl transcript: ENST00000254182
  gene symbol: ZNF211
  hgvsc: ENST00000254182.7:c.23C>T
  hgvsp: ENSP00000254182.7:p.Thr8Met
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000399193
  ensembl transcript: ENST00000420680
  gene symbol: ZNF211
  hgvsc: ENST00000420680.1:c.218C>T
  hgvsp: ENSP00000399193.1:p.Thr73Met
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000299871
  ensembl transcript: ENST00000299871
  gene symbol: ZNF211
  hgvsc: ENST00000299871.5:c.245C>T
  hgvsp: ENSP00000299871.5:p.Thr82Met
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000441386
  ensembl transcript: ENST00000544273
  gene symbol: ZNF211
  hgvsc: ENST00000544273.1:c.242C>T
  hgvsp: ENSP00000441386.1:p.Thr81Met
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000375584
  ensembl transcript: ENST00000391703
  gene symbol: ZNF211
  hgvsc: ENST00000391703.3:c.23C>T
  hgvsp: ENSP00000375584.3:p.Thr8Met
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000442740
  ensembl transcript: ENST00000535785
  gene symbol: ZNF211
  hgvsc: ENST00000535785.1:c.*300C>T
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000240731
  ensembl transcript: ENST00000240731
  gene symbol: ZNF211
  hgvsc: ENST00000240731.4:c.245C>T
  hgvsp: ENSP00000240731.4:p.Thr82Met
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000440793
  ensembl transcript: ENST00000540556
  gene symbol: ZNF211
  hgvsc: ENST00000540556.1:c.*248C>T
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000384436
  ensembl transcript: ENST00000407202
  gene symbol: ZNF211
  hgvsc: ENST00000407202.2:c.216C>T
  hgvsp: ENSP00000384436.2:p.Thr73Met
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000339562
  ensembl transcript: ENST00000347302
  gene symbol: ZNF211
  hgvsc: ENST00000347302.3:c.206C>T
  hgvsp: ENSP00000339562.3:p.Thr69Met
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000442601
  ensembl transcript: ENST00000541801
  gene symbol: ZNF211
  hgvsc: ENST00000541801.1:c.23C>T
  hgvsp: ENSP00000442601.1:p.Thr8Met
  variant of: http://identifiers.org/hgnc/13003
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 827
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1991
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 726
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6605
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2687
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1957
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2147
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 9.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 3989
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4635
  bin: 9.75e1
  variant carriers: 79
genotype depth: GenotypeDepth
  all individuals: 5196
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4502
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6922
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 997
  bin: 8.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 6353
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2936
  bin: 6.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1376
  bin: 7.75e1
  variant carriers: 7
genotype quality: GenotypeQuality
hgvs: p.Thr82Met
num of homozygotes: 0
population: South Asian
population: African
population: Other
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: ClippingRankSum

19-58146113-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58146113
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 58146113
    reference: chr 19
allele count: 3
allele frequency: 2.579934985638362e-5
allele num: 116282
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000299871
  ensembl transcript: ENST00000299871
  gene symbol: ZNF211
  hgvsc: ENST00000299871.5:c.246G>A
  hgvsp: ENST00000299871.5:c.246G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000442601
  ensembl transcript: ENST00000541801
  gene symbol: ZNF211
  hgvsc: ENST00000541801.1:c.24G>A
  hgvsp: ENST00000541801.1:c.24G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000441386
  ensembl transcript: ENST00000544273
  gene symbol: ZNF211
  hgvsc: ENST00000544273.1:c.243G>A
  hgvsp: ENST00000544273.1:c.243G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000375584
  ensembl transcript: ENST00000391703
  gene symbol: ZNF211
  hgvsc: ENST00000391703.3:c.24G>A
  hgvsp: ENST00000391703.3:c.24G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000254182
  ensembl transcript: ENST00000254182
  gene symbol: ZNF211
  hgvsc: ENST00000254182.7:c.24G>A
  hgvsp: ENST00000254182.7:c.24G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000440793
  ensembl transcript: ENST00000540556
  gene symbol: ZNF211
  hgvsc: ENST00000540556.1:c.*249G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000240731
  ensembl transcript: ENST00000240731
  gene symbol: ZNF211
  hgvsc: ENST00000240731.4:c.246G>A
  hgvsp: ENST00000240731.4:c.246G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000384436
  ensembl transcript: ENST00000407202
  gene symbol: ZNF211
  hgvsc: ENST00000407202.2:c.217G>A
  hgvsp: ENST00000407202.2:c.217G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000399193
  ensembl transcript: ENST00000420680
  gene symbol: ZNF211
  hgvsc: ENST00000420680.1:c.219G>A
  hgvsp: ENST00000420680.1:c.219G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000442740
  ensembl transcript: ENST00000535785
  gene symbol: ZNF211
  hgvsc: ENST00000535785.1:c.*301G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000339562
  ensembl transcript: ENST00000347302
  gene symbol: ZNF211
  hgvsc: ENST00000347302.3:c.207G>A
  hgvsp: ENST00000347302.3:c.207G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13003
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1994
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2219
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1989
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5577
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 653
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6933
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2662
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 992
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4571
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4506
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 827
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6362
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2934
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1373
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4000
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5207
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr82Thr
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD

19-58146123-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58146123
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 58146123
    reference: chr 19
allele count: 1
allele frequency: 8.666712889135408e-6
allele num: 115384
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000299871
  ensembl transcript: ENST00000299871
  gene symbol: ZNF211
  hgvsc: ENST00000299871.5:c.256G>C
  hgvsp: ENSP00000299871.5:p.Gly86Arg
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000441386
  ensembl transcript: ENST00000544273
  gene symbol: ZNF211
  hgvsc: ENST00000544273.1:c.253G>C
  hgvsp: ENSP00000441386.1:p.Gly85Arg
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000399193
  ensembl transcript: ENST00000420680
  gene symbol: ZNF211
  hgvsc: ENST00000420680.1:c.229G>C
  hgvsp: ENSP00000399193.1:p.Gly77Arg
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000442740
  ensembl transcript: ENST00000535785
  gene symbol: ZNF211
  hgvsc: ENST00000535785.1:c.*311G>C
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000240731
  ensembl transcript: ENST00000240731
  gene symbol: ZNF211
  hgvsc: ENST00000240731.4:c.256G>C
  hgvsp: ENSP00000240731.4:p.Gly86Arg
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000375584
  ensembl transcript: ENST00000391703
  gene symbol: ZNF211
  hgvsc: ENST00000391703.3:c.34G>C
  hgvsp: ENSP00000375584.3:p.Gly12Arg
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000384436
  ensembl transcript: ENST00000407202
  gene symbol: ZNF211
  hgvsc: ENST00000407202.2:c.227G>C
  hgvsp: ENSP00000384436.2:p.Gly77Arg
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000442601
  ensembl transcript: ENST00000541801
  gene symbol: ZNF211
  hgvsc: ENST00000541801.1:c.34G>C
  hgvsp: ENSP00000442601.1:p.Gly12Arg
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000339562
  ensembl transcript: ENST00000347302
  gene symbol: ZNF211
  hgvsc: ENST00000347302.3:c.217G>C
  hgvsp: ENSP00000339562.3:p.Gly73Arg
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000440793
  ensembl transcript: ENST00000540556
  gene symbol: ZNF211
  hgvsc: ENST00000540556.1:c.*259G>C
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000254182
  ensembl transcript: ENST00000254182
  gene symbol: ZNF211
  hgvsc: ENST00000254182.7:c.34G>C
  hgvsp: ENSP00000254182.7:p.Gly12Arg
  variant of: http://identifiers.org/hgnc/13003
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6613
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6363
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2473
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4000
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1994
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2934
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5208
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 993
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6935
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5573
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1962
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4498
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4569
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2601
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly86Arg
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
population: South Asian
population: Latino
reference allele: G
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD

19-58146126-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58146126
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 58146126
    reference: chr 19
allele count: 1
allele frequency: 8.686889745995344e-6
allele num: 115116
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000299871
  ensembl transcript: ENST00000299871
  gene symbol: ZNF211
  hgvsc: ENST00000299871.5:c.256+3A>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000399193
  ensembl transcript: ENST00000420680
  gene symbol: ZNF211
  hgvsc: ENST00000420680.1:c.229+3A>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000442601
  ensembl transcript: ENST00000541801
  gene symbol: ZNF211
  hgvsc: ENST00000541801.1:c.34+3A>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000384436
  ensembl transcript: ENST00000407202
  gene symbol: ZNF211
  hgvsc: ENST00000407202.2:c.227+3A>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000440793
  ensembl transcript: ENST00000540556
  gene symbol: ZNF211
  hgvsc: ENST00000540556.1:c.*259+3A>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000442740
  ensembl transcript: ENST00000535785
  gene symbol: ZNF211
  hgvsc: ENST00000535785.1:c.*311+3A>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000441386
  ensembl transcript: ENST00000544273
  gene symbol: ZNF211
  hgvsc: ENST00000544273.1:c.253+3A>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000339562
  ensembl transcript: ENST00000347302
  gene symbol: ZNF211
  hgvsc: ENST00000347302.3:c.217+3A>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000375584
  ensembl transcript: ENST00000391703
  gene symbol: ZNF211
  hgvsc: ENST00000391703.3:c.34+3A>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000254182
  ensembl transcript: ENST00000254182
  gene symbol: ZNF211
  hgvsc: ENST00000254182.7:c.34+3A>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000240731
  ensembl transcript: ENST00000240731
  gene symbol: ZNF211
  hgvsc: ENST00000240731.4:c.256+3A>G
  variant of: http://identifiers.org/hgnc/13003
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2529
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6611
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4000
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 993
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1900
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2934
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6935
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 826
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4498
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5573
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4569
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2585
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5208
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1372
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.256+3A>G
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: Other
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum

19-58146150-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58146150
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 58146150
    reference: chr 19
allele count: 2
allele frequency: 1.773081082997925e-5
allele num: 112798
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000442740
  ensembl transcript: ENST00000535785
  gene symbol: ZNF211
  hgvsc: ENST00000535785.1:c.*311+27C>T
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000384436
  ensembl transcript: ENST00000407202
  gene symbol: ZNF211
  hgvsc: ENST00000407202.2:c.227+27C>T
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000339562
  ensembl transcript: ENST00000347302
  gene symbol: ZNF211
  hgvsc: ENST00000347302.3:c.217+27C>T
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000375584
  ensembl transcript: ENST00000391703
  gene symbol: ZNF211
  hgvsc: ENST00000391703.3:c.34+27C>T
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000440793
  ensembl transcript: ENST00000540556
  gene symbol: ZNF211
  hgvsc: ENST00000540556.1:c.*259+27C>T
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000399193
  ensembl transcript: ENST00000420680
  gene symbol: ZNF211
  hgvsc: ENST00000420680.1:c.229+27C>T
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000240731
  ensembl transcript: ENST00000240731
  gene symbol: ZNF211
  hgvsc: ENST00000240731.4:c.256+27C>T
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000442601
  ensembl transcript: ENST00000541801
  gene symbol: ZNF211
  hgvsc: ENST00000541801.1:c.34+27C>T
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000441386
  ensembl transcript: ENST00000544273
  gene symbol: ZNF211
  hgvsc: ENST00000544273.1:c.253+27C>T
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000254182
  ensembl transcript: ENST00000254182
  gene symbol: ZNF211
  hgvsc: ENST00000254182.7:c.34+27C>T
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000299871
  ensembl transcript: ENST00000299871
  gene symbol: ZNF211
  hgvsc: ENST00000299871.5:c.256+27C>T
  variant of: http://identifiers.org/hgnc/13003
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1372
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4568
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5560
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1547
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6363
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6930
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2934
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5208
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1993
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2528
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1147
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6597
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4454
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2631
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 993
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 826
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4001
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
population: East Asian
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum

19-58146161-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58146161
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 58146161
    reference: chr 19
allele count: 1
allele frequency: 8.932718762282489e-6
allele num: 111948
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000399193
  ensembl transcript: ENST00000420680
  gene symbol: ZNF211
  hgvsc: ENST00000420680.1:c.229+38G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000441386
  ensembl transcript: ENST00000544273
  gene symbol: ZNF211
  hgvsc: ENST00000544273.1:c.253+38G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000442601
  ensembl transcript: ENST00000541801
  gene symbol: ZNF211
  hgvsc: ENST00000541801.1:c.34+38G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000339562
  ensembl transcript: ENST00000347302
  gene symbol: ZNF211
  hgvsc: ENST00000347302.3:c.217+38G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000442740
  ensembl transcript: ENST00000535785
  gene symbol: ZNF211
  hgvsc: ENST00000535785.1:c.*311+38G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000384436
  ensembl transcript: ENST00000407202
  gene symbol: ZNF211
  hgvsc: ENST00000407202.2:c.227+38G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000254182
  ensembl transcript: ENST00000254182
  gene symbol: ZNF211
  hgvsc: ENST00000254182.7:c.34+38G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000299871
  ensembl transcript: ENST00000299871
  gene symbol: ZNF211
  hgvsc: ENST00000299871.5:c.256+38G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000440793
  ensembl transcript: ENST00000540556
  gene symbol: ZNF211
  hgvsc: ENST00000540556.1:c.*259+38G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000240731
  ensembl transcript: ENST00000240731
  gene symbol: ZNF211
  hgvsc: ENST00000240731.4:c.256+38G>A
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000375584
  ensembl transcript: ENST00000391703
  gene symbol: ZNF211
  hgvsc: ENST00000391703.3:c.34+38G>A
  variant of: http://identifiers.org/hgnc/13003
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5207
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1372
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4002
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4568
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6568
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 793
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6924
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 993
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4303
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1846
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6363
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1993
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2756
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2418
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 826
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2933
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5500
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 494
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: FS

19-58146163-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58146163
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 58146163
    reference: chr 19
allele count: 1
allele frequency: 8.947424931104829e-6
allele num: 111764
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000240731
  ensembl transcript: ENST00000240731
  gene symbol: ZNF211
  hgvsc: ENST00000240731.4:c.256+40T>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000440793
  ensembl transcript: ENST00000540556
  gene symbol: ZNF211
  hgvsc: ENST00000540556.1:c.*259+40T>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000254182
  ensembl transcript: ENST00000254182
  gene symbol: ZNF211
  hgvsc: ENST00000254182.7:c.34+40T>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000441386
  ensembl transcript: ENST00000544273
  gene symbol: ZNF211
  hgvsc: ENST00000544273.1:c.253+40T>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000299871
  ensembl transcript: ENST00000299871
  gene symbol: ZNF211
  hgvsc: ENST00000299871.5:c.256+40T>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000384436
  ensembl transcript: ENST00000407202
  gene symbol: ZNF211
  hgvsc: ENST00000407202.2:c.227+40T>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000442601
  ensembl transcript: ENST00000541801
  gene symbol: ZNF211
  hgvsc: ENST00000541801.1:c.34+40T>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000399193
  ensembl transcript: ENST00000420680
  gene symbol: ZNF211
  hgvsc: ENST00000420680.1:c.229+40T>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000375584
  ensembl transcript: ENST00000391703
  gene symbol: ZNF211
  hgvsc: ENST00000391703.3:c.34+40T>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000339562
  ensembl transcript: ENST00000347302
  gene symbol: ZNF211
  hgvsc: ENST00000347302.3:c.217+40T>G
  variant of: http://identifiers.org/hgnc/13003
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000121417
  ensembl protein: ENSP00000442740
  ensembl transcript: ENST00000535785
  gene symbol: ZNF211
  hgvsc: ENST00000535785.1:c.*311+40T>G
  variant of: http://identifiers.org/hgnc/13003
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6566
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 993
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6920
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5207
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 699
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2933
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1871
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5468
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1372
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
reference allele: T

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

GenotypeDepth
all individuals: 28
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1611
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 13
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 56
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 45
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 862
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 214
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2290
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 249
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 168
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 862
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 107
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3407
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 927
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 688
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 634
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37526
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1331
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 6858
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2788
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1607
bin: 2.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11536
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10370
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.161170459823502e-4
allele num: 8612
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15730
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.023157385573493e-5
allele num: 66156
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 6.19e-1

MQ
type: SiteQuality
SIO_000300: 5.922e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.5e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.57e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.9e-1

QD
type: SiteQuality
SIO_000300: 1.374e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -2.746e0

DP
type: SiteQuality
SIO_000300: 1.455392e6

GenotypeDepth
all individuals: 36298
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 29
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1125
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 57
bin: 6.25e1
variant carriers: 1

GenotypeDepth
all individuals: 45
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 93
bin: 5.25e1
variant carriers: 2

GenotypeQuality
all individuals: 70
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1346
bin: 9.75e1
variant carriers: 7

GenotypeQuality
all individuals: 3428
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 724
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 258
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2308
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2802
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6857
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 226
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 652
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 963
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 78
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1565
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 867
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 151
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 868
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37402
bin: 6.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15706
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11538
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10372
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 9.069197980591917e-5
allele num: 66158
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -5.51e-1

QD
type: SiteQuality
SIO_000300: 1.348e1

FS
type: SiteQuality
SIO_000300: 7.171e0

MQ
type: SiteQuality
SIO_000300: 5.954e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 4.21e-1

DP
type: SiteQuality
SIO_000300: 1.454931e6

VQSLOD
type: SiteQuality
SIO_000300: 6.56e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.49e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.312e0

GenotypeDepth
all individuals: 100
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 28
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 16
bin: 9.25e1
variant carriers: 1

GenotypeDepth
all individuals: 78
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 58
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 45
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36971
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 727
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 102
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 886
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 316
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 112
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 669
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 145
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 102
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2831
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 278
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1497
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6845
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 985
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3482
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 893
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2356
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1407
bin: 9.75e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.511304558094547e-5
allele num: 66168
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11544
num of homozygotes: 0

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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 896
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15550
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 8.080000000000001e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 2.745e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.44e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.25e0

QD
type: SiteQuality
SIO_000300: 1.594e1

DP
type: SiteQuality
SIO_000300: 1.456459e6

VQSLOD
type: SiteQuality
SIO_000300: 4.44e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -3.07e-1

GenotypeDepth
all individuals: 17
bin: 9.25e1
variant carriers: 1

GenotypeDepth
all individuals: 13
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 36
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 537
bin: 4.25e1
variant carriers: 1

GenotypeDepth
all individuals: 11845
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 45
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 330
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6871
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 129
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 116
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1474
bin: 9.75e1
variant carriers: 9

GenotypeQuality
all individuals: 40
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 36807
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1437
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 71
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 321
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 674
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 105
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 909
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 722
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 971
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 909
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2385
bin: 8.25e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66206
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15506
num of homozygotes: 0

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

East Asian
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Other
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South Asian
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Latino
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African
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European (Non-Finnish)
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InbreedingCoeff
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QD
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ReadPosRankSum
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MQ
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MQRankSum
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DP
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ClippingRankSum
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BaseQRankSum
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VQSLOD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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African
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allele frequency: 0.0e0
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European (Finnish)
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Other
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South Asian
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European (Non-Finnish)
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Latino
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MQRankSum
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ClippingRankSum
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InbreedingCoeff
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VQSLOD
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DP
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FS
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QD
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BaseQRankSum
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ReadPosRankSum
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MQ
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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Latino
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European (Non-Finnish)
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East Asian
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European (Finnish)
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Other
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African
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VQSLOD
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QD
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BaseQRankSum
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ClippingRankSum
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FS
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InbreedingCoeff
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ReadPosRankSum
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MQ
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MQRankSum
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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South Asian
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Latino
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European (Non-Finnish)
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East Asian
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European (Finnish)
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DP
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MQRankSum
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ReadPosRankSum
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VQSLOD
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FS
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QD
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InbreedingCoeff
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MQ
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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Latino
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South Asian
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FS
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MQ
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QD
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African
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European (Finnish)
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South Asian
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East Asian
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European (Non-Finnish)
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FS
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DP
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QD
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VQSLOD
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MQ
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ClippingRankSum
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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African
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South Asian
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Other
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European (Finnish)
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Latino
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European (Non-Finnish)
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allele frequency: 2.326799802761341e-3
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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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ClippingRankSum
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ReadPosRankSum
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DP
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FS
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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num of homozygotes: 0

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

European (Non-Finnish)
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allele frequency: 0.0e0
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South Asian
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African
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allele frequency: 4.854368932038835e-4
allele num: 10300
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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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MQRankSum
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FS
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DP
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QD
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VQSLOD
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ReadPosRankSum
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ClippingRankSum
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InbreedingCoeff
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BaseQRankSum
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MQ
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

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

African
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allele frequency: 3.884249368809478e-4
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Other
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VQSLOD
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ClippingRankSum
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ReadPosRankSum
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BaseQRankSum
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MQRankSum
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QD
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FS
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DP
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InbreedingCoeff
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MQ
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
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num of homozygotes: 0

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

Latino
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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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South Asian
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African
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Other
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DP
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FS
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InbreedingCoeff
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MQ
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QD
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VQSLOD
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ClippingRankSum
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BaseQRankSum
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MQRankSum
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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num of homozygotes: 0

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

South Asian
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African
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allele frequency: 0.0e0
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Latino
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East Asian
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allele frequency: 1.166588894073728e-4
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European (Finnish)
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European (Non-Finnish)
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allele frequency: 0.0e0
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ReadPosRankSum
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DP
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VQSLOD
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FS
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InbreedingCoeff
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MQ
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MQRankSum
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ClippingRankSum
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BaseQRankSum
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 1.511944360447536e-4
allele num: 6614
num of homozygotes: 0

Latino
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African
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East Asian
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European (Non-Finnish)
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Other
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South Asian
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VQSLOD
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MQ
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BaseQRankSum
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DP
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QD
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FS
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MQRankSum
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InbreedingCoeff
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ClippingRankSum
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele num: 64344
num of homozygotes: 0

Other
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East Asian
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African
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European (Finnish)
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Latino
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South Asian
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InbreedingCoeff
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MQRankSum
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FS
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QD
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BaseQRankSum
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DP
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ClippingRankSum
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VQSLOD
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MQ
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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East Asian
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South Asian
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Latino
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European (Non-Finnish)
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European (Finnish)
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Other
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MQRankSum
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QD
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ClippingRankSum
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BaseQRankSum
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InbreedingCoeff
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ReadPosRankSum
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MQ
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FS
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DP
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VQSLOD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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European (Finnish)
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European (Non-Finnish)
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Latino
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Other
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South Asian
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African
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ClippingRankSum
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BaseQRankSum
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MQRankSum
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QD
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VQSLOD
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ReadPosRankSum
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DP
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MQ
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FS
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InbreedingCoeff
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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East Asian
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European (Finnish)
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African
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South Asian
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European (Non-Finnish)
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Other
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FS
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MQ
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DP
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MQRankSum
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InbreedingCoeff
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ReadPosRankSum
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QD
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BaseQRankSum
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ClippingRankSum
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VQSLOD
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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South Asian
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East Asian
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African
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European (Finnish)
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Latino
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ClippingRankSum
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InbreedingCoeff
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SIO_000300: -9.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -1.21e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.49e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.62e0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.403e1

MQ
type: SiteQuality
SIO_000300: 5.971e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.178e0

DP
type: SiteQuality
SIO_000300: 2.157778e6

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 3

GenotypeQuality
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variant carriers: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 9128
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 64016
num of homozygotes: 0

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

East Asian
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allele frequency: 3.517823639774859e-4
allele num: 8528
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 2.140911e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
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ReadPosRankSum
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QD
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VQSLOD
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SIO_000300: 7.93e-1

FS
type: SiteQuality
SIO_000300: 2.643e0

MQRankSum
type: SiteQuality
SIO_000300: -3.4e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.947e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.18e-1

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 17

East Asian
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allele frequency: 0.0e0
allele num: 8526
num of homozygotes: 0

Other
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allele frequency: 0.0e0
allele num: 796
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

African
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allele frequency: 9.786651008025054e-5
allele num: 10218
num of homozygotes: 0

European (Non-Finnish)
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allele count: 16
allele frequency: 2.499687539057618e-4
allele num: 64008
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 11466
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
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SIO_000300: -2.1e-3

QD
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SIO_000300: 1.599e1

ReadPosRankSum
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SIO_000300: 4.91e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
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SIO_000300: -4.23e-1

VQSLOD
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DP
type: SiteQuality
SIO_000300: 2.134146e6

BaseQRankSum
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SIO_000300: 3.63e0

MQRankSum
type: SiteQuality
SIO_000300: 6.900000000000001e-2

GenotypeDepth
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variant carriers: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10208
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.563330519338399e-5
allele num: 63966
num of homozygotes: 0

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

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

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 5.55e-1

QD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
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InbreedingCoeff
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SIO_000300: -1.3e-3

FS
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DP
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BaseQRankSum
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SIO_000300: -2.855e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.31e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.7e-2

GenotypeDepth
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variant carriers: 0

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

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

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10212
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 63966
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 9094
num of homozygotes: 0

Latino
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allele frequency: 8.732099196646873e-5
allele num: 11452
num of homozygotes: 0

Other
type: Population
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allele frequency: 0.0e0
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QD
type: SiteQuality
SIO_000300: 1.4e1

ClippingRankSum
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BaseQRankSum
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ReadPosRankSum
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FS
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DP
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MQRankSum
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InbreedingCoeff
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SIO_000300: -1.0e-3

MQ
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VQSLOD
type: SiteQuality
SIO_000300: -9.523e-1

GenotypeDepth
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variant carriers: 0

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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 792
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.69175190015952e-5
allele num: 63942
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8512
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10216
num of homozygotes: 0

Latino
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allele frequency: 8.730574471800244e-5
allele num: 11454
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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FS
type: SiteQuality
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DP
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MQ
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ReadPosRankSum
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InbreedingCoeff
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VQSLOD
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ClippingRankSum
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MQRankSum
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BaseQRankSum
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QD
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9048
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
type: Population
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East Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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African
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ClippingRankSum
type: SiteQuality
SIO_000300: 1.99e0

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 4693
bin: 7.75e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.699395344465679e-5
allele num: 63838
num of homozygotes: 0

African
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South Asian
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East Asian
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MQRankSum
type: SiteQuality
SIO_000300: -5.45e-1

VQSLOD
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InbreedingCoeff
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FS
type: SiteQuality
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MQ
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BaseQRankSum
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ClippingRankSum
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DP
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QD
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ReadPosRankSum
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 374
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 950
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2178
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2684
bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 134
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1215
bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.552072016141549e-5
allele num: 64430
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10182
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 822
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10258
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 3.269478e6

BaseQRankSum
type: SiteQuality
SIO_000300: -3.979e0

QD
type: SiteQuality
SIO_000300: 1.197e1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.27e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.1e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.16e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 4.47e0

MQ
type: SiteQuality
SIO_000300: 5.958e1

MQRankSum
type: SiteQuality
SIO_000300: 4.27e-1

GenotypeQuality
all individuals: 968
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 40353
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 145
bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 950
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2684
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2033
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1480
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1742
bin: 2.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10258
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10182
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.552072016141549e-5
allele num: 64430
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 822
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.958e1

VQSLOD
type: SiteQuality
SIO_000300: 4.47e0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.27e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.1e-3

QD
type: SiteQuality
SIO_000300: 1.197e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 4.27e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.979e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.16e-1

DP
type: SiteQuality
SIO_000300: 3.269478e6

GenotypeQuality
all individuals: 2035
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2715
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 393
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1480
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2408
bin: 2.25e1
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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GenotypeQuality
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 2

GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 329
bin: 3.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 2
allele frequency: 1.947798987144527e-4
allele num: 10268
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 822
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10260
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64466
num of homozygotes: 0

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

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

MQRankSum
type: SiteQuality
SIO_000300: -1.3e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.649999999999999e-1

FS
type: SiteQuality
SIO_000300: 1.51e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.24e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.9e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.2e0

DP
type: SiteQuality
SIO_000300: 3.271429e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.6e-3

QD
type: SiteQuality
SIO_000300: 1.401e1

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

GenotypeQuality
all individuals: 393
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2532
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 133
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 914
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 450
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1480
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2620
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40351
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 2174
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2722
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 392
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 328
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2035
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1217
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2826
bin: 9.25e1
variant carriers: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10292
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10260
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.739432944859976e-4
allele num: 11498
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 822
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64472
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.981e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.775e0

DP
type: SiteQuality
SIO_000300: 3.272155e6

MQRankSum
type: SiteQuality
SIO_000300: 8.54e-1

FS
type: SiteQuality
SIO_000300: 1.498e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.59e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.06e-1

QD
type: SiteQuality
SIO_000300: 1.128e1

VQSLOD
type: SiteQuality
SIO_000300: 2.03e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.2e-3

GenotypeQuality
all individuals: 77
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 425
bin: 1.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 40350
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2826
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10266
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 822
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.551060925673161e-5
allele num: 64472
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10276
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 3.272477e6

MQRankSum
type: SiteQuality
SIO_000300: -6.0e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.2e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -5.39e-1

QD
type: SiteQuality
SIO_000300: 1.182e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.6e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.11e0

VQSLOD
type: SiteQuality
SIO_000300: 1.23e0

GenotypeQuality
all individuals: 28
bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 2.25e1
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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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1480
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 5.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.548371113588505e-5
allele num: 64584
num of homozygotes: 0

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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 830
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10276
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10676
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.31e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.1e-3

MQRankSum
type: SiteQuality
SIO_000300: -1.57e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 9.320000000000001e-1

QD
type: SiteQuality
SIO_000300: 1.105e1

DP
type: SiteQuality
SIO_000300: 3.278249e6

FS
type: SiteQuality
SIO_000300: 3.663e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.18e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.52e-1

GenotypeQuality
all individuals: 22
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 411
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40349
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 380
bin: 3.25e1
variant carriers: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.164686699277894e-4
allele num: 8586
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10284
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10872
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 830
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64624
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.5e-2

VQSLOD
type: SiteQuality
SIO_000300: 9.360000000000001e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.33e-1

BaseQRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 3.280765e6

MQRankSum
type: SiteQuality
SIO_000300: -3.5e-2

FS
type: SiteQuality
SIO_000300: 1.904e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.2e-3

QD
type: SiteQuality
SIO_000300: 1.017e1

GenotypeDepth
all individuals: 3998
bin: 6.25e1
variant carriers: 0

GenotypeDepth
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 29
bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2042
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2178
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 179
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2828
bin: 9.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8592
num of homozygotes: 0

Other
type: Population
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allele frequency: 0.0e0
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European (Non-Finnish)
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European (Finnish)
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South Asian
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African
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DP
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ReadPosRankSum
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MQ
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MQRankSum
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InbreedingCoeff
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BaseQRankSum
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QD
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VQSLOD
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FS
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ClippingRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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European (Non-Finnish)
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Latino
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European (Finnish)
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African
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Other
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FS
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MQ
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MQRankSum
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DP
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ReadPosRankSum
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QD
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ClippingRankSum
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BaseQRankSum
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InbreedingCoeff
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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South Asian
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African
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Other
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European (Finnish)
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European (Non-Finnish)
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Latino
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ReadPosRankSum
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QD
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MQRankSum
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MQ
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ClippingRankSum
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FS
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DP
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InbreedingCoeff
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VQSLOD
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BaseQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele frequency: 1.540499738115044e-5
allele num: 64914
num of homozygotes: 0

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

European (Non-Finnish)
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East Asian
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Other
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African
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Latino
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South Asian
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MQRankSum
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VQSLOD
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BaseQRankSum
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ReadPosRankSum
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InbreedingCoeff
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ClippingRankSum
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FS
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MQ
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QD
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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Other
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South Asian
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African
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European (Finnish)
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Latino
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European (Non-Finnish)
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FS
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ClippingRankSum
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DP
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MQRankSum
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MQ
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BaseQRankSum
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QD
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InbreedingCoeff
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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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South Asian
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European (Finnish)
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Other
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African
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Latino
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European (Non-Finnish)
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East Asian
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VQSLOD
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ReadPosRankSum
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ClippingRankSum
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DP
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MQ
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FS
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QD
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MQRankSum
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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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African
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South Asian
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Latino
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European (Non-Finnish)
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East Asian
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European (Finnish)
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MQRankSum
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QD
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VQSLOD
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SIO_000300: 5.05e-1

ClippingRankSum
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SIO_000300: -1.7e0

MQ
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SIO_000300: 5.886e1

DP
type: SiteQuality
SIO_000300: 3.335905e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.31e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 5.23e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.043e0

GenotypeDepth
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variant carriers: 0

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.512584704743466e-5
allele num: 66112
num of homozygotes: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10384
num of homozygotes: 0

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

East Asian
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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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QD
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BaseQRankSum
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MQRankSum
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SIO_000300: 6.3e-1

ClippingRankSum
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VQSLOD
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DP
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InbreedingCoeff
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MQ
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SIO_000300: 5.88e1

FS
type: SiteQuality
SIO_000300: 1.497e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.35e-1

GenotypeDepth
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variant carriers: 0

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

African
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allele count: 1
allele frequency: 9.624639076034648e-5
allele num: 10390
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
allele num: 15326
num of homozygotes: 0

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

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

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

InbreedingCoeff
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QD
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ClippingRankSum
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ReadPosRankSum
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MQ
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SIO_000300: 5.992e1

FS
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BaseQRankSum
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DP
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SIO_000300: 3.337399e6

VQSLOD
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MQRankSum
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SIO_000300: -6.16e-1

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.515656734062869e-5
allele num: 65978
num of homozygotes: 0

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

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

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

East Asian
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Other
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num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.46e0

MQRankSum
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VQSLOD
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ClippingRankSum
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ReadPosRankSum
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QD
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InbreedingCoeff
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SIO_000300: 0.0e0

DP
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MQ
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SIO_000300: 5.957e1

BaseQRankSum
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SIO_000300: -3.12e-1

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele count: 0
allele frequency: 0.0e0
allele num: 10378
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 876
num of homozygotes: 0

Latino
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allele count: 1
allele frequency: 8.650519031141868e-5
allele num: 11560
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
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allele num: 65982
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European (Finnish)
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VQSLOD
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MQRankSum
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ReadPosRankSum
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InbreedingCoeff
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QD
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ClippingRankSum
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FS
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DP
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MQ
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BaseQRankSum
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GenotypeDepth
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variant carriers: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 13492
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10352
num of homozygotes: 0

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

Other
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East Asian
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allele frequency: 0.0e0
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Latino
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allele frequency: 8.668515950069348e-5
allele num: 11536
num of homozygotes: 0

European (Non-Finnish)
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allele count: 7
allele frequency: 1.068506533154231e-4
allele num: 65512
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FS
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VQSLOD
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ClippingRankSum
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MQRankSum
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BaseQRankSum
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QD
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DP
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MQ
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ReadPosRankSum
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InbreedingCoeff
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65458
num of homozygotes: 0

African
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allele frequency: 9.652509652509652e-5
allele num: 10360
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele num: 65458
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South Asian
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African
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Other
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ClippingRankSum
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VQSLOD
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ReadPosRankSum
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MQ
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MQRankSum
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FS
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BaseQRankSum
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DP
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InbreedingCoeff
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QD
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SIO_000300: 1.45e1

GenotypeDepth
all individuals: 1995
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 105
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 345
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1217
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2533
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3391
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 208
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3266
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 337
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2830
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40339
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2047
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1479
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2178
bin: 7.75e1
variant carriers: 0

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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 848
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13282
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.528350909368791e-5
allele num: 65430
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.569e1

MQRankSum
type: SiteQuality
SIO_000300: 1.0e0

DP
type: SiteQuality
SIO_000300: 3.296091e6

VQSLOD
type: SiteQuality
SIO_000300: 3.11e0

FS
type: SiteQuality
SIO_000300: 7.29e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.06e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.6e-3

MQ
type: SiteQuality
SIO_000300: 6.049e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.602e0

BaseQRankSum
type: SiteQuality
SIO_000300: 6.75e0

GenotypeDepth
all individuals: 5564
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 185
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variant carriers: 0

GenotypeQuality
all individuals: 3181
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2044
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2533
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 347
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 71
bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3375
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1217
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 237
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 4.25e1
variant carriers: 1

GenotypeQuality
all individuals: 40342
bin: 9.75e1
variant carriers: 111

GenotypeQuality
all individuals: 2830
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 339
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2177
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1479
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 4.75e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.634753397465261e-5
allele num: 13098
num of homozygotes: 0

African
type: Population
allele count: 102
allele frequency: 9.851265211512458e-3
allele num: 10354
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.176470588235294e-3
allele num: 850
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 6
allele frequency: 5.203816131830009e-4
allele num: 11530
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.529566520847992e-5
allele num: 65378
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.17e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.5e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.01e0

MQ
type: SiteQuality
SIO_000300: 5.969e1

QD
type: SiteQuality
SIO_000300: 1.4e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.0e0

VQSLOD
type: SiteQuality
SIO_000300: 5.12e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 3.299638e6

ClippingRankSum
type: SiteQuality
SIO_000300: -5.03e-1

GenotypeDepth
all individuals: 6616
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3456
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 32
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 269
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variant carriers: 0

GenotypeQuality
all individuals: 158
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40312
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 2180
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3078
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1485
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 181
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variant carriers: 0

GenotypeQuality
all individuals: 339
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variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2049
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variant carriers: 0

GenotypeQuality
all individuals: 350
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2837
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2536
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1219
bin: 7.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12976
num of homozygotes: 0

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

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

African
type: Population
allele count: 2
allele frequency: 1.931620629708325e-4
allele num: 10354
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.530362389813908e-5
allele num: 65344
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 844
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.974e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.771e0

FS
type: SiteQuality
SIO_000300: 3.114e0

QD
type: SiteQuality
SIO_000300: 1.256e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.91e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.2e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.13e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.2e-3

DP
type: SiteQuality
SIO_000300: 3.290678e6

VQSLOD
type: SiteQuality
SIO_000300: 8.53e-1

GenotypeDepth
all individuals: 826
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 300
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 603
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1372
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 112
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2043
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 484
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 273
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2836
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 168
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
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variant carriers: 0

GenotypeQuality
all individuals: 1216
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40311
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 9
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3592
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 127
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2180
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2531
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 328
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1485
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2885
bin: 6.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 838
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65134
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.688044952528579e-5
allele num: 10322
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12342
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.915e1

MQRankSum
type: SiteQuality
SIO_000300: 8.400000000000001e-2

DP
type: SiteQuality
SIO_000300: 3.283155e6

QD
type: SiteQuality
SIO_000300: 1.129e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.901e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.14e-1

FS
type: SiteQuality
SIO_000300: 8.51e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.4e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.6e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.43e-1

GenotypeDepth
all individuals: 1993
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6363
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 265
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 40310
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 44
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 116
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2833
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
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variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 198
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 587
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3540
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2531
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 123
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1485
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2180
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1215
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 328
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2837
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2043
bin: 6.75e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11520
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 836
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 8.210180623973728e-5
allele num: 12180
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10320
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65040
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.22e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.23e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.1e-3

FS
type: SiteQuality
SIO_000300: 6.291e0

MQRankSum
type: SiteQuality
SIO_000300: 1.0e-2

DP
type: SiteQuality
SIO_000300: 3.280937e6

QD
type: SiteQuality
SIO_000300: 1.025e1

VQSLOD
type: SiteQuality
SIO_000300: -6.69e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -2.749e0

GenotypeQuality
all individuals: 2526
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 2008
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 151
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 7
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variant carriers: 0

GenotypeQuality
all individuals: 137
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 334
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1482
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2832
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2658
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1208
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2167
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
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variant carriers: 0

GenotypeQuality
all individuals: 2507
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1650
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 401
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 40301
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 12
bin: 4.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10268
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64520
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11494
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 806
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8564
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.89897455374098e-4
allele num: 10532
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 4.52e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.3e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -1.025e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 2.96e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.481e1

DP
type: SiteQuality
SIO_000300: 3.265895e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.87e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.44e-1

GenotypeQuality
all individuals: 1477
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2150
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 185
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1950
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 656
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2404
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variant carriers: 0

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

GenotypeQuality
all individuals: 15
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variant carriers: 0

GenotypeQuality
all individuals: 2832
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 178
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1862
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1977
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2516
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1187
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 182
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40295
bin: 9.75e1
variant carriers: 1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8546
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10244
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11480
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9988
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.555790652809758e-5
allele num: 64276
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 3.255394e6

MQRankSum
type: SiteQuality
SIO_000300: -7.31e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.21e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.19e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.8e-3

MQ
type: SiteQuality
SIO_000300: 5.936e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.926e0

VQSLOD
type: SiteQuality
SIO_000300: 6.16e-1

QD
type: SiteQuality
SIO_000300: 1.371e1

FS
type: SiteQuality
SIO_000300: 0.0e0